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Updated: Jan 12, 2026

Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
Published on: May 29, 2018
Exciton relaxation modulation and lattice distortion in Rb4CdCl6:Sn2+/Bi3+ toward tunable white-light and optical
Xiangyan Yun1, Zexiang Liu2, Jingheng Nie3
1Research Center of Applied Physics and Photoelectric Information, College of Mechanical and Electrical Engineering, Chizhou University, Chizhou 247000, PR China.
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Metal halides with tunable local electronic states and excellent optical properties are indispensable for achieving single-component multi-color luminescence and solid-state healthy lighting. However, the precise regulation of dark self-trapped excitons (STEs) remains a critical challenge in achieving high-performance luminescence. This work employed zero-dimensional (0D) Rb4CdCl6 as the host to systematically investigate the spectral characteristics and underlying mechanisms of Sn2+ single-doped, Bi3+ single-doped, and Sn2+/Bi3+ co-doped samples. The results indicate that Sn2+ ions lead to the emission of blue bright STEs, while the introduction of Bi3+ effectively activates low-energy (LE) dark STEs through local lattice distortion and energy level regulation, thereby achieving the transition from single-band blue light to dual-band spectra. Sn2+ ions are the main luminescent centers, while Bi3+ ions stabilize dark-state emission by regulating exciton relaxation pathways and forming SnBi pairs. The synergistic effect of bright/dark STEs enables controllable cold-to-warm white emission and information anti-counterfeiting applications, providing new strategies for designing high-performance single-component luminescent halides via lattice strain engineering.

