Intrinsic Ion Migration Dynamics in a One- Dimensional Organic Metal Halide Hybrid

被引:6
|
作者
Hua, Zhenqi [1 ]
Ben-Akacha, Azza [2 ]
He, Qingquan [2 ]
Liu, Tianhan [1 ]
Boyce, Gillian [1 ]
van Deventer, Margaret [1 ]
Lin, Xinsong [2 ]
Gao, Hanwei [1 ]
Ma, Biwu [2 ]
Xiong, Peng [1 ]
机构
[1] Florida State Univ, Dept Phys, Tallahassee, FL 32306 USA
[2] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
基金
美国国家科学基金会;
关键词
V HYSTERESIS; SOLAR-CELL; PEROVSKITE; NANOWIRES; EFFICIENCY; ABSORBER; CRYSTALS; BEHAVIOR; IMPACT;
D O I
10.1021/acsenergylett.2c01710
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metal halide perovskites possess many physical properties amenable to optoelectronic applications, but the realization of these potentials has been hampered by their environmental and electronic instabilities. The morphological and molecular low-dimensional perovskites and perovskite-related materials have shown much promise in enhancing the chemical stability due to their unique molecular structures. Here we report on robust and reproducible four-terminal (4T) electrical measurements in a one-dimensional (1D) organic metal halide hybrid, (R)-alpha-methylbenzylammonium lead triiodide ((R-alpha-MBA)PbI3), made possible by its chemical stability. The results reveal a distinct single exponential intrinsic ion migration dynamic, which underlies the unique 4T I-V characteristics. The dynamic is directly verified by real-time measurements of the transient ionic current. Our observations are consistent with photoactivation and field-assisted ion migration. The elucidated intrinsic ion dynamics may provide the physical basis for understanding and modeling the ubiquitous hysteresis in metal halidesbased electronic devices and new insights into the dynamics of ion migration in metal halide perovskites and hybrids in general.
引用
收藏
页码:3753 / 3760
页数:8
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