Excited-State Intramolecular Proton Transfer-Driven Photon-Gating for Photoelectrochemical Sensing of CO-Releasing Molecule-3

被引:95
作者
Gao, Yuan [1 ]
Tang, Juan [2 ]
Zhou, Qian [3 ]
Yu, Zhichao [1 ]
Wu, Di [1 ]
Tang, Dianping [1 ]
机构
[1] Fuzhou Univ, Dept Chem, Key Lab Analyt Sci Food Safety & Biol MOE & Fujian, Fuzhou 350108, Peoples R China
[2] Jiangxi Normal Univ, Natl Engn Res Ctr Carbohydrate Synth, Dept Chem & Chem Engn, Key Lab Green Chem Jiangxi Prov,Key Lab Fluorine &, Nanchang 330022, Peoples R China
[3] Henan Univ, Coll Chem & Mol Sci, Henan Int Joint Lab Med Plants Utilizat, Kaifeng 475000, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON-MONOXIDE; PLATFORM; SIGNAL;
D O I
10.1021/acs.analchem.4c00324
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Different from prevalent approaches such as immunological recognition, complementary base pairing, or enzymatic regulation in current photoelectrochemical (PEC) sensing, this study reported an excited-state intramolecular proton transfer (ESIPT)-driven photon-gating PEC sensor. The sensor is developed for the detection of CO-releasing molecule-3 (CORM-3) by modifying an ESIPT-switched organic fluorescent probe molecule (NDAA) onto the surface of a p-type semiconductor (BiOI). The NDAA can be excited and exhibit strong green fluorescence after responding with CORM-3, resulting in an electrode-interface photon competitive absorption effect due to the switch on ESIPT and considerably reducing the photocurrent signal. The experimental results revealed that the as-developed PEC sensor achieved good analytical performance with high selectivity and sensitivity, with a linear range of 0.01-1000 mu M and a lower detection limit of 6.5 nM. This work demonstrates the great potential of the organic fluorescent probe molecule family in advancing PEC analysis. It is anticipated that our findings will stimulate the creation of diverse functional probes possessing distinctive characteristics for inventive PEC sensors.
引用
收藏
页码:5014 / 5021
页数:8
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