Does conjugation help exciton dissociation? a study on poly(p-phenylene)s in planar heterojunctions with C60 or TNF.
Identifieur interne : 000E85 ( Main/Exploration ); précédent : 000E84; suivant : 000E86Does conjugation help exciton dissociation? a study on poly(p-phenylene)s in planar heterojunctions with C60 or TNF.
Auteurs : RBID : pubmed:22253146English descriptors
- KwdEn :
- MESH :
- chemical , chemical synthesis : Fluorenes.
- chemical , chemistry : Cycloparaffins, Fluorenes, Fullerenes, Polystyrenes, Thiophenes, Tin Compounds.
- Quantum Theory, Solar Energy.
Abstract
Internal photocurrent quantum yields near 100% can be obtained from the separation of loosely bound geminate pairs when sufficiently large electric fields are applied to organic heterojunctions. The fields needed for complete electron-hole dissociation decrease to those prevailing in organic solar cells under operating conditions when well-conjugated polymers are employed.
DOI: 10.1002/adma.201104063
PubMed: 22253146
Links toward previous steps (curation, corpus...)
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Does conjugation help exciton dissociation? a study on poly(p-phenylene)s in planar heterojunctions with C60 or TNF.</title><author><name sortKey="Schwarz, Christian" uniqKey="Schwarz C">Christian Schwarz</name><affiliation wicri:level="3"><nlm:affiliation>Experimental Physics II and Bayreuth Institute of Macromolecular Research, University of Bayreuth, Bayreuth, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Experimental Physics II and Bayreuth Institute of Macromolecular Research, University of Bayreuth, Bayreuth</wicri:regionArea><placeName><region type="land" nuts="1">Bavière</region><region type="district" nuts="2">District de Haute-Franconie</region><settlement type="city">Bayreuth</settlement></placeName></affiliation></author><author><name sortKey="B Ssler, Heinz" uniqKey="B Ssler H">Heinz Bässler</name></author><author><name sortKey="Bauer, Irene" uniqKey="Bauer I">Irene Bauer</name></author><author><name sortKey="Koenen, Jan Moritz" uniqKey="Koenen J">Jan-Moritz Koenen</name></author><author><name sortKey="Preis, Eduard" uniqKey="Preis E">Eduard Preis</name></author><author><name sortKey="Scherf, Ullrich" uniqKey="Scherf U">Ullrich Scherf</name></author><author><name sortKey="K Hler, Anna" uniqKey="K Hler A">Anna Köhler</name></author></titleStmt><publicationStmt><date when="2012">2012</date><idno type="doi">10.1002/adma.201104063</idno><idno type="RBID">pubmed:22253146</idno><idno type="pmid">22253146</idno><idno type="wicri:Area/Main/Corpus">000F56</idno><idno type="wicri:Area/Main/Curation">000F56</idno><idno type="wicri:Area/Main/Exploration">000E85</idno></publicationStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cycloparaffins (chemistry)</term><term>Fluorenes (chemical synthesis)</term><term>Fluorenes (chemistry)</term><term>Fullerenes (chemistry)</term><term>Polystyrenes (chemistry)</term><term>Quantum Theory</term><term>Solar Energy</term><term>Thiophenes (chemistry)</term><term>Tin Compounds (chemistry)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en"><term>Fluorenes</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Cycloparaffins</term><term>Fluorenes</term><term>Fullerenes</term><term>Polystyrenes</term><term>Thiophenes</term><term>Tin Compounds</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Quantum Theory</term><term>Solar Energy</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Internal photocurrent quantum yields near 100% can be obtained from the separation of loosely bound geminate pairs when sufficiently large electric fields are applied to organic heterojunctions. The fields needed for complete electron-hole dissociation decrease to those prevailing in organic solar cells under operating conditions when well-conjugated polymers are employed.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">22253146</PMID><DateCreated><Year>2012</Year><Month>02</Month><Day>07</Day></DateCreated><DateCompleted><Year>2012</Year><Month>05</Month><Day>25</Day></DateCompleted><DateRevised><Year>2012</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1521-4095</ISSN><JournalIssue CitedMedium="Internet"><Volume>24</Volume><Issue>7</Issue><PubDate><Year>2012</Year><Month>Feb</Month><Day>14</Day></PubDate></JournalIssue><Title>Advanced materials (Deerfield Beach, Fla.)</Title><ISOAbbreviation>Adv. Mater. Weinheim</ISOAbbreviation></Journal><ArticleTitle>Does conjugation help exciton dissociation? a study on poly(p-phenylene)s in planar heterojunctions with C60 or TNF.