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Calculated exciton wave function in a hybrid organic-inorganic layered halide perovskite
Credit: Figure created with VESTA; calculations performed with the BerkeleyGW code

Marina Filip

Professor of Physics

Research theme

  • Photovoltaics and nanoscience

Sub department

  • Condensed Matter Physics

Research groups

  • Computational Condensed Matter Physics Group
  • Advanced Device Concepts for Next-Generation Photovoltaics
marina.filip@physics.ox.ac.uk
Clarendon Laboratory, room 109
  • About
  • Publications

Hot electron cooling in InSb probed by ultrafast time-resolved terahertz cyclotron resonance

Physical Review B American Physical Society 103 (2021) 245205

Authors:

Chelsea Xia, Jessica Louise Boland, Laura Herz, Marina Filip, Michael Johnston

Abstract:

Measuring terahertz (THz) conductivity on an ultrafast time scale is an excellent way to observe charge-carrier dynamics in semiconductors as a function of time after photoexcitation. However, a conductivity measurement alone cannot separate the effects of charge-carrier recombination from effective mass changes as charges cool and experience different regions of the electronic band structure. Here we present a form of time-resolved magneto-THz spectroscopy which allows us to measure cyclotron effective mass on a picosecond time scale. We demonstrate this technique by observing electron cooling in the technologically-significant narrow-bandgap semiconductor indium antimonide (InSb). A significant reduction of electron effective mass from 0.032 me to 0.017 me is observed in the first 200 ps after injecting hot electrons. Measurement of electron effective mass in InSb as a function of photo-injected electron density agrees well with conduction band non-parabolicity predictions from ab initio calculations of the quasiparticle band structure.
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Phonon Screening of Excitons in Semiconductors: Halide Perovskites and Beyond

(2021)

Authors:

Marina R Filip, Jonah B Haber, Jeffrey B Neaton
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Chemically-localized resonant excitons in silver-pnictogen halide double perovskites

Journal of Physical Chemistry Letters American Chemical Society 12:8 (2021) 2057-2063

Authors:

Raisa-Ioana Biega, Marina Filip, Linn Leppert, Jeff Neaton

Abstract:

Halide double perovskites with alternating silver and pnictogen cations are an emerging family of photoabsorber materials with robust stability and band gaps in the visible range. However, the nature of optical excitations in these systems is not yet well understood, limiting their utility. Here, we use ab initio many-body perturbation theory within the GW approximation and the Bethe-Salpeter equation approach to calculate the electronic structure and optical excitations of the double perovskite series Cs2AgBX6, with B=Bi3+, Sb3+, X = Br−, Cl−. We find that these materials exhibit strongly localized resonant excitons with energies from 170 to 434 meV below the direct band gap. In contrast to lead-based perovskites, the Cs2AgBX6 excitons are computed to be non-hydrogenic, with anisotropic effective masses and sensitive to local field effects, a consequence of their chemical heterogeneity. Our calculations demonstrate the limitations of the Wannier-Mott and Elliott models for this class of double perovskites and contribute to a detailed atomistic understanding of their light-matter interactions.
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Chemically-Localized Resonant Excitons in Silver-Pnictogen Halide Double Perovskites

(2021)

Authors:

Raisa-Ioana Biega, Marina R Filip, Linn Leppert, Jeffrey B Neaton
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Band gaps of crystalline solids from Wannier-localization based optimal tuning of a screened range-separated hybrid functional

(2020)

Authors:

Dahvyd Wing, Guy Ohad, Jonah B Haber, Marina R Filip, Stephen E Gant, Jeffrey B Neaton, Leeor Kronik
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