硼硅酸盐玻璃
材料科学
光致发光
位阻效应
离解(化学)
星团(航天器)
量子
光电子学
纳米技术
化学工程
化学
计算机科学
物理化学
复合材料
物理
有机化学
工程类
程序设计语言
量子力学
作者
Wenyan Zheng,Pengcheng Li,Chen‐Hao Wang,Xvsheng Qiao,Guodong Qian,Xianping Fan
标识
DOI:10.1016/j.jnoncrysol.2022.121910
摘要
Ag quantum clusters (Ag QCs) embedded in glasses are promising for various optoelectronic devices, but the manipulation over their aggregation states toward efficient photoluminescence (PL) is still challenging. Here, we propose two network strategies to tailor the Ag QCs aggregation and PL performance inside borate glass. Using the solubility strategy, the introduced network modifier (BaO) brings [BO3] → [BO4]− transformation and poses steric hindrance, leading to the growth of Ag QCs. Through the charge compensator strategy (Al2O3), it brings negatively charged [AlO4]− units that favor isolated Ag+ ions to meet charge balance, rendering the cluster dissociation. With further SiO2 incorporation, the borosilicate constructs a rigid network that improves the glass stability and prevents molecular motions in Ag QCs, promoting PL quantum efficiency (up to 90.55%). Based on these design principles, the glass with highly emissive and stable Ag QCs is prepared and presents potential in the spectral converter for organic solar cells.
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