Calculation of the amplitude matrix for a nonspherical particle in a fixed orientation

2000 ◽  
Vol 39 (6) ◽  
pp. 1026 ◽  
Author(s):  
Michael I. Mishchenko
2020 ◽  
Vol 2 (4) ◽  
Author(s):  
Ryan P. Jones ◽  
Julio M. Ottino ◽  
Paul B. Umbanhowar ◽  
Richard M. Lueptow

2020 ◽  
Author(s):  
MRA Majić ◽  
L Pratley ◽  
D Schebarchov ◽  
Walter Somerville ◽  
Baptiste Auguié ◽  
...  

© 2019 American Physical Society. In electromagnetic scattering, the so-called T matrix encompasses the optical response of a scatterer for any incident excitation and is most commonly defined using the basis of multipolar fields. It can therefore be viewed as a generalization of the concept of polarizability of the scatterer. We calculate here the series expansion of the T matrix for a spheroidal particle in the small-size, long-wavelength limit, up to third lowest order with respect to the size parameter, X, which we will define rigorously for a nonspherical particle. T is calculated from the standard extended boundary condition method with a linear system involving two infinite matrices P and Q, whose matrix elements are integrals on the particle surface. We show that the limiting form of the P and Q matrices, which is different in the special case of spheroid, ensures that this Taylor expansion can be obtained by considering only multipoles of order 3 or less (i.e., dipoles, quadrupoles, and octupoles). This allows us to obtain self-contained expressions for the Taylor expansion of T(X). The lowest order is O(X3) and equivalent to the quasistatic limit or Rayleigh approximation. Expressions to order O(X5) are obtained by Taylor expansion of the integrals in P and Q followed by matrix inversion. We then apply a radiative correction scheme, which makes the resulting expressions valid up to order O(X6). Orientation-averaged extinction, scattering, and absorption cross sections are then derived. All results are compared to the exact T-matrix predictions to confirm the validity of our expressions and assess their range of applicability. For a wavelength of 400 nm, the new approximation remains valid (within 1% error) up to particle dimensions of the order of 100-200 nm depending on the exact parameters (aspect ratio and material). These results provide a relatively simple and computationally friendly alternative to the standard T-matrix method for spheroidal particles smaller than the wavelength, in a size range much larger than for the commonly used Rayleigh approximation.


2021 ◽  
Vol 77 (5) ◽  
pp. 628-644
Author(s):  
Gabrielle Illava ◽  
Richard Jayne ◽  
Aaron D. Finke ◽  
David Closs ◽  
Wenjie Zeng ◽  
...  

Serial synchrotron crystallography (SSX) is enabling the efficient use of small crystals for structure–function studies of biomolecules and for drug discovery. An integrated SSX system has been developed comprising ultralow background-scatter sample holders suitable for room and cryogenic temperature crystallographic data collection, a sample-loading station and a humid `gloveless' glovebox. The sample holders incorporate thin-film supports with a variety of designs optimized for different crystal-loading challenges. These holders facilitate the dispersion of crystals and the removal of excess liquid, can be cooled at extremely high rates, generate little background scatter, allow data collection over >90° of oscillation without obstruction or the risk of generating saturating Bragg peaks, are compatible with existing infrastructure for high-throughput cryocrystallography and are reusable. The sample-loading station allows sample preparation and loading onto the support film, the application of time-varying suction for optimal removal of excess liquid, crystal repositioning and cryoprotection, and the application of sealing films for room-temperature data collection, all in a controlled-humidity environment. The humid glovebox allows microscope observation of the sample-loading station and crystallization trays while maintaining near-saturating humidities that further minimize the risks of sample dehydration and damage, and maximize working times. This integrated system addresses common problems in obtaining properly dispersed, properly hydrated and isomorphous microcrystals for fixed-orientation and oscillation data collection. Its ease of use, flexibility and optimized performance make it attractive not just for SSX but also for single-crystal and few-crystal data collection. Fundamental concepts that are important in achieving desired crystal distributions on a sample holder via time-varying suction-induced liquid flows are also discussed.


A new method for studying the de Haas–van Alphen effect in steady magnetic fields has been developed in which the field is modulated at frequency ω and a signal at frequency 2 ω is generated in a pick-up coil round the specimen because of the non-linear field dependence of magnetization. The rectified 2 ω signal is proportional to d 2 M /dH 2 and so shows de Haas–van Alphen oscillations either when H is varied for fixed orientation or when the orientation is varied in fixed H if the Fermi surface is anisotropic. Because the phase of oscillation is very high (of order 10 4 π ) even very slight anisotropy will produce a few oscillations when the orientation is varied and the method is therefore particularly sensitive for studying very nearly spherical Fermi surfaces. From the oscillations with H , values of the frequency F were found for sodium, potassium, rubidium and caesium which were close to those predicted for a free-electron sphere containing 1 electron per atom, though some small systematic deviations of order ½ % were observed which may be significant. From detailed study of the oscillations produced by rotation of single crystals in fixed H it was found possible to describe the orientation dependence of F (proportional to the area of cross-section of the Fermi surface) for potassium and rubidium consistently by a series of cubic harmonics and hence to deduce the small departures of the Fermi surfaces from spherical shape. The deviations from a sphere were found to be of the order of 1 part in 10 3 for potassium and a little less than 1 part in 10 2 for rubidium; these deviations are compared with those predicted by band structure calculations. Preliminary results for sodium suggest that it is appreciably less anisotropic than potassium. Some results are also reported on the temperature and field dependence and the absolute amplitude of the de Haas-van Alphen effect, and it is also shown how the effect can be used to measure very small variations of field with position.


2007 ◽  
Vol 35 (3) ◽  
pp. 357-364 ◽  
Author(s):  
François Clautiaux ◽  
Jacques Carlier ◽  
Aziz Moukrim

2015 ◽  
Vol 92 (3) ◽  
Author(s):  
Daniel M. Kintea ◽  
Tobias Hauk ◽  
Ilia V. Roisman ◽  
Cameron Tropea

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