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contributor authorBeaudette, Chad A.
contributor authorTu, Qiaomiao
contributor authorAli Eslamisaray, Mohammad
contributor authorKortshagen, Uwe R.
date accessioned2022-05-08T09:05:00Z
date available2022-05-08T09:05:00Z
date copyright3/7/2022 12:00:00 AM
date issued2022
identifier issn2770-3495
identifier otheraoje_1_011010.pdf
identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4284708
description abstractTitanium dioxide in its pure wide bandgap “white” form is a non-toxic, efficient, and practical photocatalyst, but predominately absorbs light in the ultraviolet range of the spectrum. The absorption range, however, can be extended into the visible by doping with oxygen vacancies or impurities, such as nitrogen, giving the material a black or brown appearance. To date, nitrogen-doped titanium dioxide has primarily been produced with approaches that require long processing times or multi-step synthesis protocols. Here, we present a fast (timescale of tens of milliseconds) all-gas-phase process, which enables the seamless tuning of the optical properties of titanium dioxide nanoparticles from white to brown. Titanium dioxide particles were synthesized through injection of tetrakis (dimethylamido)titanium (TDMAT), argon, and oxygen into a nonthermal plasma. The positions of the electrode and oxygen inlet relative to the precursor inlet are found to strongly influence particle properties. Variation of these parameters allowed for control over the produced particle optical properties from large bandgap (white) to small bandgap (brown). In addition, the particle microstructure can be tuned from amorphous to crystalline anatase phase titanium dioxide. The photocatalytic performance was tested under solar irradiation and amorphous particles exhibit the highest degree of photocatalytic decomposition of the dyes methyl orange and methylene blue.
publisherThe American Society of Mechanical Engineers (ASME)
titlePlasma-Synthesized Nitrogen-Doped Titanium Dioxide Nanoparticles With Tunable Visible Light Absorption and Photocatalytic Activity
typeJournal Paper
journal volume1
journal titleASME Open Journal of Engineering
identifier doi10.1115/1.4053338
journal fristpage11010-1
journal lastpage11010-11
page11
treeASME Open Journal of Engineering:;2022:;volume( 001 )
contenttypeFulltext


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