Understanding the interaction of an intense laser pulse with nanoparticles: Application to the quantification of single particle mass spectrometry

被引:10
作者
Zhou, L. [1 ]
Park, K. [1 ]
Milchberg, H. M. [1 ]
Zachariah, M. R. [1 ]
机构
[1] Univ Maryland, Dept Mech Engn, College Pk, MD 20852 USA
关键词
D O I
10.1080/02786820701484955
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Understanding the characteristic behavior of ions produced from the interaction of a high energy laser pulse with nanoparticles is essential for quantitative determination of composition and size of nanoparticles from single particle mass spectrometry (SPMS). We employed a one-dimensional hydrodynamic model, where the laser field is coupled to the non-equilibrium time-dependent plasma hydrodynamics of the heated particles. We focus on regimes of laser width from 0.01 ns to 10 ns (532 nm wavelength, 100 mJ/pulse) and particle size (20-400 nm in diameter) most relevant to commonly used SPMS, and determine the properties of ions generated during the interaction with a strong laser pulse. We compare the simulation results with experiments conducted on aluminum nanoparticles. The laser-particle interaction is separated into a "soft heating" regime followed by a hydrodynamic expansion. Simulation results showed that the ablation/ionization is effectively complete well before the laser ever reaches its peak intensity. As the pulse width decreased for a given pulse energy, the kinetic energy of ions increased, suggesting that too short a pulse laser (i.e., high laser intensity) would be undesirable because higher energetic ions lead to lower detection efficiency in the SPMS. Results also show that for particle sizes in the range of 100 nm similar to 400 nm, as particle size increased, the kinetic energy of ions produced from the particle increased with a power law relationship, consistent with experiment. Lastly our simulations indicated that ions from the surface of the particle are of higher energy, and therefore have lower detection efficiency.
引用
收藏
页码:818 / 827
页数:10
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