Charge Transport and Sensitized 1.5 μm Electroluminescence Properties of Full Solution-Processed NIR-OLED based on Novel Er(III) Fluorinated β-Diketonate Ternary Complex
Identifieur interne : 001063 ( Main/Repository ); précédent : 001062; suivant : 001064Charge Transport and Sensitized 1.5 μm Electroluminescence Properties of Full Solution-Processed NIR-OLED based on Novel Er(III) Fluorinated β-Diketonate Ternary Complex
Auteurs : RBID : Pascal:13-0215803Descripteurs français
- Pascal (Inist)
- Transport charge, Electroluminescence, Spectre IR proche, Spectre IR, Diode électroluminescente organique, Diode électroluminescente, Rayonnement IR proche, Verre, Oxyde d'indium, Oxyde d'étain, Thiophène polymère, Thiophène dérivé polymère, Trempe, Coordinat organique, Caractéristique électrique, Dépendance tension, Fluorène dérivé polymère, Propriété optique, Ligand, Diffraction RX, Résonance magnétique nucléaire, Spectrométrie Raman, Spectrométrie transformée Fourier, Propriété photoélectronique, Phénomène transitoire, Photoluminescence, Transfert énergie, Substrat Aluminium, 9,9-dioctylfluorène polymère, 7363, 7860F, 7830N, 8560J.
- Wicri :
- concept : Verre.
English descriptors
- KwdEn :
- Charge transport, Electrical characteristic, Electroluminescence, Energy transfer, Fluorene derivative polymer, Fourier transform spectroscopy, Glass, Indium oxide, Infrared spectra, Ligands, Light emitting diodes, Near infrared radiation, Near infrared spectrum, Nuclear magnetic resonance, Optical properties, Organic ligand, Organic light emitting diodes, Photoelectronic properties, Photoluminescence, Quenching, Raman spectroscopy, Thiophene derivative polymer, Thiophene polymer, Tin oxide, Transients, Voltage dependence, XRD.
Abstract
Solution-processed near-infrared organic light-emitting diodes (NIR-OLEDs) with structure glass/indium-tin oxide/poly(3,4-ethylenedioxythiophene)-poly(styrene sulfbnate)/Er-complex/Ca/Al based on a novel Er(III) complex, [Er(tfnb)3(bipy)] (Htfnb = 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione and bipy = 2,2'-bipyridine) have been manufactured and their properties have been studied- A complete quenching of the organic ligand visible emission is shown, and only the sensitized 1.5 μm electroluminesce from Er(III) results. From the electrical characteristic we present the mobility dependence on applied voltage using a numerical model, comparing it to poly(9,9-dioctylfluorene), a commercial semiconducting polymer with optical properties close to those of the molecular ligands. The synthesis of the novel complex together with a detailed analysis of its structure elucidated by XRD, 1H NMR, Raman, and Fourier-transform infrared spectroscopies is presented. A wide-ranging characterization of its photophysical properties in terms of absorption and steady and transient photoluminescence is used to investigate the energy-transfer process from the organic ligand to the central Er(III) ion.
