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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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Published in: | International journal of hydrogen energy 2022-04, Vol.47 (33), p.14896-14905 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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.
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•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. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2022.03.017 |