A highly efficient overall water splitting ruthenium-cobalt alloy electrocatalyst across a wide pH range via electronic coupling with carbon dots

被引:110
作者
Feng, Tanglue [1 ]
Yu, Guangtao [2 ,3 ]
Tao, Songyuan [1 ]
Zhu, Shoujun [1 ]
Ku, Ruiqi [3 ]
Zhang, Ran [3 ]
Zeng, Qingsen [1 ]
Yang, Mingxi [1 ]
Chen, Yixin [1 ]
Chen, Weihua [4 ]
Chen, Wei [2 ,3 ]
Yang, Bai [1 ,5 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Fujian Normal Univ, Coll Chem & Mat Sci, Fuzhou 350007, Peoples R China
[3] Jilin Univ, Inst Theoret Chem, Lab Theoret & Computat Chem, Changchun 130023, Peoples R China
[4] Univ Sci & Technol China, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
[5] Jilin Normal Univ, Minist Educ, Key Lab Preparat & Applicat Environm Frien4 Mater, Changchun 130103, Peoples R China
基金
美国国家科学基金会;
关键词
CATALYST;
D O I
10.1039/d0ta02496a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Efficient pH-universal overall water splitting electrocatalysts are critical but remain challenging. Herein, a highly efficient, pH-universal overall water-splitting electrocatalyst, was reported by ingeniously controlling the bulk and surface electronic structures of Ru with Co-doping and interfacial incorporation of carbon dots (CDs), respectively. The developed RuCo@CD electrocatalyst present superior hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) activities with great durability over a wide pH range, achieving a very low overpotential of 51 mV, 11 mV and 67 mV for HER, and 190 mV, 257 mV and 410 mV for OER at 10 mA cm(-2) in 0.5 M H2SO4, 1.0 M KOH and neutral 1.0 M phosphate buffer solution (PBS), respectively. A modified chemical/valence state originating from the strong electronic coupling process among Co, Ru and CDs, is revealed by combined experimental and theoretical results, which contributes to the optimization of water dissociation kinetics. A RuCo alloy was unprecedentedly endowed with efficient and stable bi-functional activities for the first time through electronic coupling with CDs. This reflects the dependence of catalytic activity on chemical/valence states and electronic structures at the atomic level. The work provides a new approach for the design of excellent Ru-based overall water splitting electrocatalysts.
引用
收藏
页码:9638 / 9645
页数:8
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