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Charge Transport and Sensitized 1.5 μm Electroluminescence Properties of Full Solution-Processed NIR-OLED based on Novel Er(III) Fluorinated β-Diketonate Ternary Complex</title><author><name sortKey="Martin Ramos, Pablo" uniqKey="Martin Ramos P">Pablo Martin-Ramos</name><affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Departamento de Teoría de la Señal y Comunicaciones e Ingeniería Telemática, Universidad de Valladolid, ETSI Telecomunicación, Paseo Belén 15, Campus Miguel Delibes</s1><s2>47011 Valladolid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Castille-et-León</region></placeName></affiliation></author><author><name sortKey="Coya, Carmen" uniqKey="Coya C">Carmen Coya</name><affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Departamento de Tecnología Electrónica, Universidad Rey Juan Carlos, Escuela Superior de Ciencias Experimentales y Tecnología (ESCET), C/Tulipán s/n</s1><s2>Móstoles, 28933 Madrid</s2><s3>ESP</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Communauté de Madrid</region></placeName></affiliation></author><author><name sortKey="Alvarez, Angel L" uniqKey="Alvarez A">Angel L. Alvarez</name><affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Departamento de Tecnología Electrónica, Universidad Rey Juan Carlos, Escuela Superior de Ciencias Experimentales y Tecnología (ESCET), C/Tulipán s/n</s1><s2>Móstoles, 28933 Madrid</s2><s3>ESP</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Communauté de Madrid</region></placeName></affiliation></author><author><name sortKey="Silva, Manuela Ramos" uniqKey="Silva M">Manuela Ramos Silva</name><affiliation wicri:level="1"><inist:fA14 i1="03"><s1>CEMDRX, Physics Department, Coimbra University, Rua Larga</s1><s2>3004-516 Coimbra</s2><s3>PRT</s3><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Portugal</country><wicri:noRegion>3004-516 Coimbra</wicri:noRegion></affiliation></author><author><name sortKey="Zaldo, Carlos" uniqKey="Zaldo C">Carlos Zaldo</name><affiliation wicri:level="2"><inist:fA14 i1="04"><s1>Instituto de Ciencia de Materiales de Madrid, Consejo Superior de Investigaciones Científicas, C/Sor Juana Inés de la Cruz 3</s1><s2>28049 Madrid</s2><s3>ESP</s3><sZ>5 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Communauté de Madrid</region></placeName></affiliation></author><author><name sortKey="Paixao, Jose A" uniqKey="Paixao J">José A. Paixao</name><affiliation wicri:level="1"><inist:fA14 i1="03"><s1>CEMDRX, Physics Department, Coimbra University, Rua Larga</s1><s2>3004-516 Coimbra</s2><s3>PRT</s3><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Portugal</country><wicri:noRegion>3004-516 Coimbra</wicri:noRegion></affiliation></author><author><name sortKey="Chamorro Posada, Pedro" uniqKey="Chamorro Posada P">Pedro Chamorro-Posada</name><affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Departamento de Teoría de la Señal y Comunicaciones e Ingeniería Telemática, Universidad de Valladolid, ETSI Telecomunicación, Paseo Belén 15, Campus Miguel Delibes</s1><s2>47011 Valladolid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Castille-et-León</region></placeName></affiliation></author><author><name sortKey="Martin Gil, Jes S" uniqKey="Martin Gil J">Jes S Martin-Gil</name><affiliation wicri:level="2"><inist:fA14 i1="05"><s1>Advanced Materials Laboratory, ETSIIAA, Universidad de Valladolid, Avenida de Madrid 44</s1><s2>34004 Palencia</s2><s3>ESP</s3><sZ>8 aut.</sZ></inist:fA14><country>Espagne</country><placeName><region nuts="2" type="communauté">Castille-et-León</region></placeName></affiliation></author></titleStmt><publicationStmt><idno type="inist">13-0215803</idno><date when="2013">2013</date><idno type="stanalyst">PASCAL 13-0215803 INIST</idno><idno type="RBID">Pascal:13-0215803</idno><idno type="wicri:Area/Main/Corpus">000B89</idno><idno type="wicri:Area/Main/Repository">001063</idno></publicationStmt><seriesStmt><idno type="ISSN">1932-7447</idno><title level="j" type="abbreviated">J. phys. chem., C</title><title level="j" type="main">Journal of physical chemistry. C</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Charge transport</term><term>Electrical