Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

One material, multiple functions: graphene/Ni(OH)2 thin films applied in batteries, electrochromism and sensors


Different nanocomposites between reduced graphene oxide (rGO) and Ni(OH)2 nanoparticles were synthesized through modifications in the polyol method (starting from graphene oxide (GO) dispersion in ethylene glycol and nickel acetate), processed as thin films through the liquid-liquid interfacial route, homogeneously deposited over transparent electrodes and spectroscopically, microscopically and electrochemically characterized. The thin and transparent nanocomposite films (112 to 513 nm thickness, 62.6 to 19.9% transmittance at 550 nm) consist of α-Ni(OH)2 nanoparticles (mean diameter of 4.9 nm) homogeneously decorating the rGO sheets. As a control sample, neat Ni(OH)2 was prepared in the same way, consisting of porous nanoparticles with diameter ranging from 30 to 80 nm. The nanocomposite thin films present multifunctionality and they were applied as electrodes to alkaline batteries, as electrochromic material and as active component to electrochemical sensor to glycerol. In all the cases the nanocomposite films presented better performances when compared to the neat Ni(OH)2 nanoparticles, showing energy and power of 43.7 W h kg−1 and 4.8 kW kg−1 (8.24 A g−1) respectively, electrochromic efficiency reaching 70 cm2 C−1 and limit of detection as low as 15.4 ± 1.2 μmol L−1.


Nickel hydroxide is a multifunctional material widely used in many areas, such as batteries1,2, electrochromic devices3,4, sensors5,6,7, fuel cells8,9 and catalysis10. All these applications involve redox reactions between Ni(OH)2 and NiOOH, both of them having two stable polymorphs: the α and β phases for Ni(OH)2, the γ and β phases for NiOOH11. The differences between these structures are the space between the layers and their organization, in which the α-Ni(OH)2 and γ-NiOOH have the larger distances and are less organized than the β-Ni(OH)2 and β-NiOOH, as can be seen in the scheme presented in Supplementary Fig. S1 (Electronic Supplementary Material). These structural differences lead to different reactivities, where the α-Ni(OH)2 and γ-NiOOH species present the better electrochemical responses. However, these phases are usually converted to the β phases during successive cycles of redox process and in highly alkaline media, decreasing their performances12,13. The phase interconversion can be avoided through the interaction between Ni(OH)2 and graphene. The preparation of graphene/Ni(OH)2 nanocomposites also increases the conductivity of the final material (comparing with neat Ni(OH)2), as well as minimizes significantly the particle aggregation and growth14,15,16,17.

Among the different methodologies employed to obtain graphene-like materials, the chemical exfoliation of graphite presents low cost and high yield. One method is based on the oxidation of graphite, followed by its exfoliation and reduction, yielding the so-called reduced graphene oxide (rGO)18. The rGO has remaining oxygenated functional groups in its structure, which are very useful for the synthesis of nanocomposites, acting as nucleating sites19,20,21.

One interesting and growing application of graphene/nickel hydroxide nanocomposites is in the field of energy storage devices, as alkaline batteries22. When compared with the lithium-ion batteries, the alkaline batteries possess a low cost and are more safety16. A great challenge in the battery field is to find materials able to associate high energy with a high power22. Some approaches to overcome this challenge are the use of nanocomposites based on conducting materials (like graphene) with nanoparticles of the electroactive material. In addition, the method employed to process the material for the application is a key step, where thick films can damage the performance of the device, blocking the access of the inner electroactive sites and avoiding the use of high charge-discharge currents. Our research group developed a very effective route to deposit thin, transparent and homogeneous films of different unprocessable materials, as carbon nanotubes23,24, graphene24,25,26, metallic nanoparticles and different kind of nanocomposites25,26,27,28,29, in which the film is stabilized at a liquid-liquid interface and easily deposited over different kind of ordinary substrates.

Besides its use in energy storage devices, Ni(OH)2 is also widely used as electrochromic material and electrochemical sensor for a several kind of analytes as glucose5, hydrogen peroxide30, methanol31, phosphate32, etc. The electrochromic properties of the Ni(OH)2 have been the focus of many studies4,33,34, because it is colorless in the reduced state and presents a deep brown color in the oxidized form, which allows its application in electronic devices displays, smart windows, glasses, among others33,35. In the same way for the batteries, the use of nanocomposites of Ni(OH)2 with graphene improves the performance of this material, increasing coloration efficiency and stability35. In which concerns its application as sensor, we demonstrate recently the use of Ni(OH)2-modified electrodes to detect glycerol, an important analyte in the pharmaceutical and biofuel fields36,37. However, to the best of our knowledge, there are no reports employing graphene/nickel hydroxide nanocomposite for this application.

Herein, we report a complete work based on different rGO/Ni(OH)2 nanocomposites, going from the synthesis till multiple-applications, passing by the fully characterization and by the processing as thin films. First, an original synthetic route is presented, in which both the components are obtained together in one step and one pot, starting from graphene oxide (GO) and nickel acetate as precursors. Afterwards, the deposition of these materials over different substrates as thin, transparent and homogeneous films through the liquid-liquid interfacial route is demonstrated. Further, the spectroscopic, microscopic and electrochemical characterization of these materials are discussed and the data correlated to their structure and morphology. Finally, the films were applied as electrodes for alkaline batteries, as electrochromic materials and as electrochemical sensors.

Results and Discussion

Structural and morphological characterization of the nanocomposites

A key point for the synthesis of Ni(OH)2 through the polyol method is the temperature of the reaction. Temperatures near the boiling point of the EG (198 °C) promote the formation of aldehyde, which will reduce the metal ions as demonstrate in the reaction (1) and (2), respectively38,39. This is an interesting way to produce graphene/metallic nickel nanocomposites, as will be demonstrated elsewhere. Otherwise, the polyalcohol generates alkoxides at slight lower temperatures, through the reaction with the acetate ions40, as represented by the reaction (3). The acetate ions react with water from the hydrated metal precursor, generating hydroxyl anions (reaction 4), which reacts with the Ni2+ cations to originate the Ni(OH)2. So, a rigorous control of temperature is necessary in order to obtain controlled samples. Also, the concentration of both OHin solution41,42 and alkoxides43 generated according equation (3) affects directly the yield and the nature of the obtained Ni(OH)2.

The proposal for the nanocomposites described here involves both the synthesis of Ni(OH)2 and the reduction of the graphene oxide (GO) concomitantly. For that, the temperature needs to be high enough to reduce the GO (according similar steps as described in equations (1) and (2)), but not too high to reduce the metallic cations. As will be shown following, the temperature of 190 °C is ideal to achieve these requirements.

The X-ray diffraction patterns for all the nanocomposite samples, as well as for the GO (used as precursor), the rGO and the Ni(OH)2 (control samples) are shown in the Fig. 1A. The GO pattern (Fig. 1A-a) shows a sharp peak at d = 8.8 Å, due the (002) planes, characteristic of the interlayer separation in oxidized graphite. This peak disappears and another one at d = 3.8 Å is observed in the diffractograms of the rGO and of all the nanocomposites, indicating that the GO was reduced in all the samples. The XRD pattern of the Ni(OH)2 sample prepared as control (Fig. 1A-g) shows peaks at d = 8.9, 2.6 and 1.5 Å, characteristics of the (001), (100) and (110) planes of α-Ni(OH)2, respectively33,44.

Figure 1

(A) X-ray diffractograms, (B) Raman spectra, (C) FT-IR spectra and (D) thermogravimetric curves of the samples GO (a), rGO (b), rGONi(OH)2-1 (c), rGONi(OH)2-2 (d), rGONi(OH)2-3 (e), rGONi(OH)2-4 (f), Ni(OH)2 (g) and ethylene glycol (h). Details of the low angle region of the XRD profiles and of the low wavenumber region of the Raman spectra are presented in the insets in (A,B), respectively. The TG data were obtained under air atmosphere at 5 °C min−1.

