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通过d轨道杂化提高镍铁基催化剂上的析氧反应性能

Boosting Oxygen Evolution Reaction Performance on NiFe-Based Catalysts Through d-Orbital Hybridization.

作者信息

Wang Xing, Pi Wei, Hu Sheng, Bao Haifeng, Yao Na, Luo Wei

机构信息

State Key Laboratory of New Textile Materials and Advanced Processing Technology, Key Laboratory of New Textile Materials and Applications of Hubei Province, School of Materials Science and Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, People's Republic of China.

出版信息

Nanomicro Lett. 2024 Sep 26;17(1):11. doi: 10.1007/s40820-024-01528-9.

Abstract

Anion-exchange membrane water electrolyzers (AEMWEs) for green hydrogen production have received intensive attention due to their feasibility of using earth-abundant NiFe-based catalysts. By introducing a third metal into NiFe-based catalysts to construct asymmetrical M-NiFe units, the d-orbital and electronic structures can be adjusted, which is an important strategy to achieve sufficient oxygen evolution reaction (OER) performance in AEMWEs. Herein, the ternary NiFeM (M: La, Mo) catalysts featured with distinct M-NiFe units and varying d-orbitals are reported in this work. Experimental and theoretical calculation results reveal that the doping of La leads to optimized hybridization between d orbital in NiFeM and 2p in oxygen, resulting in enhanced adsorption strength of oxygen intermediates, and reduced rate-determining step energy barrier, which is responsible for the enhanced OER performance. More critically, the obtained NiFeLa catalyst only requires 1.58 V to reach 1 A cm in an anion exchange membrane electrolyzer and demonstrates excellent long-term stability of up to 600 h.

摘要

用于绿色制氢的阴离子交换膜水电解槽(AEMWEs)因其使用储量丰富的镍铁基催化剂的可行性而受到广泛关注。通过在镍铁基催化剂中引入第三种金属以构建不对称的M-NiFe单元,可以调整d轨道和电子结构,这是在AEMWEs中实现足够析氧反应(OER)性能的重要策略。在此,本文报道了具有不同M-NiFe单元和不同d轨道的三元NiFeM(M:La、Mo)催化剂。实验和理论计算结果表明,La的掺杂导致NiFeM中d轨道与氧中2p之间的杂化优化,从而增强了氧中间体的吸附强度,并降低了速率决定步骤的能垒,这是OER性能增强的原因。更关键的是,所获得的NiFeLa催化剂在阴离子交换膜电解槽中仅需1.58 V即可达到1 A/cm²,并展现出高达600 h的出色长期稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5172/11427650/5183c1128c12/40820_2024_1528_Fig1_HTML.jpg

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