Zhang Zhijie, Li Liang, Jiang Ying, Xu Jiayue
School of Materials Science and Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, P. R. China.
Inorg Chem. 2022 Feb 21;61(7):3351-3360. doi: 10.1021/acs.inorgchem.2c00012. Epub 2022 Feb 9.
Heterojunction manipulation has been deemed as a promising approach in exploring efficient photocatalysts for CO reduction. In this article, a novel step-scheme (S-scheme) photocatalyst of CsPbBr quantum dots/BiOBr nanosheets (CPB/BiOBr) was fabricated via a facile self-assembly process. The strong interaction, staggered energy band alignments, and much different Fermi levels between CsPbBr and BiOBr promised the formation of an S-scheme heterojunction. The resultant CPB/BiOBr heterojunction delivered remarkable photocatalytic performance in CO reduction, with an electron consumption rate of 72.3 μmol g h, which was 4.1 and 5.7 times that of single CsPbBr and BiOBr, respectively. The superior photocatalytic performance originated from the impactful spatial separation of photoinduced electron-hole pairs, as well as the preservation of strongly reductive electrons for CO reduction. This work offers a rational strategy to design S-scheme heterojunctions based on lead halide perovskites, which are expected to have potential applications in the field of photocatalysis and solar energy utilization.
异质结调控被认为是探索用于CO还原的高效光催化剂的一种有前景的方法。在本文中,通过简便的自组装过程制备了一种新型的CsPbBr量子点/BiOBr纳米片(CPB/BiOBr)阶梯型(S型)光催化剂。CsPbBr和BiOBr之间的强相互作用、交错的能带排列以及显著不同的费米能级促成了S型异质结的形成。所得的CPB/BiOBr异质结在CO还原中表现出卓越的光催化性能,电子消耗速率为72.3 μmol g⁻¹ h⁻¹,分别是单一CsPbBr和BiOBr的4.1倍和5.7倍。优异的光催化性能源于光生电子-空穴对的有效空间分离,以及用于CO还原的强还原性电子的保留。这项工作为基于卤化铅钙钛矿设计S型异质结提供了合理策略,有望在光催化和太阳能利用领域具有潜在应用。