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Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design

A contactless method using a novel design of the experimental cell for formation of porous silicon with morphological gradient is reported. Fabricated porous silicon layers show a large distribution in porosity, pore size and depth along the radius of the samples. Symmetrical arrangements of morphol...

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Autores principales: Zhao, Mingrui, Keswani, Manish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840451/
https://www.ncbi.nlm.nih.gov/pubmed/27103508
http://dx.doi.org/10.1038/srep24864
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author Zhao, Mingrui
Keswani, Manish
author_facet Zhao, Mingrui
Keswani, Manish
author_sort Zhao, Mingrui
collection PubMed
description A contactless method using a novel design of the experimental cell for formation of porous silicon with morphological gradient is reported. Fabricated porous silicon layers show a large distribution in porosity, pore size and depth along the radius of the samples. Symmetrical arrangements of morphology gradient were successfully formulated radially on porous films and the formation was attributed to decreasing current density radially inward on the silicon surface exposed to Triton(®) X-100 containing HF based etchant solution. Increasing the surfactant concentration increases the pore depth gradient but has a reverse effect on the pore size distribution. Interestingly, when dimethyl sulfoxide was used instead of Triton(®) X-100 in the etchant solution, no such morphological gradients were observed and a homogeneous porous film was formed.
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spelling pubmed-48404512016-04-28 Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design Zhao, Mingrui Keswani, Manish Sci Rep Article A contactless method using a novel design of the experimental cell for formation of porous silicon with morphological gradient is reported. Fabricated porous silicon layers show a large distribution in porosity, pore size and depth along the radius of the samples. Symmetrical arrangements of morphology gradient were successfully formulated radially on porous films and the formation was attributed to decreasing current density radially inward on the silicon surface exposed to Triton(®) X-100 containing HF based etchant solution. Increasing the surfactant concentration increases the pore depth gradient but has a reverse effect on the pore size distribution. Interestingly, when dimethyl sulfoxide was used instead of Triton(®) X-100 in the etchant solution, no such morphological gradients were observed and a homogeneous porous film was formed. Nature Publishing Group 2016-04-22 /pmc/articles/PMC4840451/ /pubmed/27103508 http://dx.doi.org/10.1038/srep24864 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhao, Mingrui
Keswani, Manish
Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title_full Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title_fullStr Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title_full_unstemmed Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title_short Fabrication of Radially Symmetric Graded Porous Silicon using a Novel Cell Design
title_sort fabrication of radially symmetric graded porous silicon using a novel cell design
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840451/
https://www.ncbi.nlm.nih.gov/pubmed/27103508
http://dx.doi.org/10.1038/srep24864
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