Dec 4, 2024
4:00pm - 4:15pm
Sheraton, Fifth Floor, Jamaica Pond
Zhenqi Hua1,Azza Ben-Akacha1,Qingquan He1,2,Tianhan Liu1,3,Gillian Boyce1,Margaret Deventor1,Xinsong Lin1,Hanwei Gao1,Biwu Ma1,Peng Xiong1
Florida State University1,Zhejiang University of Technology2,University of California, Los Angeles3
Zhenqi Hua1,Azza Ben-Akacha1,Qingquan He1,2,Tianhan Liu1,3,Gillian Boyce1,Margaret Deventor1,Xinsong Lin1,Hanwei Gao1,Biwu Ma1,Peng Xiong1
Florida State University1,Zhejiang University of Technology2,University of California, Los Angeles3
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)-α-methylbenzylammonium lead triiodide ((R-α-MBA)PbI<sub>3</sub>), made possible by its chemical stability. The results reveal a distinct single exponential intrinsic ion migration dynamic, which underlies the unique 4T <i>I–V</i> 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 halides-based electronic devices and new insights into the dynamics of ion migration in metal halide perovskites and hybrids in general.