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Efficient hydrogen production on MoNi4 electrocatalysts with fast water dissociation kinetics

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Various platinum-free electrocatalysts have been explored for hydrogen evolution reaction in acidic solutions. However, in economical water-alkali electrolysers, sluggish water dissociation kinetics (Volmer step) on platinum-free electrocatalysts results in poor hydrogen-production activities. Here we report a MoNi4 electrocatalyst supported by MoO2 cuboids on nickel foam (MoNi4/MoO2@Ni), which is constructed by controlling the outward diffusion of nickel atoms on annealing precursor NiMoO4 cuboids on nickel foam. Experimental and theoretical results confirm that a rapid Tafel-step-decided hydrogen evolution proceeds on MoNi4 electrocatalyst. As a result, the MoNi4 electrocatalyst exhibits zero onset overpotential, an overpotential of 15 mV at 10 mA cm−2 and a low Tafel slope of 30 mV per decade in 1 M potassium hydroxide electrolyte, which are comparable to the results for platinum and superior to those for state-of-the-art platinum-free electrocatalysts. Benefiting from its scalable preparation and stability, the MoNi4 electrocatalyst is promising for practical water-alkali electrolysers.


Growing concern about the energy crisis and the seriousness of environmental contamination urgently demand the development of renewable energy sources as feasible alternatives to diminishing fossil fuels. Owing to its high energy density and environmentally friendly characteristics, molecular hydrogen is an attractive and promising energy carrier to meet future global energy demands1,2. In many of the approaches to hydrogen production, the electrocatalytic hydrogen evolution reaction (HER) from water splitting is the most economical and effective route for the future hydrogen economy3,4,5,6. To accelerate the sluggish HER kinetics, particularly in alkaline electrolytes, highly active and durable electrocatalysts are essential to lower the kinetic HER overpotential7,8. As a benchmark HER electrocatalyst with a zero HER overpotential, the precious metal platinum (Pt) plays a dominant role in present H2-production technologies, such as water-alkali electrolysers9,10,11. Unfortunately, the scarcity and high cost of Pt seriously impede its large-scale applications in electrocatalytic HERs.

To develop efficient and earth-abundant alternatives to Pt as HER electrocatalysts, great efforts have been made to understand the fundamental HER mechanisms on the surfaces of electrocatalysts in alkaline environments12,13. The HER kinetics in alkaline solutions involves two steps: electron-coupled water dissociation (the Volmer step for the formation of adsorbed hydrogen); and the concomitant combination of adsorbed hydrogen into molecular hydrogen (the Heyrovsky or Tafel step; Supplementary Note 1)12,14. Accordingly, the HER activity of an electrocatalyst in alkaline electrolytes is synergistically dominated by the prior Volmer step and subsequent Tafel step13. The low energy barrier (ΔG(H2O)=0.44 eV) of the Volmer step provides the Pt catalyst with a fast Tafel step-determined HER process (Tafel slop=30 mV per decade) in alkaline electrolytes, which is responsible for its excellent HER activity12,15. Inspired by the fundamental HER mechanism that occurs on Pt, the development of novel Pt-free electrocatalysts with a significantly accelerated Volmer step is an appealing approach. Recently, several electrocatalysts with a decreased HER overpotential, such as CoP/S (with an overpotential at 10 mA cm−2: 48 mV) and Mo2C/graphene (with an overpotential at 10 mA cm−2: 34 mV) have been reported in acidic solutions16,17. Nevertheless, under alkaline conditions, the sluggish Volmer step on these Pt-free electrocatalysts results in far lower HER activity than the Pt catalyst18,19,20,21.

