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通过表面层修饰调控相界氧化态以增强碱性氢电催化性能

Manipulation of Oxidation States on Phase Boundary via Surface Layer Modification for Enhanced Alkaline Hydrogen Electrocatalysis.

作者信息

Huang Huawei, Xu Liangliang, Zuo Shouwei, Song Lu, Zou Chen, García-Melchor Max, Li Yang, Ren Yuafu, Rueping Magnus, Zhang Huabin

机构信息

KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.

Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.

出版信息

Adv Mater. 2024 Dec;36(51):e2405128. doi: 10.1002/adma.202405128. Epub 2024 Jul 27.

DOI:10.1002/adma.202405128
PMID:39072907
Abstract

In alkaline water electrolysis and anion exchange membrane water electrolysis technologies, the hydrogen evolution reaction (HER) at the cathode is significantly constrained by a high energy barrier during the water dissociation step. This study employs a phase engineering strategy to construct heterostructures composed of crystalline NiW and amorphous WO aiming to enhance catalytic performance in the HER under alkaline conditions. This work systematically modulates the oxidation states of W within the amorphous WO of the heterostructure to adjust the electronic states of the phase boundary, the energy barriers associated with the water dissociation step, and the adsorption/desorption properties of intermediates during the alkaline HER process. The optimized catalyst, NiW/WO-2, with a quasi-metallic state of W coordinated by a low oxygen content in amorphous WO, demonstrates exceptional catalytic performance (22 mV@10 mA cm), outperforming commercial Pt/C (30 mV@10 mA cm). Furthermore, the operando X-ray absorption spectroscopy analysis and theoretical calculations reveal that the optimized W atoms in amorphous WO serve as active sites for water dissociation and the nearby Ni atoms in crystalline NiW facilitated the release of H. These findings provide valuable insights into designing efficient heterostructured materials for energy conversion.

摘要

在碱性水电解和阴离子交换膜水电解技术中,阴极的析氢反应(HER)在水离解步骤中受到高能垒的显著限制。本研究采用相工程策略构建由结晶态NiW和非晶态WO组成的异质结构,旨在提高碱性条件下HER的催化性能。这项工作系统地调节了异质结构中非晶态WO中W的氧化态,以调整相界的电子态、与水离解步骤相关的能垒以及碱性HER过程中中间体的吸附/解吸特性。优化后的催化剂NiW/WO-2,其中非晶态WO中W处于低氧含量配位的准金属态,表现出优异的催化性能(在10 mA cm时为22 mV),优于商业Pt/C(在10 mA cm时为30 mV)。此外,原位X射线吸收光谱分析和理论计算表明,非晶态WO中优化后的W原子作为水离解的活性位点,而结晶态NiW中附近的Ni原子促进了H的释放。这些发现为设计用于能量转换的高效异质结构材料提供了有价值的见解。

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