Nanoscale kinetics and dynamics during Ar+ patterning of SiO2

Mahsa Mokhtarzadeh, Jeffrey G. Ulbrandt, Peco Myint, Suresh Narayanan, Randall L. Headrick, and Karl F. Ludwig, Jr.
Phys. Rev. B 99, 165429 – Published 29 April 2019

Abstract

Broad-beam low-energy ion bombardment can lead to the spontaneous formation of nanoscale surface structures, but the dominant mechanisms driving evolution remain controversial. Using coherent x-ray scattering to examine the classic case of ion-beam rippling of SiO2 surfaces, we study the relationship between the average kinetics of ripple formation and the underlying fluctuation dynamics. The early stage growth of fluctuations is well fit with a linear theory formalism employing a viscous relaxation term with full wave-number dependence. In this regime, the x-ray photon correlation spectroscopy two-time correlation function shows distinctive behavior with memory stretching back to the beginning of the bombardment. For a given length scale, correlation times do not grow significantly beyond the characteristic time associated with the early-stage ripple growth. In the late stages of patterning, when the average surface structure on a given length scale is no longer evolving, dynamical processes continue on the surface. Nonlinear processes dominate at long length scales, leading to compressed exponential decay of the speckle correlation functions, while at short length scales the dynamics appears to approach a linear behavior consistent with viscous flow relaxation. This behavior is found to be consistent with simulations of a recent nonlinear growth model. In addition, it is shown that the surface ripple velocity, an important parameter of the ion-driven surface evolution, can be measured with coherent x-ray scattering in conjunction with use of an inhomogeneous ion beam. The change in viewpoint exemplified by this study, from a focus on only average surface kinetics to one incorporating the underlying nanoscale dynamics, is rapidly becoming more widely applicable as new and upgraded x-ray sources with higher coherent flux come online.

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  • Received 14 January 2019
  • Corrected 16 July 2019

DOI:https://doi.org/10.1103/PhysRevB.99.165429

©2019 American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied Physics

Corrections

16 July 2019

Correction: Equation (13) was misidentified in several locations as the “anisotropic Kuramoto-Sivashinsky” equation and is now properly labeled as the “Harrison-Pearson-Bradley” equation.

Authors & Affiliations

Mahsa Mokhtarzadeh1,2, Jeffrey G. Ulbrandt3, Peco Myint4, Suresh Narayanan5, Randall L. Headrick3, and Karl F. Ludwig, Jr.1,4,*

  • 1Department of Physics, Boston University, Boston, Massachusetts 02215, USA
  • 2Physics Department, Shahid Beheshti University, Evin, 19839 Tehran, Iran
  • 3Department of Physics and Materials Science Program, University of Vermont, Burlington, Vermont 05405, USA
  • 4Division of Materials Science and Engineering, Boston University, Boston, Massachusetts 02215, USA
  • 5Advanced Photon Source, Argonne National Lab, Argonne, Illinois 60439, USA

  • *ludwig@bu.edu

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Issue

Vol. 99, Iss. 16 — 15 April 2019

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