characteristic</term><term>Electroluminescence</term><term>Energy transfer</term><term>Fluorene derivative polymer</term><term>Fourier transform spectroscopy</term><term>Glass</term><term>Indium oxide</term><term>Infrared spectra</term><term>Ligands</term><term>Light emitting diodes</term><term>Near infrared radiation</term><term>Near infrared spectrum</term><term>Nuclear magnetic resonance</term><term>Optical properties</term><term>Organic ligand</term><term>Organic light emitting diodes</term><term>Photoelectronic properties</term><term>Photoluminescence</term><term>Quenching</term><term>Raman spectroscopy</term><term>Thiophene derivative polymer</term><term>Thiophene polymer</term><term>Tin oxide</term><term>Transients</term><term>Voltage dependence</term><term>XRD</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Transport charge</term><term>Electroluminescence</term><term>Spectre IR proche</term><term>Spectre IR</term><term>Diode électroluminescente organique</term><term>Diode électroluminescente</term><term>Rayonnement IR proche</term><term>Verre</term><term>Oxyde d'indium</term><term>Oxyde d'étain</term><term>Thiophène polymère</term><term>Thiophène dérivé polymère</term><term>Trempe</term><term>Coordinat organique</term><term>Caractéristique électrique</term><term>Dépendance tension</term><term>Fluorène dérivé polymère</term><term>Propriété optique</term><term>Ligand</term><term>Diffraction RX</term><term>Résonance magnétique nucléaire</term><term>Spectrométrie Raman</term><term>Spectrométrie transformée Fourier</term><term>Propriété photoélectronique</term><term>Phénomène transitoire</term><term>Photoluminescence</term><term>Transfert énergie</term><term>Substrat Aluminium</term><term>9,9-dioctylfluorène polymère</term><term>7363</term><term>7860F</term><term>7830N</term><term>8560J</term></keywords><keywords scheme="Wicri" type="concept" xml:lang="fr"><term>Verre</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Solution-processed near-infrared organic light-emitting diodes (NIR-OLEDs) with structure glass/indium-tin oxide/poly(3,4-ethylenedioxythiophene)-poly(styrene sulfbnate)/Er-complex/Ca/Al based on a novel Er(III) complex, [Er(tfnb)<sub>3</sub>(bipy)] (Htfnb = 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione and bipy = 2,2'-bipyridine) have been manufactured and their properties have been studied- A complete quenching of the organic ligand visible emission is shown, and only the sensitized 1.5 μm electroluminesce from Er(III) results. From the electrical characteristic we present the mobility dependence on applied voltage using a numerical model, comparing it to poly(9,9-dioctylfluorene), a commercial semiconducting polymer with optical properties close to those of the molecular ligands. The synthesis of the novel complex together with a detailed analysis of its structure elucidated by XRD, <sup>1</sup>H NMR, Raman, and Fourier-transform infrared spectroscopies is presented. A wide-ranging characterization of its photophysical properties in terms of absorption and steady and transient photoluminescence is used to investigate the energy-transfer process from the organic ligand to the central Er(III) ion.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1932-7447</s0></fA01><fA03 i2="1"><s0>J. phys. chem., C</s0></fA03><fA05><s2>117</s2></fA05><fA06><s2>19</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Charge Transport and Sensitized 1.5 μm Electroluminescence Properties of Full Solution-Processed NIR-OLED based on Novel Er(III) Fluorinated β-Diketonate Ternary Complex</s1></fA08><fA11 i1="01" i2="1"><s1>MARTIN-RAMOS (Pablo)</s1></fA11><fA11 i1="02" i2="1"><s1>COYA (Carmen)</s1></fA11><fA11 i1="03" i2="1"><s1>ALVAREZ (Angel L.)</s1></fA11><fA11 i1="04" i2="1"><s1>SILVA (Manuela Ramos)</s1></fA11><fA11 i1="05" i2="1"><s1>ZALDO (Carlos)</s1></fA11><fA11 i1="06" i2="1"><s1>PAIXAO (José A.)