Because of their exotic electronic properties and abundant active sites, two-dimensional (2D) materials have potential in various fields. Pursuing a general synthesis methodology of 2D materials and advancing it from the laboratory to industry is of great importance. This type of method should be low cost, rapid and highly efficient. Here, we report the high-yield synthesis of 2D metal oxides and hydroxides via a molten salts method. We obtained a high-yield of 2D ion-intercalated metal oxides and hydroxides, such as cation-intercalated manganese oxides (Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O), cation-intercalated tungsten oxides (Li2WO4 and Na2W4O13), and anion-intercalated metal hydroxides (Zn5(OH)8(NO3)2·2H2O and Cu2(OH)3NO3), with a large lateral size and nanometre thickness in a short time. Using 2D Na2W4O13 as an electrode, a high performance electrochemical supercapacitor is achieved. We anticipate that our method will enable new path to the high-yield synthesis of 2D materials for applications in energy-related fields and beyond.
Because of their thickness-dependent properties, two-dimensional (2D) atomic crystals are of great interest in various applications ranging from superconductors and field effect transistors to electrocatalysis and energy storage1,2,3,4,5,6,7,8. Current strategies for the synthesis of 2D materials primarily include exfoliation, chemical vapour deposition (CVD) and chemical synthesis9,10,11,12,13,14,15,16,17,18. Exfoliation is applied on layered compounds, such as graphene and MoS2, in which each layer is bonded by van der Waals forces9,19,20,21,22. Recently, Coleman et al. reported a shear exfoliation method for the scalable production of high-quality 2D materials9,21,22. Wu et al.23 also accomplished the mass production of oxide nanosheets by a rapid thermal annealing treatment of the hydrous-chloride compounds. However, the further centrifugation and sedimentation necessary to separate the unexfoliated bulk complicate the process, increase the cost and decrease the yield. The CVD method can obtain high-quality and large lateral size 2D materials, although the low yield of the CVD method confines its applications mainly to physics and optics10,11. High-yield chemical synthesis is widely studied in energy-related fields. Generally, a surfactant such as polyvinyl pyrrolidone (PVP) is used to guide the growth of 2D materials, however, the removal of these surfactants is time consuming and sometimes not completely successful. In addition, it should be noted that chemical synthesis usually requires a long amount of time, even several days, which is not favourable for practical applications12. Therefore, it is of crucial significance to develop a high-yield, efficient, fast and low-cost method to synthesize 2D materials.
Notably, ions always play a key role in the synthesis of 2D materials24,25,26,27,28. For example, Li+ ions are pre-intercalated into the interlayers of MoS2, increasing the interlayer distance and facilitating the exfoliation of the layered materials24,28. By contrast, for ion-intercalated 2D materials such as δ-MnO2 (birnessite), desolvated ions can serve as the template to induce the growth in the 2D plane25,26,27. Interestingly, these pre-intercalated desolvated ions are favourable for energy storage and show unique properties in optics29. However, it should be noted that when the synthesis process occurs in solution, desolvation is a necessary step because ions are in the solvated state in solution. In this context, according to the Arrhenius equation (ref. 30), the energy consumption for desolvation increases the overall activation energy, thus limiting the reaction rate. In addition, incompletely desolvated ions cause lattice distortion, which decreases the quality of 2D materials. Accordingly, we can reasonably assume that if naked ions can be directly involved in a synthesis process, the reaction limitation due to the desolvation of hydrated ions will be alleviated, which will greatly accelerate the reaction rate and enhance the quality of the generated 2D materials.
