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. Spin-polarized lasers have demonstrated many superiorities over conventional lasers. Here the authors report the identification and successful suppression of the spin relaxation mechanism in perovskites for the experimental realization of spin-polarized perovskite lasers.
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