Achievement and electrochemical responsiveness of advanced boron-doped ultrananocrystalline diamond on highly ordered titanium dioxide nanotubes

Boron-doped ultrananocrystalline diamond grown on titanium dioxide nanotubes without seeding pre-treatment (B-UNCDWS/TDNT/Ti), as a porous composite, was successfully achieved. Innovative approaches concerning the highly ordered TDNT production as well as its singular diamond formation by hot filame...

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Published in:Diamond and related materials Vol. 121; p. 108793
Main Authors: Vernasqui, Laís G., Kawata, Bianca A., Sardinha, A.F., Rodrigo, Manuel A., Ferreira, Neidenêi G.
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 01-01-2022
Elsevier BV
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Abstract Boron-doped ultrananocrystalline diamond grown on titanium dioxide nanotubes without seeding pre-treatment (B-UNCDWS/TDNT/Ti), as a porous composite, was successfully achieved. Innovative approaches concerning the highly ordered TDNT production as well as its singular diamond formation by hot filament chemical vapor deposition (CVD) were explored. The B-UNCD homogeneous cluster progress on the TDNT porous walls as a function of the growth times from 1 to 7 h led to remarkable composite morphologies, keeping the TDNT porosity, where the TiO2 – TiC conversion dominated the renucleation process facilitating the nanometric scale control. Scanning electron microscopy images confirmed the continuous ultrananocrystalline formation as nanoclusters on the TDNT walls with their size evolution as a function of growth time also showing an increase in the CVD diamond ballas clusters. Raman spectra and X-Ray patterns exhibited the diamond characteristics with defined peaks and TiC formation, as expected. The ID(220)/(111) and ID(311)/(111) ratio intensities pointed out the films governed by (220) diamond phase, due to their high renucleation process. Besides, the intensity ratios for both TiC (111) and TiC (200) phases with D(111) peak showed a carbon atoms competition between surface and bulk diffusion on the TiC layer. The electrode reversibility evaluated from cyclic voltammetry curves followed the quasi-reversible criteria for all samples, confirming their promising performance. Mott-Shottky plots are in good agreement with Raman spectra for boron-doped films from 1018 to 1019 B.cm−3 where the highest doped diamond was obtained for the thickest films of 5 and 7 h. [Display omitted] •B-UNCDWS/TDNT/Ti electrodes without seeding pre-treatment were successfully achieved.•The TDNT influence on UNCDWS formation is motivated by the TiO2 into TiC conversion.•SEM images showed a unique morphology with evolution as a function of growth time.•CVD ballas cluster were growth concomitantly, also a function of growth time.•The quasi-reversible behavior for all samples makes it a promising composite.
AbstractList Boron-doped ultrananocrystalline diamond grown on titanium dioxide nanotubes without seeding pre-treatment (B-UNCDWS/TDNT/Ti), as a porous composite, was successfully achieved. Innovative approaches concerning the highly ordered TDNT production as well as its singular diamond formation by hot filament chemical vapor deposition (CVD) were explored. The B-UNCD homogeneous cluster progress on the TDNT porous walls as a function of the growth times from 1 to 7 h led to remarkable composite morphologies, keeping the TDNT porosity, where the TiO2 – TiC conversion dominated the renucleation process facilitating the nanometric scale control. Scanning electron microscopy images confirmed the continuous ultrananocrystalline formation as nanoclusters on the TDNT walls with their size evolution as a function of growth time also showing an increase in the CVD diamond ballas clusters. Raman spectra and X-Ray patterns exhibited the diamond characteristics with defined peaks and TiC formation, as expected. The ID(220)/(111) and ID(311)/(111) ratio intensities pointed out the films governed by (220) diamond phase, due to their high renucleation process. Besides, the intensity ratios for both TiC (111) and TiC (200) phases with D(111) peak showed a carbon atoms competition between surface and bulk diffusion on the TiC layer. The electrode reversibility evaluated from cyclic voltammetry curves followed the quasi-reversible criteria for all samples, confirming their promising performance. Mott-Shottky plots are in good agreement with Raman spectra for boron-doped films from 1018 to 1019 B.cm−3 where the highest doped diamond was obtained for the thickest films of 5 and 7 h. [Display omitted] •B-UNCDWS/TDNT/Ti electrodes without seeding pre-treatment were successfully achieved.•The TDNT influence on UNCDWS formation is motivated by the TiO2 into TiC conversion.•SEM images showed a unique morphology with evolution as a function of growth time.•CVD ballas cluster were growth concomitantly, also a function of growth time.•The quasi-reversible behavior for all samples makes it a promising composite.
Boron-doped ultrananocrystalline diamond grown on titanium dioxide nanotubes without seeding pre-treatment (B-UNCDWS/TDNT/Ti), as a porous composite, was successfully achieved. Innovative approaches concerning the highly ordered TDNT production as well as its singular diamond formation by hot filament chemical vapor deposition (CVD) were explored. The B-UNCD homogeneous cluster progress on the TDNT porous walls as a function of the growth times from 1 to 7 h led to remarkable composite morphologies, keeping the TDNT porosity, where the TiO2 – TiC conversion dominated the renucleation process facilitating the nanometric scale control. Scanning electron microscopy images confirmed the continuous ultrananocrystalline formation as nanoclusters on the TDNT walls with their size evolution as a function of growth time also showing an increase in the CVD diamond ballas clusters. Raman spectra and X-Ray patterns exhibited the diamond characteristics with defined peaks and TiC formation, as expected. The ID(220)/(111) and ID(311)/(111) ratio intensities pointed out the films governed by (220) diamond phase, due to their high renucleation process. Besides, the intensity ratios for both TiC (111) and TiC (200) phases with D(111) peak showed a carbon atoms competition between surface and bulk diffusion on the TiC layer. The electrode reversibility evaluated from cyclic voltammetry curves followed the quasi-reversible criteria for all samples, confirming their promising performance. Mott-Shottky plots are in good agreement with Raman spectra for boron-doped films from 1018 to 1019 B.cm−3 where the highest doped diamond was obtained for the thickest films of 5 and 7 h.
ArticleNumber 108793
Author Vernasqui, Laís G.
Rodrigo, Manuel A.
Ferreira, Neidenêi G.
Sardinha, A.F.
Kawata, Bianca A.
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  givenname: Bianca A.
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  surname: Sardinha
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  givenname: Neidenêi G.
  surname: Ferreira
  fullname: Ferreira, Neidenêi G.
  organization: Laboratório Associado de Sensores e Materiais, Instituto Nacional de Pesquisas Espaciais (INPE), Av. dos Astronautas, 1758, 12227 010 São José dos Campos, SP, Brazil
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Keywords Boron-doped ultrananocrystalline diamond
Titanium dioxide nanotubes
Composite
CVD growth without seeding
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Snippet Boron-doped ultrananocrystalline diamond grown on titanium dioxide nanotubes without seeding pre-treatment (B-UNCDWS/TDNT/Ti), as a porous composite, was...
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StartPage 108793
SubjectTerms Boron
Boron-doped ultrananocrystalline diamond
Chemical vapor deposition
Composite
CVD growth without seeding
Diamonds
Diffusion layers
Doped films
Nanoclusters
Nanotubes
Porous walls
Raman spectra
Titanium carbide
Titanium dioxide
Titanium dioxide nanotubes
Title Achievement and electrochemical responsiveness of advanced boron-doped ultrananocrystalline diamond on highly ordered titanium dioxide nanotubes
URI https://dx.doi.org/10.1016/j.diamond.2021.108793
https://www.proquest.com/docview/2627993099
Volume 121
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