Unique S-scheme heterojunctions in self-assembled TiO2/CsPbBr3 hybrids for CO2 photoreduction
Year: 2020
Type: article
Abstract: Exploring photocatalysts to promote CO2 photoreduction into solar fuels is of great significance. We develop TiO2/perovskite (CsPbBr3) S-scheme heterojunctions synthesized by a facile electrostatic-driven self-assembling approach. Density functional theory calculation combined with experimental studies proves the electron transfer from CsPbBr3 quantum dots (QDs) to TiO2, resulting in the construction of internal electric field (IEF) directing from CsPbBr3 to TiO2 upon hybridization. The IEF drives the photoexcited electrons in TiO2 to CsPbBr3 upon light irradiation as revealed by in-situ X-ray photoelectron spectroscopy analysis, suggesting the formation of an S-scheme heterojunction in the TiO2/CsPbBr3 nanohybrids which greatly promotes the separation of electron-hole pairs to foster efficient CO2 photoreduction. The hybrid nanofibers unveil a higher CO2-reduction rate (9.02 μmol g–1 h–1) comparing with pristine TiO2 nanofibers (4.68 μmol g–1 h–1). Isotope (13CO2) tracer results confirm that the reduction products originate from CO2 source.
Source: Nature Communications
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $5,380
Funders: National Natural Science Foundation of China, China Postdoctoral Science Foundation, Wuhan University, Wuhan University of Technology, State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Australian Research Council, National Postdoctoral Program for Innovative Talents, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Awards: G1032752638, G1490685038, G2547554, G2772343490, G3042067570, 梯形太阳燃料光催化剂的设计制备与原位机理研究, G3220915221, G3353927197, CO2还原二维层状复合光催化剂的构建与机理研究, G3641612505, G6161976087, G6346494855, G6580239572, G6627639052, G6803501939, G7154186073, G7325153032, G767396088, G7755042506, G8042906021, G805028783, G8078913356, G8763490759, G8945332658
OpenAlex ID: W3085189088