Herein, we report a general and rapid molten salts method (MSM) that can synthesize various ion-intercalated 2D metal oxides and hydroxides, such as cation-intercalated manganese oxides (Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O), cation-intercalated tungsten oxides (Li2WO4 and Na2W4O13), and anion-intercalated metal hydroxides (Zn5(OH)8(NO3)2·2H2O and Cu2(OH)3NO3). The MSM is widely studied for the synthesis of nanomaterials, such as graphene and perovskite, spinel and monoclinic oxides31,32,33,34. The key feature of our method is the direct use of naked ionized ions without hydration in the molten state salt to quickly induce the growth of 2D metal oxides and hydroxides. In our technique, by adding precursors into the low-cost molten salts for only 1 min, we could obtain high-yield 2D materials simply by washing the salts without centrifugation or sedimentation, and the productivity of Na0.55Mn2O4·1.5H2O reaches up to 62% (the method of calculating the productivity is shown in Supplementary Note 1).
Synthesis of 2D metal oxides and hydroxides
Salts are common ionic crystals that can ionize in the molten state. In our experiments, we typically started by heating the nitrate to the molten state in a muffle furnace and adding the precursor into it (Fig. 1a–c). Here, the ionized species from the molten salts rapidly react with the precursor to form the 2D structured materials, at which point an apparent expansion was observed in the mixture (this mixture contains 2D materials, recrystallized salts and by-products) (Fig. 1d, Supplementary Fig. 1 and Supplementary Movie 1). After cooling down and washing the salts via filtration, we could directly obtain the 2D materials (Fig. 1e) or disperse them in deionized water (DI water) for further applications. Figure 1f shows digital image of various 2D metal oxides and hydroxides dispersions. All of these 2D materials dispersed uniformly in DI water at a concentration of 0.2 mg ml−1. As shown in Fig. 1g, we tested the zeta potential of these dispersions. Cation-intercalated 2D metal oxides show negative zeta potentials, while anion-intercalated metal hydroxides have positive zeta potentials. The highest value of about −42 mV is achieved in Na2W4O13, and the smallest value is around −22 mV in K0.27MnO2·0.54H2O.
To explore the morphology and structure of these 2D materials, we conducted scanning electron microscopy (SEM) and transmission electron microscopy (TEM). As shown in Fig. 2a,e,i,m, 2D materials are clearly seen in the representative SEM images. All of them show 2D structures, but with different morphologies, which can also be seen in TEM images (Fig. 2b,f,j,n). Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O are very flexible and have apparent wrinkles, while Li2WO4 and Na2W4O13 seem to be stiff. However, they all display high transparency and have thicknesses less than 5 nm (Supplementary Figs 2 and 3). In addition, high-resolution TEM (HRTEM) and selected area electron diffraction (SAED) images demonstrate the crystallinity of these 2D materials (Fig. 2c,g,k,o). Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O are polycrystalline, while Li2WO4 and Na2W4O13 are single crystalline. Furthermore, we used energy dispersive X-ray spectroscopy (EDS, Supplementary Fig. 4), X-ray diffraction (XRD, Supplementary Fig. 5) and X-ray photoelectron spectroscopy (XPS, Supplementary Figs 6–8) to confirm the elemental composition and atomic structure. All of these 2D metal oxides show similar layered structures with cations intercalated into the interlayer (Fig. 2d,h,l,p, Supplementary Fig. 9). Na0.55Mn2O4·1.5H2O has a monoclinic structure (a=5.175 Å, b=2.849 Å and c=7.338 Å) with Na+ and crystal water filling the interlayer. The thickness of the monolayer is 7.3 Å, and the sample we synthesized has ∼2 layers (∼1.4 nm, Supplementary Fig. 2). K0.27MnO2·0.54H2O possesses a rhombohedral structure with a=2.849 Å, b=2.849 Å and c=21.536 Å. The sample thickness of about 1.4 nm (Supplementary Fig. 2) is ∼2 layers compared with the thickness of the monolayer (7.18 Å). Li2WO4 is a rhombohedral layered material with Li+ intercalated in the interlayer (a=14.361 Å, b=14.361 Å and c=9.603 Å) and a monolayer thickness of 4.80 Å. According to measurements using atomic force microscopy (AFM, Supplementary Fig. 3), the synthesized Li2WO4 is ∼9–10 layers in thickness. Na2W4O13, however, has a different atomic structure than Li2WO4. It has an anorthic structure (a=8.381 Å, b=8.162 Å and c=3.87 Å) with a monolayer thickness of 4.19 Å. We tested the thickness of Na2W4O13 and found that it was approximately 3.79 nm, which is ∼9 layers (Supplementary Fig. 3).
