Recently, several researchers have claimed the existence of superior catalytic activity associated with topological materials belonging to the class of Dirac/Weyl semimetals, owing to the high electron conductivity and charge carrier mobility in these topological materials. By means of X-ray photoelectron spectroscopy, electrocatalytic tests, and density functional theory, we have investigated the chemical reactivity (chemisorption of ambient gases), ambient stability, and catalytic properties of PdSn4, a topological semimetal showing Dirac node arcs. We find a Tafel slope of 83 mV in the hydrogen evolution reaction (HER) dec-1 with an overpotential of 50 mV, with performances resembling those of pure Pd, regardless of its limited amount in the alloy, with a subsequent reduction in the cost of raw materials by ~80%. Remarkably, the PdSn4-based electrode shows superior robustness to CO compared to pure Pd and Pt and high stability in water media, although the PdSn4 surface is prone to oxidation with the formation of a sub-nanometric SnO2 skin. Moreover, we also assessed the significance of the role of topological electronic states in the observed catalytic properties. Actually, the peculiar atomic structure of oxidized PdSn4 enables the migration of hydrogen atoms through the Sn-O layer with a barrier comparable with the energy cost of the Heyrovsky step of HER over Pt(111) in acidic media (0.1 eV). On the other hand, the topological properties play a minor role, if existing, contrarily to the recent reports overestimating their contribution in catalytic properties.

Efficient Electrochemical Water Splitting with PdSn4 Dirac Nodal Arc Semimetal

Silvia Nappini;Andrea Marchionni;Jonathan Filippi;Silvia Mauri;Piero Torelli;Francesco Vizza;
2021

Abstract

Recently, several researchers have claimed the existence of superior catalytic activity associated with topological materials belonging to the class of Dirac/Weyl semimetals, owing to the high electron conductivity and charge carrier mobility in these topological materials. By means of X-ray photoelectron spectroscopy, electrocatalytic tests, and density functional theory, we have investigated the chemical reactivity (chemisorption of ambient gases), ambient stability, and catalytic properties of PdSn4, a topological semimetal showing Dirac node arcs. We find a Tafel slope of 83 mV in the hydrogen evolution reaction (HER) dec-1 with an overpotential of 50 mV, with performances resembling those of pure Pd, regardless of its limited amount in the alloy, with a subsequent reduction in the cost of raw materials by ~80%. Remarkably, the PdSn4-based electrode shows superior robustness to CO compared to pure Pd and Pt and high stability in water media, although the PdSn4 surface is prone to oxidation with the formation of a sub-nanometric SnO2 skin. Moreover, we also assessed the significance of the role of topological electronic states in the observed catalytic properties. Actually, the peculiar atomic structure of oxidized PdSn4 enables the migration of hydrogen atoms through the Sn-O layer with a barrier comparable with the energy cost of the Heyrovsky step of HER over Pt(111) in acidic media (0.1 eV). On the other hand, the topological properties play a minor role, if existing, contrarily to the recent reports overestimating their contribution in catalytic properties.
2021
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Istituto Officina dei Materiali - IOM -
Istituto per la Microelettronica e Microsistemi - IMM
Inglese
11
12
7311
7318
8
https://pubs.acs.org/doi/10.1021/acscatal.1c01653
Esperti anonimi
density functional theory; electrochemistry; hydrogen evolution reaction; surface science; topological materials
11
info:eu-repo/semantics/article
262
W Boukhvalov, Danil; Kuo, Chianung; Nappini, Silvia; Marchionni, Andrea; D'Olimpio, Gianluca; Filippi, Jonathan; Mauri, Silvia; Torelli, Piero; Shan L...espandi
01 Contributo su Rivista::01.01 Articolo in rivista
open
   FISR 2019 AMPERE
   AMPERE
   Ministero dell'Università e della Ricerca
   FISR 2019
   FISR2019_01294

   PRIN 2017YH9MRK
   PRIN 2017
   Ministero dell'Università e della Ricerca
   PRIN 2017
   2017YH9MRK
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/396956
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