Uncovering Self-recoverable NIR Mechanoluminescence from Cr3+ Doped Perovskite Type Aluminate

Mechanoluminescence (ML) located within the near-infrared (NIR) spectral range may hold promising applications in in-situ and real-time biomechanical imaging. This is due to the better spatial resolution and penetration depth of the biological tissues, lower optical loss, and the avoidance of autofluorescence. Historically, rare earth ions have been predominantly employed as activators in ML materials. However, adjusting the emissions of rare earth ions, especially RE3+, poses challenges, thereby limiting the practical application of NIR MLs. Therefore, the transition metal ions activated systems have been favored by more and more researchers.

Previously, Puxian Xiong and colleagues have reported a self-recoverable NIR ML material in gallate by using Cr³⁺ ions as the emission center for the first time. “Indeed, LiGa₅O₈:Cr³⁺ presents good ML repeatability and does not require a pre-irradiation process, but the intrinsic ML mechanisms are still not entirely clear,” says Xiong. “In particular, whether the remanent carriers occupied lattice traps can affect the ML repeatability is unclear.”

As is generally known, the preheating method is one of the most effective ways to remove the remanent carriers. In a new study published in Advanced Powder Materials, the team integrated the preheating method with corresponding ML results. “This work intends to actualize the analysis of the ML mechanism through eliminating the influences of stored carriers,” shares Xiong, who serves as co-corresponding author of the study.

In all, Cr³⁺ ions doped perovskite-type LaAlO₃ ML phosphor is successfully synthesized by a traditional high-temperature solid-state reaction method in air. Combined with photoluminescence, persistent luminescence, diffuse reflectance, and thermoluminescence characterizations, the inherent ML mechanism was discussed in detail by the authors.

“We observed that ML in LaAlO₃: Cr³⁺ is self-recoverable, which is different from the trap-controlled ML compounds (requiring UV light for pre-irradiation). Based on the preheating method and corresponding ML analysis, such self-recoverable ML depends more on the piezoelectricity of the non-centrosymmetric LaAlO₃: Cr³⁺,” shares Xiong.

Under mechanical stimuli, a strong piezoelectric field is built within the compound, which is large enough to generate electronically excited states of the Cr³⁺ ions, subsequently resulting in ML. This luminescence is featured with self-recoverability, implying that the compound can be applied to different applications.

“We further demonstrated great potential application prospects for the ML Bioimaging, anti-counterfeiting, and information encryption field with the encoding and decoding of ASCII code,” adds Xiong.

Contact author name, affiliation, email address: Puxian Xiong; State Key Laboratory of Luminescent Materials and Devices, School of Materials Science and Engineering, School of Physics and Optoelectronics, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices, South China University of Technology, Guangzhou 510641, China; xiongpuxian@scut.edu.cn.

Funder: We gratefully acknowledge the financial support from the National Natural Science Foundation of China (No. 52202003), Guangdong Basic and Applied Basic Research Foundation (No. 2023A1515011893), State Key Laboratory of Powder Metallurgy, Central South University, Changsha, China (No. Sklpm-KF-27) and Guangzhou Basic and Applied Basic Research Foundation (No. SL2022A04J00746).

Conflict of interest: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence them.

See the article: Peishan Shao, et al., Self-recoverable NIR mechanoluminescence from Cr³⁺ doped perovskite type aluminate, Advanced Powder Materials, 3 (2024), Page 100165. https://doi.org/10.1016/j.apmate.2023.100165.