The rGONi(OH)2-2, rGONi(OH)2-3 and rGONi(OH)2-4 diffractograms also exhibited the α-Ni(OH)2 peaks. However, a careful analysis of the XRD patterns of the nanocomposite samples demonstrates a different profile in the low angle region (inset of the Fig. 1A), when compared to the Ni(OH)2 sample. The rGONi(OH)2-2 and the rGONi(OH)2-3 possess a larger interlayer distance (11.5 Å) than the Ni(OH)2 (8.9 Å) and the rGONi(OH)2-4 shows a mixture of the structures found in the rGONi(OH)2-3 and in the Ni(OH)2. These different structural characteristics result from both the presence of the GO and the amount of nickel precursor used in the synthesis. The higher interlayer distances induced by the presence of GO in reactional medium are very interesting for electrochemical applications, since they would facilitate the access to the electroactive sites of the material, leading to a better performance in the desired application. The rGONi(OH)2-1 did not showed peaks related to α-Ni(OH)2 due the smaller amount of nickel precursor used.

Figure 1B shows the Raman spectra of the samples. All the materials present the D (1355 cm−1), G (1582 cm−1), D’ (1600 cm−1), G’ (2699 cm−1), D + G (2937 cm−1) and 2D’ (3191 cm−1) bands characteristics of graphene-based materials obtaining by the chemical exfoliation of graphite18. The spectra of rGONi(OH)2-2, rGONi(OH)2-3 and rGONi(OH)2-4 show also bands at 427 and 537 cm−1 (inset of Fig. 1B), which are attributed to the Ni-OH and Ni-O stretching, respectively44. The last band is associated to structural defects generally found in the α-Ni(OH)245,46.

The FT-IR spectra of the materials, compared to the neat ethylene glycol, are shown in the Fig. 1C. Bands at 3570/3425/3190 (νOH), 2962/2920/2850 (νCH), 1726 (νC=O), 1625 (δH-O-H), 1574 (νC=C), 1402 (δC-OH), 1220 (νC-O-C) and 1060 cm−1C-O), all related to the presence of oxygenated groups at the surface, are still present in the rGO spectra, indicating that the reduction process converting the GO to rGO was not enough to eliminate all the oxygenated groups of the surface, as previously reported18. The FT-IR spectra of the nanocomposites and of the control sample Ni(OH)2 also show bands at 665 and 586 cm−1, ascribed to δNi(OH)2 and νNi(OH)2, respectively46,47, as well as bands at 2939 (antisymmetric ν C-H), 2878 (symmetric νC-H), 1458 (δC-H), 1408 (δC-O-H), 1323 (γC-H2), 1086 (symmetric νC-O), 1039 (antisymmetric νC-O) and 865 cm−1C-C)48, related to ethylene glycol, indicating that the polyalcohol is present in the final material. As higher is the Ni(OH)2 amount in the samples, the higher the relative intensity of the ethylene glycol bands. This data suggest that the ethylene glycol is probably acting as stabilizer of the Ni(OH)2 nanoparticles, as we have previously observed for neat metallic Ni nanoparticles produced by the polyol route49.

Figure 1D shows the thermogravimetric (TG) curves of the samples, collected under air atmosphere. Comparing the TG curves of GO and rGO, the mass loss event due to the release of the oxygenate groups (120 to 400 °C) decreases from GO (36.6%) to rGO (20.9%), leading to a change of the C/O rate from 1.25 to 3.11. The TG curve of rGO also presents an increase in the oxidation temperature of the carbon backbone of 27 °C in comparison to the GO, due the restoration of the sp2 C-C bonds, as also observed in the DTG curves showed in the Supplementary Fig. S2A. Regarding to the nanocomposites, there is an increase of the residue amount as the higher the mass of nickel acetate initially used, as expected. Taking into account that the residue is composed by NiO, the Ni(OH)2 amount in the initial samples were calculate and the values are presented in the Supplementary Table S1. The Ni(OH)2 percentage increases, as expected, from 11.9 (rGONi(OH)2-1) to 56.4% (rGONi(OH)2-4). The ratio between Ni(OH)2 and rGO in the sample is also important for electrochemical applications, since excess of rGO can block the access to the Ni(OH)2 nanoparticles. There is also a decrease of the oxidation temperature of the carbon backbone with the increase of the Ni(OH)2 content in the sample, which acts as hot spots catalyzing the carbon degradation. As observed in the Supplementary Table S1, the weight loss of the first event related to the release of intercalated water is higher for the nanocomposites than for the neat Ni(OH)2, confirming the larger layer spacing of the α-Ni(OH)2 nanoparticles in the nanocomposites. The oxidation temperatures obtained from the DTG curves (Supplementary Fig. S2A) described in Supplementary Table S1 are very close to the oxidation peaks observed in the DSC curves (Supplementary Fig. S2B).

Figure 2A,B shows the FEG-SEM images of neat Ni(OH)2 and rGONi(OH)2-4, respectively. The Ni(OH)2 sample is composed by porous spherical particles with size ranging from 30 to 80 nm. In contrast, the rGONi(OH)2-4 is composed of rGO sheets decorated with many nanoparticles. Regarding to the nanocomposites with smaller Ni(OH)2 percentages (Supplementary Fig. S3), the Ni(OH)2 nanoparticles were not detectable. The TEM images of the Ni(OH)2 and rGONi(OH)2-4 are presented in the Fig. 2C,D, respectively. As seen in the FEG-SEM images, the Ni(OH)2 possesses a porous structure like a foam and the rGONi(OH)2-4 exhibits rGO sheets highly decorated by Ni(OH)2 nanoparticles. Size histogram for these nanoparticles plotted in the Fig. 2E shows a narrow size distribution with a mean size of 4.9 ± 1.8 nm. In the same way as rGONi(OH)2-4, rGONi(OH)2-3 exhibits the Ni(OH)2 nanoparticles decorating the rGO sheets, however, with fewer nanoparticles, as showed in the Supplementary Fig. S4. These data prove the GO has an important role in the Ni(OH)2 synthesis, affecting the structure and the morphology of the Ni(OH)2 nanoparticles.

Figure 2

(A,B) FEG-SEM and (C,D) TEM images of (A,C) control Ni(OH)2 and (B,D) rGONi(OH)2-4. (E) Size distribution histogram for the Ni(OH)2 nanoparticles on rGONi(OH)2-4.

The EDS spectra of the materials are shown in the Supplementary Fig. S5A. As observed in TG curves, as the higher the nickel acetate amount initially used as precursor in the synthesis, the higher the nickel and oxygen peaks intensities. The control Ni(OH)2 spectra also presents a peak related to carbon, confirming the presence of the ethylene glycol in the samples. Based on these spectra, the nickel/oxygen, nickel/carbon and oxygen/carbon peak areas ratios were calculated (Supplementary Fig. S5B). As expected, there is an increase of the nickel/carbon and oxygen/carbon peak areas ratios as the higher the Ni(OH)2 percentage in the samples.

Thin films characterization

The photographic images of the thin films prepared by the biphasic system are shown in the Fig. 3A–F. It is noted that the thin films are homogeneous and possess different transmittance values. As the rGO percentage increase in the materials, the transmittance of the thin films decreases. This behavior is due an increase of the thickness of the thin films with the rGO percentage, from 112 ± 20 (rGONi(OH)2-4) to 513 ± 108 nm (rGONi(OH)2-1), resulting in a change in the transmittance from 62.6 (rGONi(OH)2-4) to 19.9% (rGONi(OH)2-1), as exposed in the Fig. 3G. Taking into account that the rGO and Ni(OH)2 have different densities and it was used the same mass of the materials (1 mg) to prepare the thin films, as the higher the rGO percentage in the nanocomposite, the higher the volume the thin film will occupy in the liquid-liquid interface, increasing the thickness of the film over the substrate. As commented before, thicker films are not desirable, as rGONi(OH)2-1 and rGONi(OH)2-2 nanocomposites, damaging the electrochemical and electrochromic properties of the film. The UV-Vis spectra in the absorbance mode of the thin films are shown in the Supplementary Fig. S6. The spectra of the nanocomposites and the rGO thin films show typical graphene profile with a band at 270 nm attributed to the π-π* transition.

