化学
单层
半导体
自旋(空气动力学)
分子
自旋极化
化学物理
电子
极化(电化学)
过渡金属
凝聚态物理
催化作用
光电子学
量子力学
材料科学
物理化学
有机化学
物理
热力学
生物化学
作者
Yufeng Liu,Taketo Handa,Nicholas Olsen,Colin Nuckolls,Xiaoyang Zhu
摘要
Spin-polarized electrons can improve the efficiency and selectivity of photo- and electro-catalytic reactions, as demonstrated in the past with magnetic or magnetized catalysts. Here, we present a scheme in which spin-polarized charge separation occurs at the interfaces of nonmagnetic semiconductors and molecular films in the absence of a magnetic field. We take advantage of the spin-valley-locked band structure and valley-dependent optical selection rule in group VI transition metal dichalcogenide (TMDC) monolayers to generate spin-polarized electron–hole pairs. Photoinduced electron transfer from WS2 to fullerene (C60) and hole transfer from MoSe2 to phthalocyanine (H2Pc) are found to result in spin polarization lifetimes that are 1 order of magnitude longer than those in the TMDC monolayers alone. Our findings connect valleytronic properties of TMDC monolayers to spin-polarized interfacial charge transfer and suggest a viable route toward spin-selective photocatalysis.
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