4.6 Article

A multifunctional covalently linked graphene-MOF hybrid as an effective chemiresistive gas sensor

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 9, 期 32, 页码 17434-17441

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta03246a

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资金

  1. Indian Institute of Technology Jammu [SGT-100038]
  2. SERB [SRG/2020/000865, CVD/2021/000086]
  3. Operational Programme Research, Development and Education-European Regional Development Fund of the Ministry of Education, Youth and Sports of the Czech Republic [CZ.02.1.01/0.0/0.0/16_019/0000754]
  4. Czech Science Foundation [19-27454X]
  5. Council of Scienti.c & Industrial Research (CSIR), New Delhi [09/1052(0010)/2020-EMR-I]
  6. ERC from the EU Horizon 2020 Research and Innovation Programme [683024]
  7. German Research Foundation (DFG) within e-conversion (Fundamentals of Energy Conversion Processes, EXC 2089)
  8. Department of Science and Technology [PDF/2016/001193]
  9. Fonds der chemischen Industrie

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The hybrid material GA@UiO-66-NH2, synthesized by the covalent assembly of graphene acid and amine functionalized UiO-66 metal-organic framework, exhibits superior electrical resistance and rapid CO2 sensing response, showing significant potential in the development of gas sensing materials.
A hybrid of GA@UiO-66-NH2 was synthesized based on the covalent assembly of graphene acid (GA) and the amine functionalized UiO-66 metal-organic framework through amide bonds. This strategy endows the material with unique properties, such as hierarchical pores, a porous conductive network decorated with functional groups, a high specific surface area, and a good chemical and thermal stability. The resultant hybrid has an electrical resistance of similar to 10(4) omega, whereas the pristine GA and UiO-66-NH2 possess an electrical resistance of similar to 10(2) omega and similar to 10(9) omega, respectively. The hybrid GA@UiO-66-NH2 was demonstrated for CO2 chemiresistive sensing and displayed a very fast response and quick recovery time of similar to 18 s for 100% CO2, at 200 degrees C. While the pristine GA exhibits negligible response under the same conditions, GA@UiO-66-NH2 exhibited a response of 10 +/- 0.6%. Further, in situ temperature dependent Raman studies during CO2 exposure confirm the presence of strong hydrogen bonding interaction between CO2 and the amide functionality present on GA@UiO-66-NH2. The resulting gas sensing characteristics of GA@UiO-66-NH2 are majorly attributed to the better interaction of CO2 at the amide/amine functional groups and the readily accessible hierarchical pores. This design strategy opens new horizons in the development of covalently linked hybrids with hierarchical porous conductive networks which can help to improve the gas sensing properties of MOF-based materials.

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