Frias Batista Laysa M, Kaplan Ella, Weththasingha Chamari, Cook Benjamin, Harris Samuel, Nag Ashish, Tibbetts Katharine Moore
Department of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
J Phys Chem B. 2023 Jul 27;127(29):6551-6561. doi: 10.1021/acs.jpcb.3c03708. Epub 2023 Jul 18.
Laser synthesis in liquids is often carried out in organic solvents to prevent oxidation of metals during nanoparticle generation and to produce tailored carbon-based nanomaterials. This work investigates laser ablation of neat organic liquids acetone, ethanol, -hexane, and toluene with pulse widths ranging from 30 fs to 4 ps through measurements of reaction kinetics and characterization of the ablation products with optical spectroscopy and mass spectrometry. Increasing the pulse width from 30 fs to 4 ps impacts both the reaction kinetics and product distributions, suppressing the formation of solvent molecule dimers and oxidized molecules while enhancing the yields of gaseous molecules, -hybridized carbons, and fluorescent carbon dots. The observed trends are explained in the context of established ionization mechanisms and cavitation bubble dynamical processes that occur during ultrashort pulsed laser ablation of liquid media. The results of this work have important implications both for controlling the formation of carbon shells around metal nanoparticles during the ablation of solid targets in liquid and producing carbon nanomaterials directly from the ablation of organic liquids without a solid target.
液体中的激光合成通常在有机溶剂中进行,以防止在纳米颗粒生成过程中金属氧化,并生产定制的碳基纳米材料。这项工作通过测量反应动力学以及用光光谱和质谱对烧蚀产物进行表征,研究了脉冲宽度从30飞秒到4皮秒的纯有机液体丙酮、乙醇、己烷和甲苯的激光烧蚀。将脉冲宽度从30飞秒增加到4皮秒会影响反应动力学和产物分布,抑制溶剂分子二聚体和氧化分子的形成,同时提高气态分子、sp²杂化碳和荧光碳点的产率。在既定的电离机制和液体介质超短脉冲激光烧蚀过程中发生的空化泡动力学过程的背景下解释了观察到的趋势。这项工作的结果对于在液体中烧蚀固体靶材期间控制金属纳米颗粒周围碳壳的形成以及直接从无固体靶材的有机液体烧蚀中生产碳纳米材料都具有重要意义。