化学
光催化
钒
铟
固定(群体遗传学)
催化作用
纳米技术
光化学
无机化学
有机化学
材料科学
基因
生物化学
作者
Shu‐Cong Fan,Shuang-Qiu Chen,Jiawen Wang,Yongpeng Li,Peng Zhang,Ying Wang,Wenyu Yuan,Quan‐Guo Zhai
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-08-23
卷期号:61 (35): 14131-14139
被引量:26
标识
DOI:10.1021/acs.inorgchem.2c02250
摘要
The capture and fixation of CO2 under mild conditions is a cost-effective route to reduce greenhouse gases, but it is challenging because of the low conversion and selectivity issues. Metal-organic frameworks (MOFs) are promising in the fields of adsorption and catalysis because of their structural tunability and variability. However, the precise structural design of MOFs is always pursued and elusive. In this work, a metal-mixed MOF (SNNU-97-InV) was designed by precisely introducing single vanadium site into the isostructural In-MOF (SNNU-97-In). The single V sites clearly change the interactions between the MOF framework and CO2 molecules, leading to a 71.3% improvement in the CO2 adsorption capacity. At the same time, the enhanced light absorption enables SNNU-97-InV to efficiently convert CO2 into cyclic carbonates (CCs) with epoxides under illumination. Controlled experiments showed that the promoted performance of SNNU-97-InV may be that the V═O site can more easily combine with CO2 and convert them into an intermediate state under illumination, and the possible mechanism was thus speculated.
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