TY - JOUR
T1 - Excited state lifetime modulation by twisted and tilted molecular design in carbene-metal-amide photoemitters
AU - Gu, Qinying
AU - Chotard, Florian
AU - Eng, Julien
AU - Reponen, Antti-Pekka M.
AU - Vitorica-Yrezabal, Inigo J.
AU - Woodward, Adam W.
AU - Penfold, Thomas J.
AU - Credgington, Dan
AU - Bochmann, Manfred
AU - Romanov, Alexander S.
N1 - Funding Information: This work was supported by the Engineering and Physical Sciences Research Council (EPSRC, grant no. EP/M005143/1, EP/R021503/1 and EP/P012388/1), the Royal Society, the European Research Council (ERC) and Samsung Display Corp. (SDC). M.B. is an ERC Advanced Investigator Award holder (grant no. 338944-GOCAT). D.C. acknowledges support from the Royal Society (grant nos. UF130278 and RG140472). A.S.R. acknowledges support from the Royal Society (grant nos. URF\R1\180288 and RGF\EA\181008). The authors thank the National Mass Spectrometry Facility at Swansea University for measurements.
PY - 2022/8/23
Y1 - 2022/8/23
N2 - Carbene-metal-amides (CMAs) are an emerging class of photoemitters based on a linear donor-linker-acceptor arrangement. They exhibit high flexibility about the carbene-metal and metal-amide bonds, leading to a conformational freedom which has a strong influence on their photophysical properties. Herein we report CMA complexes with (1) nearly coplanar, (2) twisted, (3) tilted, and (4) tilt-twisted orientations between donor and acceptor ligands and illustrate the influence of preferred ground-state conformations on both the luminescence quantum yields and excited-state lifetimes. The performance is found to be optimum for structures with partially twisted and/or tilted conformations, resulting in radiative rates exceeding 1 × 10
6s
-1. Although the metal atoms make only small contributions to HOMOs and LUMOs, they provide sufficient spin-orbit coupling between the low-lying excited states to reduce the excited-state lifetimes down to 500 ns. At the same time, high photoluminescence quantum yields are maintained for a strongly tilted emitter in a host matrix. Proof-of-concept organic light-emitting diodes (OLEDs) based on these new emitter designs were fabricated, with a maximum external quantum efficiency (EQE) of 19.1% with low device roll-off efficiency. Transient electroluminescence studies indicate that molecular design concepts for new CMA emitters can be successfully translated into the OLED device.
AB - Carbene-metal-amides (CMAs) are an emerging class of photoemitters based on a linear donor-linker-acceptor arrangement. They exhibit high flexibility about the carbene-metal and metal-amide bonds, leading to a conformational freedom which has a strong influence on their photophysical properties. Herein we report CMA complexes with (1) nearly coplanar, (2) twisted, (3) tilted, and (4) tilt-twisted orientations between donor and acceptor ligands and illustrate the influence of preferred ground-state conformations on both the luminescence quantum yields and excited-state lifetimes. The performance is found to be optimum for structures with partially twisted and/or tilted conformations, resulting in radiative rates exceeding 1 × 10
6s
-1. Although the metal atoms make only small contributions to HOMOs and LUMOs, they provide sufficient spin-orbit coupling between the low-lying excited states to reduce the excited-state lifetimes down to 500 ns. At the same time, high photoluminescence quantum yields are maintained for a strongly tilted emitter in a host matrix. Proof-of-concept organic light-emitting diodes (OLEDs) based on these new emitter designs were fabricated, with a maximum external quantum efficiency (EQE) of 19.1% with low device roll-off efficiency. Transient electroluminescence studies indicate that molecular design concepts for new CMA emitters can be successfully translated into the OLED device.
KW - Gold complexes
KW - photoluminescence
KW - light emitting diodes
KW - organometallics
UR - http://www.scopus.com/inward/record.url?scp=85136195802&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.2c01938
DO - 10.1021/acs.chemmater.2c01938
M3 - Article
VL - 34
SP - 7526
EP - 7542
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
IS - 16
ER -