Figure 3

(A) Photographic images of Ni(OH)2, (B) rGONi(OH)2-4, (C) rGONi(OH)2-3, (D) rGONi(OH)2-2, (E) rGONi(OH)2-1 and (F) rGO thin films over glass substrates. (G) Thickness and transmittance at 550 nm as function of Ni(OH)2 percentage in the samples.

As the nanocomposites are composed of graphene-based materials, the sheet resistance of the thin films were measured over glass substrates and the values were 754 ± 33, 504 ± 50, 2800 ± 450 and 53000 ± 9500 kΩ □−1 for rGO, rGONi(OH)2-1, rGONi(OH)2-2 and rGONi(OH)2-3, respectively. The high values observed are due the synthetic method used, which does not eliminate completely the oxygenate groups of the GO, affecting the conductivity of the rGO. The increase of the resistivity with the Ni(OH)2 content happens because the Ni(OH)2 shows a poor conductivity. Due the rGONi(OH)2-4 and obviously the control Ni(OH)2 present the highest Ni(OH)2 content, leading to the highest sheet resistance values, the absolute values of the sheet resistance of these films were unable to be measured by the equipment.

Supplementary Fig. S7A–C show the FEG-SEM images of the control Ni(OH)2 and rGONi(OH)2-4 thin films over ITO substrates, respectively. As observed in the FEG-SEM image of the powder (Fig. 2A), the Ni(OH)2 thin film is composed by spherical nanoparticles, where some of them are isolated and others in large agglomerates. In contrast, besides the rGO sheets covering the substrate, the rGONi(OH)2-4 thin film does not exhibit large agglomerates, what is an advantage for electrochemical applications. The same morphology was found to the others nanocomposites. The nature of these nanoparticles as being Ni(OH)2 was confirmed by EDS, where the punctual EDS spectra over the nanoparticles exhibits the nickel signal and an increase in the oxygen signal intensity (Supplementary Fig. S8).

Electrochemical characterization of the thin films in alkaline medium

The 150th cyclic voltammograms of the thin films in 1 mol L−1 NaOH aqueous medium are presented in the Fig. 4A. With exception of the control rGO thin film, all the electrodes exhibited the Ni(OH)2/NiOOH redox pair and as the higher the Ni(OH)2 content the higher the current peak intensities. However, the normalized current peak intensities by the Ni(OH)2 percentage are higher for the nanocomposites rGONi(OH)2-4 and rGONi(OH)2-3 than the Ni(OH)2, as can be observed in the Fig. 4B. This behavior is resulted from the differences between the structure and morphologies of the Ni(OH)2 nanoparticles and the thin films for each sample. As the Ni(OH)2 control sample possess a smaller interlayer distance, a bigger nanoparticles size and the thin film possess big agglomerates, it is expected that this sample should present the lower current response. It is also noted in the Fig. 4B that the anodic current peak intensities decrease after the first cycles for the samples rGONi(OH)2-4 and neat Ni(OH)2, which can be due an increase of the nanoparticle size and/or of the crystallinity. For the rGONi(OH)2-3, rGONi(OH)2-2 and rGONi(OH)2-1 thin films, there is an increase of anodic current after the first cycle. This suggest that initially the higher rGO percentage in these films blocks the access to the Ni(OH)2 nanoparticles and as the thin films starts to be cycled these nanoparticles became exposed. This behavior also explains the lower current peak intensities even though when normalized by the Ni(OH)2 percentage. Regarding to the peak potential, after the first cycle the peak potential stabilizes for all the thin films, indicating no significant crystallinity changes.

Figure 4

(A) 150th cyclic voltammograms, (B) anodic peak current normalized by the Ni(OH)2 percentage in each sample and (C) anodic peak potential as function of cycling of rGO (a), rGONi(OH)2-1 (b), rGONi(OH)2-2 (c), rGONi(OH)2-3 (d), rGONi(OH)2-4 (e) and Ni(OH)2 (f) in aqueous solution of NaOH 1 mol L−1 at 50 mV s−1.

After the 150 cyclic voltammograms the thin films were analyzed by FEG-SEM and presented the same morphology as before cycling. However, the thin films with lower Ni(OH)2 content exhibited a higher number of nanoparticles than before cycling (Supplementary Fig. S9), confirming the exposition of these nanoparticles with the cycling as indicated by the voltammetric data.

Supplementary Fig. S10A,B show the X-ray diffraction patterns of the thin films before and after 150 voltammetric cycles. As can be seen, only the control Ni(OH)2 thin film exhibits the peak at 10° related to the (001) planes of α-Ni(OH)2 before the cycling. After the cycling, this peak shifts to 12° indicating a slightly change in the interlayer space of Ni(OH)2 nanoparticles (from 8.8 to 7.4 Å). The nanocomposites did not exhibit this peak before the cycling, which can be due to the lower amount of the Ni(OH)2 in them and the covering of the Ni(OH)2 nanoparticles by the rGO sheets. The nanocomposites and rGO thin films also present a peak at about 23° in 2θ related to rGO and it is more evident as the higher the rGO content. As seen for the Ni(OH)2control sample, the rGONi(OH)2-4 and rGONi(OH)2-3 thin films show a peak at 12° attributed to the (001) of α-Ni(OH)2 after the 150th cycle, indicating a decrease of the interlayer distance from 11.5 and 8.9 Å in the powder samples to 7.4 Å. Although the nanocomposites and the Ni(OH)2 control sample showed an increase in the crystallinity of the nanoparticles, they still present the α phase and it is an important characteristic for the further applications.

The influence of the scan rate in the Ni(OH)2/NiOOH redox pair after the pre-treatment of 150 cyclic voltammograms at 50 mV s−1 was evaluated, Supplementary Fig. S11. For all the thin films is observed a linear dependence of the current peak intensities with the root square of the scan rate (v1/2), suggesting a diffusion-controlled process for the electroactive species involved in the Ni(OH)2/NiOOH redox pair36.

Application as electrodes for alkaline and Li ion batteries

The potentiality of the thin films as electroactive materials for alkaline batteries was evaluated and the discharge curves obtaining after the voltammetric pre-treatment are presented in the Fig. 5. The capacity (C) of the thin films was calculated using the equation (5),

Figure 5

Discharge curves: (A) control Ni(OH)2, (B) rGONi(OH)2-4, (C) rGONi(OH)2-3, (D) rGONi(OH)2-2 and (E) rGONi(OH)2-1 thin films using 0.82 (a), 1.65 (b), 3.29 (c), 4.94 (d) and 8.24 A g−1 (e). (F) Time of discharge and capacity as function of the number of layers to the rGONi(OH)2-4 thin film using a charge-discharge current of 8.24 A g−1.

where I is the charge-discharge current (mA), t is the time of discharge (h) and m is the mass of material on the electrode (g), in which only the mass of the electroactive specie Ni(OH)2 was considered. As can be seen in Fig. 5, all the thin films exhibit a plateau in the range from 0.3 to 0.4 V related to the reduction of NiOOH. This behavior is typical of batteries in which the energy storage is due faradaic processes22. It is also observed that the increase of the charge-discharge current leads to a slight decrease of the capacity. This usually happens in batteries due the need of electroactive species involved in the faradaic processes diffuse through the film and as bigger the particle size and the thickness of the film, the higher is the capacity losses. The rGONi(OH)2-1 did not exhibit this decrease in the capacity with the increase of the charge-discharge current, which can be related to the exposition of the Ni(OH)2 nanoparticles with the cycling, leading to an increase in the charge stored in the material. Comparing the discharges curves, the rGONi(OH)2-4 and rGONi(OH)2-3 presented the higher capacities, as expected since they presented the higher voltammetric responses.

