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A bi-functional Co–Ni layered double hydroxide three-dimensional porous array electrode derived from ZIF-L(Co)@ZIF-L(Co, Ni) for oxygen evolution reaction and supercapacitors

Developing high-efficiency bifunctional materials for electro-catalysis and supercapacitors are urgently needed but challenging. Herein, we develop a self-supporting Co–Ni LDH electrode prepared by in-situ growing ZIF-L(Co)@ZIF-L(Co, Ni) on carbon paper followed by a pseudomorphic transformation. Th...

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Bibliographic Details
Published in:International journal of hydrogen energy 2022-04, Vol.47 (33), p.14896-14905
Main Authors: Chen, Chao, Deng, Xiaohua, Deng, Yingjie, An, Lu, Deng, Yijie, Zheng, Yuying, Dang, Dai, Yang, Xu
Format: Article
Language:English
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Summary:Developing high-efficiency bifunctional materials for electro-catalysis and supercapacitors are urgently needed but challenging. Herein, we develop a self-supporting Co–Ni LDH electrode prepared by in-situ growing ZIF-L(Co)@ZIF-L(Co, Ni) on carbon paper followed by a pseudomorphic transformation. The optimized Co–Ni LDH/carbon paper electrodes (CN-2/CP) exhibit excellent electrochemical activity and stability in oxygen evolution reactions (OER) and supercapacitors. The CN-2/CP electrode displays a low overpotential of 230 mV at 10 mA cm−2 and superior stability at 40-h chronopotentiometry for OER. For supercapacitor, the CN-2/CP electrode delivers a high specific capacitance of 1346 F g−1 at 1 A g−1 and maintains a capacitance of 88.5% after 7000 charge/discharge cycles at 20 A g−1. Based on the physical and chemical characterization results, the high performance originates from the in-situ electrochemical conversion of metal hydroxide, improved conductivity, fast charge transfer at the interface and unique layered cross morphology providing more active sites. [Display omitted] •In-situ synthesis of Co–Ni LDH 3D porous array on carbon paper.•The self-supported electrode exhibits high OER performance and stability.•The large surface area and high porosity of CoNi LDH provide abundant active sites.
ISSN:0360-3199
1879-3487
DOI:10.1016/j.ijhydene.2022.03.017