光催化
材料科学
载流子
光化学
铼
氢
分解水
光电子学
化学
催化作用
有机化学
冶金
作者
Jianmin Yu,Sohyeon Seo,Yongguang Luo,Yan Sun,Simgeon Oh,Chau T. K. Nguyen,Changwon Seo,Ji‐Hee Kim,Joonsoo Kim,Hyoyoung Lee
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-01-28
卷期号:14 (2): 1715-1726
被引量:57
标识
DOI:10.1021/acsnano.9b07366
摘要
Effective charge separation and rapid transport of photogenerated charge carriers without self-oxidation in transition metal dichalcogenide photocatalysts are required for highly efficient and stable hydrogen generation. Here, we report that a molecular junction as an electron transfer path toward two-dimensional rhenium disulfide (2D ReS2) nanosheets from zero-dimensional titanium dioxide (0D TiO2) nanoparticles induces high efficiency and stability of solar hydrogen generation by balanced charge transport of photogenerated charge carriers. The molecular junctions are created through the chemical bonds between the functionalized ReS2 nanosheets (e.g., −COOH groups) and −OH groups of two-phase TiO2 (i.e., ReS2–C6H5C(═O)–O–TiO2 denoted by ReS2–BzO–TiO2). This enhances the chemical energy at the conduction band minimum of ReS2 in ReS2–BzO–TiO2, leading to efficiently improved hydrogen reduction. Through the molecular junction (a Z-scheme charge transfer path) in ReS2–BzO–TiO2, recombination of photogenerated charges and self-oxidation of the photocatalyst are restrained, resulting in a high photocatalytic activity (9.5 mmol h–1 per gram of ReS2 nanosheets, a 4750-fold enhancement compared to bulk ReS2) toward solar hydrogen generation with high cycling stability of more than 20 h. Our results provide an effective charge transfer path of photocatalytic TMDs by preventing self-oxidation, leading to increases in photocatalytic durability and a transport rate of the photogenerated charge carriers.
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