Facile synthesis of CeO2-decorated W@Co-MOF heterostructures as a highly active and durable electrocatalyst for overall water splitting

被引:0
作者
Su, Chang [1 ]
Wang, Dan [2 ]
Wang, Wenchang [2 ,3 ]
Mitsuzaki, Naotoshi [4 ]
Chen, Zhidong [1 ,2 ]
机构
[1] Changzhou Univ, Sch Mat Sci & Engn, Changzhou 213164, Jiangsu, Peoples R China
[2] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[3] NERC Biomass Changzhou Univ, Anal & Testing Ctr, Changzhou 213032, Jiangsu, Peoples R China
[4] Qualtec Co Ltd, Osaka 5900906, Japan
基金
中国国家自然科学基金;
关键词
OXYGEN EVOLUTION; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT HYDROGEN; NANOSHEETS; ARRAYS; CARBON; CEO2;
D O I
10.1039/d4cp01350f
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
Rational coupling of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) catalysts is extremely important for practical overall water splitting; however, it is still challenging to construct such bifunctional heterostructures. Herein, a CeO2/W@Co-MOF/NF bifunctional electrocatalyst was prepared via a two-step in situ growth method involving an electrodeposition process. The incorporation of the W element enhanced the electronic interaction and enlarged the electrochemical surface area. After the electrodeposition of CeO2, the obtained CeO2/W@Co-MOF/NF possessed abundant heterointerfaces with a modulated local distribution, which promoted water dissociation and rapid electrocatalytic kinetics. In particular, it required very low overpotentials of 239 mV and 87 mV to reach a current density of 10 mA cm(-2) in OER and HER, respectively. A corresponding alkaline electrolysis cell afforded a cell voltage of 1.54 V at 10 mA cm(-2) to boost overall water splitting. This work provides a feasible strategy to fabricate MOF-based complexes and explores their possible use as bifunctional catalysts toward overall water splitting.
引用
收藏
页码:18953 / 18961
页数:9
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