Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface

We investigate surface enhancement in two-dimensional attenuated total reflectance infrared (2D ATR IR) spectroscopy from organic monolayers (MLs) at metal–liquid interfaces. We consider MLs from both aromatic and aliphatic organic samples equipped with nitrile and azide functional groups, both of w...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of physical chemistry. C 2016-02, Vol.120 (6), p.3350-3359
Hauptverfasser: Kraack, Jan Philip, Kaech, Andres, Hamm, Peter
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3359
container_issue 6
container_start_page 3350
container_title Journal of physical chemistry. C
container_volume 120
creator Kraack, Jan Philip
Kaech, Andres
Hamm, Peter
description We investigate surface enhancement in two-dimensional attenuated total reflectance infrared (2D ATR IR) spectroscopy from organic monolayers (MLs) at metal–liquid interfaces. We consider MLs from both aromatic and aliphatic organic samples equipped with nitrile and azide functional groups, both of which are widely used as local vibrational probes in ultrafast spectroscopy. Polarization-dependent 2D ATR IR spectroscopy indicates the excitation of local hot spots formed between gold (Au) nanoparticles as the dominant origin of signal enhancement. The highest enhancement factors (∼50) are observed in the case of aromatic nitrile MLs, whereas modest values (
doi_str_mv 10.1021/acs.jpcc.5b11051
format Article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_acs_jpcc_5b11051</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a153168299</sourcerecordid><originalsourceid>FETCH-LOGICAL-a346t-e9786a464e2f07e7c8a6c584b57d557af776abb597387548b125228c5bbdf4db3</originalsourceid><addsrcrecordid>eNp1kEtPwzAQhC0EEqVw5-gfQIrteOPkWJUClYqQ-jhHa8dWU7VpsJ1D_z3pQ9w4zUqzMxp9hDxzNuJM8Fc0YbRtjRmB5pwBvyEDXqQiURLg9u-W6p48hLBlDFLG0wFZLzvv0Fg6bTbYGLu3TaR1Q9e76NFhiFS80fFqQWcLumytif4QzKE9Uow0biz9shF3ybz-6eqKzppoz22P5M7hLtinqw7J-n26mnwm8--P2WQ8TzCVWUxsofIMZSatcExZZXLMDORSg6oAFDqlMtQaCpXmCmSuuQAhcgNaV05WOh0Sduk1_azgrStbX-_RH0vOyhOWssdSnrCUVyx95OUSOTuHzjf9wP_ffwGykGXI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface</title><source>ACS Publications</source><creator>Kraack, Jan Philip ; Kaech, Andres ; Hamm, Peter</creator><creatorcontrib>Kraack, Jan Philip ; Kaech, Andres ; Hamm, Peter</creatorcontrib><description>We investigate surface enhancement in two-dimensional attenuated total reflectance infrared (2D ATR IR) spectroscopy from organic monolayers (MLs) at metal–liquid interfaces. We consider MLs from both aromatic and aliphatic organic samples equipped with nitrile and azide functional groups, both of which are widely used as local vibrational probes in ultrafast spectroscopy. Polarization-dependent 2D ATR IR spectroscopy indicates the excitation of local hot spots formed between gold (Au) nanoparticles as the dominant origin of signal enhancement. The highest enhancement factors (∼50) are observed in the case of aromatic nitrile MLs, whereas modest values (&lt;10) are found for aliphatic azide and nitrile groups. Different contributions to signal enhancement are evaluated systematically and indicate the presence of both electromagnetic enhancement and contributions from molecular properties. The obtained enhancement factors are promising to allow 2D ATR IR spectroscopy to become applicable as a versatile technique for the detection of ultrafast structural dynamics in even low-absorbing organic MLs at solid–liquid interfaces.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.5b11051</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. C, 2016-02, Vol.120 (6), p.3350-3359</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a346t-e9786a464e2f07e7c8a6c584b57d557af776abb597387548b125228c5bbdf4db3</citedby><cites>FETCH-LOGICAL-a346t-e9786a464e2f07e7c8a6c584b57d557af776abb597387548b125228c5bbdf4db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jpcc.5b11051$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jpcc.5b11051$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Kraack, Jan Philip</creatorcontrib><creatorcontrib>Kaech, Andres</creatorcontrib><creatorcontrib>Hamm, Peter</creatorcontrib><title>Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>We investigate surface enhancement in two-dimensional attenuated total reflectance infrared (2D ATR IR) spectroscopy from organic monolayers (MLs) at metal–liquid interfaces. We consider MLs from