材料科学
催化作用
化学物理
氢
金属
过渡金属
原子轨道
离解(化学)
卟啉
石墨烯
活动站点
纳米技术
光化学
物理化学
化学
电子
有机化学
物理
量子力学
冶金
作者
Woon Ih Choi,Brandon C. Wood,Eric Schwegler,Tadashi Ogitsu
标识
DOI:10.1002/aenm.201501423
摘要
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
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