White-light electroluminescence from a layer incorporating a single fully-organic spiro compound with phosphine oxide substituents

被引:19
作者
Tourneur, P. [1 ]
Lucas, F. [2 ]
Quinton, C. [2 ]
Olivier, Y. [3 ,4 ]
Lazzaroni, R. [1 ,5 ]
Viville, P. [5 ]
Cornil, J. [1 ]
Poriel, C. [2 ]
机构
[1] Univ Mons, Mat Res Inst, Lab Chem Novel Mat, Mons, Belgium
[2] Univ Rennes, CNRS, ISCR UMR 6226, F-35000 Rennes, France
[3] Univ Namur, Namur Inst Struct Matter NISM, Unite Chim Phys Theor & Struct UCPTS, Namur, Belgium
[4] Univ Namur, Namur Inst Struct Matter NISM, Lab Phys Solide LPS, Namur, Belgium
[5] Mat Nova, Mat R&D Ctr, Mons, Belgium
关键词
ACTIVATED DELAYED FLUORESCENCE; EMITTING-DIODES; EXCITED-STATES; TRIPLET GAP; EFFICIENCY; EMISSION; HOSTS;
D O I
10.1039/d0tc03285a
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We have investigated the potential as an OLED emitter of a spiro compound with phosphine substituents initially designed as a host layer for triplet emitters. This is motivated by the fact that the spiro architecture is expected to reduce the detrimental impact of intermolecular interactions, thus allowing for the use of a single-component layer. Moreover, theoretical calculations suggest that this compound displays all features required for a thermally-assisted delayed fluorescence (TADF) behavior. The photophysical properties of the compound in solution are extremely unusual, as illustrated in particular by a dual emission band with relative intensities strongly depending on the experimental conditions. Although no TADF behavior is evidenced in OLED devices, the compound unexpectedly generates a white light signal, which is interpreted as the result of the formation of both intramolecular and intermolecular (exciplex) charge-transfer states.
引用
收藏
页码:14462 / 14468
页数:7
相关论文
共 39 条
[1]   Third-generation organic electroluminescence materials [J].
Adachi, Chihaya .
JAPANESE JOURNAL OF APPLIED PHYSICS, 2014, 53 (06)
[2]   Highly efficient phosphorescent emission from organic electroluminescent devices [J].
Baldo, MA ;
O'Brien, DF ;
You, Y ;
Shoustikov, A ;
Sibley, S ;
Thompson, ME ;
Forrest, SR .
NATURE, 1998, 395 (6698) :151-154
[3]   Perspective on Host Materials for Thermally Activated Delayed Fluorescence Organic Light Emitting Diodes [J].
Chatterjee, Tanmay ;
Wong, Ken-Tsung .
ADVANCED OPTICAL MATERIALS, 2019, 7 (01)
[4]   Thermally Activated Delayed Fluorescence (TADF) Path toward Efficient Electroluminescence in Purely Organic Materials: Molecular Level Insight [J].
Chen, Xian-Kai ;
Kim, Dongwook ;
Bredas, Jean-Luc .
ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (09) :2215-2224
[5]   Influence of interchain interactions on the absorption and luminescence of conjugated oligomers and polymers:: A quantum-chemical characterization [J].
Cornil, J ;
dos Santos, DA ;
Crispin, X ;
Silbey, R ;
Brédas, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (06) :1289-1299
[6]   Orthogonal Molecular Structure for Better Host Material in Blue Phosphorescence and Larger OLED White Lighting Panel [J].
Ding, Lei ;
Dong, Shou-Cheng ;
Jiang, Zuo-Quan ;
Chen, Hua ;
Liao, Liang-Sheng .
ADVANCED FUNCTIONAL MATERIALS, 2015, 25 (04) :645-650
[7]   Chemical and conformational control of the energy gaps involved in the thermally activated delayed fluorescence mechanism [J].
dos Santos, Paloma L. ;
Etherington, Marc K. ;
Monkman, Andrew P. .
JOURNAL OF MATERIALS CHEMISTRY C, 2018, 6 (18) :4842-4853
[8]   Single-reference ab initio methods for the calculation of excited states of large molecules [J].
Dreuw, A ;
Head-Gordon, M .
CHEMICAL REVIEWS, 2005, 105 (11) :4009-4037
[9]   SPIN-ORBIT COUPLING AND RADIATIONLESS PROCESSES IN NITROGEN HETEROCYCLICS [J].
ELSAYED, MA .
JOURNAL OF CHEMICAL PHYSICS, 1963, 38 (12) :2834-&
[10]   Revealing the spin-vibronic coupling mechanism of thermally activated delayed fluorescence [J].
Etherington, Marc K. ;
Gibson, Jamie ;
Higginbotham, Heather F. ;
Penfold, Thomas J. ;
Monkman, Andrew P. .
NATURE COMMUNICATIONS, 2016, 7