激发态
发光
兴奋剂
材料科学
光子上转换
纳米晶
原子物理学
光电子学
放大自发辐射
分析化学(期刊)
光学
纳米技术
激光器
物理
化学
色谱法
作者
Wei Zhang,Wei Zheng,Lingyun Li,Xiaoying Shang,Ping Huang,Xiaodong Yi,Hao Zhang,Yan Yu,Xueyuan Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-05-06
标识
DOI:10.1021/acsnano.5c05992
摘要
High-order nonlinear multiphoton absorption (MPA) is technologically important for a variety of photonic and biological applications owing to its superior advantages over linear absorption and low-order MPA such as greater spatial confinement, larger penetration depth, reduced autofluorescence, and enhanced imaging resolution. However, practical implementation beyond three-photon processes remains notoriously difficult due to the sharp reduction of absorption cross sections with increasing nonlinearity and inherent material instability under high-density irradiation. Herein, we address these challenges through rationally designed Te4+-doped Cs2SnCl6 nanocrystals (NCs), which demonstrate wideband nonlinear responsiveness across 800-2600 nm, allowing achievement of two- to seven-photon absorption (PA) with cross sections outperforming conventional nonlinear optical materials. Particularly, the engineered NCs enable 3PA-excited amplified spontaneous emission (ASE) with an ultralow excitation threshold of 0.22 μJ cm-2 under a 1300 nm femtosecond-pulsed laser excitation, representing 1-4 orders of magnitude improvement compared to existing nonlinear ASE systems. This work presents the excellent 7PA properties in metal halide NCs, positioning lead-free metal halide NCs promising as efficient light-emitting materials for extreme nonlinear nanophotonics.
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