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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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 |
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. |
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