In past decades, various Ni- or Mo-based oxides, hydroxides, layered double hydroxides, phosphides and sulfides have been reported as electrocatalysts for water splitting. Ni atoms are broadly recognized as excellent water dissociation centres, while Mo atoms have superior adsorption properties towards hydrogen13,22,23,24. Therefore, Mo–Ni-based alloy electrocatalysts (MoxNiy) can be promising candidates to effectively reduce the energy barrier of the Volmer step and speed up the sluggish HER kinetics under alkaline conditions. In this study, we demonstrate a MoNi4 electrocatalyst anchored on MoO2 cuboids, which are vertically aligned on nickel foam (MoNi4/MoO2@Ni). MoNi4 nanoparticles with a size of 20–100 nm are constructed in situ on the MoO2 cuboids by controlling the outward diffusion of Ni atoms when previously synthesized NiMoO4 cuboids are heated in a H2/Ar (v/v, 5/95) atmosphere at 500 °C. The resultant MoNi4/MoO2@Ni exhibits a high HER activity with a zero onset overpotential and a low Tafel slope of 30 mV per decade in a 1 M KOH aqueous solution, which are highly comparable to those for the Pt catalyst (onset overpotential: 0 mV; Tafel slope: 32 mV per decade). In addition, the achieved MoNi4 electrocatalyst requires low overpotentials of only 15 and 44 mV to stably deliver cathodic current densities of 10 and 200 mA cm−2, respectively, presenting state-of-the-art HER activity amongst all reported Pt-free electrocatalysts7,10,18. Experimental investigations reveal that the MoNi4 electrocatalyst behaves as the highly active centre and manifests fast Tafel step-determined HER kinetics. Furthermore, density functional theory (DFT) calculations determine that the kinetic energy barrier of the Volmer step for the MoNi4 electrocatalyst is as low as 0.39 eV. These results confirm that the sluggish Volmer step is drastically accelerated for the MoNi4 electrocatalyst.


Synthesis of the MoNi4 electrocatalyst

The synthesis of the MoNi4 electrocatalyst involves two steps, as illustrated in Fig. 1. First, the NiMoO4 cuboids were grown beforehand on a piece of nickel foam (1 × 3 cm2) via a hydrothermal reaction at 150 °C for 6 h in 15 ml of deionized water containing Ni(NO3)2·6H2O (0.04 M) and (NH4)6Mo7O24·4H2O (0.01 M). Second, when the as-synthesized NiMoO4 cuboids were calcined in a H2/Ar (v/v, 5/95) atmosphere at 500 °C for 2 h, the inner Ni atoms diffused outward due to the formation of MoO2. As a result, MoNi4 nanoparticles were directly constructed on the surfaces of the MoO2 cuboids. To probe the formation mechanism of the MoNi4 nanoparticles, different calcination temperatures and times were investigated (Supplementary Figs 1–5). In comparison with the smooth surfaces of precursor NiMoO4 at 400 °C, the appearance of numerous surface nanoparticles at 500 °C indicated the formation of MoNi4 on the resulting MoO2 cuboids (Supplementary Fig. 1a,b). When the calcination temperature reached 600 °C, MoNi3 nanoparticles on the MoO2 cuboids (MoNi3/MoO2@Ni) were produced due to the continuous reduction of MoO2 (Supplementary Fig. 1c,d). In addition, with increased calcination time at 500 °C, the MoNi4 nanoparticles gradually emerged and grew into bulk particles on the MoO2 cuboids (Supplementary Figs 2–5).

Figure 1: Synthetic scheme of MoNi4 electrocatalyst supported by the MoO2 cuboids on nickel foam.
Figure 1

Synthetic scheme of MoNi4 electrocatalyst supported by the MoO2 cuboids on nickel foam. Scale bars, Ni foam, 20 μm (top) and 1 μm (bottom); NiMoO4/Ni foam, 10 μm (top) and 2 μm (bottom); MoNi4/MoO2/Ni foam, 20 μm (top) and 1 μm (bottom).

Structural characterizations of the MoNi4 electrocatalyst

X-ray diffraction characterization reveals that the crystalline structure of the as-obtained precursor on the Ni foam can be indexed to NiMoO4 (Supplementary Fig. 6). The morphology of NiMoO4 was scrutinized by scanning electron microscopy (SEM). As shown in Supplementary Figs 7 and 8, dense NiMoO4 cuboids with sizes in the range of 0.5–1.0 μm and lengths of tens of microns are vertically aligned on the nickel foam. Elemental mapping, energy dispersive spectroscopy and X-ray photoelectron spectroscopy (XPS) confirm that the NiMoO4 cuboids consist of Ni, Mo and O elements, and the molar ratio of Ni to Mo is 1:1.01 (Supplementary Figs 9 and 10).

