Fully Reversible and Super‐Fast Photo‐Induced Morphological Transformation of Nanofilms for High‐Performance UV Detection and Light‐Driven Actuators

Author:

Liu Xiangquan1,Hu Jiahui1,Yang Jinglun12,Peng Lingya1,Tang Jiaqi13,Wang Xiaohui1,Huang Rongrong1,Liu Jianfei14,Liu Kaiqiang1,Wang Tingyi1,Liu Xiaoyan1,Ding Liping1,Fang Yu1ORCID

Affiliation:

1. Key Laboratory of Applied Surface and Colloid Chemistry Ministry of Education School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 China

2. Department of Materials Science and Engineering City University of Hong Kong Hong Kong SAR 999077 China

3. Xi'an Rare Matel Materials Institute Co. Ltd Xi'an 710016 China

4. Northwest Institute for Nonferrous Metal Research Xi'an 710016 China

Abstract

AbstractFlexible and highly ultraviolet (UV) sensitive materials garner considerable attention in wearable devices, adaptive sensors, and light‐driven actuators. Herein, a type of nanofilms with unprecedented fully reversible UV responsiveness are successfully constructed. Building upon this discovery, a new system for ultra‐fast, sensitive, and reliable UV detection is developed. The system operates by monitoring the displacement of photoinduced macroscopic motions of the nanofilms based composite membranes. The system exhibits exceptional responsiveness to UV light at 375 nm, achieving remarkable response and recovery times of < 0.3 s. Furthermore, it boasts a wide detection range from 2.85 µW cm−2 to 8.30 mW cm−2, along with robust durability. Qualitative UV sensing is accomplished by observing the shape changes of the composite membranes. Moreover, the composite membrane can serve as sunlight‐responsive actuators for artificial flowers and smart switches in practical scenarios. The photo‐induced motion is ascribed to the cis–trans isomerization of the acylhydrazone bonds, and the rapid and fully reversible shape transformation is supposed to be a synergistic result of the instability of the cis‐isomers acylhydrazone bonds and the rebounding property of the networked nanofilms. These findings present a novel strategy for both quantitative and qualitative UV detection.

Funder

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

Wiley

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