TY - JOUR
T1 - NiMo@C3N5 heterostructures with multiple electronic transmission channels for highly efficient hydrogen evolution from alkaline electrolytes and seawater
AU - Bu, Xiuming
AU - Liang, Xiongyi
AU - Bu, Yu
AU - Quan, Quan
AU - Meng, You
AU - Lai, Zhengxun
AU - Wang, Wei
AU - Liu, Chuntai
AU - Lu, Jian
AU - Lawrence Wu, Chi Man
AU - Ho, Johnny C.
N1 - Funding Information:
This work is financially supported by the Environment and Conservation Fund of Hong Kong SAR, China (ECF 2020-13), the City University of Hong Kong (project no. 9667227) and the Foshan Innovative and Entrepreneurial Research Team Program (no. 2018IT100031).
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/6/15
Y1 - 2022/6/15
N2 - Designing highly efficient and stable electrocatalysts for hydrogen evolution reaction (HER), particularly in seawater, still remains a challenging task. Herein, the unique heterostructures composed of 1D NiMo cores and 2D C3N5 shells (NiMo@C3N5) are rationally designed and demonstrated as the robust HER catalysts in both alkaline electrolytes and natural seawater, where the carbon-based shell can effectively protect the catalyst core from seawater poisoning. Based on the experimental investigation and density functional theory calculation, multiple electronic transmission channels were found to establish at the interface between NiMo cores and C3N5 shells, thus providing efficiently optimized HER pathways to achieve minimized overpotential with a reduced energy barrier of the rate-determining step. More importantly, the NiMo@C3N5 hybrids exhibit stable HER performance with a high Faradaic efficiency of 94.8% in seawater, which is superior to that of commercial Pt/C. All these results can evidently highlight a feasible strategy to develop high-performance HER electrocatalysts via interface engineering.
AB - Designing highly efficient and stable electrocatalysts for hydrogen evolution reaction (HER), particularly in seawater, still remains a challenging task. Herein, the unique heterostructures composed of 1D NiMo cores and 2D C3N5 shells (NiMo@C3N5) are rationally designed and demonstrated as the robust HER catalysts in both alkaline electrolytes and natural seawater, where the carbon-based shell can effectively protect the catalyst core from seawater poisoning. Based on the experimental investigation and density functional theory calculation, multiple electronic transmission channels were found to establish at the interface between NiMo cores and C3N5 shells, thus providing efficiently optimized HER pathways to achieve minimized overpotential with a reduced energy barrier of the rate-determining step. More importantly, the NiMo@C3N5 hybrids exhibit stable HER performance with a high Faradaic efficiency of 94.8% in seawater, which is superior to that of commercial Pt/C. All these results can evidently highlight a feasible strategy to develop high-performance HER electrocatalysts via interface engineering.
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U2 - 10.1016/j.cej.2022.135379
DO - 10.1016/j.cej.2022.135379
M3 - Article
AN - SCOPUS:85125700031
SN - 1385-8947
VL - 438
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 135379
ER -