The product of the NiMoO4 cuboids on the Ni foam calcined at 500 °C for 2 h was surveyed with X-ray diffraction using Cu-Kα radiation, SEM and high-resolution transmission electron microscopy (HRTEM). In Supplementary Fig. 11, the sharp X-ray diffraction diffraction peaks at 44.6°, 52.0° and 76.5° originate from the Ni foam (JCPDS, No. 65–2865). The peaks located at 26.3°, 37.0°, 41.5°, 49.5°, 53.7°, 60.5° and 66.9° are indexed to metallic MoO2 (JCPDS, No. 32-0671). The appearance of peaks at 31.0° and 43.5° are assigned to the (200) and (121) facets of MoNi4 (JCPDS, No. 65–5480), respectively. Thus, these result suggest that the obtained product on the nickel foam consists of MoNi4 and MoO2. As shown in Fig. 2a–c, numerous nanoparticles with sizes in the range of 20–100 nm are uniformly anchored on the cuboids, which are vertically aligned on the nickel foam. The corresponding energy-dispersive X-ray spectroscopy (EDX) analysis further confirms that the products are composed of Mo, Ni and O, and the molar ratio of Mo to Ni is 1:1.3 (Supplementary Fig. 12). Clearly, the HRTEM images of the samples show lattice fringes with lattice distances of 0.35 and 0.28 nm, which correspond to the (110) facet of MoO2 and the (200) facet of MoNi4, respectively (Fig. 2d–f). The selected-area electron diffraction pattern shows diffraction patterns of the (200) facet of MoNi4 and the (110) facet of MoO2 (the inset in Fig. 2d). Noticeably, the scanning TEM–EDX characterizations indicate that the surface nanoparticles are constituted by only Mo and Ni with an atomic ratio of 1:3.84, which well approaches to 1:4 (Fig. 2g and Supplementary Fig. 13). The XPS analysis was carried out to probe the chemical compositions and surface valence states of the MoNi4 nanoparticles and the supporting MoO2 cuboids. As illustrated in Supplementary Fig. 14, the XPS spectrum confirms the presence of Mo, Ni and O, and the molar ratio of Mo to Ni is 1:1.1. As shown in Supplementary Figs 15–17, XPS peaks of metallic Mo0 and Ni0 are observed at 229.3 and 852.5 eV, respectively, further confirming the existence of Mo0 and Ni0 in the surfaces of MoNi4/MoO2@Ni.

Figure 2: Morphology and chemical composition analyses of MoNi4/MoO2@Ni.
Figure 2

(ac) Typical SEM and (df) HRTEM images of MoNi4/MoO2@Ni; (g) corresponding elemental mapping images of the MoNi4 electrocatalyst and the MoO2 cuboids. The inset image in d is the related selected-area electron diffraction pattern of the MoNi4 electrocatalyst and the MoO2 cuboids. Scale bars, (a) 20 μm; (b) 1 μm; (c) 100 nm; (df) 2 nm; inset in d, 1 1/nm; (g) 20 nm.

