锐钛矿
材料科学
异质结
分解水
金红石
带隙
量子点
二氧化钛
氧化钛
氧化物
制氢
相(物质)
纳米颗粒
氢
化学工程
光电子学
纳米技术
光催化
化学
催化作用
有机化学
工程类
生物化学
冶金
作者
Li Shi,Daniele Benetti,Faying Li,Qin Wei,Federico Rosei
标识
DOI:10.1016/j.apcatb.2019.118317
摘要
Photoelectrochemical (PEC) water splitting is a promising and environmentally friendly approach towards sustainable hydrogen generation. Due to its excellent photostability and favorable band alignment, titanium dioxide (TiO2) is one of the most common metal oxide for water splitting. However, the efficiency in TiO2-based PEC systems is limited by the high recombination of photo-generated electron/hole pairs and large intrinsic band gap (3.2 eV) which limit the absorption of the sunlight. Herein, we explore a simple metal organic framework (MOF)-derived synthesis to obtain a controlled mixed-phase (anatase and rutile) of TiO2 nanoparticles, which retain the MOF crystal morphology. Compared with commercial TiO2 films, the MOF-derived TiO2 film sensitized by core-shell [email protected] QDs, showed an enhanced PEC device stability of +42.1% and PEC performance of +47.6%. The enhanced performance is due to the presence of the mixed rutile/anatase phases, that creates a favorable band energy alignment for the separation of the photogenerated charges. The proposed MOF-derived TiO2 is an efficient strategy to improve the efficiency of the TiO2-QDs heterojunction based PEC system for hydrogen generation.
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