Analogous to cations in cation-intercalated metal oxides, anions such as NO3− can also be used as the template to induce the synthesis of anion-intercalated metal hydroxides. Here, we used the MSM to successfully synthesize 2D NO3−-intercalated Zn hydroxide and Cu hydroxide. As shown in SEM and TEM images (Fig. 3a,b,e,f), they both exhibited typical 2D structures. In addition, HRTEM and SAED (Fig. 3c,g) demonstrated the high crystallinity of the as-synthesized anion-intercalated metal hydroxides. The atomic structures were confirmed by XRD, as shown in Fig. 3d,h and Supplementary Figs 10 and 11. Zn5(OH)8(NO3)2·2H2O has a monoclinic structure with a=19.48 Å, b=6.238 Å and c=5.517 Å. NO3− and crystal water occupied the interlayer with a monolayer thickness of 9.74 Å. Hence, the as-synthesized Zn5(OH)8(NO3)2·2H2O is ∼2 layers thick (about 2 nm) (Supplementary Fig. 12). Cu2(OH)3NO3 is also monoclinic with a=5.605 Å, b=6.087 Å and c=6.929 Å. The monolayer thickness is 6.93 Å, which suggests that our synthesized 2D Cu2(OH)3NO3 has approximately five layers (Supplementary Fig. 13).
We then examined the growth mechanism of our MSM for 2D ion-intercalated metal oxides and hydroxides. As we previously mentioned, all of these layer-like 2D metal oxides and hydroxides have similar atomic structures in which ions intercalate in the interlayer. Hence, we proposed that here, the ions play a key role in the synthesis process25,26,35,36. The formation of 2D layered metal oxides and hydroxides consists of two steps (Fig. 4). The first step is the nucleation of [MOx]octahedron or [M(OH)x]polyhedron seeds (M represents metal ion, x is the number of oxygen atoms), and the second step is the growth of crystal based on the assembly of these [MOx]octahedron or [M(OH)x]polyhedron seeds influenced by the ions from the molten salts (Fig. 4). For the synthesis of 2D Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O, [MnO6]octahedron will be formed via the following redox reaction (equation (1)) in the first step (y is the number of NO3− ions):
Then, these [MnO6]octahedron seeds assemble into a 2D plane with the cations and H2O molecules (H2O originates from the atmosphere; see details in Supplementary Note 2 and in Supplementary Fig. 14) intercalated into the interlayer to balance the charge and stabilize the layered structure25,26 and formed the 2D ion-intercalated metal oxides (Supplementary Fig. 15) according to equations (2) and (3):
For the formation of 2D Zn5(OH)8(NO3)2·2H2O, Zn2+ ions first react with H2O to form [Zn(OH)6]octahedron and [Zn(OH)4]tetrahedron via a hydrolysis reaction (equation (4), m is the number of H2O). Then, the [Zn(OH)6]octahedron and [Zn(OH)4]tetrahedron seeds assemble into a 2D plane with the anions and H2O molecules intercalated into the interlayer, which balances the charge and stabilizes the layered structure (equation (5) and Supplementary Fig. 16)37,38,39. The formation of 2D Cu2(OH)3NO3 occurs via a similar process, as shown in equations (6) and (7) and Supplementary Fig. 17.
