Loading…
Photoelectrochemical Behavior of Alizarin Modified TiO2 Films
Photocurrent voltage curves obtained under visible light excitation of alizarin molecules chemisorbed to nanoporous TiO2 films show both anodic and cathodic currents. The potential at which the sign reversal occurs depends on the electrolyte pH, the presence of acceptors, and the dye coverage, but a...
Saved in:
Published in: | Journal of physical chemistry. C 2010-07, Vol.114 (26), p.11515-11521 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 11521 |
container_issue | 26 |
container_start_page | 11515 |
container_title | Journal of physical chemistry. C |
container_volume | 114 |
creator | Di Iorio, Yesica Rodríguez, Hernán B San Román, Enrique Grela, María A |
description | Photocurrent voltage curves obtained under visible light excitation of alizarin molecules chemisorbed to nanoporous TiO2 films show both anodic and cathodic currents. The potential at which the sign reversal occurs depends on the electrolyte pH, the presence of acceptors, and the dye coverage, but as a general rule, it occurs at potentials ca. 600−700 mV more positive than the flat band potential. Negative photocurrents are accounted by efficient electron discharge to the electrolyte mediated by the ligand. Cathodic photocurrents are only observed at pH values higher than ca. 4.0 and go through a maximum at intermediate alizarin loadings. This phenomenon is ascribed to the progressive reparation of surface states by alizarin which hampers carrier transport through the TiO2 matrix and decreases electron discharge to the electrolyte solution. |
doi_str_mv | 10.1021/jp102354m |
format | article |
fullrecord | <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_jp102354m</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a508226016</sourcerecordid><originalsourceid>FETCH-LOGICAL-a251t-d7125e5403d8fcba208b978daa7641d38bccc74c9f7dc72a97f2df2f11488f1f3</originalsourceid><addsrcrecordid>eNo9j71OwzAURi0EEqUw8AZeGAO-_sHOwFAqCkhFZShz5Ni-iiOnRnFg4OlpBep0vuk7OoRcA7sFxuGu_9xDKDmckBnUgldaKnV63FKfk4tSesaUYCBm5OG9y1MOKbhpzK4LQ3Q20cfQ2e-YR5qRLlL8sWPc0bfsI8bg6TZuOF3FNJRLcoY2lXD1zzn5WD1tly_VevP8ulysK8sVTJXXwFVQkglv0LWWM9PW2nhr9b0EL0zrnNPS1ai909zWGrlHjgDSGAQUc3Lz92tdafr8Ne72tgZYc2hujs3iF2JdSU8</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Photoelectrochemical Behavior of Alizarin Modified TiO2 Films</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Di Iorio, Yesica ; Rodríguez, Hernán B ; San Román, Enrique ; Grela, María A</creator><creatorcontrib>Di Iorio, Yesica ; Rodríguez, Hernán B ; San Román, Enrique ; Grela, María A</creatorcontrib><description>Photocurrent voltage curves obtained under visible light excitation of alizarin molecules chemisorbed to nanoporous TiO2 films show both anodic and cathodic currents. The potential at which the sign reversal occurs depends on the electrolyte pH, the presence of acceptors, and the dye coverage, but as a general rule, it occurs at potentials ca. 600−700 mV more positive than the flat band potential. Negative photocurrents are accounted by efficient electron discharge to the electrolyte mediated by the ligand. Cathodic photocurrents are only observed at pH values higher than ca. 4.0 and go through a maximum at intermediate alizarin loadings. This phenomenon is ascribed to the progressive reparation of surface states by alizarin which hampers carrier transport through the TiO2 matrix and decreases electron discharge to the electrolyte solution.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp102354m</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Surfaces, Interfaces, Catalysis</subject><ispartof>Journal of physical chemistry. C, 2010-07, Vol.114 (26), p.11515-11521</ispartof><rights>Copyright © 2010 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Di Iorio, Yesica</creatorcontrib><creatorcontrib>Rodríguez, Hernán B</creatorcontrib><creatorcontrib>San Román, Enrique</creatorcontrib><creatorcontrib>Grela, María A</creatorcontrib><title>Photoelectrochemical Behavior of Alizarin Modified TiO2 Films</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>Photocurrent voltage curves obtained under visible light excitation of alizarin molecules chemisorbed to nanoporous TiO2 films show both anodic and cathodic currents. The potential at which the sign reversal occurs depends on the electrolyte pH, the presence of acceptors, and the dye coverage, but as a general rule, it occurs at potentials ca. 600−700 mV more positive than the flat band potential. Negative photocurrents are accounted by efficient electron discharge to the electrolyte mediated by the ligand. Cathodic photocurrents are only observed at pH values higher than ca. 4.0 and go through a maximum at intermediate alizarin loadings. This phenomenon is ascribed to the progressive reparation of surface states by alizarin which hampers carrier transport through the TiO2 matrix and decreases electron discharge to the electrolyte solution.