期刊
ENERGY & ENVIRONMENTAL SCIENCE
卷 13, 期 6, 页码 1799-1807出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ee00666a
关键词
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资金
- Australian Government
- Australian Research Council [FT170100224, LE190100021]
- Australian Research Council [LE190100021] Funding Source: Australian Research Council
Heterostructured catalysts with unique interfaces and properties endow distinct advantages for many electrochemical reactions. Herein, a phosphine (PH3) vapor-assisted phase and structure engineering strategy is developed for the controllable conversion of non-active NiTe into a heterostructured active Ni2P/NiTe(2)catalyst for alkaline hydrogen evolution reaction (HER). The crystalline NiTe(2)phasein situgenerated in a PH(3)vapor environment and the nanosheet morphology both contribute to the outstanding alkaline HER performance with an overpotential of only 62 mV to achieve a current density of -10 mA cm(-2). Experimental and DFT mechanistic studies suggest the Ni2P/NiTe(2)interfaces provide abundant exposed active sites. The Ni2P/NiTe(2)catalyst shows the lowest kinetic barrier for water dissociation and the adsorbed H* can simultaneously bind to two Ni atoms at the interface of Ni2P/NiTe2(011), which greatly enhances the H* binding and HER activities. DFT simulation also shows that more electrons transfer from Ni atoms to H* on Ni2P/NiTe2(011) (0.22 e(-)) than that on NiTe2(011) (0.13 e(-)), which explains the enhanced H* binding at the Ni2P/NiTe2(011) interface. The PH(3)vapor synthetic approach is also applied to treat other chalcogenide-based materials with low HER activities, such as Ni3S2, to create Ni2P/NiS(2)interfaces for significantly enhanced HER activity.
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