Co 2 P nanowire arrays anchored on a 3D porous reduced graphene oxide matrix embedded in nickel foam for a high-efficiency hydrogen evolution reaction

Regulating the structural and interfacial properties of transition metal phosphides (TMPs) by coupling carbon-based materials with large surface areas to enhance hydrogen evolution reaction (HER) performance presents significant progress for water splitting technology. Herein, we constructed a compo...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2023-08, Vol.52 (33), p.11526-11534
Hauptverfasser: Wang, Yuanqiang, Wang, Ting, Yang, Mengru, Rui, Yichuan, Xue, Zhili, Zhu, Haozhen, Wang, Chengjie, Li, Jing, Chen, Binling
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Sprache:eng
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Zusammenfassung:Regulating the structural and interfacial properties of transition metal phosphides (TMPs) by coupling carbon-based materials with large surface areas to enhance hydrogen evolution reaction (HER) performance presents significant progress for water splitting technology. Herein, we constructed a composite substrate of a three-dimensional porous graphene oxide matrix (3D-GO) embedded in nickel foam (NF) to grow a Co P electrocatalyst. Well-defined gladiolus-like Co P nanowire arrays tightly anchored on the substrate show enhanced electrochemical characteristics for the hydrogen evolution reaction (HER) based on the promoting roles of 3D porous reduced GO (3D-rGO) derived from 3D-GO, which promotes the dispersion of active components, improves the rate of electron transfer, and facilitates the transport of water molecules. As a result, the obtained Co P@3D-rGO/NF electrode exhibits superior HER activity in 1.0 M KOH media, achieving overpotentials of 36.5 and 264.7 mV at current densities of 10 and 100 mA cm , respectively. The electrode also has a low Tafel slope of 55.5 mV dec , a large electrochemical surface area, and small charge-transfer resistance, further revealing its mechanism of high intrinsic activity. Moreover, the electrode exhibits excellent HER stability and durability without surface morphology and chemical state changes.
ISSN:1477-9226
1477-9234
DOI:10.1039/D3DT01367G