Electrocatalytic HER performance

To evaluate the electrocatalytic HER activities of the electrocatalysts, a three-electrode system in an Ar-saturated 1 M KOH aqueous solution was used using a Hg/HgO electrode and a graphite rod as the reference and counter electrodes, respectively (Supplementary Fig. 18). All potentials are referenced to the reversible hydrogen electrode (RHE), and the ohmic potential drop loss from the electrolyte resistance has been subtracted (Supplementary Figs 19 and 20). For comparison, pure Ni nanosheets and MoO2 cuboids were also prepared on the nickel foam using the hydrothermal reactions (Supplementary Figs 21–25). As displayed in Fig. 3a and Supplementary Fig. 26, a commercial Pt/C electrocatalyst deposited on the nickel foam (weight density: 1 mg cm−2) using Nafion as a binder exhibited a zero HER onset overpotential and delivered a current density of 10 mV cm−2 at an overpotential of 10 mV. However, the maximum current density only reached 80 mA cm−2 due to the Pt catalyst significantly peeling off from the support, caused by the generated H2 bubbles. Although the Ni nanosheets on the nickel foam could act as an HER electrocatalyst, the HER occurred at a very high overpotential of 253 mV. For the MoO2 cuboids on the nickel foam, the cathodic current density of 10 mA cm−2 was delivered at an overpotential as large as 48 mV. In comparison to the Ni nanosheets and the MoO2 cuboids, the NiMoO4 cuboids and MoNi3/MoO2 cuboids on the nickel foam exhibited a similar onset overpotential of 10 mV and an overpotential of 30 and 37 mV at 10 mA cm−2, respectively (Supplementary Figs 27–29). Remarkably, MoNi4/MoO2@Ni exhibited an onset overpotential of 0 mV, which was highly comparable to that of the Pt catalyst. In addition, for the supported MoNi4 electrocatalyst, the overpotential at current densities of 10 and 200 mA cm−2 was as low as 15 and 44 mV, respectively, which were significantly lower than the values for the Ni nanosheets, MoO2 cuboids, NiMoO4 cuboids, MoNi3/MoO2 cuboids and state-of-the-art Pt-free HER electrocatalysts such as NiO/Ni heterostructures (85 mV at 10 mA cm−2)25, pyrite-type CoPS nanowires (48 mV at 10 mA cm−2)16, nickel doped carbon (34 mV at 10 mA cm−2)26, a Mo2C/carbon/graphene hybrid (34 mV at 10 mA cm−2)17, MoSSe/NiSe2 foam (69 mV at 10 mA cm−2)27, Fe0.9Co0.1S2/carbon nanotubes (100 mV at 10 mA cm−2)28, Ni2P nanoparticles (120 mV at 10 mA cm−2)29 and strained MoS2 nanosheets (170 mV at 10 mA cm−2)30 (Supplementary Table 1)31,32,33,34,35,36,37,38,39.

Figure 3: Electrocatalytic activities of different catalysts.
Figure 3

(a) Polarization curves and (b) Tafel plots of the MoNi4 electrocatalyst supported by the MoO2 cuboids, pure Ni nanosheets and MoO2 cuboids on the nickel foam. (c) Comparison with selected state-of-the-art HER electrocatalysts. (d) Polarization curves of the MoNi4 electrocatalyst before and after 2,000 cyclic voltammetry cycles; inset: long-term stability tests of the MoNi4 electrocatalyst at different current densities: 10; 100; and 200 mA cm−2. Electrolyte: 1 M KOH aqueous solution; scan rate: 1 mV s−1.

Figure 3b displays the Tafel plots of the corresponding polarization curves, which provide profound insights into the fundamental HER kinetic mechanism occurring on the surfaces of the electrocatalysts. As a result of the low energy barrier (0.44 eV on Pt) of the Volmer step, the kinetic rate-limiting step for the Pt catalyst is the Tafel process, and the theoretical Tafel slope is 30 mV per decade (here the Tafel slope of the commercial Pt catalyst was measured to be 32 mV per decade)12. Remarkably, the Tafel slope of the MoNi4 electrocatalyst was as low as 30 mV per decade, which is far lower than the values of 129 mV per decade for the Ni nanosheets and 75 mV per decade for the MoO2 cuboids and highly comparable to that of the Pt-based catalyst (Fig. 3c and Supplementary Table 1). This result indicated that the electrocatalytic HER kinetics on the MoNi4 electrocatalyst were determined by the Tafel step rather than a coupled Volmer–Tafel or Volmer–Heyrovsky process. In other words, the prior Volmer step has been significantly accelerated. The exchange current density of the MoNi4 electrocatalyst was estimated to be 1.24 mA cm−2 (Supplementary Fig. 30). To clarify the influence of the active surface area on the electrocatalytic HER activity, the corresponding electrochemical double-layer capacitances (Cps) of the electrocatalysts were analysed by applying cyclic voltammetry cycles at different scan rates40. The Cps of the Ni nanosheets and MoO2 cuboids were 0.001 and 0.640 F, respectively, while the MoNi4 electrocatalyst had a high Cp of 2.220 F (Supplementary Fig. 31). On the basis of its Cp, the MoNi4 electrocatalyst was calculated to have a turnover frequency of 0.4 s−1 at a low overpotential of 50 mV, which was higher than the turnover frequency values of the previously reported Pt-free electrocatalysts (Supplementary Fig. 32 and Supplementary Table 1)41,42,43,44.