The liquid-liquid interfacial route can be easily used to produce films with several superposed layers, which is an advantage for the construction of final energy storage device and leads to a higher charge stored. Therefore, the influence of the number of layers on the time of discharge and the capacity for the rGONi(OH)2-4 nanocomposite was evaluated (Fig. 5F). It is clear a proportional increase on the time of discharge after the deposition of a second layer, maintaining the capacity. For the third layer there is a non-proportional increase on the time of discharge and for the fourth layer no significant increase has been detected, followed by a decrease in the capacity, probably due the covering of the inner layers by the rGO sheets, blocking the access to the Ni(OH)2 nanoparticles. As the time of discharge still increase till the deposition of three layers thin film, this could be considered the ideal configuration. The photographic images of thin films varying the number of layers of rGONi(OH)2-4, as well as the ITO are present in the Supplementary Fig. S12A. As expected, the increase of the number of layers leads to a decrease in the transmittance from 75 to 38% at 550 nm (Supplementary Fig. S12B).

The specific energy (E) and power (P) values for the thin films were calculated using the equations (6) and (7), respectively, where C is the capacity (mA h g−1), V is the plateau voltage (V) and t is the time of discharge (h). The obtained values for the thin films prepared in this work compared with other data involving Ni(OH)2 nanoparticles and nanocomposites with different carbonaceous materials are demonstrated in the Rogone’s plot present in Fig. 6A. As can be seen, the rGONi(OH)2-4 and rGONi(OH)2-3 exhibited the higher specific energy and power values among the thin films developed in this work and impressive values comparing with the literature (Fig. 6A). Other important characteristic is the high energy values even though when using high charge-discharge currents, demonstrating their potentiality for fast energy devices.

Figure 6

(A) Specific power as function of the specific energy (Ragone’s plot) for the rGONi(OH)2-1 (a), rGONi(OH)2-2 (b), rGONi(OH)2-3 (m), rGONi(OH)2-4 (n), control Ni(OH)2 (e) and for reports from literature using Ni(OH)2 nanoparticles (c55, o56, q)1, activated carbon-NiO-Ni(OH)2 (d)57, rGO-NiO-Ni(OH)2 (f)57, MWCNT-NiO-Ni(OH)2 (g)57, SWCNT-NiO-Ni(OH)2 (h)57, rGO-Ni(OH)2 nanocomposites (i58, j59, l56, p)16 and aluminum-substituted Ni(OH)2 (k)60. (B) Capacity as function of cycling for control Ni(OH)2 (a), rGONi(OH)2-4 (b), rGONi(OH)2-3 (c) and rGONi(OH)2-2 (d) using 8.24 A g−1.

Figure 6B shows the stability of the capacity applying 2000 charge-discharge cycles using a current of 8.24 A g−1 for the nanocomposites and for the neat Ni(OH)2 thin films. Except for the rGONi(OH)2-2, all the thin films presented a decrease in the capacity with the exhaustive cycling, where the rGONi(OH)2-3, rGONi(OH)2-4 and control Ni(OH)2 exhibited 73, 62 and 66% of the initial capacity, respectively. This loss of capacity can be attributed to structural and morphological changes in the Ni(OH)2 nanoparticles, decreasing the number of electroactive sites. The increase in the capacity of the rGONi(OH)2-2 (200% of the initial capacity) is related to the exposition of the Ni(OH)2 nanoparticles with the cycling, as discussed before. These structural and morphological changes also affected the voltammetric behavior and the EIS spectra of the thin films, as can be seen in Supplementary Figs S13 and S14, respectively. As seen in the Supplementary Fig. S13, the rGONi(OH)2-3, rGONi(OH)2-4 and control Ni(OH)2 presented a shift and an intensity decrease of the peaks. The EIS spectra of the thin films before the charge-discharge cycling present semicircles in the high-frequency range, which are related to the oxidation process of the Ni(OH)2 (Supplementary Fig. S14A,B). The curves were fitted using the equivalent circuit illustrated in the inset of the Supplementary Fig. S14B. Rb is the resistance resulting from the contact resistance between the nanomaterial and the current collector, the intrinsic resistance of the substrate and the electrolyte resistance; CPE is the constant phase element and represents the double-layer capacitance; Rct is the charge-transfer resistance resulting from the faradaic reaction; Zw is the Warburg element related to the ion diffusion resistance; and Cint is the capacitance originated from the ion intercalation in the Ni(OH)2 layers50,51. The values of Rct to rGONi(OH)2-3, rGONi(OH)2-4 and control Ni(OH)2 thin films before the charge-discharge cycling were 30, 28 and 23 Ω, respectively. The low values of Rct are resulting of the high surface area of the Ni(OH)2 nanoparticles50,51. However, after the 2000 charge-discharge cycles there is a drastic change in the EIS profile for the three thin films, as seen in the Supplementary Fig. S14C. This high increase of the semicircle length indicates a very high Rct and it is also associated to structural and morphological changes after this long cycling. Due the very high Rct, the EIS spectra after charge-discharge cycling were not fitted.

To evaluate possible changes in the Ni(OH)2 structure, the thin films were analyzed by X-ray diffraction before and after the 2000 charge-discharge cycles (Supplementary Fig. S15). Both patterns present the broad peak at around 11° (001) related to the α-Ni(OH)2. Nevertheless, the thin films after the charge-discharge cycling also exhibit a broad and low intensity peak at around 21° (001), which could be related to a defective β-Ni(OH)2 formed in the films44. This slight change in the crystallinity of the α-Ni(OH)2 indicate that probably morphological changes as particle agglomeration happened after the 2000 charge-discharge cycles and they should be responsible by the decrease of the capacity.

Aiming evaluate the potentiality of the nanocomposites as electroactive materials for Li-ion batteries, the rGONi(OH)2-4 thin film was cycled in LiClO4/propylenecarbonate solution. Supplementary Fig. S16 shows the second voltammetric cycle using a scan rate of 1 mV s−1. It is clear to note the presence of two anodic and two cathodic peaks. As describe by others52,53, the reduction processes are related to both the formation of the solid electrolyte interface (SEI) film on the nanocomposite electrode (at −0.408 V, which consist of several lithium species as Li2CO3 and RCO2Li)54 and the reduction of the Ni(OH)2 to Ni (at −0.062 V, with consequent production of LiOH). In opposite, the anodic processes are attributed to the decomposition of the SEI (at 1.640 V) and the oxidation of the metallic Ni (at 1.374 V, with consequent decomposition of the LiOH). In this way, the lithium intercalation process can be described as:

This result indicates the potentiality of use the rGONi(OH)2 nanocomposites for this purpose.

Application as electrochromic material in alkaline medium

Since the rGONi(OH)2-4, rGONi(OH)2-3 and control Ni(OH)2thin films have the higher transmittances, they were also evaluated as electrochromic electrodes. For this purpose, after the pre-treatment of 150 voltammetric cycles, the thin films were periodically submitted to potentials of 0.1 and 0.5 V and simultaneously analyzed by UV-Vis spectroscopy. As seen in the Fig. 7A, the change of the applied potential from 0.1 to 0.5 V leads to an increase of the absorbance. This happens because the NiOOH generated at 0.5 V is darker than the Ni(OH)2 generated at 0.1 V. However, the thin films presented different absorbance variations (optical densities), where the values at 550 nm were 0.047, 0.154 and 0.090 to the Ni(OH)2, rGONi(OH)2-4 and rGONi(OH)2-3 thin films, respectively. In the same way that observed during the data related to the application in batteries, the nanocomposite thin films present a better response than the neat Ni(OH)2. Figure 7B shows the transmittance at 550 nm of the thin films as function of time, where 100 colored-bleached cycles were applied. As can be seen in the UV-Vis spectra (Fig. 7A), the rGONi(OH)2-4 thin film exhibited the higher transmittance variation (Fig. 7C), which is due the higher percentage of Ni(OH)2 and the smaller particle size comparing with the rGONi(OH)2-3 and control Ni(OH)2, respectively. The response time was considered as the time to reach 2/3 of the total transmittance change. The obtained values were 3.9, 1.7 and 1.7 s to the rGONi(OH)2-4, rGONi(OH)2-3 and control Ni(OH)2 thin films, respectively. The higher response time to the rGONi(OH)2-4 can be related to the higher amount of particles decorating the rGO. Taking into account the optical density (OD) and the charge (Q) of the last colored-bleached cycle and using the equation (9), the electrochromic efficiency (η) for the rGONi(OH)2-4, rGONi(OH)2-3 and control Ni(OH)2 thin films were 52, 70 and 58 cm2 C−1, respectively. Once more the nanocomposites exhibited a better performance than the neat Ni(OH)2. These η values are very close to the results of literature reports that use Ni(OH)2 nanoparticles (80 cm2 C−1)34, Ni(OH)2 thin films (111 cm2 C−1)4 and rGO/Ni(OH)2 nanocomposites (76 cm2 C−1)35.

