Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 124, Issue 8, Pages 4414-4420Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.9b11172
Keywords
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Funding
- Global Frontier R&D Program of the Center for Multiscale Energy System - National Research Foundation under the Ministry of Science, ICT Future, Korea [NRF-2012M3A6A7054861]
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Lead halide perovskites have received much attention as light emitting materials owing to their excellent photoelectronic properties. Despite their high efficiency as light-emitting diodes (LEDs), only a few lead bromide perovskite (APbBr(3))-based devices have been developed due to their low stabilities and/or the formation of undesirable phases under ambient condition. This work demonstrates that the addition of a small quantity of guanidinium (GUA) A-site cations into an all inorganic CsPbBr3 perovskite framework leads to the formation of multidimensional perovskites, with enhanced photoluminescence efficiency due to charge carrier funneling and a pinhole-free surface morphology. All-inorganic 3D CsPbBr3 perovskite films and GUA-incorporated multidimensional quasi-2D films are employed in the fabrication of green LED devices with an inverted structure of glass substrate/indium tin oxide (ITO)/zinc oxide (ZnO)/poly(ethylenimine) (PEI)/perovskite/poly(9-vinylcarbazole) (PVK)/WO3/Al. With the addition of GUA A-site cations, the LEDs based on GUA-incorporated perovskite thin films exhibited much higher brightness of similar to 10000 cd m(-2) and current efficiency of 9.4 cd A(-1) compared to those of Cs-only perovskite thin film LEDs (similar to 400 cd m(-2) and 0.2 Cd A(-1), respectively).
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