Loading…
First-principles theoretical analysis of silyl radical diffusion on silicon surfaces
We report results from a detailed analysis of the fundamental radical precursor diffusion processes on silicon surfaces and discuss their implications for the surface smoothness of hydrogenated amorphous silicon (a-Si:H) thin films. The analysis is based on a synergistic combination of first-princip...
Saved in:
Published in: | The Journal of chemical physics 2006-09, Vol.125 (10), p.104702-104702 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993 |
---|---|
cites | cdi_FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993 |
container_end_page | 104702 |
container_issue | 10 |
container_start_page | 104702 |
container_title | The Journal of chemical physics |
container_volume | 125 |
creator | Bakos, Tamas Valipa, Mayur S Maroudas, Dimitrios |
description | We report results from a detailed analysis of the fundamental radical precursor diffusion processes on silicon surfaces and discuss their implications for the surface smoothness of hydrogenated amorphous silicon (a-Si:H) thin films. The analysis is based on a synergistic combination of first-principles density functional theory (DFT) calculations of SiH(3) radical migration on the hydrogen-terminated Si(001)-(2 x 1) surface with molecular-dynamics (MD) simulations of SiH(3) radical precursor migration on surfaces of a-Si:H films. Our DFT calculations yield activation energies for SiH(3) migration that range from 0.18 to 0.89 eV depending on the local electronic environment on the Si(001)-(2 x 1):H surface. In particular, when no substantial surface relaxation (Si-Si bond breaking or formation) accompanies the hopping of the SiH(3) radical the activation barriers are highest, whereas hopping between nearest-neighbor overcoordinated surface Si atoms results in the lowest radical diffusion barrier of 0.18 eV; this low barrier is consistent with the activation barrier for SiH(3) migration through overcoordinated sites on the a-Si:H surface. Specifically, the analysis of the MD simulations of SiH(3) radical migration on a-Si:H surfaces yields an effective diffusion barrier of 0.16 eV, allowing for the rapid migration of the SiH(3) radical prior to its incorporation in surface valleys; rapid migration and subsequent incorporation constitute the two-step mechanism responsible for the smoothness of plasma deposited a-Si:H thin films. |
doi_str_mv | 10.1063/1.2345064 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68893744</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68893744</sourcerecordid><originalsourceid>FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993</originalsourceid><addsrcrecordid>eNpFkE9Lw0AUxBdRbK0e_AKSk-Ah9W12s3-OUloVCl7qOWw2u7iyTeq-5NBvb2oDwsAc5vcG3hByT2FJQbBnuiwYL0HwCzKnoHQuhYZLMgcoaK4FiBm5QfwGACoLfk1mVGitS87mZLcJCfv8kEJrwyE6zPov1yXXB2tiZloTjxgw63yGIR5jlkzzlzTB-wFD12ajxijYkw_JG-vwllx5E9HdTb4gn5v1bvWWbz9e31cv29wWivV5A0b7shTGKclrqK3VXnlRghOyrLUH66gpnPTSW2GUYEXNLB8lxXipNVuQx3PvIXU_g8O-2ge0LkbTum7ASiilmeR8BJ_OoE0dYnK-Gh_em3SsKFSnCStaTROO7MNUOtR71_yT02bsF5DSbKk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68893744</pqid></control><display><type>article</type><title>First-principles theoretical analysis of silyl radical diffusion on silicon surfaces</title><source>American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list)</source><source>AIP_美国物理联合会现刊(与NSTL共建)</source><creator>Bakos, Tamas ; Valipa, Mayur S ; Maroudas, Dimitrios</creator><creatorcontrib>Bakos, Tamas ; Valipa, Mayur S ; Maroudas, Dimitrios</creatorcontrib><description>We report results from a detailed analysis of the fundamental radical precursor diffusion processes on silicon surfaces and discuss their implications for the surface smoothness of hydrogenated amorphous silicon (a-Si:H) thin films. The analysis is based on a synergistic combination of first-principles density functional theory (DFT) calculations of SiH(3) radical migration on the hydrogen-terminated Si(001)-(2 x 1) surface with molecular-dynamics (MD) simulations of SiH(3) radical precursor migration on surfaces of a-Si:H films. Our DFT calculations yield activation energies for SiH(3) migration that range from 0.18 to 0.89 eV depending on the local electronic