兴奋剂
化学物理
氧气
氧原子
材料科学
格子(音乐)
氢
化学
电荷(物理)
氢原子
结晶学
Atom(片上系统)
光化学
分子
光电子学
物理
有机化学
计算机科学
嵌入式系统
量子力学
声学
烷基
作者
Yi Ding,Fei Lu,Fengchu Zhang,Shoujie Liu,Bo Zhou,Denglei Gao,Xi Wang,Jiannian Yao
标识
DOI:10.1002/anie.202004510
摘要
Abstract Single‐atom catalysts have attracted much attention. Reported herein is that regulating charge transfer of lattice oxygen atoms in serial single‐atom‐doped titania enables tunable hydrogen evolution reaction (HER) activity. First‐principles calculations disclose that the activity of lattice oxygen for the HER can be regularly promoted by substituting its nearest metal atom, and doping‐induced charge transfer plays an essential role. Besides, the realm of the charge transfer of the active site can be enlarged to the second nearest atom by creating oxygen vacancies, resulting in further optimization for the HER. Various single‐atom‐doped titania nanosheets were fabricated to validate the proposed model. Taking advantage of the localized charge transfer to the lattice atom is demonstrated to be feasible for realizing precise regulation of the electronic structures and thus catalytic activity of the nanosheets.
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