arXiv subjects

Dmitri R. Yakovlev

Publications and source records attributed to Dmitri R. Yakovlev.

At least 19 recordsLinked to original sources

arXiv2026

Interaction between Rydberg Excitons in Cuprous Oxide Revealed through Resonant Second Harmonic Generation

We report experimental and theoretical investigations of interacting excitons of the yellow series in cuprous oxide (Cu$_2$O) with principal quantum numbers up to by means of second harmonic generation (SHG). Using picosecond pulsed laser excitation up to 10 GW/cm$^2$ peak intensity we observe a pronounced change of the spectra with increasing pump laser intensity: an energetic shift to lower absolute energies and a spectral broadening. The absolute intensities of the spectral lines scale for low powers with the square of the pump power, but saturates at higher powers. At still higher powers the SHG intensity is actually reduced. To explain these results quantitively, we developed a semi-classical theory of resonant SHG where the process of SHG is fully coherent. The excitons are assumed to be bosons interacting by a distance dependent potential giving rise to both the changes in spectral line shape and the saturation by a $\it{Rydberg}$ blockade. The concomitant measurement of two-photon absorption allows to derive quantitative values for the exciton-exciton interaction. While the results agree in order of magnitude with those calculated by state-of-the art atomic-like van der Waals interaction theory, the scaling with principle quantum number is quite different. As a possible screening by an electron-hole plasma created by three-photon absorption into blue and violet band states could be ruled out, our results point toward fundamental differences between excitons and atoms.

cond-mat.mes-hall↗

arXiv2026

Resonant cooling of nuclear spins by optically-oriented holes in MAPbI$_3$ perovskite crystals

Resonant cooling of nuclear spins by photogenerated spin-oriented holes is demonstrated for MAPbI$_3$ perovskite crystals. It is evidenced by Hanle-effect measurements under helicity-modulated excitation with variable frequency. The resonance position in magnetic field shifts toward higher fields with increasing modulation frequency. The invariance of the Hanle curve upon in-plane sample rotation is consistent with the involvement of $^{207}$Pb nuclei with spin $I = 1/2$, which do not exhibit quadrupolar splitting. The shape of the resonance feature in the Hanle curve reveals that the nuclear spins are cooled by carriers with a negative $g$-factor, consistent with holes. The resonance fields associated with the modulation frequencies exceed the half-width of the weakly localized hole contribution to the Hanle curve, indicating that strongly localized holes are the primary carriers responsible for the nuclear spin cooling.

cond-mat.mes-hall↗

arXiv2026

Hyperfine versus exchange interaction in the spin dynamics of spatially indirect excitons in CsPbI$_{3}$ perovskite nanocrystals

We study the dynamics of recombination, optical orientation, and optical alignment of excitons in ensembles of CsPbI$_{3}$ nanocrystals (NCs), synthesized in a glass matrix. In large NCs with size exceeding 16 nm, the low-energy photoluminescence is contributed by the emission of indirect in real space excitons formed by spatially separated electrons and holes, which are localized at the NC/glass interface. The recombination dynamics of an ensemble of such excitons extends from tens of nanoseconds to microseconds and exhibits a power-law dependence. Their optical alignment and optical orientation reveal a peculiar spin dynamics caused by excitons influenced by the exchange interaction, varying by orders of magnitude. We develop a theory of the polarized photoluminescence of triplet excitons, taking into account the interplay between the electron-hole exchange interaction, their Zeeman effect, and their hyperfine interaction with the nuclei. This model reveals that for the excitons with the smallest exchange splitting we reach the regime, where the exciton fine structure becomes dominated by the hyperfine interaction with the random nuclear spin fluctuations in the NCs.

cond-mat.mes-hall↗

arXiv2026

Layer-dependent Landé $g$-factors of electrons, holes, and excitons in two-dimensional Ruddlesden-Popper lead halide perovskites

