Rapid Spin Depolarization in the Layered 2D Ruddlesden-Popper Perovskite (BA)(MA)PbI

被引:1
|
作者
Kempf, Michael Andreas [1 ]
Moser, Philipp [2 ]
Tomoscheit, Maximilian [1 ]
Schroer, Julian [1 ]
Blancon, Jean-Christophe [3 ]
Schwartz, Rico [1 ]
Deb, Swarup [1 ]
Mohite, Aditya [3 ]
Stier, Andreas V. [2 ]
Finley, Jonathan J. [2 ]
Korn, Tobias [1 ]
机构
[1] Rostock Univ, Inst Phys, D-18059 Rostock, Germany
[2] Tech Univ Munich, Walter Schottky Inst, TUM Sch Nat Sci, D-85748 Garching, Germany
[3] Rice Univ, Dept Chem & Biomol Engn, 6100 Main St, Houston, TX 77005 USA
关键词
layered perovskites; (BA)(MA)PbI; spin dynamics; photocarrier dynamics; time-resolved spectroscopy; HIGH-EFFICIENCY; LIGHT; DYNAMICS; CARRIER; SUPERCONDUCTIVITY; PHYSICS;
D O I
10.1021/acsnano.3c09001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report temperature-dependent spectroscopy on the layered (n = 4) two-dimensional (2D) Ruddlesden-Popper perovskite (BA)-(MA)-PbI. Helicity-resolved steady-state photoluminescence (PL) reveals no optical degree of polarization. Time-resolved PL shows a photocarrier lifetime on the order of nanoseconds. From simultaneously recorded time-resolved differential reflectivity (TR Delta R) and time-resolved Kerr ellipticity (TRKE), a photocarrier lifetime of a few nanoseconds and a spin relaxation time on the order of picoseconds was found. This stark contrast in lifetimes clearly explains the lack of spin polarization in steady-state PL. While we observe clear temperature-dependent effects on the PL dynamics that can be related to structural dynamics, spin relaxation is nearly T-independent. Our results highlight that spin relaxation in 2D (BA)-(MA)-PbI occurs at time scales faster than the exciton recombination time, which poses a bottleneck for applications aiming to utilize this degree of freedom.
引用
收藏
页码:25459 / 25467
页数:9
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