Anchoring of Ni12P5 Microbricks in Nitrogen- and Phosphorus-Enriched Carbon Frameworks: Engineering Bifunctional Active Sites for Efficient Water-Splitting Systems

The demand for developing high-efficiency multifunctional electrocatalysts with a long-term stability rapidly increases for achieving the commercialization of sustainable hydrogen (H2) production via cost-effective water electrolysis systems. This study describes single-phase metal-rich nickel phosp...

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Veröffentlicht in:ACS sustainable chemistry & engineering 2022-01, Vol.10 (3), p.1182-1194
Hauptverfasser: Janani, Gnanaprakasam, Surendran, Subramani, Choi, Hyeonuk, An, Tae-Yong, Han, Mi-Kyung, Song, Sun-Ju, Park, Woosung, Kim, Jung Kyu, Sim, Uk
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Sprache:eng
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Zusammenfassung:The demand for developing high-efficiency multifunctional electrocatalysts with a long-term stability rapidly increases for achieving the commercialization of sustainable hydrogen (H2) production via cost-effective water electrolysis systems. This study describes single-phase metal-rich nickel phosphide (Ni12P5)-incorporated carbon composites for a highly efficient water-splitting system. The distinct Ni12P5 is anchored in nitrogen (N)- and phosphorus (P)-rich carbon matrices (Ni12P5@N,P-C); the creation of the matrices entails a facile hydrothermal-followed pyrolysis treatment to explore their bifunctional activities in the water-splitting system. Owing to the superior activity of the rich Ni (δ+) component for the production of molecular oxygen and that of P (δ−)­and N species in the carbon framework for hydrogen adsorption, the optimized Ni12P5@N,P-C composites contribute effectively toward both high oxygen evolution and hydrogen evolution reactions. Consequently, the Ni12P5@N,P-C composite-based two-electrode water-splitting system shows a low operating potential of 1.57 V at 10 mA cm–2 and achieves the commercially required high current density of 500 mA cm–2 at a stable potential of 2 V. The functionalization of composite electrocatalysts based on strategical engineering and the intrusion of multiple active sites can help develop enhanced electrochemical energy systems.
ISSN:2168-0485
2168-0485
DOI:10.1021/acssuschemeng.1c06514