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用于高效碱性析氢反应、析氧反应和全水解的MoO@N/Mo‒ReS杂化物中的异质界面驱动电子调制

Heterointerface-Driven Electronic Modulation in MoO@N/Mo‒ReS Hybrid for Efficient Alkaline HER, OER, and Overall Water Splitting.

作者信息

Singh Manjinder, Park Jaejun, Kim Hayoung, Kim Gyuchan, Cha Dunchan, Paudel Dasu Ram, Kim Byung-Hyun, Lee Seunghyun

机构信息

Department of Energy and Bio Sciences, Hanyang University ERICA, Ansan, 15588, Republic of Korea.

Center for Bionano Intelligence Education and Research, Hanyang University ERICA, Ansan, 15588, Republic of Korea.

出版信息

Small. 2025 Aug;21(34):e2505906. doi: 10.1002/smll.202505906. Epub 2025 Jul 11.

Abstract

Alkaline water electrolysis is an efficient technical pathway for producing high-purity green hydrogen (H). However, rational design and fabrication of efficient electrocatalysts are essential for energy conversion. Herein, MoO nanoclusters on N/Mo dual-doped ReS nanosheets (MoO@N/Mo-ReS) develops through a hydrothermal and CVD-nitridation process. This novel strategy leads to modifying the electronic properties of metastable ReS through metal/nonmetal doping, heterostructure formation, and basal plane activation, thus increasing the number of electrochemically active sites. The MoO@N/Mo-ReS catalyst is effective at hydrogen-adsorption, has a low energy barrier for water dissociation, and exhibits high electrical conductivity, as demonstrated by density functional theory (DFT) studies. The optimal MoO@N/Mo-ReS heterostructure shows exceptional endurance at low overpotentials of -93 and 249 mV, respectively, and catalytic activity for the evolution of both H and oxygen (O) at a current density of 10 mA cm in an alkaline electrolyte. The performance of the MoO@N/Mo-ReS electrolyzer is 1.54 V at 10 mA cm, which is comparable to a commercial Pt/C||RuO (1.56 V at 10 mA cm) electrocatalyst. This study offers a promising strategy for the development of scalable and efficient electrocatalysts, aiming to enhance their suitability for energy applications.

摘要

碱性水电解是生产高纯度绿色氢气(H)的有效技术途径。然而,合理设计和制造高效电催化剂对于能量转换至关重要。在此,通过水热和化学气相沉积氮化过程在N/Mo双掺杂的ReS纳米片上制备了MoO纳米团簇(MoO@N/Mo-ReS)。这种新策略通过金属/非金属掺杂、异质结构形成和基面活化来改变亚稳态ReS的电子性质,从而增加电化学活性位点的数量。密度泛函理论(DFT)研究表明,MoO@N/Mo-ReS催化剂在氢吸附方面有效,水离解的能垒低,并且具有高电导率。最佳的MoO@N/Mo-ReS异质结构在-93和249 mV的低过电位下分别表现出优异的耐久性,并且在碱性电解质中,在10 mA cm的电流密度下对氢气(H)和氧气(O)的析出均具有催化活性。MoO@N/Mo-ReS电解槽在10 mA cm时的性能为1.54 V,与商业Pt/C||RuO(在10 mA cm时为1.56 V)电催化剂相当。这项研究为开发可扩展且高效的电催化剂提供了一种有前景的策略,旨在提高它们在能源应用中的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af6/12393017/97f7558f768e/SMLL-21-2505906-g004.jpg

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