光激发
工作职能
材料科学
电子
带材弯曲
欧姆接触
辐照
金属
光化学
化学
原子物理学
纳米技术
光电子学
激发态
物理
量子力学
核物理学
冶金
图层(电子)
作者
Rong Fu,Zewen Wu,Ziye Pan,Zhuoyang Gao,Zhen Li,Xianghua Kong,Lu Li
标识
DOI:10.1002/anie.202100572
摘要
Abstract The first observation of surface metallization of TiO 2− x induced by fluoride ions is presented. The emerging metallic states are contributed by the 3d orbital of surface Ti and the 2p orbital of surface bridging F, which are intrinsically originated from the strong electron repulsion between F − and adjacent Ti 3+ . The metalized TiO 2− x with reduced work function and downward band bending possesses high electron‐donating power to supported Ru species via atomic‐scale ohmic contacts, exhibiting unprecedented photocatalytic performances for ammonia synthesis across the entire solar spectrum region (200–1550 nm) at room temperature. Mechanism and kinetic analysis revealed that the loaded Ru could behave as efficient electron sinks to accumulate photogenerated electrons and that the metallic surface markedly enhanced the dissociation of H 2 and N 2 by the hot electrons generated by the visible or even infrared light irradiation.
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