Crystal Field Stabilization Energy Asymmetrically Constructed Built-in Electric Fields for Efficient Water Cracking

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-04-24 DOI:10.1002/smll.202502250
Dengji Xu, Xinran Li, Zhenyan Liu, Qiang Wang, Di Tian, Wei Liu, Zhiguo Qu
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Abstract

Efficient bifunctional electrocatalysts for hydrogen and oxygen evolution reactions (HER and OER) play crucial roles in water electrolysis. However, the discrepancy in binding affinities of catalytic sites to O/H-contained intermediates makes it difficult to achieve OER and HER bifunctional catalysis simultaneously. Multi-component heterostructures have been demonstrated to be an effective solution to realize bifunctional electrocatalysts, but the division of labor and action mechanism of each component are not fully elucidated. Therefore, based on asymmetrical crystal field stabilization energy (CFSE) between NiS and Ni2P, the heterogeneous catalyst (NiS/Ni2P@NF) with built-in electric field (BEF) is constructed in this paper, which showed efficient bifocal water cracking. DFT calculation has confirmed that BEF causes the directional movement of electrons in the material, thus optimizing the OER/HER reaction path. Further control experiments indicated that NiS and Ni2P serves as the active species for the corresponding OER and HER, thus NiS/Ni2P@NF delivers a remarkably reduced cell voltage of 1.62 V (10 mA cm−2) within a H-type electrolyzer as both anode and cathode electrodes. The strategy of constructing BEF based on asymmetrical CFSE has the potential to precisely induce the local electron flow of the catalytic site and accurately design multifunctional catalysts with composition-function contrast.

Abstract Image

晶体场稳定能量不对称构造内置电场高效水裂解
高效的氢析氧双功能电催化剂(HER和OER)在水电解过程中起着至关重要的作用。然而,由于催化位点对含O/ h中间体的结合亲合力存在差异,使得OER和HER双功能催化难以同时实现。多组分异质结构已被证明是实现双功能电催化剂的有效解决方案,但各组分的分工和作用机理尚未完全阐明。因此,基于NiS和Ni2P之间的不对称晶体场稳定能(CFSE),本文构建了内置电场(BEF)的非均相催化剂(NiS/Ni2P@NF),该催化剂具有高效的双焦点水裂解。DFT计算证实了BEF引起材料中电子的定向运动,从而优化了OER/HER反应路径。进一步的控制实验表明,NiS和Ni2P作为相应的OER和HER的活性物质,因此NiS/Ni2P@NF在h型电解槽内作为阳极和阴极都提供了1.62 V (10 mA cm−2)的显著降低的电池电压。基于非对称CFSE构建BEF的策略可以精确地诱导催化部位的局部电子流,并精确地设计具有组成-功能对比的多功能催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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