A Silane‐Based Bipolar Host with High Triplet Energy for High Efficiency Deep‐Blue Phosphorescent OLEDs with Improved Device Lifetime

A high triplet energy host is developed using a silane moiety, 9‐(4‐(triphenylsilyl)dibenzo[b,d]furan‐2‐yl)‐9H‐carbazole (SiDBFCz), is designed through extensive density functional theory (DFT) calculations to obtain appropriate hole and electron injection barriers. The chemical hardness and the cha...

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Veröffentlicht in:Chemistry : a European journal 2020-06, Vol.26 (35), p.7767-7773
Hauptverfasser: Ko, Soo‐Byung, Kang, Sunwoo, Kim, Taekyung
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creator Ko, Soo‐Byung
Kang, Sunwoo
Kim, Taekyung
description A high triplet energy host is developed using a silane moiety, 9‐(4‐(triphenylsilyl)dibenzo[b,d]furan‐2‐yl)‐9H‐carbazole (SiDBFCz), is designed through extensive density functional theory (DFT) calculations to obtain appropriate hole and electron injection barriers. The chemical hardness and the charge transport characteristics are comprehensively investigated to realize a bipolar host with high triplet energy over 2.9 eV for deep blue phosphorescent organic light‐emitting diodes (PHOLEDs). The synthesized SiDBFCz clearly exhibits the bipolar characteristics especially with emitter molecules doped. An external quantum efficiency over 19 % without any microcavity optimization is achieved thanks to the good charge balance in the SiDBFCz PHOLED. The device lifetime of the SiDBFCz PHOLED is improved more than 1000 %, compared to the unipolar control devices at an initial luminance of 500 cd m−2. The dramatic enhancement of the operational stability of the deep blue PHOLED is also thoroughly investigated in terms of electrochemical stability of host molecules in charged or excited states. The results clearly indicate that the device lifetime is strongly correlated with the bond dissociation energy and the activation energy for the bond dissociation reaction in triplet excited state. High efficiency and dramatic improvement of device lifetime were simultaneously and successfully realized with a silane‐based bipolar host, SiDBFCz. The dramatic enhancement of the operational stability was attributed to the bond dissociation energy and the activation energy for the bond dissociation reaction in the triplet excited state.
doi_str_mv 10.1002/chem.202000018
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The chemical hardness and the charge transport characteristics are comprehensively investigated to realize a bipolar host with high triplet energy over 2.9 eV for deep blue phosphorescent organic light‐emitting diodes (PHOLEDs). The synthesized SiDBFCz clearly exhibits the bipolar characteristics especially with emitter molecules doped. An external quantum efficiency over 19 % without any microcavity optimization is achieved thanks to the good charge balance in the SiDBFCz PHOLED. The device lifetime of the SiDBFCz PHOLED is improved more than 1000 %, compared to the unipolar control devices at an initial luminance of 500 cd m−2. The dramatic enhancement of the operational stability of the deep blue PHOLED is also thoroughly investigated in terms of electrochemical stability of host molecules in charged or excited states. The results clearly indicate that the device lifetime is strongly correlated with the bond dissociation energy and the activation energy for the bond dissociation reaction in triplet excited state. High efficiency and dramatic improvement of device lifetime were simultaneously and successfully realized with a silane‐based bipolar host, SiDBFCz. 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The chemical hardness and the charge transport characteristics are comprehensively investigated to realize a bipolar host with high triplet energy over 2.9 eV for deep blue phosphorescent organic light‐emitting diodes (PHOLEDs). The synthesized SiDBFCz clearly exhibits the bipolar characteristics especially with emitter molecules doped. An external quantum efficiency over 19 % without any microcavity optimization is achieved thanks to the good charge balance in the SiDBFCz PHOLED. The device lifetime of the SiDBFCz PHOLED is improved more than 1000 %, compared to the unipolar control devices at an initial luminance of 500 cd m−2. The dramatic enhancement of the operational stability of the deep blue PHOLED is also thoroughly investigated in terms of electrochemical stability of host molecules in charged or excited states. The results clearly indicate that the device lifetime is strongly correlated with the bond dissociation energy and the activation energy for the bond dissociation reaction in triplet excited state. High efficiency and dramatic improvement of device lifetime were simultaneously and successfully realized with a silane‐based bipolar host, SiDBFCz. The dramatic enhancement of the operational stability was attributed to the bond dissociation energy and the activation energy for the bond dissociation reaction in the triplet excited state.