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Deuterium Effect of Dinuclear Pt(II) Complex in Prolonging Operational Lifetime of OLEDs

Authors
Lee, Gyeong SeokJeong, YeonjuPark, Jeong YongLee, HakjunKim, SungbumKang, SunwooKo, Soo-ByungKim, TaekyungKim, Yun-Hi
Issue Date
Jan-2026
Publisher
American Chemical Society
Keywords
deuterium; dinuclear Pt(II) complexes; radiativerate; PS TADF OLED; device lifetime
Citation
ACS Applied Materials & Interfaces, v.18, no.1, pp 2315 - 2323
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
ACS Applied Materials & Interfaces
Volume
18
Number
1
Start Page
2315
End Page
2323
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/82051
DOI
10.1021/acsami.5c22470
ISSN
1944-8244
1944-8252
Abstract
The butterfly-shaped dinuclear platinum complex, Pt-dinu-D 20 , is composed of nonfluorinated NHC ligands with N-deuterated methyl groups in the imidazole ring, as well as a deuterated ancillary ligand. Pt-dinu-D20 , with a further deuterated ancillary ligand, can increase the device lifetime by about 2.5 times compared with Pt-dinu-D 6 while maintaining an EQEmax of approximately 20%. DFT calculations demonstrate that a high deuterium ratio may play a beneficial role in effectively suppressing the formation of the 3MC state. To elucidate the crucial role of deuterium in prolonging the operational lifetime of OLEDs using dinuclear Pt(II), the stability is studied from both the device and material perspectives through exciton dynamics and HPLC measurements. An increased number of deuterium atoms suppresses the hole trapping of the dinuclear Pt dopant within the EML, thereby mitigating the hole-induced quenching process. This improvement results from the lowering of the HOMO energy level due to deuterium, which facilitates hole injection and minimizes trapping. Additionally, the increasing presence of C-D bonds improves the intrinsic stability of the material by reducing the hole-induced dissociation.
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