</s1></fA11><fA11 i1="07" i2="1"><s1>CHAMORRO-POSADA (Pedro)</s1></fA11><fA11 i1="08" i2="1"><s1>MARTIN-GIL (Jesús)</s1></fA11><fA14 i1="01"><s1>Departamento de Teoría de la Señal y Comunicaciones e Ingeniería Telemática, Universidad de Valladolid, ETSI Telecomunicación, Paseo Belén 15, Campus Miguel Delibes</s1><s2>47011 Valladolid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Tecnología Electrónica, Universidad Rey Juan Carlos, Escuela Superior de Ciencias Experimentales y Tecnología (ESCET), C/Tulipán s/n</s1><s2>Móstoles, 28933 Madrid</s2><s3>ESP</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>CEMDRX, Physics Department, Coimbra University, Rua Larga</s1><s2>3004-516 Coimbra</s2><s3>PRT</s3><sZ>4 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="04"><s1>Instituto de Ciencia de Materiales de Madrid, Consejo Superior de Investigaciones Científicas, C/Sor Juana Inés de la Cruz 3</s1><s2>28049 Madrid</s2><s3>ESP</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Advanced Materials Laboratory, ETSIIAA, Universidad de Valladolid, Avenida de Madrid 44</s1><s2>34004 Palencia</s2><s3>ESP</s3><sZ>8 aut.</sZ></fA14><fA20><s1>10020-10030</s1></fA20><fA21><s1>2013</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>549C</s2><s5>354000503005330550</s5></fA43><fA44><s0>0000</s0><s1>© 2013 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>53 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>13-0215803</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of physical chemistry. C</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Solution-processed near-infrared organic light-emitting diodes (NIR-OLEDs) with structure glass/indium-tin oxide/poly(3,4-ethylenedioxythiophene)-poly(styrene sulfbnate)/Er-complex/Ca/Al based on a novel Er(III) complex, [Er(tfnb)<sub>3</sub>(bipy)] (Htfnb = 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione and bipy = 2,2'-bipyridine) have been manufactured and their properties have been studied- A complete quenching of the organic ligand visible emission is shown, and only the sensitized 1.5 μm electroluminesce from Er(III) results. From the electrical characteristic we present the mobility dependence on applied voltage using a numerical model, comparing it to poly(9,9-dioctylfluorene), a commercial semiconducting polymer with optical properties close to those of the molecular ligands. The synthesis of the novel complex together with a detailed analysis of its structure elucidated by XRD, <sup>1</sup>H NMR, Raman, and Fourier-transform infrared spectroscopies is presented. A wide-ranging characterization of its photophysical properties in terms of absorption and steady and transient photoluminescence is used to investigate the energy-transfer process from the organic ligand to the central Er(III) ion.</s0></fC01><fC02 i1="01" i2="3"><s0>001B70C63</s0></fC02><fC02 i1="02" i2="3"><s0>001B70H60F</s0></fC02><fC02 i1="03" i2="3"><s0>001B70H30N</s0></fC02><fC02 i1="04" i2="X"><s0>001D03F15</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Transport charge</s0><s5>01</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Charge transport</s0><s5>01</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Electroluminescence</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Electroluminescence</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Spectre IR proche</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Near infrared spectrum</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Espectro IR próximo</s0><s5>03</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Spectre IR</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Infrared spectra</s0><s5>04</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Diode électroluminescente organique</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Organic light emitting diodes</s0><s5>05</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Diode électroluminescente</s0><s5>06</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Light emitting diodes</s0><s5>06</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Rayonnement IR proche</s0><s5>07</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Near infrared radiation</s0><s5>07</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Verre</s0><s5>08</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Glass</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Oxyde d'indium</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Indium oxide</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Indio