Long-term electrocatalytic stability is another important criterion for HER electrocatalysts. To investigate the durability of the MoNi4 electrocatalyst, continuous cyclic voltammetry scans were performed between 0.2 and −0.2 V at a scan rate of 50 mV s−1 in a 1 M KOH solution. As depicted in Fig. 3d, the HER overpotential of the MoNi4 electrocatalyst at 200 mA cm−2 increased by only 6 mV after 2,000 cyclic voltammetry cycles. In addition, a long-term electrocatalytic HER process was successively carried out at current densities of 10, 100 and 200 mA cm−2 (Supplementary Movie 1). The inset in Fig. 3d demonstrates that the MoNi4 electrocatalyst retained a steady HER activity, and only an increase of 3 mV in potential was observed at a current density of 10 mA cm−2 after a period of 10 h of hydrogen production. The overpotential required for large current densities of 100 and 200 mA cm−2 was augmented by only 2 and 5 mV, respectively. After a series of HER durability assessments, the structure of the MoNi4 electrocatalyst was examined using SEM and HRTEM. MoNi4/MoO2@Ni showed no structural variations, highlighting the superior structural robustness of the MoNi4 electrocatalyst during the electrocatalytic HER process (Supplementary Figs 33–36).

The approach to the synthesis of MoNi4/MoO2@Ni is scalable on the nickel foam. The MoNi4 electrocatalyst was thus prepared on commercially available nickel foam with dimensions of 6 × 20 cm2. As shown in Supplementary Fig. 37, the MoNi4 electrocatalyst supported by the MoO2 cuboids on the nickel foam was free-standing and highly flexible. It is notable that the MoNi4 electrocatalyst unveiled a steady HER activity even though the supporting Ni foam was deformed to various degrees (Supplementary Fig. 38). For reported Raney nickel and nickel–molybdenum alloy electrodes, concentrated alkaline solutions (30 wt%) and high electrolyte temperatures (70 °C) are generally demanded to achieve high cathodic current densities of 200–500 mA cm−2 (ref. 45). Here high cathodic current densities of up to 200 and 500 mA cm−2 were delivered by the MoNi4 electrocatalyst at extremely low overpotentials of 44 and 65 mV in a 5.3 wt% KOH solution at room temperature.

Afterward, a water-alkali electrolyser was built up in a 1 M KOH solution using MoNi4/MoO2@Ni as the cathode and a previously reported MoS2/Ni3S2 hybrid as the anode (Supplementary Fig. 39)38. As exhibited in Supplementary Fig. 40a, for a noble metal-based Pt–Ir/C couple, a cell voltage of 1.7 V was applied for a current density of 10 mA cm−2. In contrast, the MoNi4–MoS2/Ni3S2 couple required a low cell voltage of only 1.47 V to deliver a current density of 10 mA cm−2, which is much lower than that for the noble metal-based Pt–Ir/C couple. Over 10 h of galvanostatic electrolysis at 10 mA cm−2, the applied voltage of the MoNi4–MoS2/Ni3S2 couple had an augmentation of 0.02 V, which is much lower than the value of 0.07 V for the Pt–Ir/C couple (Supplementary Fig. 40b). Moreover, the electrolyser with a high current density of 200 mA cm−2 was durably driven by the MoNi4–MoS2/Ni3S2 couple at a low voltage of 1.70 V (Supplementary Movie 2).

