A one-stone-two-birds strategy to construct metal-organic framework-derived cobalt phosphide as an efficient bifunctional electrocatalyst for oxygen electrode reactions
Materials derived from metal-organic frameworks (MOFs) are promising oxygen electrocatalysts for zinc-air batteries (ZABs). Rational design of precursors and introduction of heteroatoms are effective strategies for optimizing the performance of MOF-derived catalysts. Herein, a facile one-stone-two-b...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-07, Vol.11 (27), p.156-1513 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Materials derived from metal-organic frameworks (MOFs) are promising oxygen electrocatalysts for zinc-air batteries (ZABs). Rational design of precursors and introduction of heteroatoms are effective strategies for optimizing the performance of MOF-derived catalysts. Herein, a facile one-stone-two-birds strategy is proposed to achieve dual-regulation on geometric and electronic structures by constructing a phytic acid cross-linked metal ion (M-PA) network film on the surface of 2D Zn/Co ZIF-L, followed by an annealing procedure. The resultant catalyst composed of cobalt phosphide nanoparticles and N, P co-doped carbon substrates (denoted as Co
2
P@NPC) exhibits high bifunctional activity towards the oxygen reduction reaction (
E
1/2
= 0.852 V) and oxygen evolution reaction (
η
10
= 336 mV). Moreover, the quasi-solid-state ZAB assembled with Co
2
P@NPC also delivers a promising power density and long cycling stability. The present work demonstrates an effective strategy to develop MOF-derived materials with a protected morphology and optimized electronic structures.
A MOF-derived electrocatalyst composed of N, P co-doped carbon and cobalt phosphide (Co
2
P@NPC) is fabricated as an efficient bifunctional electrocatalyst towards the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta02434b |