异质结
光催化
纳米片
钙钛矿(结构)
卤化物
材料科学
光电子学
氧化物
化学工程
纳米技术
化学
无机化学
催化作用
冶金
生物化学
工程类
作者
Su‐Xian Yuan,Ke Su,You‐Xiang Feng,Min Zhang,Tong‐Bu Lu
标识
DOI:10.1016/j.cclet.2022.07.025
摘要
The elaborate regulation of heterostructure interface to accelerate the interfacial charge separation is one of practicable approaches to improve the photocatalytic CO2 reduction performance of halide perovskite (HP) materials. Herein, we report an in-situ growth strategy for the construction of 2D CsPbBr3 based heterostructure with perovskite oxide (SrTiO3) nanosheet as substrate (CsPbBr3/SrTiO3). Lattice matching and matchable energy band structures between CsPbBr3 and SrTiO3 endow CsPbBr3/SrTiO3 heterostructure with an efficient interfacial charge separation. Moreover, the interfacial charge transfer rate can be further accelerated by etching SrTiO3 with NH4F to form flat surface capped with Ti−O bonds. The resultant 2D/2D T-SrTiO3/CsPbBr3 heterostructure exhibits an impressive photocatalytic activity for CO2 conversion with a CO yield of 120.2 ± 4.9 µmol g−1 h−1 at the light intensity of 100 mW/cm2 and water as electron source, which is about 10 and 7 times higher than those of the pristine SrTiO3 and CsPbBr3 nanosheets, surpassing the reported halide perovskite-based photocatalysts under the same conditions.
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