HER active centres

To understand the intrinsic contributions of the surface MoNi4 nanoparticles and the underlying MoO2 cuboids to the HER activity, pure MoO2 nanosheets and MoNi4 nanoparticles supported by MoO2 cuboids were also synthesized on carbon cloth. Thus, the contribution of the underlying Ni foam could be excluded (Supplementary Fig. 41). Clearly, the pristine MoO2 nanosheets on carbon cloth showed a very high HER onset potential of 240 mV in 1 M KOH and 200 mV in 0.5 M H2SO4, suggesting that the MoO2 electrocatalyst inherently presented a very sluggish Volmer step and a poor Tafel process (Supplementary Fig. 42). In contrast, the MoNi4 electrocatalyst supported by the MoO2 cuboids on the carbon cloth (MoNi4/MoO2@C) exhibited a zero onset potential, which was similar to that for MoNi4/MoO2@Ni. When the surface MoNi4 nanoparticles of MoNi4/MoO2@C were etched away using 2 M H2SO4 aqueous solution. Obviously, the produced MoO2@C showed a largely increased onset potential of 133 mV (Supplementary Figs 43–46). These results demonstrate that the excellent HER activity of the MoNi4/MoO2@Ni unambiguously originates from the surface MoNi4 nanoparticles rather than from the supporting MoO2 cuboids.

To gain profound insight into the electrocatalytic HER active sites, we also analysed the surface electrochemical behaviour of the MoNi4 electrocatalyst on the MoO2 cuboids. For a freshly prepared MoNi4 electrocatalyst, an electrochemical cyclic voltammetry cycle between −0.025 and 0.275 V (versus RHE) was initially performed with a scan rate of 1 mV s−1. Obviously, the positions of the electrochemically reversible peaks shifted from 0.175 V/0.113 V to 0.215 V/0.064 V when the KOH concentration was changed from 1 to 0.1 M (Supplementary Fig. 47a). The strong dependence on the concentration of KOH as the electrolyte revealed that the electrochemically reversible peaks originated from an ad-/desorption process of water molecules or hydrogen (between 0.05 and 0.35 V, as reported) rather than from the surface redox reactions of the MoNi4 electrocatalyst and supporting MoO2 cuboids12. In addition, in contrast to the results on pure Ni nanosheets (0.150 V) and MoO2 (0.164 V) cuboids, the water or hydrogen adsorption peak of the MoNi4 electrocatalyst showed an anodic shift to 0.175 V, reflecting a superior water or hydrogen adsorption property (Supplementary Fig. 47b).

To evaluate the intrinsic electrocatalytic HER activity of the MoNi4 electrocatalyst, the recorded cathodic current density was normalized versus the related Brunauer Emmett Teller specific surface area of the MoNi4 electrocatalyst (32 m2 g−1) (Supplementary Fig. 48). As described in Supplementary Fig. 49, when the current density was below 0.38 A m−2, the polarization curve of the MoNi4 electrocatalyst nearly overlapped with that of the Pt catalyst. However, the HER overpotential of the MoNi4 electrocatalyst was much lower than that of the Pt catalyst at large current densities (>0.38 A m−2). These results illustrate that the intrinsic HER activity associated with the specific surface area of the MoNi4 electrocatalyst is even higher than that of the Pt catalyst under alkaline conditions.

Theoretical calculations

To understand the fundamental mechanism of the outstanding HER activity on MoNi4/MoO2@Ni, the kinetic energy barrier of the prior Volmer step (ΔG(H2O)) and the concomitant combination of adsorbed H into molecular hydrogen (ΔG(H), Tafel step) were studied using the DFT calculations according to the as-built electrocatalyst models including the (111) facet of Ni metal, the (110) facet of Mo metal, the (110) facet of MoO2 and the (200) facet of MoNi4 (Supplementary Fig. 50). As shown in Fig. 4, MoO2 has a large energy barrier for the Volmer step (ΔG(H2O)=1.01 eV) and a strong hydrogen adsorption free energy (|ΔG(H)|=1.21 eV), indicating a very sluggish Volmer–Tafel mechanism. Thus, MoO2 is not the highly active centre for the HER, which agrees well with the experimental results. The ΔG(H2O) values on pure Ni metal and Mo metal are as high as 0.91 and 0.65 eV, respectively (Fig. 4b and Supplementary Fig. 51). In contrast, the ΔG(H2O) on MoNi4 is significantly decreased to 0.39 eV, which is even lower than the value of 0.44 eV on Pt (ref. 15). In addition, MoNi4 has a lower |ΔG(H)| of 0.74 eV than the value of 1.21 eV for MoO2, which corresponds to a superior hydrogen adsorption capability (Fig. 4c). Thereby, the HER reaction on MoNi4 is associated with a process defined by a fast Tafel step rather than a sluggish Volmer–Tafel step (Supplementary Fig. 52).