Figure 7

(A) UV-Vis spectra applying 0.1 () and 0.5 V (), (B,C) transmittance as function of the time for the 100 colored-bleached cycles, (D) chronoamperograms for the potentials applied and (E) transmittance variation as function of the number of cycles for the control Ni(OH)2 (a), rGONi(OH)2-3 (b) and rGONi(OH)2-4 (c) thin films.

Figure 7E presents the stability of the transmittance variation as function of the cycling. All the thin films presented a decrease of the transmittance variation with the cycling, reaching to 73.3, 79 and 77.6% of initial value for the rGONi(OH)2-4, rGONi(OH)2-3 and control Ni(OH)2, respectively. This decrease is expected, since morphological changes in the Ni(OH)2 nanoparticles happen with the cycling of the materials.

Application as chronoamperometric sensor for glycerol

Ni(OH)2 is also widely used as electroactive material for electrochemical sensors. For this reason, the rGONi(OH)2-4, rGONi(OH)2-3 and control Ni(OH)2 thin films were evaluated as sensors for glycerol. For that, after the pre-treatment of 150 voltammetric cycles, three additions of 1 mmol L−1 of glycerol have been done to the electrochemical cell and after each addition the electrodes were cycled. Figure 8A shows the voltammograms for the rGONi(OH)2-4 thin film in the absence and in the presence of glycerol. Both the increase of the anodic current peak and the decrease of the cathodic current peak indicate a typical electrocatalysis profile, where the NiOOH oxidizes the analyte generating Ni(OH)2 and products. Since the potential that this chemical step occurs is high, the resulting Ni(OH)2 is reoxidized leading to the current increment. Concomitantly, as the NiOOH is consumed the cathodic current peak decreases. The same behavior was found to the other thin films (Supplementary Fig. S17) and confirms the electroactivity of these nanomaterials for detection of glycerol. However, the rGONi(OH)2-3 exhibits an expressive decrease of the cathodic current, indicating a higher electrocatalytic behavior.

Figure 8

(A) Cyclic voltammograms of rGONi(OH)2-4 thin film in the absence (a) and presence of 1 (b), 2 (c) and 3 (d) mmol L−1 glycerol. (B) Chronoamperogram for rGONi(OH)2-4 thin film with four additions of 100 μmol L−1 glycerol using 0.45 V. (C) Sensitivity as function of the potential used in the chronoamperometry. (D) Chronoamperogram for rGONi(OH)2-4 thin film with glycerol additions from 10 to 800 μmol L−1. (E) Analytical curves constructed from chronoamperograms. (a–c)in (C,E) represent rGONi(OH)2-3 (a), rGONi(OH)2-4 (b) and control Ni(OH)2(c) thin films. The analyses were carried out in 1 mol L−1 NaOH aqueous solution.

To optimize the potential for the glycerol detection, the thin films were submitted to chronoamperometry using the potentials of 0.4, 0.45 and 0.5 V and for each potential four additions of 100 μmol L−1 glycerol were carried out (Supplementary Fig. S18). Figure 8B shows a typical chronoamperogram, showing the increases of the current according the glycerol additions, as expected. Using the current increments after each glycerol addition, the sensitivity for the thin films in each potential evaluated was calculated (Fig. 8C) and the best sensitivity for all the thin films was found at 0.45 V. So, the potential of 0.45 V was employed for the detection of glycerol in the concentration range from 10 to 800 μmol L−1. All the thin films showed a similar chronoamperogram (Fig. 8D and Supplementary Fig. S19) characterized by current increments for all the glycerol additions. Figure 8E exhibits the analytical curves constructed from the chronoamperograms. It is clear to note the linear responses for the whole glycerol concentration range, with R2 of 0.9987, 0.9978 and 0.9961 to the control Ni(OH)2, rGONi(OH)2-4 and rGONi(OH)2-3 thin films, respectively. However, the rGONi(OH)2-3 leads to the higher sensitivity, where the values found to the concentration range from 10 to 50 μmol L−1 were 0.28 ± 0.01, 0.24 ± 0.06 and 0.36 ± 0.02 μA (μmol L−1)−1 to control Ni(OH)2, rGONi(OH)2-4 and rGONi(OH)2-3, respectively. The limit of detection (LOD) and the limit of quantification (LOQ) were calculated using the Equations (10) and (11), respectively, where s is the standard deviation from the blank (1.9, 2.0 and 1.9 μA to Ni(OH)2, rGONi(OH)2-4 and rGONi(OH)2-3, respectively) and α is the sensitivity. The rGONi(OH)2-3 thin film presented the lower LOD and LOQ (15.4 ± 1.2 and 51.3 ± 4.1 μmol L−1), than the Ni(OH)2 (20.2 ± 0.6 and 67.5 ± 2.1 μmol L−1) and the rGONi(OH)2-4 thin films (25.0 ± 3.1 and 83.2 ± 10.5 μmol L−1). Despite the Ni(OH)2 control sample showed a better performance than the rGONi(OH)2-4, it is important to notice that this last one possesses a lower amount of electroactive material. The higher electroactivity of the rGONi(OH)2-3 can be associated to smaller nanoparticles sizes and a better distribution of them through the film. These low LOD values and the wide linear detection range (10 to 800 μmol L−1) reveal a good performance of the thin films developed in this work when compared with the literature, where LOD values vary from 1.49 to 95 μmol L−1, as seen in the Supplementary Table S2.


Different nanocomposites between reduced graphene oxide and Ni(OH)2 nanoparticles have been synthesized by an innovative modification in the polyol method, starting from both graphene oxide and nickel acetate as precursors, in one pot and one single step. Comparing to neat Ni(OH)2 nanoparticles obtained by the same route, the hydroxide nanoparticles obtained in the nanocomposites are smaller and present a more open structure, which are very desirable characteristics for electrochemical applications. The concomitant occurrence of both the synthesis of Ni(OH)2 and the reduction of GO represent a new pathway for both reactions, in which the oxygenates groups of the GO surface can act as nucleating points for the Ni(OH)2 nanoparticles growth, resulting in nanocomposites with a strong interaction between the components.

All the materials prepared were processed as thin, homogenous and transparent films through a liquid-liquid biphasic system and homogeneously deposited over transparent electrodes. These thin films presented a multifunctional character and they were applied as electrodes for alkaline batteries, electrochromic materials and active component in electrochemical sensors. For all these applications the performances of the nanocomposites were much superior than the observed for neat Ni(OH)2 prepared as control sample, which is attributed to: i) the smaller Ni(OH)2 particle size; ii) the better Ni(OH)2 distribution through the film; and iii) the presence of the rGO in the nanocomposites. Also, the performance for each application is better or comparable to the best results found in literature, with a particular emphasis to the application as electrodes for alkaline batteries, in which the responses of the nanocomposite films occupy a privileged position in the Ragone’s plot due the impressive and desirable relationship between the specific energy and power of the materials.


H2SO4 (Carlo Erba), graphite (Graflake 99580, 99%, Nacional de Grafite SA), NaNO3 (Vetec), KMnO4 (Synth), HCl (Impex), H2O2 aqueous solution (Vetec), ethylene glycol (Carlo Erba), toluene (Carlo Erba), glycerol (CAAL) and NaOH (Vetec) were used as received. Ni(CH3COO)2·4H2O (Vetec) was previously dried under low pressure at 100 C for 5 hours before used. The aqueous solutions were prepared using deionized Milli-Q water.

