Nanochannel Engineering in Metal-Organic Frameworks by Grafting Sulfonic Groups for Boosting Proton Conductivity

被引:13
作者
Yang, Fan [1 ,2 ]
Shi, Ruimin [1 ,2 ]
Huang, Hongliang [1 ,2 ]
Zhang, Zhengqing [1 ,2 ]
Guo, Xiangyu [1 ,2 ]
Qiao, Zhihua [1 ,2 ]
Zhong, Chongli [1 ,2 ]
机构
[1] Tiangong Univ, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[2] Tiangong Univ, Sch Chem Engn & Technol, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金;
关键词
benzene-1,3,5-trisulfonic acid; water adsorption; metal-organic framework; functionalization; proton conductivity; POROUS COORDINATION POLYMERS; ACID GROUPS; CONSTRUCTION; MOFS;
D O I
10.1021/acsaem.1c03852
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Constructing highly proton-conducting metal-organic frameworks (MOFs) remains a difficult challenge. Hence, we developed an effective nanochannel engineering strategy by grafting sulfonic-abundant benzene-1,3,5-trisulfonic acid (BTSA) onto the Zr-6-clusters of PCN-222 to act as a proton-conducting intensifier. Although the introduced BTSA dramatically reduced the pore volume, the resultant MOF (PCN-222-BTSA) exhibited strong water affinity and thus significantly enhanced water uptake at low RH values, reaching up to an almost equivalent water adsorption capacity at a high RH value compared with the capacity of pristine PCN-222. Benefiting from the enhanced water adsorption behavior and the proton-donating capability of sulfonic groups, PCN-222-BTSA displayed 2-3 orders of magnitude higher proton conductivity than pristine PCN-222. Our work is the first to report on postsynthetic modification in the nanochannel of MOFs for proton conduction, which demonstrates a strategy to design functional MOFs with abundant sulfonic groups and provides a bright avenue for constructing proton-conducting materials.
引用
收藏
页码:3235 / 3241
页数:7
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