</ArticleTitle><Pagination><MedlinePgn>922-5</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/adma.201104063</ELocationID><Abstract><AbstractText>Internal photocurrent quantum yields near 100% can be obtained from the separation of loosely bound geminate pairs when sufficiently large electric fields are applied to organic heterojunctions. The fields needed for complete electron-hole dissociation decrease to those prevailing in organic solar cells under operating conditions when well-conjugated polymers are employed.</AbstractText><CopyrightInformation>Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schwarz</LastName><ForeName>Christian</ForeName><Initials>C</Initials><Affiliation>Experimental Physics II and Bayreuth Institute of Macromolecular Research, University of Bayreuth, Bayreuth, Germany.</Affiliation></Author><Author ValidYN="Y"><LastName>Bässler</LastName><ForeName>Heinz</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Bauer</LastName><ForeName>Irene</ForeName><Initials>I</Initials></Author><Author ValidYN="Y"><LastName>Koenen</LastName><ForeName>Jan-Moritz</ForeName><Initials>JM</Initials></Author><Author ValidYN="Y"><LastName>Preis</LastName><ForeName>Eduard</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Scherf</LastName><ForeName>Ullrich</ForeName><Initials>U</Initials></Author><Author ValidYN="Y"><LastName>Köhler</LastName><ForeName>Anna</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType>Journal Article</PublicationType><PublicationType>Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>01</Month><Day>18</Day></ArticleDate></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Adv Mater</MedlineTA><NlmUniqueID>9885358</NlmUniqueID><ISSNLinking>0935-9648</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Cycloparaffins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Fluorenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Fullerenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Polystyrenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Thiophenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>Tin Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance>poly-para-phenylene</NameOfSubstance></Chemical><Chemical><RegistryNumber>71243-84-0</RegistryNumber><NameOfSubstance>indium tin oxide</NameOfSubstance></Chemical><Chemical><RegistryNumber>NP9U26B839</RegistryNumber><NameOfSubstance>fullerene C60</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N">Cycloparaffins</DescriptorName><QualifierName MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Fluorenes</DescriptorName><QualifierName MajorTopicYN="N">chemical synthesis</QualifierName><QualifierName MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Fullerenes</DescriptorName><QualifierName MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Polystyrenes</DescriptorName><QualifierName MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Quantum Theory</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Solar Energy</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Thiophenes</DescriptorName><QualifierName MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N">Tin Compounds</DescriptorName><QualifierName MajorTopicYN="N">chemistry</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year><Month>10</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2011</Year><Month>12</Month><Day>6</Day></PubMedPubDate><PubMedPubDate PubStatus="aheadofprint"><Year>2012</Year><Month>1</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>1</Month><Day>19</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>1</Month><Day>19</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>5</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="doi">10.1002/adma.201104063</ArticleId><ArticleId IdType="pubmed">22253146</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=IndiumV2/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000E85 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000E85 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= *** parameter Area/wikiCode missing ***
|area= IndiumV2
|flux= Main
|étape= Exploration
|type= RBID
|clé= pubmed:22253146
|texte= Does conjugation help exciton dissociation? a study on poly(p-phenylene)s in planar heterojunctions with C60 or TNF.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:22253146" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a IndiumV2
| This area was generated with Dilib version V0.5.76. |  |