Figure 4: DFT calculations.
Figure 4

(a) Calculated free energies of H2O adsorption, activated H2O adsorption, OH adsorption and H adsorption. (b) Calculated adsorption free energy diagram for the Volmer step. (c) Calculated adsorption free energy diagram for the Tafel step. Blue balls: Ni; aqua balls: Mo; red balls: O.


In summary, we have demonstrated a MoNi4 electrocatalyst supported by MoO2 cuboids on nickel foam or carbon cloth. As favoured by a largely reduced energy barrier of the Volmer step, the achieved MoNi4 electrocatalyst exhibits a high HER activity under alkaline conditions, which is highly comparable to that for Pt and outperforms any reported results for Pt-free electrocatalysts, to the best of our knowledge. Moreover, the large-scale preparation and excellent catalytic stability provide MoNi4/MoO2@Ni with a promising utilization in water-alkali electrolysers for hydrogen production. Therefore, the exploration and understanding of the MoNi4 electrocatalyst provide a promising alternative to Pt catalysts for emerging applications in energy generation.


Material synthesis

To synthesize the MoNi4 electrocatalyst, NiMoO4 cuboids were first constructed on nickel foam through a hydrothermal reaction46. First, the commercial nickel foam was successively washed with ethanol, a 1 M HCl aqueous solution and deionized water. Second, one piece of nickel foam (1 × 3 cm2) was immersed into 15 ml of H2O containing Ni(NO3)2·6H2O (0.04 M) and (NH4)6Mo7O24·4H2O (0.01 M) in a Teflon autoclave. Third, the autoclave was heated at 150 °C for 6 h in a drying oven. After washing with deionized water, the NiMoO4 cuboids were achieved on the nickel foam. Finally, the as-constructed NiMoO4 cuboids were heated at 500 °C for 2 h in a H2/Ar (4:96) atmosphere, and then, the MoNi4 electrocatalyst anchored on the MoO2 cuboids was obtained. The loading weight of the formed MoNi4 nanoparticles and MoO2 cuboids on the nickel foam was 43.4 mg cm2. The pure Ni nanosheets and MoO2 cuboids on the nickel foam, as well as the pure MoO2 nanosheets and MoN4 nanoparticles supported by MoO2 cuboids on carbon cloth, were also prepared following the same procedure for MoNi4 by changing the precursors and substrates.

Structure characterizations

SEM, as well as corresponding elemental mapping, and EDX analysis were carried out with a Gemini 500 (Carl Zeiss) system. HRTEM was performed using a LIBRA 200 MC Cs scanning TEM (Carl Zeiss) operating at an accelerating voltage of 200 kV. XPS experiments were carried out on an AXIS Ultra DLD (Kratos) system using Al Kα radiation. XRD patterns were recorded on a PW1820 powder diffractometer (Phillips) using Cu-Kα radiation. The electrochemical tests were carried out on WaveDriver 20 (Pine Research Instrumentation) and CHI 660E Potentiostat (CH Instruments) systems.

