Boosting the photocatalytic activity of CdLa2S4 for hydrogen production using Ti3C2 MXene as a co-catalyst

被引:177
|
作者
Cheng, Lin [1 ]
Chen, Qian [1 ]
Li, Juan [1 ]
Liu, Hong [1 ]
机构
[1] Shanghai Univ, Sch Environm & Chem Engn, Dept Chem Engn, 99 Shangda Rd, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
CdLa2S4; Ti3C2; Photocatalytic; Co-catalyst; H-2; evolution; NANOSHEETS; HETEROJUNCTION; NANOCRYSTALS; COMPOSITE; EVOLUTION; HYBRIDS; G-C3N4;
D O I
10.1016/j.apcatb.2019.118379
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
Exploring efficient, stable and low-cost photocatalysts for photocatalytic hydrogen production remains a challenge in the field of energy conversion. Here, two-dimensional Ti3C2 nanosheets were fabricated via etching Ti3AlC2 with HF, followed by ultrasonic exfoliation. Then CdLa2S4/Ti3C2 nanocomposites were fabricated by growing CdLa2S4 nanoparticles in situ on the surface of these Ti3C2 nanosheets. The resultant CdLa2S4/Ti3C2 nanocomposites exhibited an excellent photocatalytic activity for H-2 production from water splitting under visible light illumination. When the content of Ti3C2 was 1.0 wt%, the CdLa2S4/Ti3C2 nanocomposites presented maximum hydrogen production rate of 11182.4 mu mol.g(-1).h(-1), which was 13.4 times as high as that of pristine CdLa2S4 and even outperformed Pt-loaded CdLa2S4. The apparent quantum efficiency reached 15.6% at 420 nm. In addition, the CdLa2S4/Ti3C2 photocatalyst still maintained high photocatalytic activity after six cycles. The exceptional performance of CdLa2S4/Ti3C2 originated from the superior electrical conductivity of Ti3C2 MXene, which facilitated the separation of photo-generated electron-hole pairs. This work presents the potential of earth-abundant MXene materials in the construction of high efficiency and low-cost photocatalysts toward solar energy conversion.
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页数:9
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