Local photothermal and photoelectric effect synergistically boost hollow CeO2/CoS2 heterostructure electrocatalytic oxygen evolution reaction

被引:96
作者
Tian, Lin [1 ,2 ,3 ]
Chen, Hongyu [1 ]
Lu, Xinhua [1 ]
Liu, Dongsheng [1 ]
Cheng, Wenjing [2 ,3 ]
Liu, Yuanyuan [1 ]
Li, Jing [1 ]
Li, Zhao [1 ,2 ]
机构
[1] Xuzhou Univ Technol, Sch Mat & Chem Engn, Xuzhou 221018, Peoples R China
[2] Yili Normal Univ, Sch Chem & Environm Sci, Univ & Coll Key Lab Nat Prod Chem & Applicat Xinji, Yining 835000, Peoples R China
[3] Yili Normal Univ, Sch Chem & Environm Sci, Key Lab Pollutant Chem & Environm Treatment, Yining 835000, Peoples R China
关键词
CeO2/CoS(2 )heterostructures; Local photothermal effect; Oxygen evolution reaction; Photo-assisted electrocatalysis;
D O I
10.1016/j.jcis.2022.07.125
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
Solar-assisted electrocatalytic oxygen evolution reaction (OER) plays a key role in energy conversion and storage technology. Herein, we provide the novel design and synthesis of an advanced category of CeO2/ CoS2 heterostructures, which combines the local photothermal effect (LPTE) action of CeO2 and the pho-toelectric effect CoS2 to boost OER. Interestingly, the hollow framework, rich heterointerface, coupled local photothermal effect and photoelectric effect equip CeO2/CoS(2 )with remarkably excellent electrocatalytic OER performance. As a result, the optimized CeO2/CoS2-6 only needs an overpotential of 283 mV to reach 10 mA cm(-2) as well as a smaller Tafel slop of 33.2 mV dec(-1), outperforming the RuO2 catalyst (323 mA @ 10 mA cm(-2)). Upon combination of experimental data and mechanistic study, it is revealed that the enhanced OER performance is primarily ascribed to the photo-induced local thermal. partly resulting from photoelectric effect, where the photogenerated electron flow from CeO2 to CoS2 can photogenerated holes in CeO2 to boost water oxidation. This work is extremely expected to offer a novel avenue for the rational design and fabrication of outstanding OER electrocatalysts upon LPTE. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:663 / 672
页数:10
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