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Highly dispersed NiMo@rGO nanocomposite catalysts fabricated by a two-step hydrothermal method for hydrogen evolution

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Abstract

Exploring and designing a high-performance non-noble metal catalyst for hydrogen evolution reaction (HER) are crucial for the large-scale application of H2 by water electrolysis. Here, novel catalysts with NiMo nanoparticles decorated on reduced graphene oxide (NiMo@rGO) synthesized by a two-step hydrothermal method were reported. Physical characterization results showed that the prepared NiMo@rGO-1 had an irregular lamellar structure, and the NiMo nanoparticles were uniformly dispersed on the rGO. NiMo@rGO-1 exhibited outstanding HER performance in an alkaline environment and required only 93 and 180 mV overpotential for HER in 1.0 M KOH solution to obtain current densities of −10 and −50 mA·cm2, respectively. Stability tests showed that NiMo@rGO-1 had a certain operating stability for 32 h. Under the same condition, the performance of NiMo@rGO-1 can be comparable with that of commercial Pt/C catalysts at high current density. The synergistic effect between NiMo particles and lamellate graphene can remarkably promote charge transfer in electrocatalytic reactions. As a result, NiMo@rGO-1 presented the advantages of high intrinsic activity, large specific surface area, and small electrical impedance. The lamellar graphene played a role in dispersion to prevent the aggregation of nanoparticles. The prepared NiMo@rGO-1 can be used in an-ion exchange membrane water electrolysis to produce hydrogen. This study provides a simple preparation method for efficient and low-cost water electrolysis to produce hydrogen in the future.

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Acknowledgement

This research was financially supported by the National Natural Science Foundation of China (No. 22278125).

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Correspondence to Chao Xu.

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Cao, D., Ma, X., Zhang, Y. et al. Highly dispersed NiMo@rGO nanocomposite catalysts fabricated by a two-step hydrothermal method for hydrogen evolution. Int J Miner Metall Mater 30, 2432–2440 (2023). https://doi.org/10.1007/s12613-023-2677-7

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  • DOI: https://doi.org/10.1007/s12613-023-2677-7

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