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Unveiling the Mechanisms Ruling the Efficient Hydrogen Evolution Reaction with Mitrofanovite Pt3Te4
Author(s) -
Danil W. Boukhvalov,
Jia Cheng,
Gianluca D’Olimpio,
François Bocquet,
Chia-Nung Kuo,
Anan Bari Sarkar,
Barun Ghosh,
I. Vobornik,
Jun Fujii,
Kuan H. Hsu,
Li-Min Wang,
Ori Azulay,
Gopi Nath Daptary,
Doron Naveh,
C. S. Lue,
Mykhailo Vorokhta,
Amit Agarwal,
Lixue Zhang,
Antonio Politano
Publication year - 2021
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.1c01261
Subject(s) - overpotential , tafel equation , electrocatalyst , catalysis , hydrogen , electrode , materials science , density functional theory , conductivity , chemistry , chemical engineering , chemical physics , computational chemistry , electrochemistry , organic chemistry , engineering
By means of electrocatalytic tests, surface-science techniques and density functional theory, we unveil the physicochemical mechanisms ruling the electrocatalytic activity of recently discovered mitrofanovite (Pt 3 Te 4 ) mineral. Mitrofanovite represents a very promising electrocatalyst candidate for energy-related applications, with a reduction of costs by 47% compared to pure Pt and superior robustness to CO poisoning. We show that Pt 3 Te 4 is a weak topological metal with the Z 2 invariant, exhibiting electrical conductivity (∼4 × 10 6 S/m) comparable with pure Pt. In hydrogen evolution reaction (HER), the electrode based on bulk Pt 3 Te 4 shows a very small overpotential of 46 mV at 10 mA cm -2 and a Tafel slope of 36-49 mV dec -1 associated with the Volmer-Heyrovsky mechanism. The outstanding ambient stability of Pt 3 Te 4 also provides durability of the electrode and long-term stability of its efficient catalytic performances.

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