催化作用
煅烧
甲醇
纳米颗粒
材料科学
化学工程
金属有机骨架
选择性
色散(光学)
金属
热分解
降水
无机化学
纳米技术
化学
有机化学
冶金
吸附
工程类
物理
光学
气象学
作者
Jialing Song,Bin Chen,Juanjuan Bian,Yanmei Cai,Sajid Ali,Dongren Cai,Bingyun Zheng,Jiale Huang,Guowu Zhan
标识
DOI:10.1021/acsanm.4c03801
摘要
ZnZrOx solid solution is a promising catalyst for the hydrogenation of CO2 to methanol, but precise design of the nanostructure to enhance catalytic performance remains a significant challenge. Herein, a ZnZrOx-based solid solution (ZnZrOx-MD) nanoparticle catalyst with uniform metal dispersion and remarkable CO2 activation ability was developed via calcination of metal–organic frameworks [MOFs, viz., PCN-223(Zn)] with mixed metal (Zr and Zn) as solid precursors. It was found that the ZnZrOx-MD nanoparticle catalyst outperformed its counterparts prepared using a traditional deposition–precipitation method (ZnZrOx-TD). Furthermore, the effects of the micromorphology and crystal composition on the catalytic performance of ZnZrOx-MD were systematically investigated. Comprehensive characterization results reveal that ZnZrOx-MD contained abundant oxygen vacancies, large specific surface area, and uniform metal dispersion, which collectively contributed to its excellent CO2 hydrogenation performance, resulting in a high methanol selectivity of 77.2% at 320 °C. In situ DRIFTS experiments confirm the mechanism for the CO2 hydrogenation to methanol over the ZnZrOx nanoparticle catalysts involved the initial formation of HCOO* species, followed by subsequent hydrogenation to generate CH3O* and ultimately produce methanol. Overall, this work highlights the potential benefits of MOFs as thermal decomposition precursors for the fabrication of solid-state catalysts with unique properties.
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