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,Jun-Yi Ding,Li‐Jun Hu,Sizhuan Li,Shuai Zhang,Minghua Wang,Linghao He,Miao Du
出处
期刊:Chemcatchem
[Wiley]
日期:2023-05-03
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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