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JOURNAL OF LUMINESCENCE · 2019 · IF 2.961

Microwave synthesis of amphiphilic carbon dots from xylose and construction of luminescent composites with shape recovery performance

Ziqi Zhu,Pei Yang,Minzhi Chen,Tao Zhang,Yizhong Cao,Wei Zhang,Xiaoyan Zhou,Weimin Chen

Carbon dots (CDs) have sparked tremendous attention owing to their unique properties and great potential in various fields. Herein, novel amphiphilic CDs (ACDs) were synthesized solvothermally by microwave heating a mixture of xylose and ethylenediamine in N, N-dimethylacetamide. The xylose-derived ACDs were monodisperse nanoparticles with an average diameter of about 1.81 nm, and exhibited excitation-dependent emission behavior in both aqueous and several common organic solvents . Furthermore, the synthesized ACDs can be uniformly dispersed into polyvinyl alcohol (PVA) solution to fabricate transparent luminescent composites, the as-prepared PVA/ACDs composites not only exhibited excellent fluorescence with excitation-dependent emission performance, but also achieved water-induced shape memory behavior. The intrinsic reason and pH sensitivity of shape recovery were investigated, the results confirmed that a faster shape recovery can be obtained in water at pH 4 within 180 s. Further investigation illustrated that the sensitivity of additional hydrogen bonding between PVA and ACDs to the water molecular was highly related to the shape recovery of the luminescent composite. The green synthesis route for xylan-derived ACDs and fabrication of smart luminescent composite will open many possibilities for the valuable application of low-cost biomass.

研究领域: 纳米材料学 · 高分子科学 · 生物医学工程 · 功能材料 · 绿色化学 · 智能材料
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JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS · 2018 ·Vol. 56 ·期 19 ·1281-1286 · IF 2.499

Hydrogen bond-reinforced double-network hydrogels with ultrahigh elastic modulus and shape memory property

Yan Jie Wang,Chen Yu Li,Zhi Jian Wang,Yiping Zhao,Li Chen,Zi Liang Wu,Qiang Zheng

Development of tough hydrogels has greatly expanded their applications as load-bearing materials. However, the elastic modulus of tough hydrogels is usually lower than 1 MPa. It remains a challenge to design tough hydrogels with high modulus. We report here a series of tough double-network (DN) hydrogels with ultrahigh elastic modulus (up to 200 MPa) by forming robust hydrogen bonds between the first poly(acrylic acid) network and the second poly( N -isopropyl acrylamide) network. The dense cooperative hydrogen bonds greatly reduce the segmental mobility and thus improve the rigidity of gel matrix. Owing to the dynamic nature of hydrogen bonds, the modulus of hydrogels is strongly influenced by temperature and pH, affording the gels shape memory property. The strategy by forming robust noncovalent bonds between interpenetrating networks should be applicable to other systems for designing tough and versatile hydrogels with diverse promising applications. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56 , 1281–1286

研究领域: 高分子物理 · 生物材料 · 软物质科学 · 智能响应材料 · 组织工程
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