Document Type

Article

Original Publication Date

2023

Journal/Book/Conference Title

The Journal of Physical Chemistry B

Volume

127

Issue

29

First Page

6551

Last Page

6661

DOI of Original Publication

10.1021/acs.jpcb.3c03708

Comments

This document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of Physical Chemistry B, copyright © 2023 American Chemical Society, after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/full/10.1021/acs.jpcb.3c03708

Date of Submission

December 2024

Abstract

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, n-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, sp-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.

Rights

© 2023 American Chemical Society

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VCU Chemistry Publications

Included in

Chemistry Commons

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