z-logo
Premium
Tuning the Bandgap and Cytotoxicity of ZnO by Tailoring the Nanostructures
Author(s) -
Zhang Jianhui,
Dong Guanjun,
Thurber Aaron,
Hou Yayi,
Tenne Dmitri A.,
Hanna Charles B.,
Gu Min,
Pan Zhongda,
Wang Kaiyu,
Du Youwei,
Punnoose Alex
Publication year - 2015
Publication title -
particle and particle systems characterization
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 56
eISSN - 1521-4117
pISSN - 0934-0866
DOI - 10.1002/ppsc.201400188
Subject(s) - cytotoxicity , band gap , materials science , polyvinylpyrrolidone , nanostructure , nanotechnology , nanoparticle , reagent , chemical engineering , optoelectronics , chemistry , organic chemistry , polymer chemistry , in vitro , biochemistry , engineering
Tuning the bandgap and cytotoxicity of ZnO nanoparticles (NPs) is very important, not only for customizing their optoelectronic and biomedical applications, but also for their cytotoxicity assay and safe usage. A unique soft‐template of polyvinylpyrrolidone has been developed here to realize a rapid room‐temperature neutral synthesis of ZnO with controlled nanostructures for tuning the bandgap and cytotoxicity of ZnO. By simply changing the reagent stoichiometry and the soft‐template shape, high‐purity ZnO rods, tripods, tubes, and unique T‐like tubes with tunable size, surface composition/charge, bandgap, and cytotoxicity are obtained. It has been revealed that the ZnO bandgap can be remarkably reduced by introducing the surface nonstoichiometry; and the ZnO‐induced cytotoxicity can be tuned by the size, shape, surface charge/composition, and bandgap of ZnO NPs at different degrees. Significantly, both the photochemistry reaction and the reactive oxygen species induced by ZnO NPs are not necessary for the ZnO‐induced cytotoxicity.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here