MXenes have demonstrated potential for various applications owing to their tunable surface chemistry and metallic conductivity. However, high temperatures can accelerate MXene film oxidation in air. Understanding the mechanisms of MXene oxidation at elevated temperatures, which is still limited, is critical in improving their thermal stability for high-temperature applications. Here, we demonstrate that Ti C T MXene monoflakes have exceptional thermal stability at temperatures up to 600 C in air, while multiflakes readily oxidize in air at 300 C. Density functional theory calculations indicate that confined water between Ti C T flakes has higher removal energy than surface water and can thus persist to higher temperatures, leading to oxidation. We demonstrate that the amount of confined water correlates with the degree of oxidation in stacked flakes. Confined water can be fully removed by vacuum annealing Ti C T films at 600 C, resulting in substantial stability improvement in multiflake films (can withstand 600 C in air). These findings provide fundamental insights into the kinetics of confined water and its role in Ti C T oxidation. This work enables the use of stable monoflake MXenes in high-temperature applications and provides guidelines for proper vacuum annealing of multiflake films to enhance their stability. 
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                    This content will become publicly available on March 18, 2026
                            
                            Eco-friendly synthesis and stability analysis of CsPbBr 3 and poly(methyl methacrylate)-CsPbBr 3 films
                        
                    
    
            Abstract This study presents an eco-friendly mechanochemical synthesis of cesium lead bromide (CsPbBr3), eliminating the need of organic solvents and high temperatures. The synthesized CsPbBr3powder is used to fabricate poly(methyl methacrylate) (PMMA)-CsPbBr3films and CsPbBr3nanocrystals (NCs). The photoluminescence (PL) peaks of the emission light are centered at 541 nm, 538 nm, and 514 nm for the CsPbBr3powder, PMMA-CsPbBr3films, and CsPbBr3NCs, respectively, correlating with crystal sizes of 0.96, 0.56, and 0.12μm, respectively. The PL lifetime analysis reveals decay times ( ) of (4.18, 20.08), (5.7, 46.99), and (5.81, 23.14) in the units (ns, ns) for the CsPbBr3powder, PMMA-CsPbBr3films, and CsPbBr3NCs, respectively. The PL quantum yield of the CsPbBr3NCs in toluene is 61.3%. Thermal activation energies for thermal quenching are 217.48 meV (films) and 178.15 meV (powder), indicating improved thermal stability with the PMMA encapsulation. The analysis of the PL intensity decay from water diffusion in the PMMA-CsPbBr3films yields 1.70 × 10−12m2s−1for the diffusion coefficient of water, comparable to that for water diffusion in pure PMMA. This work demonstrates a scalable, sustainable strategy for CsPbBr3synthesis and stability enhancement for optoelectronic applications. 
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                            - Award ID(s):
- 2018411
- PAR ID:
- 10621108
- Publisher / Repository:
- IOP
- Date Published:
- Journal Name:
- Nanotechnology
- Volume:
- 36
- Issue:
- 17
- ISSN:
- 0957-4484
- Page Range / eLocation ID:
- 175601
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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