摘要
Using CO2 (or aqueous-CO2, HCO3−) and biomass as feedstock to produce chemicals under solar irradiation represents a promising approach to achieving the net-zero emission goal. In this study, we employed a highly efficient •H-forming photocatalyst to convert HCO3−, demonstrating the occurrence of C[sbnd]C coupling to produce C2-species. Under simulated solar illumination, the photocatalytic system consistently reduces HCO3− into acetate through the coupling of •CO2− radicals. Additionally, in the photoreforming of xylose, acetate emerges as the predominant product, likely resulting from the coupling of •CO2− derived from the interaction of formate and •OH. Notably, a C6-compound is generated through C[sbnd]C coupling of radicals originating from HCO3− and xylose. Achieving an overall apparent quantum efficiency of 26% under 420-nm irradiation, our work underscores the feasibility of concurrently photocatalyzing the conversion of CO2 and biomass into chemicals through C[sbnd]C coupling. This study not only highlights the significance of our approach in contributing to the net-zero emission goal but also emphasizes the novelty of achieving concurrent photocatalytic conversion.
| 原文 | English |
|---|---|
| 文章編號 | 150318 |
| 期刊 | Chemical Engineering Journal |
| 卷 | 486 |
| DOIs | |
| 出版狀態 | Published - 2024 4月 15 |
All Science Journal Classification (ASJC) codes
- 一般化學
- 環境化學
- 一般化學工程
- 工業與製造工程
指紋
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