both aromatic and aliphatic organic samples equipped with nitrile and azide functional groups, both of which are widely used as local vibrational probes in ultrafast spectroscopy. Polarization-dependent 2D ATR IR spectroscopy indicates the excitation of local hot spots formed between gold (Au) nanoparticles as the dominant origin of signal enhancement. The highest enhancement factors (∼50) are observed in the case of aromatic nitrile MLs, whereas modest values (&lt;10) are found for aliphatic azide and nitrile groups. Different contributions to signal enhancement are evaluated systematically and indicate the presence of both electromagnetic enhancement and contributions from molecular properties. The obtained enhancement factors are promising to allow 2D ATR IR spectroscopy to become applicable as a versatile technique for the detection of ultrafast structural dynamics in even low-absorbing organic MLs at solid–liquid interfaces.</description><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kEtPwzAQhC0EEqVw5-gfQIrteOPkWJUClYqQ-jhHa8dWU7VpsJ1D_z3pQ9w4zUqzMxp9hDxzNuJM8Fc0YbRtjRmB5pwBvyEDXqQiURLg9u-W6p48hLBlDFLG0wFZLzvv0Fg6bTbYGLu3TaR1Q9e76NFhiFS80fFqQWcLumytif4QzKE9Uow0biz9shF3ybz-6eqKzppoz22P5M7hLtinqw7J-n26mnwm8--P2WQ8TzCVWUxsofIMZSatcExZZXLMDORSg6oAFDqlMtQaCpXmCmSuuQAhcgNaV05WOh0Sduk1_azgrStbX-_RH0vOyhOWssdSnrCUVyx95OUSOTuHzjf9wP_ffwGykGXI</recordid><startdate>20160218</startdate><enddate>20160218</enddate><creator>Kraack, Jan Philip</creator><creator>Kaech, Andres</creator><creator>Hamm, Peter</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20160218</creationdate><title>Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface</title><author>Kraack, Jan Philip ; Kaech, Andres ; Hamm, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a346t-e9786a464e2f07e7c8a6c584b57d557af776abb597387548b125228c5bbdf4db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kraack, Jan Philip</creatorcontrib><creatorcontrib>Kaech, Andres</creatorcontrib><creatorcontrib>Hamm, Peter</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kraack, Jan Philip</au><au>Kaech, Andres</au><au>Hamm, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2016-02-18</date><risdate>2016</risdate><volume>120</volume><issue>6</issue><spage>3350</spage><epage>3359</epage><pages>3350-3359</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>We investigate surface enhancement in two-dimensional attenuated total reflectance infrared (2D ATR IR) spectroscopy from organic monolayers (MLs) at metal–liquid interfaces. We consider MLs from both aromatic and aliphatic organic samples equipped with nitrile and azide functional groups, both of which are widely used as local vibrational probes in ultrafast spectroscopy. Polarization-dependent 2D ATR IR spectroscopy indicates the excitation of local hot spots formed between gold (Au) nanoparticles as the dominant origin of signal enhancement. The highest enhancement factors (∼50) are observed in the case of aromatic nitrile MLs, whereas modest values (&lt;10) are found for aliphatic azide and nitrile groups. Different contributions to signal enhancement are evaluated systematically and indicate the presence of both electromagnetic enhancement and contributions from molecular properties. The obtained enhancement factors are promising to allow 2D ATR IR spectroscopy to become applicable as a versatile technique for the detection of ultrafast structural dynamics in even low-absorbing organic MLs at solid–liquid interfaces.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.5b11051</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1932-7447
ispartof Journal of physical chemistry. C, 2016-02, Vol.120 (6), p.3350-3359
issn 1932-7447
1932-7455
language eng
recordid cdi_crossref_primary_10_1021_acs_jpcc_5b11051
source ACS Publications
title Surface Enhancement in Ultrafast 2D ATR IR Spectroscopy at the Metal-Liquid Interface
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T22%3A18%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Surface%20Enhancement%20in%20Ultrafast%202D%20ATR%20IR%20Spectroscopy%20at%20the%20Metal-Liquid%20Interface&rft.jtitle=Journal%20of%20physical%20chemistry.%20C&rft.au=Kraack,%20Jan%20Philip&rft.date=2016-02-18&rft.volume=120&rft.issue=6&rft.spage=3350&rft.epage=3359&rft.pages=3350-3359&rft.issn=1932-7447&rft.eissn=1932-7455&rft_id=info:doi/10.1021/acs.jpcc.5b11051&rft_dat=%3Cacs_cross%3Ea153168299%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true