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通过光异构化诱导半结晶聚(偶氮苯)熔融实现可逆驱动

Reversible Actuation via Photoisomerization-Induced Melting of a Semicrystalline Poly(Azobenzene).

作者信息

Kuenstler Alexa S, Clark Kyle D, Read de Alaniz Javier, Hayward Ryan C

机构信息

Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.

Department of Chemistry and Biochemistry, University of California Santa Barbara Santa Barbara, California 93106, United States.

出版信息

ACS Macro Lett. 2020 Jun 16;9(6):902-909. doi: 10.1021/acsmacrolett.0c00328. Epub 2020 Jun 4.

Abstract

Photoisomerization of azobenzene in polymer matrices is a powerful method to convert photon energy into mechanical work. While most previous studies have focused on incorporating azobenzene within amorphous or liquid crystalline materials, the limited extents of molecular ordering and correspondingly modest enthalpy changes upon switching in such systems has limited the achievable energy densities. In this work, we introduce a semicrystalline main-chain poly(azobenzene), where photoisomerization is capable of reversibly triggering melting and recrystallization under essentially isothermal conditions. These materials can be drawn into aligned fibers, yielding optically driven two-way shape memory actuators capable of reversible bending.

摘要

聚合物基质中偶氮苯的光异构化是将光能转化为机械功的有效方法。尽管此前的大多数研究都集中在将偶氮苯引入无定形或液晶材料中,但此类体系中分子有序化程度有限,且切换时相应的焓变适度,限制了可实现的能量密度。在这项工作中,我们引入了一种半结晶主链聚(偶氮苯),其中光异构化能够在基本等温的条件下可逆地引发熔融和重结晶。这些材料可以被拉制成排列整齐的纤维,从而产生能够可逆弯曲的光驱动双向形状记忆致动器。

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