材料科学
钙钛矿(结构)
光电子学
光致发光
放射发光
闪烁体
纳米晶
纳米颗粒
量子点
纳米技术
纳米复合材料
氧化物
纳米材料
钝化
发光
闪烁
光子学
量子效率
超短脉冲
纳米尺度
纳米结构
悬空债券
作者
Francesco Bruni,Saptarshi Chakraborty,Andrea Fratelli,Abdessamad El Adel,Jordi Llusar,Francesco Carulli,Matteo L. Zaffalon,Chenger Wang,Vojtěch Zabloudil,Etiennette Auffray,Francesco Meinardi,Leonardo Poletti,Laura Lazzarini,Daniela Manno,Anna Galli,Francesca Rossi,Ivan Infante,Sergio Brovelli
标识
DOI:10.1002/adfm.202520228
摘要
Abstract Lead halide perovskite nanocrystals (NCs), such as CsPbBr 3 , are promising candidates for next‐generation scintillators due to their ultrafast radiative kinetics and high emission efficiency. However, their integration in composite scintillators is limited by poor compatibility with high‐Z sensitizers, reabsorption losses at high loading, and low radiation stopping power due to their nanoscale dimensions. Here, a robust strategy is demonstrated to hybridize CsPbBr 3 NCs with hafnium oxide (HfO 2 ) nanoparticles (NPs) as transparent, high‐Z electromagnetic sensitizers. Surface oxygen dangling bonds on HfO 2 NPs are identified as the main source of perovskite degradation and it is shown that a PbBr 2 pre‐treatment effectively passivates these sites. This enables stable NC–NP hybrids, preserving optical quality and scintillation properties. Co‐synthesis in the presence of treated HfO 2 NPs suppresses NC degradation and enhances both photoluminescence efficiency and thermal robustness. The hybrids can be embedded in polymer nanocomposites via thermal radical polymerization, a process typically detrimental to perovskites. Under X‐ray excitation, HfO 2 NPs significantly enhance radioluminescence intensity without compromising the ultrafast response of CsPbBr 3 NCs, confirming efficient electromagnetic sensitization via electron cascade. This work offers a viable pathway for designing hybrid nanoscintillators with enhanced stopping power and stable optical performance for practical radiation detection technologies.
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