塔菲尔方程
过电位
析氧
材料科学
钴
电子转移
催化作用
化学工程
氢氧化物
纳米颗粒
分解水
循环伏安法
无机化学
纳米技术
电化学
光催化
化学
光化学
有机化学
电极
冶金
物理化学
工程类
作者
Wei Wang,Sainan Zhu,Xingliang Chen,Xinyu Zhang,Yourong Tao,Yanxin Zhang,Ruizhi Xiang,Xingcai Wu
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2020-09-04
卷期号:31 (47): 475402-475402
被引量:11
标识
DOI:10.1088/1361-6528/abaf80
摘要
Herein, a novel composite of small amounts of Ag nanoparticles (NPs) decorated urchin-like cobalt carbonate hydroxide hydrate (CCHH) was developed for highly-efficient alkaline oxygen evolution reaction (OER). Not only can Ag colloids, as template agents, modify the morphologies of urchin-like CCHH microspheres to expose more active sites available, but also the supported Ag NPs formed by Ag colloids can transfer the electron to CCHH surfaces, accelerating the transformation of surface CoII to CoIII/CoIV (proton-coupled electron transfer (PCET) process). The urchin-like Ag/CCHH (0.013 mmol) precatalyst (before cyclic voltammetry (CV) activation) exhibits a better OER performance (a low overpotential of 273 mV at 10 mA cm-2 and small Tafel slope of 65 mV dec-1) as compared with commercial RuO2. Furthermore, the dynamic surface self-reconstruction (surface CO32- and OH - exchange) can further enhance the activities of Ag/CCHH precatalysts. Consequently, the optimal Ag/CCHH (0.013 mmol) catalyst presents a superior activity (a lower overpotential of 267 mV at 10 mA cm-2 and markedly reduced Tafel slope to 56 mV dec-1) along with an excellent stability after CV cycles. The study provides a feasible strategy to fully realize the low overpotential of CCHH-based OER electrocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI