Phase-junction design of MOF-derived TiO2 photoanodes sensitized with quantum dots for efficient hydrogen generation

被引:82
作者
Shi, Li [1 ,2 ]
Benetti, Daniele [1 ]
Li, Faying [1 ,2 ]
Wei, Qin [2 ]
Rosei, Federico [1 ]
机构
[1] Inst Natl Rech Sci, Ctr Energy Mat & Telecommun, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
[2] Univ Jinan, Key Lab Interfacial React & Sensing Anal Univ Sha, Sch Chem & Chem Engn, Jinan 250022, Peoples R China
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Photoelectrochemical water splitting; Hydrogen generation; Metal organic framework; Mixed-phase TiO2; Quantum dots; ENHANCED PHOTOCATALYTIC ACTIVITY; PHOTOELECTROCHEMICAL CELLS; CHARGE-TRANSFER; WATER; CDSE; NH2-MIL-125(TI); PHOTOACTIVITY; NANOCRYSTALS; NANOHYBRIDS; PERFORMANCE;
D O I
10.1016/j.apcatb.2019.118317
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 CdSe@CdS 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.
引用
收藏
页数:10
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