Two-dimensional Ruddlesden-Popper lead halide perovskites provide a valuable platform for tailoring charge and spin properties through quantum confinement and reduced symmetry. While the electron and hole Landé $g$-factors in bulk lead halide perovskites exhibit a universal dependence on the band gap energy, their evolution in two-dimensional perovskites has remained largely unexplored. Here, the Zeeman splittings of electrons and holes in (PEA)$_2$MA$_{n-1}$Pb$_n$I$_{3n+1}$ perovskites with the number of inorganic layers ovarying in the range $n=1,...,8$ are measured by means of the spin-flip Raman scattering and time-resolved Kerr rotation magneto-optical techniques. A systematic evolution of the electron and hole $g$-factors with decreasing layer thickness, which deviates from the universal bulk behavior and reveals confinement-driven trends similar to those observed in perovskite nanocrystals, is found. The experimental results are in good qualitative agreement with empirical tight-binding calculations. The exciton $g$-factors are evaluated from the Zeeman splittings of the exciton resonances in reflectivity measured in pulsed magnetic fields up to 55~T. These results provide comprehensive insight into the spin properties of two-dimensional lead halide perovskites and establish them as a tunable platform for engineering spin-dependent phenomena in quantum-confined semiconductors.

cond-mat.other↗

arXiv2026

Millisecond spin relaxation times of distinct electron and hole subensembles in MA$_x$FA$_{1-x}$PbI$_3$ perovskite crystals

The unique combination of outstanding optical quality and attractive spin properties opens new avenues for optical spin control in hybrid organic-inorganic perovskite semiconductors. Using the optically detected magnetic resonance technique, we study the spins of electrons and holes in mixed-cation MA$_x$FA$_{1-x}$PbI$_3$ single crystals with $x = 0.4$ and 0.8. Multiple distinct spin subensembles with $g$-factors spanning from 2.9 to 3.6 for electrons and from 0.5 to 1.2 for holes are resolved, revealing diverse localization environments. We measure the longitudinal spin relaxation times, $T_1$, reaching 2 ms and remaining in the $μ$s range even for weakly localized carriers at the cryogenic temperature of 1.6 K. The magnetic-field dependence of $T_1$ is dominated by the random nuclear (Overhauser) fields with strengths of $\sim 0.4-0.8$ mT for electrons and $\sim 4-12$ mT for holes, corresponding to $μ$s-long correlation times of the hyperfine field determined by carrier hopping between shallow localization sites. The temperature dependence of $T_1$ reveals a weak localization potential of the charge carriers and shows a correlation between $T_1$ and the inhomogeneity of the spin ensemble. These results establish mixed-A-site perovskite single crystals as a promising solid-state platform with long-lived spin states for quantum information applications.

cond-mat.mes-hall↗

arXiv2026

Assessing the classicality of photon echo from excitons in lead halide perovskite nanocrystals

Photon echo (PE) spectroscopy is a powerful technique for probing decoherence mechanisms and charge carrier dynamics in semiconductor systems. Beyond traditional coherence measurements, characterizing the photon statistics of the echo signal is important for assessing its potential in quantum information applications and understanding the underlying quantum mechanical processes. Here, we study the photon statistics of PE signals generated by excitons in ensembles of lead halide perovskite CsPbI$_3$ nanocrystals at cryogenic temperature of 2 K using continuous-variable quantum state optical tomography based on homodyne detection. Pronounced Rabi oscillations of the PE amplitude allow us to evaluate the statistics for various pulse areas in the excitation sequence. The damping of the oscillations with increasing pulse area is attributed to spatial excitation inhomogeneity and excitation-induced dephasing. Despite the large ensemble of optically addressed excitons, the efficiency of generated PE signals is low which is attributed to the complex energy level structure of excitons and non-radiative recombination channels in CsPbI$_3$ nanocrystals. We analyze the statistical characteristics of PE via the second-order correlation function $g^{(2)}(0)$ and the characteristic function for different combinations of the areas of the excitation pulses. Our results show that $g^{(2)}(0) = 1$, and the characteristic function of the PE signal corresponds to classical behavior. The formation of photon echoes as well as $g^{(2)}(0) = 1$ at the echo time is reproduced by a quantized free-space multimode model. Despite the relatively low efficiency, the photon echo exhibits a high degree of coherence and minimal classical noise, consistent with Poissonian statistics.

