吸附
光敏剂
乙烯
光催化
动力学
材料科学
催化作用
原位
化学工程
化学
光化学
联轴节(管道)
金属有机骨架
纳米技术
工作(物理)
产量(工程)
化学动力学
生产率
可见光谱
反应中间体
多相催化
作者
Yu He,Wenjuan Zheng,Yong Liu,Wenxue Zhang,Huan Pang,Jiangwei Zhang,Wang‐Kang Han,Zhi‐Guo Gu
标识
DOI:10.1002/ange.202516438
摘要
Abstract The development of efficient direct air capture (DAC) systems coupled with photocatalytic CO 2 conversion is still an appealing challenge. Here, we engineered a series of defective Cu 3 ‐based metal–organic frameworks (Cu 3 ‐MOFs) for integrated atmospheric CO 2 capture and in situ photoreduction. The defective Cu 3 ‐MOFs were constructed through selective removal of coordinated CO 3 2− from pristine MOFs with HCl etching, generating unsaturated Cu active sites for CO 2 harvesting, and the Cu 3 ‐MOFs demonstrated enhanced CO 2 capture kinetics and capacity that compared to their pristine counterpart. Remarkably, the captured CO 2 could be directly photoreduced to C 2 H 4 with an optimal production rate of 18.25 µmol·g −1 ·h −1 without additional photosensitizer or sacrificial agent. The experimental and theoretical results revealed that the defective sites not only facilitated CO 2 adsorption but also promoted C–C coupling of *CO intermediates, thereby enhancing C 2 H 4 production. This work provides deep insights for designing advanced materials toward direct air‐to‐fuel conversion.
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