Unusual self-assembly of chloroaluminium phthalocyanine on graphite
•The unusual ClAlPc molecular self-assembled layer on a buffer layer have large deformations compared with the common ClAlPc bilayer.•Almost freestanding environment is provided for the molecules when the influence from the substrate is shielded by the buffer layer.•The dominated intermolecular inte...
Gespeichert in:
Veröffentlicht in: | Surface science 2019-03, Vol.681, p.104-110 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 110 |
---|---|
container_issue | |
container_start_page | 104 |
container_title | Surface science |
container_volume | 681 |
creator | Ma, Hai-yang Zhao, Yan-ling Zaw, Myo Win Jia, Jin-feng Zhang, Rui-qin Van Hove, Michel A. |
description | •The unusual ClAlPc molecular self-assembled layer on a buffer layer have large deformations compared with the common ClAlPc bilayer.•Almost freestanding environment is provided for the molecules when the influence from the substrate is shielded by the buffer layer.•The dominated intermolecular interaction is likely to be the dispersion forces via Reduced Density Gradient analysis.
We report an unusual self-assembled layer structure of chloroaluminium phthalocyanine (ClAlPc) molecules on highly ordered pyrolytic graphite (HOPG), in which a close-packed well-ordered monolayer is separated from the substrate by a relatively disordered buffer layer, as revealed using scanning tunneling microscopy (STM). Our close-packed monolayer has a nearly rectangular lattice, instead of the distinctly different square lattice for the more commonly observed well-ordered bilayer structure. This may be due to the dominance of intermolecular interactions within the monolayer when the influence from the substrate is shielded by the buffer layer. Density Functional Theory (DFT) calculations and Reduced Density Gradient (RDG) analysis indicate that the dominant intermolecular interaction within the unusual layer is likely the London dispersion force.
[Display omitted] |
doi_str_mv | 10.1016/j.susc.2018.11.010 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2211924360</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0039602818304953</els_id><sourcerecordid>2211924360</sourcerecordid><originalsourceid>FETCH-LOGICAL-c328t-33a09402d072a031ddce2ea293b67f7731d22d21691eda615f33a2c1f5a4d08b3</originalsourceid><addsrcrecordid>eNp9kE1LxDAQhoMouK7-AU8Fz60zk36CF1n8ggUveg7ZJLUp3aYmrbD_3izr2bkMDO8zMzyM3SJkCFje91lYgsoIsM4QM0A4YyusqyalqqjP2QqAN2kJVF-yqxB6iJU3xYptPsclLHJIghnaVIZg9rvhkLg2Ud3gvJPDsrejXfbJ1M2dHJw6yNGOJnFj8uXl1NnZXLOLVg7B3Pz1Nft8fvrYvKbb95e3zeM2VZzqOeVcQpMDaahIAketlSEjqeG7smqrKk6INGHZoNGyxKKNBClsC5lrqHd8ze5OeyfvvhcTZtG7xY_xpCBCbCjnJcQUnVLKuxC8acXk7V76g0AQR1miF0dZ4ihLIIooK0IPJ8jE_3-s8SIoa0ZltPVGzUI7-x_-C7Z_cwE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2211924360</pqid></control><display><type>article</type><title>Unusual self-assembly of chloroaluminium phthalocyanine on graphite</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Ma, Hai-yang ; Zhao, Yan-ling ; Zaw, Myo Win ; Jia, Jin-feng ; Zhang, Rui-qin ; Van Hove, Michel A.</creator><creatorcontrib>Ma, Hai-yang ; Zhao, Yan-ling ; Zaw, Myo Win ; Jia, Jin-feng ; Zhang, Rui-qin ; Van Hove, Michel A.</creatorcontrib><description>•The unusual ClAlPc molecular self-assembled layer on a buffer layer have large deformations compared with the common ClAlPc bilayer.•Almost freestanding environment is provided for the molecules when the influence from the substrate is shielded by the buffer layer.•The dominated intermolecular interaction is likely to be the dispersion forces via Reduced Density Gradient analysis.
