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Switchable biomimetic nanochannels for on-demand SO(2) detection by light-controlled photochromism

In contrast to the conventional passive reaction to analytes, here, we create a proof-of-concept nanochannel system capable of on-demand recognition of the target to achieve an unbiased response. Inspired by light-activatable biological channelrhodopsin-2, photochromic spiropyran/anodic aluminium ox...

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Detalles Bibliográficos
Autores principales: Zhang, Dan, Sun, Yongjie, Wang, Zhichao, Liu, Fang, Zhang, Xuanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076267/
https://www.ncbi.nlm.nih.gov/pubmed/37019894
http://dx.doi.org/10.1038/s41467-023-37654-y
Descripción
Sumario:In contrast to the conventional passive reaction to analytes, here, we create a proof-of-concept nanochannel system capable of on-demand recognition of the target to achieve an unbiased response. Inspired by light-activatable biological channelrhodopsin-2, photochromic spiropyran/anodic aluminium oxide nanochannel sensors are constructed to realize a light-controlled inert/active-switchable response to SO(2) by ionic transport behaviour. We find that light can finely regulate the reactivity of the nanochannels for the on-demand detection of SO(2). Pristine spiropyran/anodic aluminium oxide nanochannels are not reactive to SO(2). After ultraviolet irradiation of the nanochannels, spiropyran isomerizes to merocyanine with a carbon‒carbon double bond nucleophilic site, which can react with SO(2) to generate a new hydrophilic adduct. Benefiting from increasing asymmetric wettability, the proposed device exhibits a robust photoactivated detection performance in SO(2) detection in the range from 10 nM to 1 mM achieved by monitoring the rectified current.