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Hydrazine Hydrate and Dissolved Oxygen-Triggered Near-Infrared Chemiluminescence from CuInS 2 @ZnS Nanocrystals for Bioassays.

Authors :
Li Z
Deng X
Wu S
Dong S
Zou G
Source :
Analytical chemistry [Anal Chem] 2021 Jun 29; Vol. 93 (25), pp. 8931-8936. Date of Electronic Publication: 2021 Jun 17.
Publication Year :
2021

Abstract

The overwhelming majority of commercially available chemiluminescence (CL) assays are conducted in the eye-visible region. Herein, a near-infrared (NIR) aqueous CL strategy was proposed with CuInS <subscript>2</subscript> @ZnS nanocrystals (CIS@ZnS NCs) as emitters. Hydrazine hydrate (N <subscript>2</subscript> H <subscript>4</subscript> ·H <subscript>2</subscript> O) could inject electrons into the conduction band of the CIS@ZnS NCs and simultaneously transformed to the intermediate radical N <subscript>2</subscript> H <subscript>3</subscript> <superscript>•</superscript> . N <subscript>2</subscript> H <subscript>3</subscript> <superscript>•</superscript> reduced dissolved oxygen (O <subscript>2</subscript> ) to O <subscript>2</subscript> <superscript>-•</superscript> , while the O <subscript>2</subscript> <superscript>-•</superscript> could inject holes into the valence band of the CIS@ZnS NCs. The recombination of electrons and holes at Cu <superscript>+</superscript> defects in CIS@ZnS NCs eventually yielded efficient NIR CL at around 824.1 nm, which is the longest waveband for NCs CL to the best of our knowledge. The NIR CL could be conveniently performed in the neutral aqueous medium (pH 7.0) with a quantum yield of 0.0155 Einstein/mol and was successfully employed for constructing a signal-off CL biosensor with ascorbic acid as the analyte as well as a signal-on CL biosensor for determining ascorbate oxidase, which indicates that this NIR CL system has a promising potential for bioassays in diverse ways.

Details

Language :
English
ISSN :
1520-6882
Volume :
93
Issue :
25
Database :
MEDLINE
Journal :
Analytical chemistry
Publication Type :
Academic Journal
Accession number :
34137591
Full Text :
https://doi.org/10.1021/acs.analchem.1c01380