The GO was obtained as follows18: 46 mL of concentrated H2SO4 was added to a 500 mL round flask under ice bath. Next, 2 g of graphite and 1 g of NaNO3 were added to the round flask. After 15 minutes of magnetic stirring, which was maintained during the whole process, 6 g of KMnO4 was added slowly to the round flask. Afterwards, the ice bath was removed and the system was maintained under magnetic stirring for 180 minutes. After this time, 92 mL of water was added slowly and then 280 mL of hot water was added. To the consumption of oxidize agent, 10 mL of H2O2 (30% v v−1) were slowly added and kept 30 minutes under stirring. Next, the mixture was transfer to 1 L beaker and it was added 500 mL of a HCl solution (10% v v−1). The system was magnetic stirred for 10 minutes and it was left to sediment. Finally, the solid was washed with deionized water until neutral pH, filtrated and dried at 60 °C for 24 hours generating the graphite oxide (Gr-O). 150 mg of Gr-O was exfoliated in 50 mL of deionized water using a tip ultrasound for 10 min (Cole Parmer CP505 - 20 kHz–200 W). This mixture was centrifuged for 90 minutes at 3000 rpm to remove the not dispersed material, leading to the GO dispersion. After that, the water was removed from the GO dispersion by heating at 80 °C and the resulting solid (GO) remained drying at this temperature overnight.

To the synthesis of the nanocomposites, 5 mg of GO was dispersed in 20 mL of ethylene glycol in a 250 mL round flask using a bath ultrasound (Unique USC 1880 - 37 kHz) for 60 minutes. Next, nickel acetate was added to the system leading to the GO/Ni2+ weight ratios of 1/0.1 (starting from 2.2 mg of nickel acetate, yielding the sample rGONi(OH)2-1), 1/0.25 (5.5 mg of nickel acetate, sample rGONi(OH)2-2), 1/0.5 (11.1 mg of nickel acetate, sample rGONi(OH)2-3) and 1/1 (22.1 mg of nickel acetate, sample rGONi(OH)2-4). Then, a condenser was adapted to the system, which was maintained at vigorous magnetic stirring and heated for 2 hours at 190 °C. After this time, the solid material was filtrated, washed with 200 mL of deionized water and dried at 70 °C for 2 hours. Other two control samples were prepared starting from just GO (producing the sample rGO) or the nickel precursor (sample Ni(OH)2), where the amount of nickel acetate used was the same that in the sample rGONi(OH)2-4.

To the processing of the materials as thin films, 1 mg of each material was dispersed in 40 mL of deionized water in a 100 mL round flask using a bath ultrasound for 60 minutes. Next, 40 mL of toluene was added and the system was kept under magnetic stirring (2500 rpm) for 20 hours. After this time, the magnetic stirring was interrupted and a thin film was spontaneously deposited at the water/toluene interface. The entire round flask content was transferred with a micropipette to a 100 mL beaker containing the desired substrates. As the thin film is self-assembled, it reorganizes itself at the liquid-liquid interface. So, the substrates were pulled from the bottom of the beaker to the interface direction, aiming a homogeneous deposition of the film over them. Finally, the thin films over the substrates were dried at 100 °C for 60 minutes. All the steps involved in the thin film preparation are illustrated in the Supplementary Fig. S20.

Thermogravimetric analyses (TGA) were carried out in a TGA/SDT Q 600, using a heating rate of 5 °C min−1 in air atmosphere.

X-ray diffraction patterns were obtaining using a Shimadzu XRD-6000 diffractometer with Cu-Kα radiation (λ = 1.5418 Å) operating at 40 kV and 30 mA. The thin films were analyzed using a low angle accessory with 0.1° incident angle operating at 40 kV and 40 mA.

FT–IR spectra of the samples were recorded using a FT-IR Bomem spectrophotometer with 32 scans and 4 cm−1 of resolution. The samples were prepared in KBr pellets.

UV-Vis data of the thin films over quartz substrates were obtaining using a Shimadzu UV-2450 spectrophotometer. The UV-Vis spectroelectrochemical measurements were carried out in the same equipment using a home-made electrochemical cell.

Raman spectra were obtaining in a Renishaw Raman Imaging Microprobe System 3000 spectrophotometer using a 514.5 nm (Ar+ laser) excitation line.

TEM measurements were performed in a JEOL JEM 120 kV instrument. For the analysis, one drop of the samples dispersed in deionized water was evaporated onto carbon films supported on holey carbon copper grids.

SEM images were recorded using a MIRA-3 FEG-SEM Tescan with 10 kV voltage and a secondary electrons detector. The samples were analyzed either as powders sprinkled on Cu adhesive tape or as the thin films deposited over ITO substrates. EDS spectra were obtaining in the same equipment using an Oxford accessory.

The thicknesses of the films were analyzed using a Dektak 150 Veeco surface profilometer with 1 nm resolution.

Resistivity measurements of the films were carried out using a four-point Jandel Universal Probe, directly from the thin films over glass substrates.

The mass of the thin films was evaluated by measuring the mass of four layers deposited onto the same substrate with an area of 7.5 cm2. After each deposition the substrates were dried at 100 °C for 60 minutes under low pressure. The mass found for one thin film layer was 8.5 μg cm−2.

Cyclic voltammetry measurements were carried out in a Autolab potentiostat in a conventional three-electrode cell, where the thin films deposited over ITO, with a 1 cm2 electroactive area, were used as working electrodes, an Ag/AgCl (3 mol L−1 KCl) as the reference electrode and a platinum wire as the counter electrode. The cyclic voltammetry for the lithium intercalation test was carried out in 1 mol L−1 LiClO4 (Vetec) propylenecarbonate (Aldrich) solution using a scan rate of 1 mV s−1. The UV-Vis spectroelectrochemical measurements were carried out with the films deposited over ITO with a 1.5 cm2 electroactive area. The charge-discharge measurements were performed using cut-off potentials of 0 and 0.5 V and 3 cycles for each charge-discharge current. The charge-discharge currents were calculated using the whole mass of the film.

The chronoamperograms for the glycerol detection were recorded under magnetic stirring (1100 rpm). The EIS data were obtaining using the NOVA software. For that, the thin films were first submitted to 150 voltammetric cycles at 50 mV s−1 and then a potential of 0.39 V was applied for 5 minutes. Next, impedance analyses were carried out at frequencies ranging from 10−1 to 104 Hz, using a standard potential of 0.39 V and an amplitude potential of 10 mV. These analyses were also performed after the 2000 cycles of charge-discharge. The data were fitted using the ZView software. All the electrochemical measurements were carried out in 1 mol L−1 NaOH aqueous solution.

Additional Information

How to cite this article: Neiva, E. G. C. et al. One material, multiple functions: graphene/Ni(OH)2 thin films applied in batteries, electrochromism and sensors. Sci. Rep. 6, 33806; doi: 10.1038/srep33806 (2016).


  1. Sun, J. et al. Assembly and electrochemical properties of novel alkaline rechargeable Ni/Bi battery using Ni(OH)2 and (BiO)4CO3(OH)2 microspheres as electrode materials. J. Power Sources 274, 1070–1075 (2015).

    ADS  CAS  Google Scholar 

  2. Kiani, M. A., Mousavi, M. F. & Ghasemi, S. Size effect investigation on battery performance: Comparison between micro- and nano-particles of β-Ni(OH)2 as nickel battery cathode material. J. Power Sources 195, 5794–5800 (2010).

    ADS  CAS  Google Scholar 

  3. Inamdar, A. I. et al. Electrochromic and electrochemical properties of amorphous porous nickel hydroxide thin films. Appl. Surf. Sci. 257, 9606–9611 (2011).

    ADS  CAS  Google Scholar 

  4. Liu, H., Yan, G., Liu, F., Zhong, Y. & Feng, B. Structural, electrochemical and optical properties of NiOxHy thin films prepared by electrochemical deposition. J. Alloys Compd. 481, 385–389 (2009).

    CAS  Google Scholar 

  5. Yang, H. et al. Nickel hydroxide nanoflowers for a nonenzymatic electrochemical glucose sensor. J. Electrochem. Soc. 161, B216–B219 (2014).