</description><subject>bond dissociation energies</subject><subject>Carbazole</subject><subject>Carbazoles</subject><subject>Charge transport</subject><subject>Chemistry</subject><subject>Density functional theory</subject><subject>Electrochemistry</subject><subject>Emitters</subject><subject>Emitters (electron)</subject><subject>Energy of dissociation</subject><subject>Excitation</subject><subject>Free energy</subject><subject>Heat of formation</subject><subject>high triplet bipolar host</subject><subject>OLEDs</subject><subject>Optimization</subject><subject>Organic light emitting diodes</subject><subject>Phosphorescence</subject><subject>Quantum efficiency</subject><subject>Service life assessment</subject><subject>Stability</subject><subject>Transport properties</subject><subject>triplet excited states</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkT9v1DAYhy1ERa-FlRFZYmHJ1X_iczK2d4GrdKhIlNlKnNeNqyQOdtLqNla2fkY-SX1KWyQW7MGS9fh5f_IPofeULCkh7Ew30C0ZYSQumr1CCyoYTbhciddoQfJUJivB82N0EsJtRPIV52_QMWeU5YKlC_T7HH-3bdnDn18PF2WAGl_YwbWlx1sXRnxvxwZv7U2Dr70dWhhx0YO_2WPj_HxfGGO1hV7v8QZgOGjaCfC3xoWhcR6Chn7EV7tiE2bbZTd4dxcHbeDOasA7a2C0HbxFR6ZsA7x7Ok_Rj8_F9Xqb7K6-XK7Pd4nmkmcJ1PWKMpHqVEJOZE5LnRFjhIaKG0k1KTMuKiEqSDNeGi5SMFWm67il0ILwU_Rp9sYYPycIo-psDNkePsFNQTEuKU1TwrKIfvwHvXWT72M6xVIqJGMyk5FazpT2LgQPRg3edqXfK0rUoSR1KEm9lBQffHjSTlUH9Qv-3EoE8hm4ty3s_6NT623x9a_8EdztoC8</recordid><startdate>20200623</startdate><enddate>20200623</enddate><creator>Ko, Soo‐Byung</creator><creator>Kang, Sunwoo</creator><creator>Kim, Taekyung</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7632-8756</orcidid></search><sort><creationdate>20200623</creationdate><title>A Silane‐Based Bipolar Host with High Triplet Energy for High Efficiency Deep‐Blue Phosphorescent OLEDs with Improved Device Lifetime</title><author>Ko, Soo‐Byung ; Kang, Sunwoo ; Kim, Taekyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3738-edd61254c47e90791ac80ff5ceb3f71c0a835b55be483af354efb8cdcdc75c503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>bond dissociation energies</topic><topic>Carbazole</topic><topic>Carbazoles</topic><topic>Charge transport</topic><topic>Chemistry</topic><topic>Density functional theory</topic><topic>Electrochemistry</topic><topic>Emitters</topic><topic>Emitters (electron)</topic><topic>Energy of dissociation</topic><topic>Excitation</topic><topic>Free energy</topic><topic>Heat of formation</topic><topic>high triplet bipolar host</topic><topic>OLEDs</topic><topic>Optimization</topic><topic>Organic light emitting diodes</topic><topic>Phosphorescence</topic><topic>Quantum efficiency</topic><topic>Service life assessment</topic><topic>Stability</topic><topic>Transport properties</topic><topic>triplet excited states</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ko, Soo‐Byung</creatorcontrib><creatorcontrib>Kang, Sunwoo</creatorcontrib><creatorcontrib>Kim, Taekyung</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ko, Soo‐Byung</au><au>Kang, Sunwoo</au><au>Kim, Taekyung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Silane‐Based Bipolar Host with High Triplet Energy for High Efficiency Deep‐Blue Phosphorescent OLEDs with Improved Device Lifetime</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2020-06-23</date><risdate>2020</risdate><volume>26</volume><issue>35</issue><spage>7767</spage><epage>7773</epage><pages>7767-7773</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>A high triplet energy host is developed using a silane moiety, 9‐(4‐(triphenylsilyl)dibenzo[b,d]furan‐2‐yl)‐9H‐carbazole (SiDBFCz), is designed through extensive density functional theory (DFT) calculations to obtain appropriate hole and electron injection barriers. The chemical hardness and the charge transport characteristics are comprehensively investigated to realize a bipolar host with high triplet energy over 2.9 eV for deep blue phosphorescent organic light‐emitting diodes (PHOLEDs). The synthesized SiDBFCz clearly exhibits the bipolar characteristics especially with emitter molecules doped. An external quantum efficiency over 19 % without any microcavity optimization is achieved thanks to the good charge balance in the SiDBFCz PHOLED. The device lifetime of the SiDBFCz PHOLED is improved more than 1000 %, compared to the unipolar control devices at an initial luminance of 500 cd m−2. The dramatic enhancement of the operational stability of the deep blue PHOLED is also thoroughly investigated in terms of electrochemical stability of host molecules in charged or excited states. The results clearly indicate that the device lifetime is strongly correlated with the bond dissociation energy and the activation energy for the bond dissociation reaction in triplet excited state. High efficiency and dramatic improvement of device lifetime were simultaneously and successfully realized with a silane‐based bipolar host, SiDBFCz. The dramatic enhancement of the operational stability was attributed to the bond dissociation energy and the activation energy for the bond dissociation reaction in the triplet excited state.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32129524</pmid><doi>10.1002/chem.202000018</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7632-8756</orcidid></addata></record>
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subjects bond dissociation energies
Carbazole
Carbazoles
Charge transport
Chemistry
Density functional theory
Electrochemistry
Emitters
Emitters (electron)
Energy of dissociation
Excitation
Free energy
Heat of formation
high triplet bipolar host
OLEDs
Optimization
Organic light emitting diodes
Phosphorescence
Quantum efficiency
Service life assessment
Stability
Transport properties
triplet excited states
title A Silane‐Based Bipolar Host with High Triplet Energy for High Efficiency Deep‐Blue Phosphorescent OLEDs with Improved Device Lifetime
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