Electrochemical measurements

All electrochemical tests were performed at room temperature. The electrochemical HER was carried out in a three-electrode system. A standard Hg/HgO electrode and a graphite rod were used as the reference and counter electrodes, respectively. The Hg/HgO electrode was calibrated using bubbling H2 gas on a Pt coil electrode. Potentials were referenced to an RHE by adding 0.923 V (0.099+0.059 × pH) in a 1 M KOH aqueous solution. For comparison, Pt/C (20 wt%, FuelCellStore; loaded on the nickel foam at 1 mg cm−2) was used as an HER electrocatalyst. The impedance spectra of the electrocatalysts in a three-electrode set-up were recorded at different HER overpotentials in a 1 M KOH electrolyte. All voltages and potentials were corrected to eliminate electrolyte resistances unless noted. Electrolyte resistance: 0.94 Ω; scan rate: 1 mV s−1.

Theoretical calculations

All computations were performed by applying the plane-wave-based DFT method with the Vienna Ab Initio Simulation Package and periodic slab models. The electron ion interaction was described with the projector augmented wave method. The electron exchange and correlation energy were treated within the generalized gradient approximation in the Perdew–Burke–Ernzerhof formalism. The cut-off energy of 400 eV and Gaussian electron smearing method with σ=0.05 eV were used. The geometry optimization was performed when the convergence criterion on forces became smaller than 0.02 eV Å−1 and the energy difference was <10−4 eV. The adsorption energy (Eads) of species X is calculated by Eads=E(X/slab)−E(X)−E(slab), and a more negative Eads indicates a more stable adsorption. For the DFT calculations, the reactant (H2O) and intermediates (OH and H) are first adsorbed on all possible active sites of the catalyst. Afterwards, the VASP software is utilized to optimize the adsorption. For evaluating the energy barrier (Ea=ETSEIS), the transitional state (TS) was located using the Nudged Elastic Band method. All transition states were verified by vibration analyses with only one imaginary frequency. The p(3 × 3)-Ni(111), p(3 × 3)-Mo(110), p(3 × 3)-MoO2(110) and p(1 × 1)-MoNi4(200) surfaces were utilized to simulate the properties of these electrocatalysts.

Data availability

The data that support the findings of this study are available from the corresponding author on reasonable request.

Additional information

How to cite this article: Zhang, J. et al. Efficient hydrogen production on MoNi4 electrocatalysts with fast water dissociation kinetics. Nat. Commun. 8, 15437 doi: 10.1038/ncomms15437 (2017).

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This work was financially supported by the ERC Grant on 2DMATER and EC under Graphene Flagship (No. CNECT-ICT-604391). We also acknowledge the Cfaed (Center for Advancing Electronics Dresden), the Dresden Center for Nanoanalysis (DCN) at TU Dresden and Dr Horst Borrmann for the X-ray diffraction characterizations in Max Planck Institute for Chemical Physics of Solids.

Author information


  1. Center for Advancing Electronics Dresden (Cfaed) and Department of Chemistry and Food Chemistry, Technische Universitaet Dresden, 01062 Dresden, Germany

    • Jian Zhang
    • , Shaohua Liu
    • , Xiaodong Zhuang
    •  & Xinliang Feng
  2. Univ Lyon, Ens de Lyon, CNRS, Université Lyon 1, Laboratoire de Chimie, UMR 5182, F-69342 Lyon, France

    • Tao Wang
  3. WPI Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577, Japan

    • Pan Liu
    •  & Mingwei Chen
  4. CREST, JST, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan

    • Pan Liu
    •  & Mingwei Chen
  5. Fraunhofer Institute for Ceramic Technologies and Systems (IKTS), 01109 Dresden, Germany

    • Zhongquan Liao
    •  & Ehrenfried Zschech


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J.Z. and X.F. conceived and designed the experiments and wrote the paper; J.Z. carried out the synthesis and characterization of electrocatalysts; T.W. performed the DFT calculations; P.L., S.L., Z.L., X.Z., M.C. and E.Z. assisted with the HRTEM and XPS characterizations. All authors discussed the results and commented on the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Xinliang Feng.

Supplementary information

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    Supplementary Information

    Supplementary Figures, Supplementary Table, Supplementary Note and Supplementary References

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  1. 1.

    Supplementary Movie 1

    Electrocatalytic hydrogen evolution in a three-electrode cell.

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    Supplementary Movie 2

    Alkaline water splitting electrolyzer.


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