Metal-organicframeworkswithdinuclearmetalcentersforsynergisticallyboostingCO2photoreduction<iclass="icon-zqcb"></i>

被引:0
作者
HuiFeng Wang [1 ,2 ]
WenJie Shi [2 ]
YuXin Yang [2 ]
BaoXia Dong [1 ]
TongBu Lu [2 ]
DiChang Zhong [2 ]
机构
[1] School of Chemistry and Chemical Engineering, Yangzhou University
[2] Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science and Engineering, Tianjin University of
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X701 [废气的处理与利用]; O643.36 [催化剂]; O644.1 [光化学];
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摘要
Dinuclear metal synergistic catalysis (DMSC) has been proved powerful in boosting CO2reduction,while this has not been achieved in heterogeneous catalysts with long-range order structures.In this study,we,by introduction of metal catalytic centers into an indium-based metal-organic framework (MOF),obtained a series of isostructural In-MOFs,including three MOFs with mononuclear metal catalytic center (M-In),three MOFs with dinuclear homometallic catalytic centers (MM-In),and three MOFs with dinuclear heterometallic catalytic centers (MM’-In,M/M’=Co(II),Ni(II),Zn(II)).It was found that all these MOFs can serve as catalysts for photochemical CO2reduction to CO.Compared with M-In,the catalytic activities of MM-In were obviously enhanced,and that of MM’-In was further significantly enhanced.For example,the CO yield of Co Zn-In reaches a record value of 12,700μmol g-1h-1,which is 4.0,8.1,9.4,and 18.6-fold higher than that of Co Co-In,Zn Zn-In,Co-In,and Zn-In,respectively.Similarly,the catalytic activities of Co Ni-In and Ni Zn-In also show different fold increase than those of corresponding dinuclear homometallic and mononuclear metallic MOFs.The results of control experiments and theoretical calculation reveal that the higher catalytic activities of MM-In over M-In can be ascribed to the DMSC effect,and the higher catalytic activity of MM’-In over MM-In can be ascribed to the strengthened DMSC effect.The work reveals the relationship between DMSC effect and bimetal centers in CO2reduction,which provides new insights into the DMSC and paves a new way to design highly active catalysts for photochemical CO2reduction.
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页码:201 / 208
页数:8
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