cond-mat.mes-hall↗

arXiv2026

Millisecond-long electron spin lifetime in CsPbI$_3$ perovskite nanocrystals revealed by optically detected magnetic resonance

Perovskite nanocrystals are a convenient model system for optical spin orientation and manipulation. However, its real potential might be underestimated due to the incomplete knowledge on spin relaxation times, which are obscured by the limited sensitivity of measurement techniques as well as by the insufficient understanding of the spin relaxation mechanisms in perovskites. In this work, we study the spin relaxation of charge carriers in perovskite nanocrystals both experimentally and theoretically. We address the electron and hole spins in CsPbI$_3$ nanocrystals embedded in a glass matrix by the resonant spin inertia technique based on optically detected magnetic resonance. It allows us to determine the longitudinal spin relaxation time $T_1$ separately for electrons and holes, the $g$ factors, and the effective Overhauser field of the nuclear spin bath. At a temperature of 1.6 K, the $T_1$ time for electrons can be as long as 0.9 ms. We reveal the effect of the time-varying nuclear field fluctuations, which enhances the electron spin relaxation at low magnetic fields, and measure a rather long nuclear spin correlation time of about 60 $μ$s. We develop a model of the spin relaxation in nanocrystals based on a two-LO-phonon Raman process, which explains the observed temperature dependence of the time $T_1$.

cond-mat.mes-hall↗

arXiv2026

Hyperfine interaction of electrons and holes with nuclei probed by optical orientation in MAPbI$_3$ perovskite crystals

Optical orientation of electron and hole spins by circularly polarized light is investigated for MAPbI$_3$ single crystals. The Hanle and polarization recovery effects measured in transverse and longitudinal magnetic fields, respectively, evidence the hyperfine interaction with nuclear spins as the main factor determining the spin dynamics of charge carriers at cryogenic temperatures. The parameters of the nuclear spin fluctuations within the carrier localization volume are evaluated. Dynamic polarization of the nuclear spins is demonstrated by the Overhauser field reaching 5 mT for acting on the electrons and -30 mT for acting on the holes.

cond-mat.mes-hall↗

arXiv2026

Millisecond spin coherence of electrons in semiconducting perovskites revealed by spin mode locking

Long spin coherence times of carriers are essential for implementing quantum technologies using semiconductor devices for which, however, a possible obstacle is spin relaxation. For the spin dynamics, decisive features are the band structure, crystal symmetry, and quantum confinement. Perovskite semiconductors recently have come into focus of studies of their spin states, notivated by efficient optical access and potentially long-living coherence. Here, we report an electron spin coherence time $T_2$ of the order of 1 ms, measured for a bulk FA$_{0.95}$Cs$_{0.05}$PbI$_3$ lead halide perovskite crystal. Using periodic laser pulses, we synchronize the electron spin Larmor precession about an external magnetic field in an inhomogeneous ensemble, the effect known as spin mode locking. It appears as a decay of the optically created ensemble spin polarization within the dephasing time $T_2^*$ of up to 20 ns and its revival during the spin coherence time $T_2$ reaching the millisecond range. This exceptionally long spin coherence time in a bulk crystal is complemented by millisecond-long longitudinal spin relaxation times $T_1$ for electrons and holes, measured by optically-detected magnetic resonance. These long-lasting spin dynamics highlight perovskites as promising platform for the quantum devices with all-optical control.

cond-mat.mtrl-sci↗

arXiv2026

Spin-dependent Raman and Brillouin light scattering on excitons in CsPbBr$_3$ perovskite crystals

The spin properties of excitons and charge carriers in CsPbBr$_3$ lead halide perovskite crystals are investigated by spin-dependent light scattering in magnetic fields up to 10 T. Spin-flip Raman scattering spectra measured under resonant excitation of exciton-polaritons show a rich variety of features provided by the Zeeman splittings of excitons and of electrons and holes interacting with the excitons. The magnitudes and anisotropies of their Landé $g$-factors are measured. A detailed consideration of the responsible mechanisms is presented and discussed in relation to the experimental data, in particular on the polarization properties of the Raman spectra. We consider several mechanisms for the combined spin-flip Raman scattering processes involving resident carriers and photoexcited excitons and suggest new ones, involving trions in the intermediate scattering state. A double electron spin-flip caused by the exciton interaction with two localized or donor-bound electrons is revealed. The spectral lines of Brillouin light scattering on exciton-polaritons shift in energy and become polarization-sensitive in magnetic field, evidencing the splitting of the exciton-polariton dispersion.