óxido</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Oxyde d'étain</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Tin oxide</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estaño óxido</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Thiophène polymère</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Thiophene polymer</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Tiofeno polímero</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Thiophène dérivé polymère</s0><s2>NK</s2><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Thiophene derivative polymer</s0><s2>NK</s2><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Tiofeno derivado polímero</s0><s2>NK</s2><s5>12</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Trempe</s0><s5>13</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Quenching</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Coordinat organique</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Organic ligand</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Ligando orgánico</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Caractéristique électrique</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Electrical characteristic</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Característica eléctrica</s0><s5>29</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Dépendance tension</s0><s5>30</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Voltage dependence</s0><s5>30</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Fluorène dérivé polymère</s0><s5>31</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Fluorene derivative polymer</s0><s5>31</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Fluoreno derivado polímero</s0><s5>31</s5></fC03><fC03 i1="18" i2="3" l="FRE"><s0>Propriété optique</s0><s5>32</s5></fC03><fC03 i1="18" i2="3" l="ENG"><s0>Optical properties</s0><s5>32</s5></fC03><fC03 i1="19" i2="3" l="FRE"><s0>Ligand</s0><s5>33</s5></fC03><fC03 i1="19" i2="3" l="ENG"><s0>Ligands</s0><s5>33</s5></fC03><fC03 i1="20" i2="3" l="FRE"><s0>Diffraction RX</s0><s5>34</s5></fC03><fC03 i1="20" i2="3" l="ENG"><s0>XRD</s0><s5>34</s5></fC03><fC03 i1="21" i2="3" l="FRE"><s0>Résonance magnétique nucléaire</s0><s5>35</s5></fC03><fC03 i1="21" i2="3" l="ENG"><s0>Nuclear magnetic resonance</s0><s5>35</s5></fC03><fC03 i1="22" i2="3" l="FRE"><s0>Spectrométrie Raman</s0><s5>36</s5></fC03><fC03 i1="22" i2="3" l="ENG"><s0>Raman spectroscopy</s0><s5>36</s5></fC03><fC03 i1="23" i2="3" l="FRE"><s0>Spectrométrie transformée Fourier</s0><s5>37</s5></fC03><fC03 i1="23" i2="3" l="ENG"><s0>Fourier transform spectroscopy</s0><s5>37</s5></fC03><fC03 i1="24" i2="X" l="FRE"><s0>Propriété photoélectronique</s0><s5>38</s5></fC03><fC03 i1="24" i2="X" l="ENG"><s0>Photoelectronic properties</s0><s5>38</s5></fC03><fC03 i1="24" i2="X" l="SPA"><s0>Propiedad fotoelectrónica</s0><s5>38</s5></fC03><fC03 i1="25" i2="3" l="FRE"><s0>Phénomène transitoire</s0><s5>39</s5></fC03><fC03 i1="25" i2="3" l="ENG"><s0>Transients</s0><s5>39</s5></fC03><fC03 i1="26" i2="3" l="FRE"><s0>Photoluminescence</s0><s5>40</s5></fC03><fC03 i1="26" i2="3" l="ENG"><s0>Photoluminescence</s0><s5>40</s5></fC03><fC03 i1="27" i2="3" l="FRE"><s0>Transfert énergie</s0><s5>41</s5></fC03><fC03 i1="27" i2="3" l="ENG"><s0>Energy transfer</s0><s5>41</s5></fC03><fC03 i1="28" i2="3" l="FRE"><s0>Substrat Aluminium</s0><s4>INC</s4><s5>46</s5></fC03><fC03 i1="29" i2="3" l="FRE"><s0>9,9-dioctylfluorène polymère</s0><s4>INC</s4><s5>47</s5></fC03><fC03 i1="30" i2="3" l="FRE"><s0>7363</s0><s4>INC</s4><s5>71</s5></fC03><fC03 i1="31" i2="3" l="FRE"><s0>7860F</s0><s4>INC</s4><s5>72</s5></fC03><fC03 i1="32" i2="3" l="FRE"><s0>7830N</s0><s4>INC</s4><s5>73</s5></fC03><fC03 i1="33" i2="3" l="FRE"><s0>8560J</s0><s4>INC</s4><s5>74</s5></fC03><fN21><s1>196</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard></inist></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= Charge Transport and Sensitized 1.5 μm Electroluminescence Properties of Full Solution-Processed NIR-OLED based on Novel Er(III) Fluorinated β-Diketonate Ternary Complex
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