    CAS  Google Scholar 

  6. Niu, X., Lan, M., Zhao, H. & Chen, C. Highly sensitive and selective nonenzymatic detection of glucose using three-dimensional porous nickel nanostructures. Anal. Chem. 85, 3561–3569 (2013).

    CAS  PubMed  Google Scholar 

  7. Mathew, M. & Sandhyarani, N. A highly sensitive electrochemical glucose sensor structuring with nickel hydroxide and enzyme glucose oxidase. Electrochim. Acta 108, 274–280 (2013).

    CAS  Google Scholar 

  8. Abdel Rahim, M. A., Abdel Hameed, R. M. & Khalil, M. W. Nickel as a catalyst for the electro-oxidation of methanol in alkaline medium. J. Power Sources 134, 160–169 (2004).

    ADS  CAS  Google Scholar 

  9. Tehrani, R. M. A. & Ghani, S. A. The nanocrystalline nickel with catalytic properties on methanol oxidation in alkaline medium. Fuel Cells 9, 579–587 (2009).

    CAS  Google Scholar 

  10. Gao, M. et al. Efficient water oxidation using nanostructured α-nickel-hydroxide as an electrocatalyst. J. Am. Chem. Soc. 136, 7077–7084 (2014).

    CAS  PubMed  Google Scholar 

  11. Bode, H., Dehmelt, K. & Witte, J. Zur kenntnis der nickelhydroxidelektrode–I. Über das nickel (II)-hydroxidhydrat. Electrochim. Acta 11, 1079–1087 (1966).

    CAS  Google Scholar 

  12. Bernard, M. C., Bernard, P., Keddam, M., Senyarich, S. & Takenouti, H. Characterisation of new nickel hydroxides during the transformation of αNi(OH)2 to βNi(OH)2 by ageing. Electrochim. Acta 41, 91–93 (1996).

    CAS  Google Scholar 

  13. Wehrens-Dijksma, M. & Notten, P. H. L. Electrochemical quartz microbalance characterization of Ni(OH)2-based thin film electrodes. Electrochim. Acta 51, 3609–3621 (2006).

    CAS  Google Scholar 

  14. Zhu, X. et al. Amperometric nonenzymatic determination of glucose based on a glassy carbon electrode modified with nickel(II) oxides and graphene. Microchim Acta 180, 477–483 (2013).

    CAS  Google Scholar 

  15. Zhu, J., Chen, S., Zhou, H. & Wang, X. Fabrication of a low defect density graphene-nickel hydroxide nanosheet hybrid with enhanced electrochemical performance. Nano Res. 5, 11–19 (2012).

    ADS  CAS  Google Scholar 

  16. Sun, J. et al. Ni/Bi battery based on Ni(OH)2 nanoparticles/graphene sheets and Bi2O3 rods/graphene sheets with high performance. J. Alloys Compd. 643, 231–238 (2015).

    CAS  Google Scholar 

  17. Wang, X., Liu, J., Wang, Y., Zhao, C. & Zheng, W. Ni(OH)2 nanoflakes electrodeposited on Ni foam-supported vertically oriented graphene nanosheets for application in asymmetric supercapacitors. Mater. Res. Bull. 52, 89–95 (2014).

    CAS  Google Scholar 

  18. Mehl, H., Matos, C. F., Neiva, E. G. C., Domingues, S. H. & Zarbin, A. J. G. Efeito da variação de parâmetros reacionais na preparação de grafeno via oxidação e redução do grafite. Quím. Nova 37, 1639–1645 (2014).

    CAS  Google Scholar 

  19. Fonsaca, J. E. S. et al. Graphene nanoribbons inducing cube-shaped Ag nanoparticle assemblies. Carbon 93, 800–811 (2015).

    CAS  Google Scholar 

  20. Zhang, H. et al. One-step electrophoretic deposition of reduced graphene oxide and Ni(OH)2 composite films for controlled syntheses supercapacitor electrodes. J. Phys. Chem. B 117, 1616–1627 (2013).

    CAS  PubMed  Google Scholar 

  21. Xiao, J. & Yang, S. Nanocomposites of Ni(OH)2/reduced graphene oxides with controllable composition, size and morphology: performance variations as pseudocapacitor electrodes. ChemPlusChem 77, 807–816 (2012).

    CAS  Google Scholar 

  22. Dubal, D. P., Ayyad, O., Ruiz, V. & Gomez-Romero, P. Hybrid energy storage: the merging of battery and supercapacitor chemistries. Chem. Soc. Rev. 44, 1777–1790 (2015).

    CAS  Google Scholar 

  23. Salvatierra, R. V., Souza, V. H. R., Matos, C. F., Oliveira, M. M. & Zarbin, A. J. G. Graphene chemically synthesized from benzene at liquid–liquid interfaces. Carbon 93, 924–932 (2015).

    CAS  Google Scholar 

  24. Souza, V. H. R. et al. Flexible, Transparent and Thin Films of Carbon Nanomaterials as Electrodes for Electrochemical Applications. Electrochim. Acta 197, 200–209 (2016).

    CAS  Google Scholar 

  25. Mehl, H., Oliveira, M. M. & Zarbin, A. J. G. Thin and transparent films of graphene/silver nanoparticles obtained at liquid–liquid interfaces: Preparation, characterization and application as SERS substrates. J. Colloid Interface Sci. 438, 29–38 (2015).

    ADS  CAS  PubMed  Google Scholar 

  26. Domingues, S. H., Salvatierra, R. V., Oliveira, M. M. & Zarbin, A. J. G. Transparent and conductive thin films of graphene/polyaniline nanocomposites prepared through interfacial polymerization. Chem. Commun. 47, 2592–2594 (2011).

    CAS  Google Scholar 

  27. de Souza, V. H. R., Oliveira, M. M. & Zarbin, A. J. G. Thin and flexible all-solid supercapacitor prepared from novel single wall carbon nanotubes/polyaniline thin films obtained in liquid–liquid interfaces. J. Power Sources 260, 34–42 (2014).

    ADS  Google Scholar 

  28. Salvatierra, R. V., Cava, C. E., Roman, L. S. & Zarbin, A. J. G. ITO-free and flexible organic photovoltaic device based on high transparent and conductive polyaniline/carbon nanotube thin films. Adv. Funct. Mater. 23, 1490–1499 (2013).

    CAS  Google Scholar 

  29. Salvatierra, R. V., Oliveira, M. M. & Zarbin, A. J. G. One-pot synthesis and processing of transparent, conducting and freestanding carbon nanotubes/polyaniline composite films. Chem. Mater. 22, 5222–5234 (2010).

    CAS  Google Scholar 

  30. Martins, P. R., Motta, A. G. N., Nakamura, M., Araki, K. & Angnes, L. Nanostructured alpha-nickel hydroxide electrodes for high performance hydrogen peroxide sensing. Electroanal. 25, 2060–2066 (2013).

    CAS  Google Scholar 

  31. Toghill, K., Xiao, L., Stradiotto, N. & Compton, R. The determination of methanol using an electrolytically fabricated nickel microparticle modified boron doped diamond electrode. Electroanal. 22, 491–500 (2010).

    CAS  Google Scholar 

  32. Cheng, W.-L., Sue, J.-W., Chen, W.-C., Chang, J.-L. & Zen, J.-M. Activated nickel platform for electrochemical sensing of phosphate. Anal. Chem. 82, 1157–1161 (2009).

    Google Scholar 

  33. Vidotti, M., Torresi, R. & Córdoba de Torresi, S. I. Eletrodos modificados por hidróxido de níquel: Um estudo de revisão sobre suas propriedades estruturais e eletroquímicas visando suas aplicações em eletrocatálise, eletrocromismo e baterias secundárias. Quím. Nova 33, 2176–2186 (2010).

    CAS  Google Scholar 

  34. Vidotti, M., van Greco, C., Ponzio, E. A. & Córdoba de Torresi, S. I. Sonochemically synthesized Ni(OH)2 and Co(OH)2 nanoparticles and their application in electrochromic electrodes. Electrochem. Commun. 8, 554–560 (2006).

