纳米晶
材料科学
纳米技术
微尺度化学
光子学
热分解
量子点
光电子学
化学
数学
数学教育
有机化学
作者
Fu Li,Changhao Chen,Shaoyong Lu,Xueguang Chen,Wangyu Liu,Kangkang Weng,Zhong Fu,Dan Liu,Lipeng Zhang,Hannikezi Abudukeremu,Linhan Lin,Yuanyuan Wang,Minlin Zhong,Hao Zhang,Jinghong Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-07-22
卷期号:16 (9): 13674-13683
被引量:26
标识
DOI:10.1021/acsnano.2c04033
摘要
Precise patterning with microscale lateral resolution and widely tunable heights is critical for integrating colloidal nanocrystals into advanced optoelectronic and photonic platforms. However, patterning nanocrystal layers with thickness above 100 nm remains challenging for both conventional and emerging direct photopatterning methods, due to limited light penetration depths, complex mechanical and chemical incompatibilities, and others. Here, we introduce a direct patterning method based on a thermal mechanism, namely, the thermally activated ligand chemistry (or TALC) of nanocrystals. The ligand cross-linking or decomposition reactions readily occur under local thermal stimuli triggered by near-infrared lasers, affording high-resolution and nondestructive patterning of various nanocrystals under mild conditions. Patterned quantum dots fully preserve their structural and photoluminescent quantum yields. The thermal nature allows for TALC to pattern over 10 μm thick nanocrystal layers in a single step, far beyond those achievable in other direct patterning techniques, and also supports the concept of 2.5D patterning. The thermal chemistry-mediated TALC creates more possibilities in integrating nanocrystal layers in uniform arrays or complex hierarchical formats for advanced capabilities in light emission, conversion, and modulation.
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