We report an unusual self-assembled layer structure of chloroaluminium phthalocyanine (ClAlPc) molecules on highly ordered pyrolytic graphite (HOPG), in which a close-packed well-ordered monolayer is separated from the substrate by a relatively disordered buffer layer, as revealed using scanning tunneling microscopy (STM). Our close-packed monolayer has a nearly rectangular lattice, instead of the distinctly different square lattice for the more commonly observed well-ordered bilayer structure. This may be due to the dominance of intermolecular interactions within the monolayer when the influence from the substrate is shielded by the buffer layer. Density Functional Theory (DFT) calculations and Reduced Density Gradient (RDG) analysis indicate that the dominant intermolecular interaction within the unusual layer is likely the London dispersion force.
[Display omitted]</description><identifier>ISSN: 0039-6028</identifier><identifier>EISSN: 1879-2758</identifier><identifier>DOI: 10.1016/j.susc.2018.11.010</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>2D self-assembly ; Bilayers ; Buffer layers ; Density functional theory ; Dispersion forces ; Molecular structure ; Monolayers ; Pyrolytic graphite ; Self-assembly ; Substrates ; Weak interactions</subject><ispartof>Surface science, 2019-03, Vol.681, p.104-110</ispartof><rights>2018</rights><rights>Copyright Elsevier BV Mar 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-33a09402d072a031ddce2ea293b67f7731d22d21691eda615f33a2c1f5a4d08b3</citedby><cites>FETCH-LOGICAL-c328t-33a09402d072a031ddce2ea293b67f7731d22d21691eda615f33a2c1f5a4d08b3</cites><orcidid>0000-0001-6897-4010 ; 0000-0001-5840-9149</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.susc.2018.11.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Ma, Hai-yang</creatorcontrib><creatorcontrib>Zhao, Yan-ling</creatorcontrib><creatorcontrib>Zaw, Myo Win</creatorcontrib><creatorcontrib>Jia, Jin-feng</creatorcontrib><creatorcontrib>Zhang, Rui-qin</creatorcontrib><creatorcontrib>Van Hove, Michel A.</creatorcontrib><title>Unusual self-assembly of chloroaluminium phthalocyanine on graphite</title><title>Surface science</title><description>•The unusual ClAlPc molecular self-assembled layer on a buffer layer have large deformations compared with the common ClAlPc bilayer.•Almost freestanding environment is provided for the molecules when the influence from the substrate is shielded by the buffer layer.•The dominated intermolecular interaction is likely to be the dispersion forces via Reduced Density Gradient analysis.
We report an unusual self-assembled layer structure of chloroaluminium phthalocyanine (ClAlPc) molecules on highly ordered pyrolytic graphite (HOPG), in which a close-packed well-ordered monolayer is separated from the substrate by a relatively disordered buffer layer, as revealed using scanning tunneling microscopy (STM). Our close-packed monolayer has a nearly rectangular lattice, instead of the distinctly different square lattice for the more commonly observed well-ordered bilayer structure. This may be due to the dominance of intermolecular interactions within the monolayer when the influence from the substrate is shielded by the buffer layer. Density Functional Theory (DFT) calculations and Reduced Density Gradient (RDG) analysis indicate that the dominant intermolecular interaction within the unusual layer is likely the London dispersion force.
[Display omitted]</description><subject>2D self-assembly</subject><subject>Bilayers</subject><subject>Buffer layers</subject><subject>Density functional theory</subject><subject>Dispersion forces</subject><subject>Molecular structure</subject><subject>Monolayers</subject><subject>Pyrolytic graphite</subject><subject>Self-assembly</subject><subject>Substrates</subject><subject>Weak interactions</subject><issn>0039-6028</issn><issn>1879-2758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouK7-AU8Fz60zk36CF1n8ggUveg7ZJLUp3aYmrbD_3izr2bkMDO8zMzyM3SJkCFje91lYgsoIsM4QM0A4YyusqyalqqjP2QqAN2kJVF-yqxB6iJU3xYptPsclLHJIghnaVIZg9rvhkLg2Ud3gvJPDsrejXfbJ1M2dHJw6yNGOJnFj8uXl1NnZXLOLVg7B3Pz1Nft8fvrYvKbb95e3zeM2VZzqOeVcQpMDaahIAketlSEjqeG7smqrKk6INGHZoNGyxKKNBClsC5lrqHd8ze5OeyfvvhcTZtG7xY_xpCBCbCjnJcQUnVLKuxC8acXk7V76g0AQR1miF0dZ4ihLIIooK0IPJ8jE_3-s8SIoa0ZltPVGzUI7-x_-C7Z_cwE</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Ma, Hai-yang</creator><creator>Zhao, Yan-ling</creator><creator>Zaw, Myo Win</creator><creator>Jia, Jin-feng</creator><creator>Zhang, Rui-qin</creator><creator>Van Hove, Michel A.