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Combinatorial Search for High‐Activity Hydrogen Catalysts Based on Transition‐Metal‐Embedded Graphitic Carbons
Author(s) -
Choi Woon Ih,
Wood Brandon C.,
Schwegler Eric,
Ogitsu Tadashi
Publication year - 2015
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.201501423
Subject(s) - materials science , catalysis , chemical physics , hydrogen , metal , transition metal , atomic orbital , dissociation (chemistry) , porphyrin , graphene , active site , nanotechnology , photochemistry , chemistry , electron , organic chemistry , physics , quantum mechanics , metallurgy
Transition metal (TM) atoms in porphyrin‐like complexes play important roles in many protein and enzymetic systems, where crystal‐field effects are used to modify d‐orbital levels. Inspired by the tunable electronic structure of these motifs, a high‐throughput computational search for synthetic hydrogen catalysts is performed based on a similar motif of TM atoms embedded into the lattice of graphene. Based on an initial list of 300 possible embedding geometries, binders, and host atoms, descriptors for stability and catalytic activity are applied to extract ten promising candidates for hydrogen evolution, two of which are expected to exhibit high activity for hydrogen oxidation. In several instances, the active TM atoms are earth‐abundant elements that show no activity in the bulk phase, highlighting the importance of the coordination environment in tuning the d‐orbitals. In addition, it is found that the most active candidates involve a hitherto unreported surface reaction pathway that involves a Kubas‐complex intermediate, which significantly lowers the kinetic barrier associated with hydrogen dissociation and association