Now, we discuss why only 2D morphology, not one-dimensional (1D) or three-dimensional (3D) morphologies, was obtained in this study. Here, we further explain the example of birnessite (K0.27MnO2·0.54H2O) in detail. MnO2 exists as various types of crystal structures, such as α, β, γ and δ phases, all of which can be considered as kinetically stable phases. It is agreed that birnessite-type MnO2 is the kinetically favoured product and is always formed first, while tunnelled-structure MnO2 species, such as α phase and β phase, are the thermodynamically favoured products and can be formed from δ-MnO2 (ref. 40). After the reaction time was extended to 10 min, the crystal structure and 2D morphology features of δ-MnO2 remain unchanged (Supplementary Fig. 18). Hence, 2D ion-intercalated MnO2 is stable under the reaction conditions in this work.
Compared to previously reported hydrothermal syntheses of birnessite26,35, there are two obvious differences in our method: relatively higher temperature (∼350 °C) and ionized species (without hydration). Generally, the reaction temperature and the ion state can directly influence the morphology of the products. Thus, we discuss the influence of these two factors on the morphology of the 2D materials in detail. First, we determined the relationship between reaction temperature (K) and reaction rate constant (ka and kb, which represent the reaction rate constant in growth direction  (thickness) and  (lateral size), respectively). In a typical 2D structured material, the reaction rate constant in different growth directions determines the thickness and lateral size.
where Ea and Eb are the activation energy in different growth directions (J mol−1), R is the molar gas constant (8.314 J mol−1 K−1) and T is the reaction temperature (K). According to equation (8), if we only increase the reaction temperature, the value of kb/ka will decrease (see details in Supplementary Note 4), signifying that the thickness of 2D δ-MnO2 increases faster than the lateral size increases. Thus, a large lateral size with a subnanometer thickness cannot be obtained, which is not consistent with our experimental results, as shown in Figs 2 and 3. Hence, we could exclude the temperature as the main factor.
Second, we compared the activation energy along the  direction in our method (Eb′) to that in ref. 41 (Eb) (see details in Supplementary Note 5): Eb−Eb′=23.9–32.0 kJ mol−1. As the total hydration energy of K+ is −312.2 kJ mol−1 (that is, a fully hydrated K+ ion requires 312.2 kJ mol−1 of energy to form a naked ion; see details in Supplementary Note 6), the K+ number is 0.27 in our work, thus, the dehydration energy is ∼84.3 kJ mol−1 for the sample of K0.27MnO2·0.54H2O. Considering that the dehydration process does not go to completion in the hydrothermal system, this value has the same order of magnitude as the value of (Eb−Eb′), for example, the actual dehydration energy would be lower than 84.3 kJ mol−1. Accordingly, it is reasonable that the ionized species in our method affect the size of the 2D materials by accelerating the reaction rate (do not need the dehydration process).
In addition, we also noted that the type of ion is important for the synthesis of 2D birnessite. Other types of ion-intercalated 2D manganese oxides can be obtained by choosing the appropriate molten salts, that is, those beyond NaNO3 and KNO3. By using MnSO4 as the precursor, 2D Cs4Mn14O27·xH2O and 2D Ba2Mn14O27·xH2O can be synthesized from the molten salts of CsNO3 and Ba(NO3)2 (Supplementary Fig. 19), respectively. However, if we use LiNO3 as the molten salt, β-MnO2 nanowires instead of 2D nanosheets will be obtained (Supplementary Fig. 20). This is maybe because the radius size of the desolvated Li+ is too small to support the interlayer of birnessite (about 0.7 nm), which demonstrates that the template effect of ions is of great importance to the synthesis of 2D materials26,27.
