催化作用
材料科学
纳米颗粒
电催化剂
微观结构
化学工程
可逆氢电极
纳米技术
纳米复合材料
碳纳米管
纳米材料基催化剂
电极
电化学
化学
复合材料
工作电极
物理化学
有机化学
工程类
作者
Moujie Huang,Yongsong Ma,Jingbo Yang,Lingyun Xu,Hangqi Yang,Miao Wang,Xin Ma,Xin Xia,Junhao Yang,Deli Wang,Chuang Peng
标识
DOI:10.1016/j.apsusc.2023.158834
摘要
Strong metal-support interactions (SMSIs) play a pivotal role in enhancing the catalytic activity and stability of supported metal catalysts in heterogeneous thermal catalysis, but construction of effective SMSIs remains challenging in electrocatalysis. As a ubiquitous and versatile support for electrocatalysts, carbon materials are generally too inert to generate SMSIs with the loaded metal active sites. We hereby report a CVD-based method to prepare Ru nanoparticles on arrays of oxygen- and nitrogen-doped CNTs grown on the fibers of carbon paper (Ru/ONCNT@CP). The SMSIs were manifested by electronic structure tuning of Ru nanoparticles and their partial embedment in the carbon support. The SMSIs result in optimized Gibbs free energy of H*, lowered energy barrier of H2O dissociation, and enhanced catalyst robustness. Combined with the hierarchical microstructure, high surface area and hydrophilic/aerophobic nature, the Ru/ONCNT@CP electrode displays excellent HER catalytic activity in 1 M KOH, requiring overpotentials of only 73, 180, and 252 mV to achieve current densities of 100, 500, and 800 mA cm−2, respectively. Moreover, the Ru/ONCNT@CP electrode exhibits outstanding stability, with negligible current decay after 120 h HER operation at 100 mA cm−2. This work features an effective and scalable approach for preparation of metal-loaded-carbon electrocatalysts with engineered microstructure and SMSIs.
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