SrTiO3 中二氧化碳压力诱导的自俘获激子

IF 3.7 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Lianyu Li, Zongwei Chen, Bo Gao, Qun Xu
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引用次数: 0

摘要

在强电子-声子耦合作用下,包晶材料中通常会形成自俘获激子(STE),STE 的辐射重组可产生具有较大斯托克斯偏移的宽带发射。要进一步提高材料的光电特性,STEs 至关重要。令人惊讶的是,二维体系是一种边缘情况,其自阱壁垒很低,甚至没有自阱壁垒,因此可以毫不费力地形成 STE。本研究利用超临界二氧化碳(SC CO2)制备了具有缺陷的二维钛酸锶(SrTiO3),并对其载流子输运和转变进行了研究。飞秒瞬态吸收光谱中出现的宽光诱导正吸收信号是 STE 形成的直接证据。稳态光致发光光谱中增加的斯托克斯偏移和半最大全宽进一步证明了 STE 的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CO2 Pressure-Induced Self-Trapped Excitons in SrTiO3

CO2 Pressure-Induced Self-Trapped Excitons in SrTiO3

With strong electron–phonon coupling, self-trapped excitons (STEs) are typically formed in perovskite materials, and radiative recombination of STEs can produce broadband emission with large Stokes shifts. STEs are essential to further improve the optoelectronic properties of materials. Surprisingly, 2D system is the edge case, with low even no self-trapping barriers, leading to effortless formation of STEs. In this work, 2D strontium titanate (SrTiO3) with defects is prepared using supercritical carbon dioxide (SC CO2) and its carrier transport and transition are studied. The appearance of wide photoinduced positive absorption signals in the femtosecond transient absorption spectra is direct evidence for the formation of STEs. The presence of STEs is further supported by the increased Stokes shift and full width at half maximum in the steady-state photoluminescence spectra.

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