TY - JOUR
T1 - Zero-Dimensional Cs4PbBr6 Perovskite Nanocrystals
AU - Zhang, Yuhai
AU - Saidaminov, Makhsud I.
AU - Dursun, Ibrahim
AU - Yang, Haoze
AU - Banavoth, Murali
AU - Alarousu, Erkki
AU - Yengel, Emre
AU - Alshankiti, Buthainah
AU - Bakr, Osman
AU - Mohammed, Omar F.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We gratefully acknowledge funding support from KAUST, Technology Innovation Center for Solid-State Lighting at KAUST.
PY - 2017/2/14
Y1 - 2017/2/14
N2 - Perovskite nanocrystals (NCs) have become leading candidates for solution-processed optoelectronics applications. While substantial work has been published on 3-D perovskite phases, the NC form of the zero-dimensional (0-D) phase of this promising class of materials remains elusive. Here we report the synthesis of a new class of colloidal semiconductor NCs based on Cs4PbBr6, the 0-D perovskite, enabled through the design of a novel low-temperature reverse microemulsion method with 85% reaction yield. These 0-D perovskite NCs exhibit high photoluminescence quantum yield (PLQY) in the colloidal form (PLQY: 65%), and, more importantly, in the form of thin film (PLQY: 54%). Notably, the latter is among the highest values reported so far for perovskite NCs in the solid form. Our work brings the 0-D phase of perovskite into the realm of colloidal NCs with appealingly high PLQY in the film form, which paves the way for their practical application in real devices.
AB - Perovskite nanocrystals (NCs) have become leading candidates for solution-processed optoelectronics applications. While substantial work has been published on 3-D perovskite phases, the NC form of the zero-dimensional (0-D) phase of this promising class of materials remains elusive. Here we report the synthesis of a new class of colloidal semiconductor NCs based on Cs4PbBr6, the 0-D perovskite, enabled through the design of a novel low-temperature reverse microemulsion method with 85% reaction yield. These 0-D perovskite NCs exhibit high photoluminescence quantum yield (PLQY) in the colloidal form (PLQY: 65%), and, more importantly, in the form of thin film (PLQY: 54%). Notably, the latter is among the highest values reported so far for perovskite NCs in the solid form. Our work brings the 0-D phase of perovskite into the realm of colloidal NCs with appealingly high PLQY in the film form, which paves the way for their practical application in real devices.
UR - http://hdl.handle.net/10754/623936
UR - http://pubs.acs.org/doi/abs/10.1021/acs.jpclett.7b00105
UR - http://www.scopus.com/inward/record.url?scp=85014333876&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.7b00105
DO - 10.1021/acs.jpclett.7b00105
M3 - Article
C2 - 28181438
SN - 1948-7185
VL - 8
SP - 961
EP - 965
JO - The Journal of Physical Chemistry Letters
JF - The Journal of Physical Chemistry Letters
IS - 5
ER -