锰
钙钛矿(结构)
兴奋剂
激光阈值
材料科学
自旋(空气动力学)
凝聚态物理
光电子学
化学
物理
结晶学
波长
冶金
热力学
作者
Penghao Li,Zhonghao Zhou,Guangliu Ran,Tongjin Zhang,Zhengjun Jiang,Haidi Liu,Wenkai Zhang,Yongli Yan,Jiannian Yao,Haiyun Dong,Yong Sheng Zhao
标识
DOI:10.1038/s41467-024-55234-6
摘要
Spin-polarized lasers have demonstrated many superiorities over conventional lasers in both performance and functionalities. Hybrid organic-inorganic perovskites are emerging spintronic materials with great potential for advancing spin-polarized laser technology. However, the rapid carrier spin relaxation process in hybrid perovskites presents a major bottleneck for spin-polarized lasing. Here we report the identification and successful suppression of the spin relaxation mechanism in perovskites for the experimental realization of spin-polarized perovskite lasers. The electron-hole exchange interaction is identified as the decisive spin relaxation mechanism hindering the realization of spin-polarized lasing in perovskite microcrystals. An ion doping strategy is employed accordingly to introduce a new energy level in perovskites, which enables a long carrier spin lifetime by suppressing the electron-hole exchange interaction. As a result, spin-polarized lasing is achieved in the doped perovskite microcrystals. Moreover, the doped cation is a magnetic species allowing for the magnetic field control of the spin-polarized perovskite lasing. This work unlocks the potential of perovskites for spin-polarized lasers, providing guidance for the design of perovskites towards spintronic devices.
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