Abstract

We compare the discrete dipole approximation (DDA) and the finite difference time domain (FDTD) method for simulating light scattering of spheres in a range of size parameters x up to 80 and refractive indices m up to 2. Using parallel implementations of both methods, we require them to reach a certain accuracy goal for scattering quantities and then compare their performance. We show that relative performance sharply depends on m. The DDA is faster for smaller m, while the FDTD for larger values of m. The break-even point lies at m = 1.4. We also compare the performance of both methods for a few particular biological cells, resulting in the same conclusions as for optically soft spheres.

Highlights

  • The discrete dipole approximation (DDA) [1,2] and the finite difference time domain method (FDTD) [3,4] are two of the most popular methods to simulate light scattering of arbitrarily shaped inhomogeneous particles

  • As an intermediate case between homogeneous spheres and real biological cells, we consider a coated sphere model consisting of two concentric spheres, which is an approximation for the B-cell precursor (BCP) shape described above

  • Values of dpl cannot be directly compared between both methods because the typical values for the DDA [1] are twice as small as for the FDTD [4]

Read more

Summary

Introduction

The discrete dipole approximation (DDA) [1,2] and the finite difference time domain method (FDTD) [3,4] are two of the most popular methods to simulate light scattering of arbitrarily shaped inhomogeneous particles. These methods have a very similar region of applicability; they are rarely used together. We focus on particles with negligible absorption, e.g. biological particles This covers a broad range of slightly absorbing materials, e.g. water and ice, because performance of both methods do not depend significantly on small imaginary part of the refractive index.

DDA and FDTD implementations
Test objects
Results for spheres
Sample applications to biological cells
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call