Carbon nanodot-induced Eu3+-based fluorescent polymeric hydrogel for excellent phase-separation absorption of VOC

Hydrogels with environment remediation function have attracted increasing interest in the past decades. Herein, we report the in situ preparation of heat-set fluorescent Eu3+ hydrogels derived from terpyridine-modified PEI polymers (PEI-LysTPY) via sol–gel transition. We demonstrate that carbon dots...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 10; no. 14; pp. 7941 - 7947
Main Authors Li, Heng, Guo, Jiangbo, Ren, Jujie, Li, Yajuan, Yu, Xudong
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 24.02.2022
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Summary:Hydrogels with environment remediation function have attracted increasing interest in the past decades. Herein, we report the in situ preparation of heat-set fluorescent Eu3+ hydrogels derived from terpyridine-modified PEI polymers (PEI-LysTPY) via sol–gel transition. We demonstrate that carbon dots with abundant amine groups, which are formed by pyrolysis of PEI derivatives, behave as efficient linkers to trigger the hydrogelation process of the Eu3+/PEI-LysTPY assembly. The aggregation-induced emission enhancement (AIE) phenomena of Eu3+ is observed in the hydrogelation process. As applications for environment remediation, the hydrogel exhibits an excellent absorption (acetone: 2.58 g g−1 and methanol: 2.04 g g−1) for acetone gas or methanol gas (kinds of volatile organic compounds). Interestingly, the hybrid carbon dot-based hydrogel could selectively absorb acetone or methanol gas to form two phases, including the acetone-lean phase as the gel state and the acetone-rich phase as the solution state. The two phases could be easily separated. Additionally, the hydrogel could be reused by the reabsorption of solution and solute. This work supplies a unique method for the phase-separation absorption of VOCs using carbon dot-accelerated hydrogels with high absorption capacity, good stability and reusability ability.
ISSN:2050-7488
2050-7496
DOI:10.1039/d1ta10858a