environment on the Si(001)-(2 x 1):H surface. In particular, when no substantial surface relaxation (Si-Si bond breaking or formation) accompanies the hopping of the SiH(3) radical the activation barriers are highest, whereas hopping between nearest-neighbor overcoordinated surface Si atoms results in the lowest radical diffusion barrier of 0.18 eV; this low barrier is consistent with the activation barrier for SiH(3) migration through overcoordinated sites on the a-Si:H surface. Specifically, the analysis of the MD simulations of SiH(3) radical migration on a-Si:H surfaces yields an effective diffusion barrier of 0.16 eV, allowing for the rapid migration of the SiH(3) radical prior to its incorporation in surface valleys; rapid migration and subsequent incorporation constitute the two-step mechanism responsible for the smoothness of plasma deposited a-Si:H thin films.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.2345064</identifier><identifier>PMID: 16999543</identifier><language>eng</language><publisher>United States</publisher><subject>Chemical Phenomena ; Chemistry, Physical ; Dimerization ; Hydrogen - chemistry ; Models, Molecular ; Molecular Conformation ; Silanes - chemistry ; Silicon Compounds - chemistry ; Surface Properties</subject><ispartof>The Journal of chemical physics, 2006-09, Vol.125 (10), p.104702-104702</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993</citedby><cites>FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,782,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16999543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bakos, Tamas</creatorcontrib><creatorcontrib>Valipa, Mayur S</creatorcontrib><creatorcontrib>Maroudas, Dimitrios</creatorcontrib><title>First-principles theoretical analysis of silyl radical diffusion on silicon surfaces</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>We report results from a detailed analysis of the fundamental radical precursor diffusion processes on silicon surfaces and discuss their implications for the surface smoothness of hydrogenated amorphous silicon (a-Si:H) thin films. The analysis is based on a synergistic combination of first-principles density functional theory (DFT) calculations of SiH(3) radical migration on the hydrogen-terminated Si(001)-(2 x 1) surface with molecular-dynamics (MD) simulations of SiH(3) radical precursor migration on surfaces of a-Si:H films. Our DFT calculations yield activation energies for SiH(3) migration that range from 0.18 to 0.89 eV depending on the local electronic environment on the Si(001)-(2 x 1):H surface. In particular, when no substantial surface relaxation (Si-Si bond breaking or formation) accompanies the hopping of the SiH(3) radical the activation barriers are highest, whereas hopping between nearest-neighbor overcoordinated surface Si atoms results in the lowest radical diffusion barrier of 0.18 eV; this low barrier is consistent with the activation barrier for SiH(3) migration through overcoordinated sites on the a-Si:H surface. Specifically, the analysis of the MD simulations of SiH(3) radical migration on a-Si:H surfaces yields an effective diffusion barrier of 0.16 eV, allowing for the rapid migration of the SiH(3) radical prior to its incorporation in surface valleys; rapid migration and subsequent incorporation constitute the two-step mechanism responsible for the smoothness of plasma deposited a-Si:H thin films.</description><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Dimerization</subject><subject>Hydrogen - chemistry</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Silanes - chemistry</subject><subject>Silicon Compounds - chemistry</subject><subject>Surface Properties</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpFkE9Lw0AUxBdRbK0e_AKSk-Ah9W12s3-OUloVCl7qOWw2u7iyTeq-5NBvb2oDwsAc5vcG3hByT2FJQbBnuiwYL0HwCzKnoHQuhYZLMgcoaK4FiBm5QfwGACoLfk1mVGitS87mZLcJCfv8kEJrwyE6zPov1yXXB2tiZloTjxgw63yGIR5jlkzzlzTB-wFD12ajxijYkw_JG-vwllx5E9HdTb4gn5v1bvWWbz9e31cv29wWivV5A0b7shTGKclrqK3VXnlRghOyrLUH66gpnPTSW2GUYEXNLB8lxXipNVuQx3PvIXU_g8O-2ge0LkbTum7ASiilmeR8BJ_OoE0dYnK-Gh_em3SsKFSnCStaTROO7MNUOtR71_yT02bsF5DSbKk</recordid><startdate>20060914</startdate><enddate>20060914</enddate><creator>Bakos, Tamas</creator><creator>Valipa, Mayur