Coordination mode engineering in stacked-nanosheet metal–organic frameworks to enhance catalytic reactivity and structural robustness

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作者
Chuanhui Huang
Juncai Dong
Weiming Sun
Zhenjie Xue
Jun Ma
Lirong Zheng
Cong Liu
Xiao Li
Kang Zhou
Xuezhi Qiao
Qian Song
Wende Ma
Lan Zhang
Zhenyu Lin
Tie Wang
机构
[1] Beijing National Laboratory for Molecular Sciences,Ministry of Education Key Laboratory for Analytical Science of Food Safety and Biology
[2] Key Laboratory of Analytical Chemistry for Living Biosystems and Colloid,The Department of Basic Chemistry, The School of Pharmacy
[3] Interface and Chemical Thermodynamics,undefined
[4] Institute of Chemistry,undefined
[5] Chinese Academy of Sciences,undefined
[6] #2 Zhongguancun,undefined
[7] Fuzhou University,undefined
[8] University of Chinese Academy of Sciences,undefined
[9] Beijing Synchrotron Radiation Facility,undefined
[10] Institute of High Energy Physics,undefined
[11] Chinese Academy of Sciences,undefined
[12] Fujian Medical University,undefined
[13] State Key Laboratory of Structure Chemistry,undefined
[14] Fujian Institute of Research on the Structure of Matter,undefined
[15] Chinese Academy of Sciences,undefined
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摘要
Optimising the supported modes of atom or ion dispersal onto substrates, to synchronously integrate high reactivity and robust stability in catalytic conversion, is an important yet challenging area of research. Here, theoretical calculations first show that three-coordinated copper (Cu) sites have higher activity than four-, two- and one-coordinated sites. A site-selective etching method is then introduced to prepare a stacked-nanosheet metal–organic framework (MOF, CASFZU-1)-based catalyst with precisely controlled coordination number sites on its surface. The turnover frequency value of CASFZU-1 with three-coordinated Cu sites, for cycloaddition reaction of CO2 with epoxides, greatly exceed those of other catalysts reported to date. Five successive catalytic cycles reveal the superior stability of CASFZU-1 in the stacked-nanosheet structure. This study could form a basis for the rational design and construction of highly efficient and robust catalysts in the field of single-atom or ion catalysis.
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