Molten state synthesis of nickel phosphides: mechanism and composition-activity correlation for electrochemical applications

Nickel phosphides are highly attractive low-cost (electro)catalysts, thanks to their unique electronic structure, versatile phase diagram, and chemical stability. Herein, we describe a single-step, simple, and scalable synthesis of nickel phosphides, with good control over phase composition, size, a...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-12, Vol.9 (48), p.27629-27638
Hauptverfasser: Geva, Rotem, Levy, Natasha Ronith, Tzadikov, Jonathan, Cohen, Reut, Weitman, Michal, Xing, Lidan, Abisdris, Liel, Barrio, Jesús, Xia, Jiawei, Volokh, Michael, Ein-Eli, Yair, Shalom, Menny
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Sprache:eng
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Zusammenfassung:Nickel phosphides are highly attractive low-cost (electro)catalysts, thanks to their unique electronic structure, versatile phase diagram, and chemical stability. Herein, we describe a single-step, simple, and scalable synthesis of nickel phosphides, with good control over phase composition, size, and catalytic activity, by a direct thermal reaction of nickel nitrate hexahydrate and triphenylphosphine (PPh 3 ). Advanced analytic tools combined with theoretical calculations reveal that upon heating, nickel ions are dissolved and coordinated by PPh 3 , enabling the synthesis of fine-tuned particles, with nickel phosphide phases ranging from Ni 3 P to Ni 2 P. The new synthetic method enables comprehending the correlation between phase composition and the phosphides' catalytic activity. This work shows a clear composition-activity trend of the optimized nickel phosphides both as electrocatalysts for the hydrogen evolution reaction in acidic media and as anode materials in Li-ion batteries. A straightforward, benign, scalable and low-cost molten-state synthesis of nickel phosphides with tunable phase composition, applied both as electrocatalysts for hydrogen evolution reaction and as anode materials for Li-ion batteries.
ISSN:2050-7488
2050-7496
DOI:10.1039/d1ta08455k