Journal
SMALL
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202302685
Keywords
amorphous structures; hydrogen evolution reaction; nanocages; P doping; PtTe2
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In this work, phosphorus-doped (P-doped) PtTe2 nanocages with abundant amorphous and crystalline interface (A/C-P-PtTe2) were successfully synthesized via a simple template-free hydrothermal method. The P doping induced atomic Te vacancies on the basal planes of PtTe2, resulting in unsaturated Pt atoms as active sites for the hydrogen evolution reaction (HER) in the amorphous layer. The defective structure of A/C-P-PtTe2 catalysts exhibited fast Tafel step kinetics, leading to an ultralow overpotential and a small Tafel slope in HER.
PtTe2, a member of the noble metal dichalcogenides (NMDs), has aroused great interest in exploring its behavior in the hydrogen evolution reaction (HER) due to the unique type-II topological semimetallic nature. In this work, a simple template-free hydrothermal method to obtain the phosphorus-doped (P-doped) PtTe2 nanocages with abundant amorphous and crystalline interface (A/C-P-PtTe2) is developed. Revealed by density functional theory calculations, the atomic Te vacancies can spontaneously form on the basal planes of PtTe2 by the P doping, which results in the unsaturated Pt atoms exposed as the active sites in the amorphous layer for HER. Owing to the defective structure, the A/C-P-PtTe2 catalysts have the fast Tafel step determined kinetics in HER, which contributes to an ultralow overpotential (eta = 28 mV at 10 mA cm(-2)) and a small Tafel slope of 37 mV dec(-1). More importantly, benefiting from the inner stable crystalline P-PtTe2 nanosheets, limited decay of the performance is observed after chronopotentiometry test. This work reveals the important role of the inherent relationship between structure and activity in PtTe2 for HER, which may bring another enlightenment for the design of efficient catalysts based on NMDs in the near future.
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