    CAS  Google Scholar 

  35. Cai, G.-f. et al. An efficient route to a porous NiO/reduced graphene oxide hybrid film with highly improved electrochromic properties. Nanoscale 4, 5724–5730 (2012).

    ADS  CAS  PubMed  Google Scholar 

  36. Neiva, E. G. C., Bergamini, M. F., Oliveira, M. M., Marcolino Jr, L. H. & Zarbin, A. J. G. PVP-capped nickel nanoparticles: Synthesis, characterization and utilization as a glycerol electrosensor. Sens. Actuators B Chem. 196, 574–581 (2014).

    CAS  Google Scholar 

  37. Neiva, E. G. C., Oliveira, M. M., Marcolino Jr, L. H. & Zarbin, A. J. G. Nickel nanoparticles with hcp structure: Preparation, deposition as thin films and application as electrochemical sensor. J. Colloid Interface Sci. 468, 34–41 (2016).

    ADS  CAS  PubMed  Google Scholar 

  38. Fievet, F., Lagier, J. P. & Figlarz, M. Preparing monodisperse metal powders in micrometer and submicrometer sizes by the polyol process. MRS Bull. 14, 29–34 (1989).

    CAS  Google Scholar 

  39. Sun, Y., Yin, Y., Mayers, B. T., Herricks, T. & Xia, Y. Uniform silver nanowires synthesis by reducing AgNO3 with ethylene glycol in the presence of seeds and poly(vinyl pyrrolidone). Chem. Mater. 14, 4736–4745 (2002).

    CAS  Google Scholar 

  40. Larcher, D., Sudant, G., Patrice, R. & Tarascon, J. M. Some insights on the use of polyols-based metal alkoxides powders as precursors for tailored metal-oxides particles. Chem. Mater. 15, 3543–3551 (2003).

    CAS  Google Scholar 

  41. Du, H., Jiao, L., Cao, K., Wang, Y. & Yuan, H. Polyol-mediated synthesis of mesoporous α-Ni(OH)2 with enhanced supercapacitance. ACS Appl. Mater. Interfaces 5, 6643–6648 (2013).

    CAS  PubMed  Google Scholar 

  42. Yang, L.-X. et al. Hydrothermal synthesis of nickel hydroxide nanostructures in mixed solvents of water and alcohol. J. Solid State Chem. 180, 2095–2101 (2007).

    ADS  CAS  Google Scholar 

  43. Prevot, V., Forano, C. & Besse, J. P. Hydrolysis in polyol: New route for hybrid-layered double hydroxides preparation. Chem. Mater. 17, 6695–6701 (2005).

    CAS  Google Scholar 

  44. Deabate, S., Fourgeot, F. & Henn, F. X-ray diffraction and micro-Raman spectroscopy analysis of new nickel hydroxide obtained by electrodialysis. J. Power Sources 87, 125–136 (2000).

    ADS  CAS  Google Scholar 

  45. Ni, X., Zhao, Q., Li, B., Cheng, J. & Zheng, H. Interconnected β-Ni(OH)2 sheets and their morphology-retained transformation into mesostructured Ni. Solid State Commun. 137, 585–588 (2006).

    ADS  CAS  Google Scholar 

  46. Bantignies, J. L. et al. New insight into the vibrational behavior of nickel hydroxide and oxyhydroxide using inelastic neutron scattering, far/mid-infrared and Raman spectroscopies. J. Phys. Chem. C 112, 2193–2201 (2008).

    CAS  Google Scholar 

  47. Li, Y. et al. Synthesis of α-Ni(OH)2 with hydrotalcite-like structure: Precursor for the formation of NiO and Ni nanomaterials with fibrous shapes. Chem. Eng. J. 136, 398–408 (2008).

    CAS  Google Scholar 

  48. Sawodny, W., Niedenzu, K. & Dawson, J. W. The vibrational spectrum of ethylene glycol. Spectrochim. Acta, Part A 23, 799–806 (1967).

    ADS  CAS  Google Scholar 

  49. Couto, G. G. et al. Nickel nanoparticles obtained by a modified polyol process: Synthesis, characterization and magnetic properties. J. Colloid Interface Sci. 311, 461–468 (2007).

    ADS  CAS  PubMed  Google Scholar 

  50. Fang, D.-L., Chen, Z.-D., Liu, X., Wu, Z.-F. & Zheng, C.-H. Homogeneous growth of nano-sized β-Ni(OH)2 on reduced graphene oxide for high-performance supercapacitors. Electrochim. Acta 81, 321–329 (2012).

    CAS  Google Scholar 

  51. Neiva, E. G. C., Souza, V. H. R., Huang, K., Pénicaud, A. & Zarbin, A. J. G. Graphene/nickel nanoparticles composites from graphenide solutions. J. Colloid Interface Sci. 453, 28–35 (2015).

    ADS  CAS  PubMed  Google Scholar 

  52. Tian, J. et al. PH-driven dissolution-precipitation: A novel route toward ultrathin Ni(OH)2 nanosheets array on nickel foam as binder-free anode for Li-ion batteries with ultrahigh capacity. CrystEngComm 15, 8300–8305 (2013).

    CAS  Google Scholar 

  53. Zhu, Y. & Cao, C. Remarkable electrochemical lithium storage behaviour of two-dimensional ultrathin α-Ni(OH)2 nanosheets. RSC Adv. 5, 83757–83763 (2015).

    CAS  Google Scholar 

  54. Su, L., Zhou, Z. & Shen, P., Ni/C Hierarchical Nanostructures with Ni Nanoparticles Highly Dispersed in N-Containing Carbon Nanosheets: Origin of Li Storage Capacity. J. Phys. Chem. C 116, 23974–23980 (2012).

    CAS  Google Scholar 

  55. Chang, J., Xu, H., Sun, J. & Gao, L. High pseudocapacitance material prepared via in situ growth of Ni(OH)2 nanoflakes on reduced graphene oxide. J. Mater. Chem. 22, 11146–11150 (2012).

    CAS  Google Scholar 

  56. Kong, D.-S., Wang, J.-M., Shao, H.-B., Zhang, J.-Q. & Cao, C.-n. Electrochemical fabrication of a porous nanostructured nickel hydroxide film electrode with superior pseudocapacitive performance. J. Alloys Compd. 509, 5611–5616 (2011).

    CAS  Google Scholar 

  57. Kim, B. K., Chabot, V. & Yu, A. Carbon nanomaterials supported Ni(OH)2/NiO hybrid flower structure for supercapacitor. Electrochim. Acta 109, 370–380 (2013).

    CAS  Google Scholar 

  58. Wang, H. et al. Advanced asymmetrical supercapacitors based on graphene hybrid materials. Nano Res. 4, 729–736 (2011).

    CAS  Google Scholar 

  59. Yan, J. et al. Advanced asymmetric supercapacitors based on Ni(OH)2/graphene and porous graphene electrodes with high energy density. Adv. Funct. Mater. 22, 2632–2641 (2012).

    CAS  Google Scholar 

  60. Lang, J.-W., Kong, L.-B., Liu, M., Luo, Y.-C. & Kang, L. Asymmetric supercapacitors based on stabilized α-Ni(OH)2 and activated carbon. J. Solid State Electrochem. 14, 1533–1539 (2010).

    CAS  Google Scholar 

Download references


The authors acknowledge the financial support by CAPES, CNPq, NENNAM (PRONEX, Fund. Araucária/CNPq), National Institute of Science and Technology of Carbon Nanomaterials and the CME-UFPR by the TEM images. E.G.C.N. thanks CAPES for a research fellowship.

Author information




E.G.C.N. and A.J.G.Z. conceived and designed the experiments. E.G.C.N. performed the experiments. M.M.O. was responsible for the TEM images. M.L.B. and L.H.M.J. conceived and designed experiments related to the electrochemical sensor. A.J.G.Z. coordinated and supervised the project. All authors discussed the results and commented on the manuscript.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Electronic supplementary material

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Neiva, E., Oliveira, M., Bergamini, M. et al. One material, multiple functions: graphene/Ni(OH)2 thin films applied in batteries, electrochromism and sensors. Sci Rep 6, 33806 (2016).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing