Shih Cheng-Yu, Gnilitskyi Iaroslav, Shugaev Maxim V, Skoulas Evangelos, Stratakis Emmanuel, Zhigilei Leonid V
Department of Materials Science and Engineering, University of Virginia, 395 McCormick Road, Charlottesville, Virginia 22904-4745, USA.
Nanoscale. 2020 Apr 14;12(14):7674-7687. doi: 10.1039/d0nr00269k. Epub 2020 Mar 24.
The effect of a liquid environment on the fundamental mechanisms of surface nanostructuring and generation of nanoparticles by single pulse laser ablation is investigated in a closely integrated computational and experimental study. A large-scale molecular dynamics simulation of spatially modulated ablation of Cr in water reveals a complex picture of the dynamic interaction between the ablation plume and water. Ablation plume is found to be rapidly decelerated by the water environment, resulting the formation and prompt disintegration of a hot metal layer at the interface between the ablation and water. A major fraction of the ablation plume is laterally redistributed and redeposited back to the target, forming smooth frozen surface features. Good agreement between the shapes of the surface features predicted in the simulation and the ones generated in single pulse laser ablation experiments performed for Cr in water supports the mechanistic insights revealed in the simulation. The results of this study suggest that the presence of a liquid environment can eliminate the sharp features of the surface morphology, reduce the amount of the material removed from the target by more than an order of magnitude, and narrow down the nanoparticle size distribution as compared to laser ablation under vacuum. Moreover, the computational predictions of the effective incorporation of molecules constituting the liquid environment into the surface region of the irradiated target and the generation of high vacancy concentrations, exceeding the equilibrium levels by more than an order of magnitude, suggest a potential for hyperdoping of laser-generated surfaces by solutes present in the liquid environment.
在一项紧密结合计算与实验的研究中,探究了液体环境对单脉冲激光烧蚀表面纳米结构化基本机制及纳米颗粒生成的影响。对水中Cr的空间调制烧蚀进行的大规模分子动力学模拟揭示了烧蚀羽流与水之间动态相互作用的复杂图景。发现烧蚀羽流被水环境迅速减速,导致在烧蚀与水的界面处形成并迅速分解一个热金属层。大部分烧蚀羽流横向重新分布并重新沉积回靶材,形成光滑的冻结表面特征。模拟预测的表面特征形状与在水中对Cr进行单脉冲激光烧蚀实验所产生的表面特征形状之间的良好一致性,支持了模拟中揭示的机理见解。这项研究的结果表明,与真空下的激光烧蚀相比,液体环境的存在可以消除表面形态的尖锐特征,将从靶材去除的材料量减少一个多数量级,并缩小纳米颗粒尺寸分布。此外,对构成液体环境的分子有效掺入被辐照靶材表面区域以及产生高空位浓度(超过平衡水平一个多数量级)的计算预测表明,液体环境中存在的溶质有可能对激光生成的表面进行超掺杂。