吸附
光敏剂
材料科学
乙烯
光催化
动力学
原位
联轴节(管道)
纳米技术
化学工程
工作(物理)
催化作用
光化学
生产率
化学
金属有机骨架
产量(工程)
光电子学
可见光谱
直接耦合
化学动力学
降级(电信)
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/anie.202516438
摘要
The development of efficient direct air capture (DAC) systems coupled with photocatalytic CO2 conversion is still an appealing challenge. Here, we engineered a series of defective Cu3-based metal-organic frameworks (Cu3-MOFs) for integrated atmospheric CO2 capture and in situ photoreduction. The defective Cu3-MOFs were constructed through selective removal of coordinated CO3 2- from pristine MOFs with HCl etching, generating unsaturated Cu active sites for CO2 harvesting, and the Cu3-MOFs demonstrated enhanced CO2 capture kinetics and capacity that compared to their pristine counterpart. Remarkably, the captured CO2 could be directly photoreduced to C2H4 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 CO2 adsorption but also promoted C-C coupling of *CO intermediates, thereby enhancing C2H4 production. This work provides deep insights for designing advanced materials toward direct air-to-fuel conversion.
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