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Ni‐Metalloid (B, Si, P, As, and Te) Alloys as Water Oxidation Electrocatalysts
Author(s) -
Masa Justus,
Piontek Stefan,
Wilde Patrick,
Antoni Hendrik,
Eckhard Till,
Chen YenTing,
Muhler Martin,
Apfel UlfPeter,
Schuhmann Wolfgang
Publication year - 2019
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201900796
Subject(s) - metalloid , materials science , nickel , oxygen evolution , metal , catalysis , inorganic chemistry , electrolyte , adsorption , chemical engineering , electronic structure , chemistry , metallurgy , electrode , electrochemistry , computational chemistry , engineering , biochemistry
Breakthroughs toward effective water‐splitting electrocatalysts for mass hydrogen production will necessitate material design strategies based on unexplored material chemistries. Herein, Ni‐metalloid (B, Si, P, As, Te) alloys are reported as an emergent class of highly promising electrocatalysts for the oxygen evolution reaction (OER) and insight is offered into the origin of activity enhancement on the premise of the surface electronic structure, the OER activation energy, influence of the guest metalloid elements on the lattice structure of the host metal (Ni), and surface‐oxidized metalloid oxoanions. The metalloids modify the lattice structure of Ni, causing changes in the nearest Ni–Ni interatomic distance ( d Ni–Ni ). The activation energy E a scales with d Ni–Ni indicating an apparent dependence of the OER activity on lattice properties. During the OER, surface Ni atoms are oxidized to nickel oxyhydroxide, which is the active state of the catalyst, meanwhile, the surface metalloids are oxidized to the corresponding oxoanions that affect the interfacial electrode/electrolyte properties and hence the adsorption/desorption interaction energies of the reacting species.