A novel UV-curable molecular-modified graphene oxide for high-resolution printed electronics
Autor: | Keke Wang, Shuyuan Zhang, Feng Xueming, Yu Luo, Pei Yuechen, Bingheng Lu, Li Wang, Li Yingtao, Zhaofa Zhang |
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Rok vydání: | 2021 |
Předmět: |
Materials science
Graphene Oxide Nanotechnology 02 engineering and technology General Chemistry 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences law.invention chemistry.chemical_compound chemistry law Printed electronics Electrode Molecule General Materials Science Electronics Photolithography 0210 nano-technology Electrical conductor |
Zdroj: | Carbon. 176:470-479 |
ISSN: | 0008-6223 |
DOI: | 10.1016/j.carbon.2021.01.150 |
Popis: | The development of graphene-based materials with good light-curing ability and excellent electrical conductivity is the key to next-generation electronic devices. Herein, we demonstrate the molecular structure modification of photocurable graphene oxide (PGO) by reacting hydroxyl groups with isocyano groups, which is referred to as grafting of the photosensitive group on pristine GO, resulting in photosensitive PGO flakes that can be photocured during 3D printing using water as a solvent and a developer. Complex-shaped and highly precise 2D and 3D structures of GO as well as thin single-layer or few-layer GO films are obtained by optimizing the concentration and photocuring parameters of the PGO precursor. After thermal reduction of PGO microarchitectures, the reduced cross-linked GO (rCGO) exhibits a minimum square resistance of 213.74 mΩ sq−1, which is similar to that of graphene. Moreover, rCGO demonstrates excellent cell compatibility during cell culture experiments and superior hydrophilicity. The latter property can be exploited to prepare solution-based detection electrodes. The proposed strategy is used to print circuits and 3D bulk conductors, and can facilitate the formation of various electronic devices via photocuring 3D printing or photolithography process. |
Databáze: | OpenAIRE |
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