Yuan Zhenting, Huang Huoshuai, Li Najun, Chen Dongyun, Xu Qingfeng, Li Hua, He Jinghui, Lu Jianmei
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215123, China.
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215123, China; National Center of International Research on Intelligent New Nanomaterials and Detection Technologies in Environmental Protection, Suzhou 215123, China.
J Hazard Mater. 2021 May 5;409:125027. doi: 10.1016/j.jhazmat.2020.125027. Epub 2021 Jan 2.
TiC quantum dots (TQDs) derived from ultrathin few-layered TiC nanosheets were served as the low-cost solid electron mediator of photogenerated carriers at the semiconductor interfaces, which could greatly reserve the reductive and oxidative reaction sites on the surface of heterojunctions and accelerate the reduction and oxidation reactions. The all-solid-state TQDs-bridge WO/TQDs/InS Z-scheme photocatalysts exhibited extremely promoted photocatalytic reduction of Cr (VI) and photocatalytic oxidation of Bisphenol A (BPA) under visible light irradiation, which are 4 and 3 times higher than that of WO/InS heterojunctions, respectively. The favorable photocatalytic activities of WO/TQDs/InS should attribute to the effective electron transfer and charges separation with introduction of TQDs as the electron mediators in the Z-scheme system. In addition, the stability of WO/TQDs/InS was investigated and the possible mechanisms during photo-reduction of Cr (VI) and photo-oxidation of BPA were proposed. This work provides a new strategy for fabrication of all-solid-state Z-scheme heterojunctions using TiC quantum dots as the low-cost solid electron mediator for efficient environmental remediation.
源自超薄少层TiC纳米片的TiC量子点(TQDs)作为半导体界面光生载流子的低成本固体电子介质,可极大地保留异质结表面的还原和氧化反应位点,并加速还原和氧化反应。全固态TQDs桥连的WO/TQDs/InS Z型光催化剂在可见光照射下对Cr(VI)的光催化还原和双酚A(BPA)的光催化氧化表现出极大的促进作用,分别比WO/InS异质结高4倍和3倍。WO/TQDs/InS良好的光催化活性应归因于在Z型体系中引入TQDs作为电子介质实现了有效的电子转移和电荷分离。此外,研究了WO/TQDs/InS的稳定性,并提出了Cr(VI)光还原和BPA光氧化过程中的可能机理。这项工作为使用TiC量子点作为低成本固体电子介质制备全固态Z型异质结以进行高效环境修复提供了一种新策略。