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Correlation of ETL in perovskite light-emitting diodes and the ultra-long rise time in time-resolved electroluminescence


Indexed by:Journal Papers

First Author:Wang, Minhuan

Correspondence Author:Bian, JM (reprint author), Dalian Univ Technol, Sch Phys, Key Lab Mat Modificat Laser Ion & Electron Beams, Minist Educ, Dalian 116024, Peoples R China.; Shi, YT (reprint author), Dalian Univ Technol, Sch Chem, State Key Lab Fine Chem, Dalian 116024, Peoples R China.

Co-authors:Bian, Jiming,Feng, Yulin,Zhang, Yadong,Liu, Hongzhu,Shi, Yantao

Date of Publication:2018-06-15


Included Journals:SCIE、EI


Page Number:131-136

ISSN No.:1369-8001

Key Words:Perovskite; Light-emitting diodes; Delayed electroluminescence; Electron transport layers

Abstract:Here, two series CH3NH3PbI3 based perovskite light-emitting diodes (Pe-LEDs) were synthesized with TiO2 and SnO2 as electron transport layer (ETL), respectively. An exceptional ultra-long rise time (T-r) persisting to tens of seconds was observed in time-resolved electroluminescence (EL) characteristics from the Pe-LEDs as driven with constant voltage, which might be intrinsic to the MAPbI(3) perovskite layer regardless of the ETL materials. Qualitatively, SnO2 based ETL was preferred than the TiO2 ETL counterpart for faster response Pe-LED devices with lower T-r. Moreover, the T-r of Pe-LED can be adjusted in the range of 10-28 s by precisely controlling the thickness of SnO2 ETL. In addition, the similar trend was also confirmed in the SnO2 ETL thickness dependent hysteresis index deduced from current-voltage (J-V) characteristics. The mechanism was interpreted by means of dynamics of carrier injection and transport at the perovskite/ETL interface. These achievement may contribute to better understanding of the origin and mechanism of the slow process in EL characteristics, and hence favorable for minimizing this detrimental effects.

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