材料科学
纳米材料基催化剂
二硫化钼
铼
兴奋剂
钼
降级(电信)
氢
化学工程
光化学
纳米技术
纳米颗粒
光电子学
冶金
有机化学
化学
计算机科学
电信
工程类
作者
Raquel Aymerich‐Armengol,Miquel Vega‐Paredes,Zhenbin Wang,Andrea M. Mingers,Luca Camuti,Jeeung Kim,Jeongwook Bae,Ilias Efthimiopoulos,Rajib Sahu,Filip Podjaski,Martin Rabe,Christina Scheu,Joohyun Lim,Siyuan Zhang
标识
DOI:10.1002/adfm.202413720
摘要
Abstract Molybdenum disulfide (MoS 2) nanostructures are promising catalysts for proton‐exchange‐membrane (PEM) electrolyzers to replace expensive noble metals. Their large‐scale application demands high activity for the hydrogen evolution reaction (HER) as well as robust durability. Doping is commonly applied to enhance the HER activity of MoS 2 ‐based nanocatalysts, but the effect of dopants on the electrochemical and structural stability is yet to be discussed. Herein, operando electrochemical measurements to the structural evolution of the materials down to the nanometric scale are correlated by identical location electron microscopy and spectroscopy. The range of stable operation for MoS 2 nanocatalysts with and without rhenium doping is experimentally defined. The responsible degradation mechanisms at first electrolyte contact, open circuit stabilization, and HER conditions are experimentally identified and confirmed with the calculated Pourbaix diagram of Re‐doped MoS 2 . Doping MoS 2 ‐based nanocatalysts is validated as a promising strategy for continuing the improvement of high‐performance and durable PEM electrolyzers.
科研通智能强力驱动
Strongly Powered by AbleSci AI