S</creator><creator>Maroudas, Dimitrios</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060914</creationdate><title>First-principles theoretical analysis of silyl radical diffusion on silicon surfaces</title><author>Bakos, Tamas ; Valipa, Mayur S ; Maroudas, Dimitrios</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Chemical Phenomena</topic><topic>Chemistry, Physical</topic><topic>Dimerization</topic><topic>Hydrogen - chemistry</topic><topic>Models, Molecular</topic><topic>Molecular Conformation</topic><topic>Silanes - chemistry</topic><topic>Silicon Compounds - chemistry</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bakos, Tamas</creatorcontrib><creatorcontrib>Valipa, Mayur S</creatorcontrib><creatorcontrib>Maroudas, Dimitrios</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bakos, Tamas</au><au>Valipa, Mayur S</au><au>Maroudas, Dimitrios</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First-principles theoretical analysis of silyl radical diffusion on silicon surfaces</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2006-09-14</date><risdate>2006</risdate><volume>125</volume><issue>10</issue><spage>104702</spage><epage>104702</epage><pages>104702-104702</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>We report results from a detailed analysis of the fundamental radical precursor diffusion processes on silicon surfaces and discuss their implications for the surface smoothness of hydrogenated amorphous silicon (a-Si:H) thin films. The analysis is based on a synergistic combination of first-principles density functional theory (DFT) calculations of SiH(3) radical migration on the hydrogen-terminated Si(001)-(2 x 1) surface with molecular-dynamics (MD) simulations of SiH(3) radical precursor migration on surfaces of a-Si:H films. Our DFT calculations yield activation energies for SiH(3) migration that range from 0.18 to 0.89 eV depending on the local electronic environment on the Si(001)-(2 x 1):H surface. In particular, when no substantial surface relaxation (Si-Si bond breaking or formation) accompanies the hopping of the SiH(3) radical the activation barriers are highest, whereas hopping between nearest-neighbor overcoordinated surface Si atoms results in the lowest radical diffusion barrier of 0.18 eV; this low barrier is consistent with the activation barrier for SiH(3) migration through overcoordinated sites on the a-Si:H surface. Specifically, the analysis of the MD simulations of SiH(3) radical migration on a-Si:H surfaces yields an effective diffusion barrier of 0.16 eV, allowing for the rapid migration of the SiH(3) radical prior to its incorporation in surface valleys; rapid migration and subsequent incorporation constitute the two-step mechanism responsible for the smoothness of plasma deposited a-Si:H thin films.</abstract><cop>United States</cop><pmid>16999543</pmid><doi>10.1063/1.2345064</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9606 |
ispartof | The Journal of chemical physics, 2006-09, Vol.125 (10), p.104702-104702 |
issn | 0021-9606 1089-7690 |
language | eng |
recordid | cdi_proquest_miscellaneous_68893744 |
source | American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); AIP_美国物理联合会现刊(与NSTL共建) |
subjects | Chemical Phenomena Chemistry, Physical Dimerization Hydrogen - chemistry Models, Molecular Molecular Conformation Silanes - chemistry Silicon Compounds - chemistry Surface Properties |
title | First-principles theoretical analysis of silyl radical diffusion on silicon surfaces |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T07%3A41%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=First-principles%20theoretical%20analysis%20of%20silyl%20radical%20diffusion%20on%20silicon%20surfaces&rft.jtitle=The%20Journal%20of%20chemical%20physics&rft.au=Bakos,%20Tamas&rft.date=2006-09-14&rft.volume=125&rft.issue=10&rft.spage=104702&rft.epage=104702&rft.pages=104702-104702&rft.issn=0021-9606&rft.eissn=1089-7690&rft_id=info:doi/10.1063/1.2345064&rft_dat=%3Cproquest_cross%3E68893744%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c283t-d0a9f556ae874b0bcc9f8f650e675b9f0ce1a2e7f7fc6a8632b3c43c4760a9993%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=68893744&rft_id=info:pmid/16999543&rfr_iscdi=true |