</description><subject>C: Surfaces, Interfaces, Catalysis</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9j71OwzAURi0EEqUw8AZeGAO-_sHOwFAqCkhFZShz5Ni-iiOnRnFg4OlpBep0vuk7OoRcA7sFxuGu_9xDKDmckBnUgldaKnV63FKfk4tSesaUYCBm5OG9y1MOKbhpzK4LQ3Q20cfQ2e-YR5qRLlL8sWPc0bfsI8bg6TZuOF3FNJRLcoY2lXD1zzn5WD1tly_VevP8ulysK8sVTJXXwFVQkglv0LWWM9PW2nhr9b0EL0zrnNPS1ai909zWGrlHjgDSGAQUc3Lz92tdafr8Ne72tgZYc2hujs3iF2JdSU8</recordid><startdate>20100708</startdate><enddate>20100708</enddate><creator>Di Iorio, Yesica</creator><creator>Rodríguez, Hernán B</creator><creator>San Román, Enrique</creator><creator>Grela, María A</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20100708</creationdate><title>Photoelectrochemical Behavior of Alizarin Modified TiO2 Films</title><author>Di Iorio, Yesica ; Rodríguez, Hernán B ; San Román, Enrique ; Grela, María A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a251t-d7125e5403d8fcba208b978daa7641d38bccc74c9f7dc72a97f2df2f11488f1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>C: Surfaces, Interfaces, Catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Iorio, Yesica</creatorcontrib><creatorcontrib>Rodríguez, Hernán B</creatorcontrib><creatorcontrib>San Román, Enrique</creatorcontrib><creatorcontrib>Grela, María A</creatorcontrib><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Iorio, Yesica</au><au>Rodríguez, Hernán B</au><au>San Román, Enrique</au><au>Grela, María A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoelectrochemical Behavior of Alizarin Modified TiO2 Films</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2010-07-08</date><risdate>2010</risdate><volume>114</volume><issue>26</issue><spage>11515</spage><epage>11521</epage><pages>11515-11521</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Photocurrent voltage curves obtained under visible light excitation of alizarin molecules chemisorbed to nanoporous TiO2 films show both anodic and cathodic currents. The potential at which the sign reversal occurs depends on the electrolyte pH, the presence of acceptors, and the dye coverage, but as a general rule, it occurs at potentials ca. 600−700 mV more positive than the flat band potential. Negative photocurrents are accounted by efficient electron discharge to the electrolyte mediated by the ligand. Cathodic photocurrents are only observed at pH values higher than ca. 4.0 and go through a maximum at intermediate alizarin loadings. This phenomenon is ascribed to the progressive reparation of surface states by alizarin which hampers carrier transport through the TiO2 matrix and decreases electron discharge to the electrolyte solution.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp102354m</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-7447 |
ispartof | Journal of physical chemistry. C, 2010-07, Vol.114 (26), p.11515-11521 |
issn | 1932-7447 1932-7455 |
language | eng |
recordid | cdi_acs_journals_10_1021_jp102354m |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | C: Surfaces, Interfaces, Catalysis |
title | Photoelectrochemical Behavior of Alizarin Modified TiO2 Films |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T04%3A13%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photoelectrochemical%20Behavior%20of%20Alizarin%20Modified%20TiO2%20Films&rft.jtitle=Journal%20of%20physical%20chemistry.%20C&rft.au=Di%20Iorio,%20Yesica&rft.date=2010-07-08&rft.volume=114&rft.issue=26&rft.spage=11515&rft.epage=11521&rft.pages=11515-11521&rft.issn=1932-7447&rft.eissn=1932-7455&rft_id=info:doi/10.1021/jp102354m&rft_dat=%3Cacs%3Ea508226016%3C/acs%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a251t-d7125e5403d8fcba208b978daa7641d38bccc74c9f7dc72a97f2df2f11488f1f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |