Accelerating Electron-Transfer Dynamics by TiO2 -Immobilized Reversible Single-Atom Copper for Enhanced Artificial Photosynthesis of Urea

© 2022 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 51 vom: 10. Dez., Seite e2207793
1. Verfasser: Li, Dong (VerfasserIn)
Weitere Verfasser: Zhao, Yunxuan, Miao, Yingxuan, Zhou, Chao, Zhang, Li-Ping, Wu, Li-Zhu, Zhang, Tierui
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article electron-transfer dynamics photocatalysis reversible variation single-atom copper urea synthesis Copper 789U1901C5 titanium dioxide 15FIX9V2JP mehr... Carbon Dioxide 142M471B3J
Beschreibung
Zusammenfassung:© 2022 Wiley-VCH GmbH.
Photocatalysis as a sustainable technology is expected to provide a novel sight for the green synthesis of urea directly using N2 , CO2 , and H2 O under mild conditions. However, the fundamental issue of inefficient electron transfer in photocatalysis strongly hinders its feasibility, especially for the above multi-electron-demanding urea synthesis. Herein, an effective strategy of accelerating electron-transfer dynamics is reported by TiO2 -immobilized reversible single-atom copper (denoted as Cu SA-TiO2 ) to enhance the performance for photosynthesis of urea from N2 , CO2 , and H2 O. As revealed by a series of quasi-in-situ characterizations (e.g., electron paramagnetic resonance, and wavelength-resolved and femtosecond time-resolved spectroscopies), the expedited dynamics behaviors originating from reversible single-atom copper in as-designed Cu SA-TiO2 (electron extraction rate: over 30 times faster than the reference photocatalysts) allow the assurance of abundant and continual photogenerated electrons for multi-electron-demanding co-photoactivation of N2 and CO2 , resulting in considerable rates of urea production. The strategy above for improving the photoelectron-extraction ability of photocatalysts will offer a high-efficiency and promising route for artificial urea photosynthesis and other multi-electron-demanding photocatalytic reactions
Beschreibung:Date Completed 26.12.2022
Date Revised 26.12.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202207793