A Dual‐Ligand Porous Coordination Polymer Chemiresistor with Modulated Conductivity and Porosity

Single‐ligand‐based electronically conductive porous coordination polymers/metal–organic frameworks (EC‐PCPs/MOFs) fail to meet the requirements of numerous electronic applications owing to their limited tunability in terms of both conductivity and topology. In this study, a new 2D π‐conjugated EC‐M...

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Published inAngewandte Chemie International Edition Vol. 59; no. 1; pp. 172 - 176
Main Authors Yao, Ming‐Shui, Zheng, Jia‐Jia, Wu, Ai‐Qian, Xu, Gang, Nagarkar, Sanjog S., Zhang, Gen, Tsujimoto, Masahiko, Sakaki, Shigeyoshi, Horike, Satoshi, Otake, Kenichi, Kitagawa, Susumu
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 02.01.2020
EditionInternational ed. in English
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Summary:Single‐ligand‐based electronically conductive porous coordination polymers/metal–organic frameworks (EC‐PCPs/MOFs) fail to meet the requirements of numerous electronic applications owing to their limited tunability in terms of both conductivity and topology. In this study, a new 2D π‐conjugated EC‐MOF containing copper units with mixed trigonal ligands was developed: Cu3(HHTP)(THQ) (HHTP=2,3,6,7,10,11‐hexahydrotriphenylene, THQ=tetrahydroxy‐1,4‐quinone). The modulated conductivity (σ≈2.53×10−5 S cm−1 with an activation energy of 0.30 eV) and high porosity (ca. 441.2 m2 g−1) of the Cu3(HHTP)(THQ) semiconductive nanowires provided an appropriate resistance baseline and highly accessible areas for the development of an excellent chemiresistive gas sensor. Makes sense: As two ligands offer more opportunity than one to tune MOF conductivity and topology, a 2D π‐conjugated copper‐based electronically conductive MOF with two different trigonal organic ligands was developed (see structure). The semiconductivity and high porosity of the resulting nanowires provided a low conductivity baseline and highly accessible surface areas, thus resulting in excellent room‐temperature chemiresistive sensing properties.
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ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.201909096