4.7 Article

Bioinduced Surface Oxygen Vacancies on Bismuth Trioxide Nanocrystals for Photocathodic Bioassays

Journal

ACS APPLIED NANO MATERIALS
Volume 6, Issue 13, Pages 11309-11316

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.3c01359

Keywords

cathodic photoelectrochemistry; bioinduced surface oxygenvacancy; bismuth trioxide nanocrystal; surface effectengineering; glucose-6-phosphate dehydrogenase; p-hydroxybenzoate hydroxylase

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This study discloses a new mechanism of introducing surface oxygen vacancies (V(O)) in bismuth trioxide (Bi2O3) nanocrystals, which enables superior photostability and anti-interference capability in cathodic photoelectrochemical (PEC) bioanalysis. The surface V(O) can act as a separation center for charge carriers, facilitating the generation of cathodic photocurrent that is linearly correlated with the concentrations of targets, glucose-6-phosphate (G-6-P) and G6PD. This research not only provides a method to introduce surface V(O), but also enriches the toolbox of cathodic PEC bioassays and stimulates further interest in surface effect engineering in other fields.
Cathodic photoelectrochemistry withsuperior photostability andanti-interference capability has been shown to be appealing in thefield of bioanalysis. However, a major challenge regarding this technologyis the limited photoinduced electron transfer signal transductionmechanism. Herein, we disclose a finding of the bioinduced surfaceoxygen vacancy (V (O)) on bismuth trioxide(Bi2O3) nanocrystals, which underlies an innovativemechanism for cathodic photoelectrochemical (PEC) bioanalysis. Theprotocatechuic acid engendered from the tandem enzymatic reactionof p-hydroxybenzoate hydroxylase (PHBH) and glucose-6-phosphatedehydrogenase (G6PD) can coordinate with the surface of Bi2O3 nanocrystals through forming binary Bi-O-Cbonds, which breaks the initial Bi-O bonds and enables theescape of O2- from the lattice to form surface V (O) in situ. The surface V (O) can function as a separation center for chargecarriers, which is favorable to the generation of cathodic photocurrent.In such a system, the cathodic signal is linearly correlated withthe targets, glucose-6-phosphate (G-6-P) and G6PD, in concentrationranges of 8.0 to 8.0 x 10(5) & mu;M and 0.1 to 1.0x 10(4) U/L, achieving detection limits of 2.0 & mu;Mand 0.03 U/L, respectively. This study not only offers a way of introducingsurface V (O) in situ butalso enriches the current toolbox of cathodic PEC bioassays and promisesto stimulate further interest in exploring surface effect engineeringin other fields.

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