Logo image
Interface Engineering Effected Charge Redistribution within High Entropy Alloy-Metal Heterostructured Catalyst Enables High Performance Anion Exchange Membrane Water Electrolysis
期刊文章   同儕審查

Interface Engineering Effected Charge Redistribution within High Entropy Alloy-Metal Heterostructured Catalyst Enables High Performance Anion Exchange Membrane Water Electrolysis

Chiung-Wen Chang, Yu-Chieh Ting, Kai-An Lee, Shao Chang, Tsung-Wei Hsueh, Kun-Han Lin 和 Shih-Yuan Lu
Small (Weinheim an der Bergstrasse, Germany), 卷.22(5), 頁碼.e10665-n/a
01/01/2026
PMID: 41294015
Web of Science ID: WOS:001623176200001

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
Development of low-cost, highly efficient and stable catalysts is critical for the prevalence of anion exchange membrane water electrolysis (AEMWE) technology for green hydrogen production. High entropy alloy (HEA)-metal heterostructures (HEA-Mo), taking advantage of the versatile active sites and multiple synergies between constituent elements of HEA and interfacial electronic interactions between HEA and metal, are promising bifunctional catalysts for high-performance water electrolysis. Here, a FeCoNiCuMo HEA-Mo heterostructured catalyst is synthesized, through supersaturation-induced phase separation, for both anode and cathode of an AEMWE. The catalyst exhibits outstanding hydrogen evolution reaction (HER) (eta 10/eta 500 of 24/140 mV) and oxygen evolution reaction (OER) (eta 10/eta 500 of 175/325 mV) activities in 1 m KOH. The HEA-Mo//HEA-Mo based AEMWE delivers an ultrahigh current density of 2207 mA cm-2 at 2.0 V and maintains stable operations at a commercially relevant high current density of 500 mA cm-2 for 100 h with only 3.1% decay, demonstrating its excellent operation stability. HER activities are greatly enhanced through modulation of charge distributions with the decorated Mo, leading to better balanced hydrogen adsorption/desorption, together with the team up of Mo, a strong OH- adsorbent, for enhanced water dissociation to accelerate both the Volmer and Heyrovsky steps.

相關連結

指標

1 檢視次數

詳細資料

Logo image