Amorphous Metallic Cobalt-Based Organophosphonic Acid Compounds as Novel Photocatalysts to Boost Photocatalytic CO2 Reduction

C Pub Date : 2024-01-24 DOI:10.3390/c10010012
Chengwei Zhou, Fan Wu, Yonggong Tang, Boyuan Chai, Jiaxin Liang, Jiangang Han, Weinan Xing, Yudong Huang, Guangyu Wu
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Abstract

Photocatalytic carbon dioxide conversion is a promising method for generating carbon fuels, in which the most important thing is to adjust the catalyst material to improve the photocatalytic efficiency and selectivity to conversion products, but it is still very challenging. In order to enhance the efficiency of CO2 photoreduction, it is important to develop an appropriate photocatalyst. The present study focuses on developing a simple and effective hydrothermal reaction treatment to improve the catalytic efficiency of transition metal cobalt (Co) and organophosphonates. Photoexcited charge carriers are separated and transferred efficiently during this treatment, which enhances CO2 chemisorption. Under visible light exposure, the best performing catalyst, CoP-4, showed 2.4 times higher activity than Co3O4 (19.90 μmol h−1 g−1) for reducing CO2 into CO, with rates up to 47.16 μmol h−1 g−1. This approach provides a viable route to enhancing the efficiency of CO2 photoreduction.
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无定形金属钴基有机膦酸化合物作为新型光催化剂促进光催化二氧化碳还原作用
光催化二氧化碳转化是一种很有前景的生成碳燃料的方法,其中最重要的是调整催化剂材料,以提高光催化效率和对转化产物的选择性,但这仍然非常具有挑战性。为了提高二氧化碳的光催化效率,开发一种合适的光催化剂非常重要。本研究的重点是开发一种简单有效的水热反应处理方法,以提高过渡金属钴(Co)和有机膦酸盐的催化效率。在这种处理过程中,光激发的电荷载流子被有效分离和转移,从而增强了二氧化碳的化学吸附。在可见光照射下,性能最好的催化剂 CoP-4 将 CO2 还原成 CO 的活性比 Co3O4(19.90 μmol h-1 g-1)高 2.4 倍,速率高达 47.16 μmol h-1 g-1。这种方法为提高 CO2 光还原效率提供了一条可行的途径。
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