Near Infrared to Visible Upconversion Polarization Imaging Enabled by Cs 2 NaScCl 6 :Er 3+ Composite Film
Résumé fourni par la source
ABSTRACT Current near‐infrared (NIR) polarization imaging relys on expensive, cryogenically cooled infrared detectors with resolution, toxicity, and system complexity limitations. Herein, we propose a NIR polarization imaging system based on Cs 2 NaScCl 6 :Er 3+ upconversion emissive film and a commercial visible camera. Cs 2 NaScCl 6 , a lead‐free double perovskite, was selected as the host matrix for its non‐toxicity, wide bandgap, and ability to accommodate high‐concentration Er 3+ doping. We optimized the Er 3+ doping concentration to 12%, achieving a high photoluminescence quantum yield (PLQY) of 5.98% under 980 nm excitation, with emission peaks located at 551 nm. The as‐fabricated powder was 600‐mesh sieved for refinement. Subsequently, the post‐processing Cs 2 NaScCl 6 :Er 3+ powders were dissolved in polydimethylsiloxane (PDMS) to fabricate uniform, flexible, and environmentally stable composite films, which maintain retained excellent upconversion emission even after 30‐day storage. The NIR polarization imaging system combines the upconversion film with the dual‐orthogonal linear polarization detection scheme, enabling the extraction of the full Stokes vector, degree of linear polarization (DOLP), and angle of polarization (AOP). This system outperforms traditional NIR cameras in background suppression and material distinction, and operates without cryogenic cooling. This modular, low‐cost approach expands the application of perovskite optoelectronics and provides a practical path for high‐resolution NIR polarization imaging across multiple fields.
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Contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé, mais le titre doit être comparé manuellement.
- Titre Crossref
- Near Infrared to Visible Upconversion Polarization Imaging Enabled by Cs <sub>2</sub> NaScCl <sub>6</sub> :Er <sup>3+</sup> Composite Film
- Date Crossref
- 25/06/2026
- Éditeur
- Wiley
- Type
- journal-article
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