过电位
电催化剂
塔菲尔方程
双金属片
析氧
材料科学
化学工程
催化作用
金属
量子点
无机化学
化学
纳米技术
电极
物理化学
冶金
电化学
有机化学
工程类
作者
Fufeng Yan,Junyi Ding,Li‐Jun Hu,Sizhuan Li,Shuai Zhang,Minghua Wang,Linghao He,Miao Du
出处
期刊:Chemcatchem
[Wiley]
日期:2023-04-01
卷期号:15 (10)
被引量:4
标识
DOI:10.1002/cctc.202300115
摘要
Abstract To accelerate the reaction kinetics of electrocatalytic oxygen evolution reaction (OER), a multicomponent CDs@(PdFeNiCo)Nb x nanohybrid comprising multiple metal nanoalloys and carbon quantum dots (CDs) was in situ generated by treating the mixture of Nb 2 C quantum dots (Nb 2 C QDs) and a variety of metal ions (M 2+ =Pd 2+ , Fe 2+ , Co 2+ , Ni 2+ ) through the solution plasma (SP) modification technique. The CDs@(PdFeNiCo)Nbx catalyst was further explored as an electrocatalyst for OER in alkaline solution. Under nitrogen plasma irradiation with high input power (200 W), diverse bimetallic nanoalloy particles, including NbPd 3 , FeNb, NbNi 3 , and CoNbO 4 nanoalloys, were generated, accompanied with the decomposition of Nb 2 C QDs into CDs. In view of the synergic effect between multivariate metal active sites and highly conjugated CD network, the developed CDs@(PdFeNiCo)Nb x electrocatalyst showed a small overpotential of 240 mV for achieving the current density of 10 mA cm −2 , together with a very low Tafel slope of 62 mV dec −1 , which substantially outperformed those of the state‐of‐the‐art metal electrocatalysts and was competitive with most metal oxides. The CDs@(PdFeNiCo)Nb x electrocatalyst also showed a negligible overpotential change during 30 h chronopotentiometry measurement. The present work can provide a feasible alternative strategy for the development of an excellent OER electrocatalyst using the SP modification method.
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