Applications of 2D Na2W4O13
Because of the large interlayer spacing of these 2D materials, the ions could easily diffuse in or out, which is beneficial for energy storage application. Moreover, 2D morphologies have a quite large specific surface area (Supplementary Fig. 21, Supplementary Table 1) that can provide more active sites. Here, we investigate the electrochemical properties of 2D Na2W4O13 as an example (Supplementary Figs. 22,23 and Supplementary Note 7). First, we used a three-electrode configuration in Swagelok cell to test electrochemical performance. An electrode was fabricated by vacuum-filtrating the 2D Na2W4O13 dispersion onto a Celgard film. The thickness of the film was ∼1 μm (inset of Supplementary Fig. 22b). The Na2W4O13 electrode has excellent wetting behaviour (Supplementary Fig. 24), which provides favourable contact with the electrolyte (0.5 mol l−1 Na2SO4 solution). The restacked 2D Na2W4O13 was tested as a positive electrode and revealed typical pseudocapacitive behaviour, as shown in cyclic voltammetry (CV) curves at sweep rates ranging from 5 to 100 mV s−1 (Supplementary Fig. 22a). The largest volumetric capacitance is ∼310 F cm−3 at 5 mV s−1, whereas 200 F cm−3 is still obtained at 100 mV s−1, thus showing a good rate capability. Moreover, the restacked 2D Na2W4O13 electrode demonstrated good stability since after 10,000 cycles at 10 mV s−1, the capacitance still remained at 93% of its initial value (Supplementary Fig. 22c).
In addition, the 2D Na2W4O13 dispersion is uniform enough that the colloidal state of the dispersion was demonstrated by an obvious Tyndall effect (Supplementary Fig. 25a). This dispersion is very suitable for printable electronics. Accordingly, we fabricated a flexible paper-based electrode by coating the 2D Na2W4O13 dispersion on A4 paper. First, we used the Mayer rod method42 to coat a uniform CNT layer onto the A4 paper, as a current collector (Fig. 5a). Then, the 2D Na2W4O13 dispersion was coated onto the A4 paper@CNT by the same process (Fig. 5b). Finally, we obtained the flexible A4 paper@CNT@Na2W4O13 electrode, as shown in Fig. 5c,d. The resistivity of the electrode was also measured to be 52.88 Ω, as shown in Supplementary Fig. 25b. The structure schematic of the solid-state SC is illustrated in Fig. 5e. Two A4 paper@CNT@Na2W4O13 electrodes were sandwiched by a Celgard film and a H3PO4/Polyvinyl Alcohol (PVA) solid-state electrolyte, which resulted in a flexible solid-state supercapacitor (Fig. 5f). According to the CV curves at different sweep rates, this solid-state supercapacitor worked at a stable voltage window from 0 to 0.8 V with typical capacitive behaviour. Even at a high sweep rate of 100 mV s−1, only a little distortion could be seen in the CV curve, implying a high ion and electron transport rate (Fig. 5g). Similar to the results from the three-electrode configuration, the solid-state supercapacitor also shows an excellent rate capability as 69% of the initial volumetric capacitance was maintained from 5 to 100 mV s−1 (Supplementary Fig. 26). In addition, comparing the CV curves of the A4 paper@CNT electrodes to those of the A4 paper@CNT@Na2W4O13 electrodes under the same sweep rates (Supplementary Fig. 27) suggested very little capacitance contribution from the CNT substrate. The power and energy density are summarized in a Ragone plot, as shown in Fig. 5h. The highest energy density is 3.83 mWh cm−3 (1.33 Wh kg−1) with a power density of 1.2 W cm−3 (598.4 W kg−1) (Supplementary Fig. 28 and Supplementary Note 8), comparable to those of a 4 V/500 μAh Li thin-film battery and WO3@MoO3-ASCs and much higher than those of VOx/VN-ASCs and an Al electrolytic capacitor43,44,45. Furthermore, we connected four solid-state supercapacitors in series to expand the working voltage window to 3.2 V, as shown in Fig. 5i. After being fully charged, the energy pack could power a commercial red light-emitting-diode (LED, inset of Fig. 5f), revealing the potential applications of the supercapacitors in wearable and portable electronics.
Ion-intercalated tungsten oxide is also a good candidate for ion adsorption. Therefore, we tested the ion adsorption ability of 2D Na2W4O13 in solution. As shown in Supplementary Fig. 29, 2D Na2W4O13 demonstrated an obvious adsorption of Mg2+, Cd2+, Ca2+ and Pb2+.
To promote the translation of 2D materials from the laboratory to industry, pursuing a high-efficiency and low-cost synthesis is of great importance. Our MSM was inspired by the low cost of the salts we used, as well as the fact that ionized species naturally exist in the molten state salts and can rapidly induce the growth of 2D materials. Although a certain temperature of 300–400 °C is required, the whole reaction time is just 1 min due to fast ion transport, which decreases the cost. Importantly, we have calculated the productivity of Na0.55Mn2O4·1.5H2O to be as high as 62%. In addition, the final mixtures consist of the targeted products (2D materials), unreacted precursors and other salts. The 2D materials can be easily separated from the other species by rinsing the mixtures with DI water. Even without centrifugation or sedimentation, we do not observe particles or nanowires in the final products (SEM images in Figs 2 and 3). This could dramatically simplify the process which is preferable for commercialization. Although we only reported eight 2D ion-intercalated metal oxides and hydroxides, the versatility of this molten salt synthesis process gives us confidence that reasonably tuning the precursors and molten salts will allow various 2D oxides and hydroxides to be synthesized and the scope of the accessible oxides and hydroxides to expand to other 2D materials with attractive properties.
In conclusion, we have reported a rapid mass production molten salts method that can rapidly provide 2D ion-intercalated metal oxides and hydroxides. The ionized species in the molten salts were directly involved in the reaction with the precursors, guiding the growth of the 2D structures within only 1 min. The as-synthesized 2D metal oxides and hydroxides have a large lateral size with an atomic scale thickness. When used as supercapacitor electrodes, these oxides and hydroxides can be fabricated into a flexible solid-state supercapacitor based on A4 paper@CNT@Na2W4O13 electrodes. These show good electrochemical performance with an excellent rate capability, demonstrating the potential applications of these 2D ion-intercalated metal oxides and hydroxides in energy storage and beyond.
Synthesis of 2D Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O
The 2D Na0.55Mn2O4·1.5H2O and K0.27MnO2·0.54H2O were synthesized by the MSM. Typically, 5 g of nitrate powder was added into a crucible and transferred to the muffle furnace at a temperature of 350 °C (for sodium nitrate, NaNO3) or 380 °C (for potassium nitrate, KNO3) for ∼10 min. As the nitrate became molten, 0.2 g of manganese sulfate (MnSO4) powder was added into the molten salt for 1 min. Then, the product was removed from the muffle furnace and cooled to room temperature under ambient conditions. Finally, the product was washed with DI water to remove NaNO3 or KNO3.
Synthesis of 2D Li2WO4 and Na2W4O13
The 2D Li2WO4 and Na2W4O13 were synthesized by the MSM. Typically, 5 g of nitrate powder was added into a crucible and transferred to the muffle furnace at a temperature of 420 °C (for lithium nitrate, LiNO3) or 350 °C (for NaNO3) for approximately 10 min. As the nitrate became molten, 0.2 g of ammonium tungstate hydrate (H40N10O41W12·xH2O) powder was added into the molten salt for 1 min. Then, the product was removed from the muffle furnace and cooled to room temperature. Finally, the product was washed with DI water to remove LiNO3 or NaNO3.
Synthesis of 2D Zn5(OH)8(NO3)2·2H2O
The 2D Zn5(OH)8(NO3)2·2H2O was synthesized by the MSM. Typically, 5 g of KNO3 was added into a crucible and transferred to the muffle furnace at a temperature of 380 °C for ∼10 min. As the KNO3 became molten, 0.2 g zinc chloride (ZnCl2) powder was added into the molten salt for 1 min. Then, the product was removed from the muffle furnace and cooled to room temperature. Finally, the product was washed by DI water to remove KNO3.
Synthesis of 2D Cu2(OH)3NO3
The 2D Cu2(OH)3NO3 was synthesized by MSM. Typically, 5 g KNO3 was added into the crucible and transferred to the muffle furnace with a temperature of 380 °C for ∼10 min. As the KNO3 became the molten state, 0.2 g copper nitrate trihydrate powder (Cu(NO3)2·3H2O) was added into the molten salt for 1 min. Then, the product was removed from muffle furnace and cooled to room temperature. Finally, the product was washed with DI water to remove KNO3.
