过电位
离解(化学)
电化学
催化作用
钌
材料科学
分解水
无机化学
纳米片
化学工程
电催化剂
纳米颗粒
纳米技术
物理化学
化学
电极
有机化学
工程类
光催化
作者
Liming Zeng,Yongyang Zhu,Daifeng Wu,Dongxing Wang,Qing Zhou
标识
DOI:10.1016/j.surfin.2024.103903
摘要
The hydrogen evolution reaction (HER) in alkaline medium is much sluggish than that in acidic medium due to the limited water dissociation step, thus accelerating the water dissociation kinetics is critical. Herein, we designed a MoOx species-modified ruthenium nanoparticle catalyst (MoOx/Ru/C-3) based on the unique electrostatic interaction between carboxymethylcellulose sodium salt (CMC) and metal ions, where an heterophase structure is formed between MoOx and Ru. The obvious electronic interaction between them allows the formation of synergistic promotion relationship involving the water dissociation on MoOx and the adsorbed hydrogen recombination on Ru. At a metal loading of 6.98 μgRu cm-2 geo, the overpotential of 82 mV is just required to reach a current density of 10 mA cm−2, exhibiting a significantly better apparent electrochemical activity than Ru/C (98 mV) without introduction of MoOx, which demonstrates superior or comparable alkaline HER activity to the recently reported Ru-based electrocatalysts. Meanwhile, the overpotential for Ru/C increased by 113 mV after 24 h of chronopotentiometric test, whereas only 61 mV elevates for MoOx/Ru/C-3, and even just 98 mV generates after 120 h. Thereof, introduction of MoOx species into Ru matrix can also markedly improve the electrochemical stability. The proposed material construction strategy in this study provides a feasible idea for the rational design of highly cost-performance alkaline hydrogen evolution catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI