Metal-organic framework derived CoSe2 nanoparticles anchored on carbon fibers as bifunctional electrocatalysts for efficient overall water splitting

被引:214
作者
Sun, Chencheng [1 ,2 ]
Dong, Qiuchun [1 ,2 ]
Yang, Jun [1 ,2 ]
Dai, Ziyang [1 ,2 ]
Lin, Jianjian [1 ,2 ]
Chen, Peng [3 ]
Huang, Wei [1 ,2 ]
Dong, Xiaochen [1 ,2 ]
机构
[1] Nanjing Tech Univ NanjingTech, Key Lab Flexible Elect KLOFE, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[2] Nanjing Tech Univ NanjingTech, IAM, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[3] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
基金
中国国家自然科学基金;
关键词
metal-organic framework; cobalt selenide; electrocatalyst; overall water splitting; HYDROGEN EVOLUTION REACTION; OXYGEN REDUCTION; HIGH-PERFORMANCE; CATALYSTS; MOLYBDENUM; NANOSHEETS; MECHANISM; GRAPHENE; STORAGE; DESIGN;
D O I
10.1007/s12274-016-1110-1
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
The development of efficient, low-cost, stable, non-noble-metal electrocatalysts for water splitting, particularly those that can catalyze both the hydrogen evolution reaction (HER) at the cathode and oxygen evolution reaction (OER) at the anode, is a challenge. We have developed a facile method for synthesizing CoSe2 nanoparticles uniformly anchored on carbon fiber paper (CoSe2/CF) via pyrolysis and selenization of in situ grown zeolitic imidazolate framework-67 (ZIF-67). CoSe2/CF shows high and stable catalytic activity in both the HER and OER in alkaline solution. At a low cell potential, i.e., 1.63 V, a water electrolyzer equipped with two CoSe2/CF electrodes gave a water-splitting current of 10 mA center dot cm(-2). At a current of 20 mA center dot cm(-2), it can operate without degradation for 30 h. This study not only offers a cost-effective solution for water splitting but also provides a new strategy for developing various catalytic nanostructures by changing the metal-organic framework precursors.
引用
收藏
页码:2234 / 2243
页数:10
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