Fabrication of aqueous and solid-state devices for electrochemical tests
We used a typical three-electrode configuration in Swagelok cells (Swagelok, USA) for aqueous electrolyte testing. In this setup, YP-50 (Kuraray, Japan) was the counter electrode, Ag/AgCl (CHI, USA) was the reference electrode, 0.5 mol l−1 Na2SO4 solution was the electrolyte and a Celgard film served as the separator (Celgard, USA). The electrode was prepared by vacuum filtering the Na2W4O13 suspension (1 mg ml−1) on a Celgard film with a loading mass of 0.31 mg cm−2. The thickness of the Na2W4O13 film was 1 μm. The CNT ink was prepared by probe-sonicating 50 ml of a CNT (5 mg l−1) and sodium dodecylbenzenesulfonate (0.1 mg l−1) dispersion for 20 min. Na2W4O13 suspension (1 mg l−1) was prepared using a similar probe-sonication method. After coating the CNT ink and Na2W4O13 suspension on A4 paper separately, the SC electrode was prepared successfully. H3PO4/PVA gel electrolyte was fabricated by mixing 6 g of H3PO4 and 6 g of PVA powder with 60 ml DI water. The mixture was heated to 85 °C under vigorous stirring. The solid-state device was fabricated in two steps. First, two A4 paper@CNT@Na2W4O13 electrodes were dipped into H3PO4/PVA gel electrolyte for 5 min and sandwiched with a Celgard film as separator. Second, after drying at room temperature for 24 h, the solid-state device was successfully assembled. The mass loading of Na2W4O13 on the A4 paper@CNT was 1.2 mg cm−2. The thickness of the Na2W4O13 film was 6 μm. All of the electrochemical tests were carried out using EC-Lab and CHI660E, and electrochemical impedance was measured with a potential amplitude of 10 mV from 1 to 1 MHz.
X-ray diffraction (XRD, X’Pert Pro, PANalytical) was used to determine the crystal structure and stoichiometric ratio of the 2D materials, and X-ray photoelectron spectroscopy (XPS, ESCALab 250), field-emission scanning electron microscopy (FE-SEM, FEI Nova 450 Nano), transmission electron microscopy with energy dispersive X-ray spectroscopy (Tecnai G2 20 U-Twin and Titan G2 60-300), and atomic force microscopy (AFM, Shimadzu) were used to explore the structure and morphology of the samples. Zeta potential was measured using a Zetasizer (Nano ZSP, Malvern Instruments Limited, UK). N2 adsorption-desorption isotherms were measured on a Micrometrics ASAP 2000 to confirm the specific surface area. An SL200B contact angle metre (Kino Industry, USA) was employed to measure the surface wettability with electrolyte. The mass loading of the electrode was measured by a microbalance (CPA225D, Sartorius).
The authors declare that the data supporting the findings of this study are available within the paper.
How to cite this article: Hu, Z. et al. Rapid mass production of two-dimensional metal oxides and hydroxides via the molten salts method. Nat. Commun. 8, 15630 doi: 10.1038/ncomms15630 (2017).
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This work was supported by the National Natural Science Foundation of China (grants 51322210, 51672097, 61434001 and 51602115) and the National Program for Support of Top-notch Young Professionals and Director Fund of WNLO. We wish to thank M.H. Wu for helpful discussion on atomic structure. We also wish to acknowledge facility support from the Center for Nanoscale Characterization & Devices, WNLO of Huazhong University of Science and Technology (HUST) and the Analytical and Testing Center of HUST.
Process for synthesis of two-dimensional metal oxides and hydroxides via the molten salts method
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N-doped mesoporous carbon integrated on carbon cloth for flexible supercapacitors with remarkable performance
Journal of Materials Science (2018)