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Open AccessDOI: 10.1007/s40843-025-3373-5Original Research

Glass Network Structure Adjustment and Particle Size Screening to Obtain Ultra-Stable Luminescent Perovskite Glass and Its Application

College of Chemistry and Materials Engineering, Wenzhou University

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Glass Network Structure Adjustment and Particle Size Screening to Obtain Ultra-Stable Luminescent Perovskite Glass and Its Application
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SCIENCE CHINA Materials
Published:January 15, 2025Edition:Vol. 68, Issue 7 • pp. 100-112Citation:Enrou Mei et al. (2025), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料
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Perovskite Solar Cells: Silicon/Perovskite Tandem Cells, 2D/3D Passivation & Module Stability
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Key Takeaways & Executive Findings

  • • • B2O3 addition to GeO2-SiO2 glass network yields CsPbBr3@Glass with 85% PLQY, enabling high-efficiency downconverters for LCD backlights; industrial impact: reduces energy consumption and extends display lifetime. • • Glass powder content of 4% in AB glue maximizes fluorescence intensity; higher content improves blue light stability, with green samples retaining superior stability after 120 h irradiation (red samples degrade faster), critical for long-term color fidelity in displays. • • In situ heating-cooling cycles show thermal recovery >90% for green and >86% for red CsPbX3@Glass, indicating robust reversible thermal stability essential for high-power LED applications. • • CsPbX3@Glass@PS films maintain >90% initial PL intensity after 15 days in 95% ethanol, demonstrating dual glass-polymer protection that enables polar solvent resistance, a key requirement for solution-processed display manufacturing.
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Abstract

Halide perovskite nanocrystals (PNCs) exhibit high photoluminescence quantum yield (PLQY), narrow full width at half maximum (FWHM), and high color purity, yet their intrinsic instability under ambient, thermal, and photonic stress restricts deployment in optoelectronic devices. Embedding CsPbX3 (X = Br, I) PNCs within inorganic glass matrices mitigates degradation, but dense glass networks impede nucleation and growth. This work adjusts the GeO2-SiO2-B2O3 glass network via B2O3 addition to create loose, compact structures that facilitate PNC precipitation. Optimized CsPbBr3@Glass achieves a PLQY of 85%. Glass powders with varying particle sizes are screened for stability, identifying an optimal size range. Composite films of CsPbX3@Glass@PS (X = Br, I) with polymer materials yield light conversion films. Under 120 h blue light irradiation, green-light samples outperform red-light samples in stability. In situ heating-cooling cycles show thermal recovery exceeding 90% for green and 86% for red samples. A white light-emitting diode (WLED) constructed with CsPbBr3@Glass, CsPbBrI2@Glass, and a 460 nm InGaN chip achieves a color gamut covering 123% of NTSC 1953 and 91.8% of Rec 2020. An LCD incorporating green CsPbBr3@Glass@PS and red CsPbBrI2@Glass@PS films with a 450 nm mini-blue chip retains >90% of initial PL intensity after 15 days in 95% ethanol, demonstrating dual protection from glass and polymer. These results establish a pathway for stable, wide-gamut display backlights.

1. Introduction

Halide perovskite nanocrystals (PNCs) offer high photoluminescence quantum yield (PLQY), narrow full width at half maximum (FWHM), and high color purity, making them ideal for wide-gamut liquid crystal displays (LCDs). However, their intrinsic instability under moisture, heat, air, and blue light irradiation has stalled commercialization. Coating PNCs with inorganic glass matrices effectively improves stability, but dense glass networks often prevent sufficient nucleation and growth of PNCs during heat treatment. Existing glass systems require precise compositional tuning to balance network connectivity and ion migration.

This study optimizes a GeO2-SiO2-B2O3 glass network by introducing B2O3 as a network intermediate, which loosens the glass structure and promotes in situ crystallization of CsPbX3 (X = Br, I) PNCs. The adjusted network enables a high PLQY of 85% for CsPbBr3@Glass. Furthermore, particle size screening identifies the optimal glass powder range for stability, and composite films with polystyrene (PS) provide dual protection. The resulting CsPbX3@Glass@PS films exhibit >90% PL intensity retention after 15 days in 95% ethanol, and a WLED device achieves 123% NTSC 1953 color gamut. These findings address the stability bottleneck and offer a scalable route for stable, wide-color-gamut LCD backlights.

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Cite This Research Paper
Enrou Mei, Han Zhao, Ziyi Jiang, Shuo Wang, Xiaojuan Liang, Weidong Xiang (2025). Glass Network Structure Adjustment and Particle Size Screening to Obtain Ultra-Stable Luminescent Perovskite Glass and Its Application. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-025-3373-5
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Frequently Asked Questions

What is the failure mechanism of CsPbX3@Glass under prolonged blue light irradiation, and how does particle size screening mitigate it?

Under 120 h blue light irradiation, red-light samples degrade faster than green-light samples, likely due to iodide oxidation and phase segregation. Particle size screening identifies a range where glass powders with optimal surface-to-volume ratio reduce defect sites and ion migration, enhancing stability. Higher glass powder content (e.g., 4% in AB glue) improves blue light stability by increasing scattering and reducing local heating.

How does the B2O3 additive concentration affect the glass network structure and PNC nucleation, and what is the optimal range?

B2O3 acts as a network intermediate that loosens the glass structure by reducing network former connectivity. An appropriate amount (not specified in excerpt) promotes PNC nucleation and growth while inhibiting non-radiative recombination, achieving 85% PLQY. Excessive B2O3 may over-loosen the network, leading to PNC aggregation or reduced stability. The optimal range balances sufficient space for nucleation and adequate encapsulation.

What are the thermal recovery rates for green and red CsPbX3@Glass, and what do they imply for device reliability?

In situ heating-cooling cycles show thermal recovery >90% for green samples and >86% for red samples. These values indicate reversible thermal degradation with minimal hysteresis, suggesting that the glass matrix effectively confines PNCs and prevents permanent sintering or ion migration. For device reliability, this translates to stable performance under thermal cycling, essential for high-power LED backlights.

How does the dual protection of glass and PS film enhance stability in polar solvents, and what is the measured retention?

CsPbX3@Glass@PS films retain >90% of initial PL intensity after 15 days in 95% ethanol. The glass matrix provides primary encapsulation against ion and moisture ingress, while the PS film acts as a hydrophobic barrier, preventing polar solvent penetration. This dual mechanism is critical for solution-processed display manufacturing where polar solvents may be used.

What are the color gamut metrics of the WLED device, and how do they compare to industry standards?

The WLED, constructed with CsPbBr3@Glass, CsPbBrI2@Glass, and a 460 nm InGaN chip, achieves 123% of NTSC 1953 and 91.8% of Rec 2020 color gamut. These metrics exceed typical commercial LCD backlights, enabling ultra-wide color reproduction for high-definition displays. The narrow FWHM of PNCs contributes to the wide gamut.

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