</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-6897-4010</orcidid><orcidid>https://orcid.org/0000-0001-5840-9149</orcidid></search><sort><creationdate>201903</creationdate><title>Unusual self-assembly of chloroaluminium phthalocyanine on graphite</title><author>Ma, Hai-yang ; Zhao, Yan-ling ; Zaw, Myo Win ; Jia, Jin-feng ; Zhang, Rui-qin ; Van Hove, Michel A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-33a09402d072a031ddce2ea293b67f7731d22d21691eda615f33a2c1f5a4d08b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>2D self-assembly</topic><topic>Bilayers</topic><topic>Buffer layers</topic><topic>Density functional theory</topic><topic>Dispersion forces</topic><topic>Molecular structure</topic><topic>Monolayers</topic><topic>Pyrolytic graphite</topic><topic>Self-assembly</topic><topic>Substrates</topic><topic>Weak interactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Hai-yang</creatorcontrib><creatorcontrib>Zhao, Yan-ling</creatorcontrib><creatorcontrib>Zaw, Myo Win</creatorcontrib><creatorcontrib>Jia, Jin-feng</creatorcontrib><creatorcontrib>Zhang, Rui-qin</creatorcontrib><creatorcontrib>Van Hove, Michel A.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Surface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Hai-yang</au><au>Zhao, Yan-ling</au><au>Zaw, Myo Win</au><au>Jia, Jin-feng</au><au>Zhang, Rui-qin</au><au>Van Hove, Michel A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unusual self-assembly of chloroaluminium phthalocyanine on graphite</atitle><jtitle>Surface science</jtitle><date>2019-03</date><risdate>2019</risdate><volume>681</volume><spage>104</spage><epage>110</epage><pages>104-110</pages><issn>0039-6028</issn><eissn>1879-2758</eissn><abstract>•The unusual ClAlPc molecular self-assembled layer on a buffer layer have large deformations compared with the common ClAlPc bilayer.•Almost freestanding environment is provided for the molecules when the influence from the substrate is shielded by the buffer layer.•The dominated intermolecular interaction is likely to be the dispersion forces via Reduced Density Gradient analysis.
We report an unusual self-assembled layer structure of chloroaluminium phthalocyanine (ClAlPc) molecules on highly ordered pyrolytic graphite (HOPG), in which a close-packed well-ordered monolayer is separated from the substrate by a relatively disordered buffer layer, as revealed using scanning tunneling microscopy (STM). Our close-packed monolayer has a nearly rectangular lattice, instead of the distinctly different square lattice for the more commonly observed well-ordered bilayer structure. This may be due to the dominance of intermolecular interactions within the monolayer when the influence from the substrate is shielded by the buffer layer. Density Functional Theory (DFT) calculations and Reduced Density Gradient (RDG) analysis indicate that the dominant intermolecular interaction within the unusual layer is likely the London dispersion force.
[Display omitted]</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.susc.2018.11.010</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6897-4010</orcidid><orcidid>https://orcid.org/0000-0001-5840-9149</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0039-6028 |
ispartof | Surface science, 2019-03, Vol.681, p.104-110 |
issn | 0039-6028 1879-2758 |
language | eng |
recordid | cdi_proquest_journals_2211924360 |
source | ScienceDirect Journals (5 years ago - present) |
subjects | 2D self-assembly Bilayers Buffer layers Density functional theory Dispersion forces Molecular structure Monolayers Pyrolytic graphite Self-assembly Substrates Weak interactions |
title | Unusual self-assembly of chloroaluminium phthalocyanine on graphite |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T13%3A08%3A12IST&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=Unusual%20self-assembly%20of%20chloroaluminium%20phthalocyanine%20on%20graphite&rft.jtitle=Surface%20science&rft.au=Ma,%20Hai-yang&rft.date=2019-03&rft.volume=681&rft.spage=104&rft.epage=110&rft.pages=104-110&rft.issn=0039-6028&rft.eissn=1879-2758&rft_id=info:doi/10.1016/j.susc.2018.11.010&rft_dat=%3Cproquest_cross%3E2211924360%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2211924360&rft_id=info:pmid/&rft_els_id=S0039602818304953&rfr_iscdi=true |