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3-d Element Induced Charge Redistribution Within Bimetallic η-Phase Carbides Leads to High Performance Electrocatalysts for Highly Efficient Anion Exchange Membrane Water Electrolysis
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3-d Element Induced Charge Redistribution Within Bimetallic η-Phase Carbides Leads to High Performance Electrocatalysts for Highly Efficient Anion Exchange Membrane Water Electrolysis

Tzu-Hsiang Lin, Yu-Chieh Ting, Chiung-Wen Chang, Shao Chang, Kai-An Lee, Tsung-Wei Hsueh, Kun-Han LinShih-Yuan Lu
Small (Weinheim an der Bergstrasse, Germany), 卷.21(50), e11280
01/12/2025
PMID: 41014242

摘要

Chemistry Chemistry, Multidisciplinary Chemistry, Physical Materials Science, Multidisciplinary Nanoscience & Nanotechnology Physics, Applied Physics, Condensed Matter Science & Technology Science & Technology - Other Topics Materials Science Physical Sciences Physics Technology
Cost-effective, highly efficient, and robust electrocatalysts are critical for prevailing of anion exchange membrane water electrolysis technology for green hydrogen production. Here, Ni and Fe are incorporated into tungsten carbides to form bimetallic eta-phase carbides Ni6W6C and Fe6W6C, respectively, achieving remarkably low overpotentials of 37/204 and 203/296 mV at current densities of 10/500 mA cm-2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, in 1 m KOH. With Ni6W6C and Fe6W6C serving as the cathode and anode catalysts, respectively, the anion exchange membrane water electrolyzer exhibits outstanding water electrolysis performances, achieving an ultrahigh current density of 2.8 A cm-2 at 2 V and exhibiting ultra-stability of a continuous operation at a commercially relevant high current density of 0.5 A cm-2 for 100 h without appreciable decay. Incorporation of Ni in Ni6W6C induces charge redistribution between Ni and W, leading to an upshift in hydrogen adsorption energy to near-ideal value of zero and a downshift in hydrogen desorption energy for fast release of hydrogen, both contributing to the high HER activities of Ni6W6C. In situ surface reconstruction of Fe6W6C to highly OER-active (Fe,W)OOH during OER operations gives rise to high OER activities of Fe6W6C.

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