阳极
晶界
溶解
材料科学
析氧
电解
电解水
溶解度
分解水
化学工程
纳米晶
电池电压
阴极
氧气
纳米技术
电流密度
电解质
电化学
电流(流体)
无机化学
电压
电催化剂
制氢
工作(物理)
结构稳定性
电解槽
电极
作者
Yaojia Cheng,Tingting Zhai,Xue Yong,Ran Zhang,Da Pan,Yong Yuan,Zhiyong Tang,Hao Wang,Siyu Lu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-17
卷期号:19 (38): 34329-34340
被引量:17
标识
DOI:10.1021/acsnano.5c12133
摘要
RuO2-based oxygen evolution reaction electrocatalysts have gained considerable attention as promising alternatives to replace expensive iridium-based materials in proton-exchange-membrane water electrolysis (PEMWE). Nevertheless, the structural destruction of RuO2 and the dissolution of Ru atoms under high current densities hinder its instability. In this work, we introduced Mo into the RuO2 lattice, which not only disrupted the long-range periodic structure but also the "site blocking" effect of Mo enabling the formation of ultrafine nanocrystals (4.3 nm) of RuO2 with abundant grain boundaries (GB-Mo-RuO2) at a higher temperature (500 °C). The developed GB-Mo-RuO2 exhibited lower overpotentials of 185 and 280 mV and excellent stability of 450 and 150 h at 10 and 100 mA cm-2, respectively. The introduction of Mo and GBs reduced the energy barrier in the rate-determining step and the solubility of Ru, thereby boosting both the activity and the stability of the catalyst. The PEMWE with GB-Mo-RuO2 as the anode exhibited cell voltages of 1.65 and 1.85 V at 1 and 2 A cm-2, respectively, and an extremely low decay rate (56.4 μV h-1) at 1 A cm-2 during 160 h.
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