cond-mat.mtrl-sci↗

arXiv2026

Magnetoluminescence of ZnMnSe/BeMnTe heterostructures with type-II band alignment at millikelvin temperatures

The magneto-optical properties of a Zn$_{0.99}$Mn$_{0.01}$Se/Be$_{0.93}$Mn$_{0.07} $Te diluted magnetic semiconductor heterostructure with type-II band alignment are investigated at cryogenic temperatures down to 16 mK. The temperature of the Mn spin system, which at the lowest possible laser power reaches 270 mK, is evaluated from the giant Zeeman splitting of the direct exciton in the Zn$_{0.99}$Mn$_{0.01}$Se layers subject to an external magnetic field. The degree of circular polarization of the direct and indirect optical transitions, induced by the magnetic field, is a sensitive indicator for the laser heating of the Mn spin system. Evidence of spin glass formation in the Mn spin system of the Be$_{0.93}$Mn$_{0.07}$Te layers with the critical temperature of $T_{SG}=400$ mK is found.

cond-mat.mtrl-sci↗

arXiv2025

Exciton spin structure in lead halide perovskite semiconductors explored via the spin dynamics in magnetic field

We theoretically investigate the spin structure and spin dynamics of excitons in bulk lead halide perovskite semiconductors with cubic, tetragonal, and orthorhombic crystal symmetry. The exciton spin structure and its modification by an external magnetic field are modeled for different regimes defined by the relative magnitude of the electron-hole exchange interaction (splitting between dark and bright states) and the Zeeman spin splitting. The effects of crystal symmetry and magnetic field orientation with respect to the crystal axes are considered for lead halide perovskite crystals with band gaps in the range 1.4 - 3.5 eV, having different ratios of electron and hole g-factors. For cubic symmetry, in a longitudinal magnetic field, our theory predicts quantum beats between the bright exciton states under linearly polarized excitation and detection, while the dark exciton remains optically inactive. In a transverse magnetic field, all exciton spin states become optically active and can be excited by circularly polarized light. Reduction of the crystal symmetry leads to a zero-field offset of the exciton Larmor precession frequencies, modifying the Zeeman splitting energy dependence on magnetic field. This theoretical framework allows for the extraction of the strength of the exchange interaction and the crystal symmetry. Experimentally, we measure the exciton spin coherence via time-resolved photoluminescence at a temperature of 1.6 K in longitudinal and transverse magnetic fields in orthorhombic MAPbI3 crystals. Polarization beats at the frequency of the bright exciton are observed in both configurations. Comparison with theory indicates that the excitons are in the strong exchange interaction regime, and the reduction of symmetry does not lead to a significant splitting of the exciton spin levels.

cond-mat.other↗

arXiv2025

Dynamic polarization of nuclear spins by optically-oriented electrons and holes in lead halide perovskite semiconductors

A theory of dynamic polarization of the nuclear spin system via optically-oriented charge carriers in lead halide perovskites is developed and compared with the experiments performed on a FA$_{0.9}$Cs$_{0.1}$PbI$_{2.8}$Br$_{0.2}$ crystal. The spin Hamiltonians of the electron and hole hyperfine interaction with the nuclear spins of lead and halogen are derived. The hyperfine interaction of the halogen spins with charge carriers is shown to be anisotropic and depending on the position of the halogen nucleus in the cubic elementary cell. The quadrupole splitting is absent for the lead spins, but plays an important role for the halogen spins and affects their dynamic polarization by charge carriers. The Overhauser fields of the dynamically polarized nuclei are calculated as functions of the tilting angle of an external magnetic field and compared with the experimentally measured angular dependence of the Hanle effect. The comparison of the theoretical model with the experimental data reveals an enhanced spin polarization of the lead nuclei, whose mean spin exceeds several times the mean spins of localized electrons and holes. This unexpectedly strong spin polarization is explained by the interaction of the lead nuclei with excitons having a high degree of spin orientation due to their short lifetime after excitation by circularly-polarized light. The dynamic polarization of the quadrupole-split halogen spins manifests itself via the magnetic field they produce at the lead nuclei. This field maintains the magnetization of the lead nuclei at zero external magnetic field. The dynamics of the nuclear spin polarization is measured under optical pumping and in the dark, yielding a nuclear spin-lattice relaxation time on the order of 10 seconds.

cond-mat.mes-hall↗

arXiv2025

Hyperfine interaction of electrons confined in CsPbI$_3$ nanocrystals with nuclear spin fluctuations

The coherent spin dynamics of electrons are investigated for CsPbI$_3$ perovskite nanocrystals in a glass matrix using time-resolved Faraday ellipticity. In nanocrystals with a diameter of about 11 nm, the Larmor precession frequency has a linear dependence on magnetic field corresponding to the electron Landé $g$-factor of 2.07. We find a finite Larmor precession frequency at zero magnetic field, corresponding to the electron spin splitting of $0.8$ $μ$eV. This splitting is explained by the hyperfine interaction with nuclear spin fluctuations. Our model analysis shows that the hyperfine interaction for the conduction band electrons is contributed both by the $p$-orbitals of the lead atoms and by the $s$-orbitals of the iodine atoms, with the leading contribution to the hyperfine field fluctuations coming from iodine. This fact agrees well with the 9% iodine contribution to the Bloch amplitude of the conduction band, obtained by DFT calculations. From these findings, the atomic hyperfine constant for the $5s$-orbital of iodine is evaluated as 190 $μ$eV.

cond-mat.mes-hall↗

arXiv2025

Polarization- and time-resolved nonlinear multi-photon spectroscopy for confocal microscopy of semiconductor nanostructures

We present a versatile confocal microscopy setup for optical second harmonic generation (SHG) and multi-photon spectroscopy that enables polarization-resolved studies of semiconductor bulk crystals and low-dimensional structures. The system offers full polarization control in both excitation and detection, spatial scanning with micrometer resolution, and spectrally tunable excitation over a broad energy range from 0.5 to 4.0 eV, using femtosecond and picosecond laser pulses. Samples are mounted in a helium-flow cryostat, allowing temperature control from 4 to 300 K. Magnetic fields up to 0.625 T can be applied in the Voigt geometry via an electromagnet. The nonlinear optical signals are analyzed using a high-resolution spectrometer with a spectral resolution of 60 $μ$eV. We demonstrate the potential of the setup by means of SHG polarization tomography measurements on a Cu$_2$O crystal as well as through a SHG spectral scan of a ZnSe crystal over a wide energy range from 1.4 to 3.1 eV. Polarization-resolved confocal SHG mapping of various twisted mono- and bilayer MoS$_2$ structures is also presented. In addition, time-resolved two-color pump-probe experiments are shown for a Cs$_2$AgBiBr$_6$ crystal, illustrating the potential of the system for investigating coherent exciton and phonon dynamics.

cond-mat.mtrl-sci↗

arXiv2025

Interaction between Rydberg Excitons in Cuprous Oxide Revealed through Second Harmonic Generation

We report experimental and theoretical investigations of interacting excitons of the yellow series in cuprous oxide (Cu$_2$O) with principal quantum numbers up to $n=7$ by means of second harmonic generation (SHG). Using picosecond pulsed laser excitation up to 10 GW/cm$^2$ peak intensity we observe a pronounced change of the spectra with increasing pump laser intensity: an energetic shift to lower absolute energies and a spectral broadening, while the absolute intensity for low powers scales with the square of the pump power, but saturates at higher powers. Concomitant with SHG we determined the density of the excitons excited by the ps pulse by measuring the two-photon absorption directly. This allows to derive quantitative values for the exciton-exciton interaction. Surprisingly, the results disagree both in magnitude and scaling with principal quantum number with those calculated by state-of-the art atomic-like van der Waals interaction theory. As a possible screening by an electron-hole plasma created by three-photon absorption into blue and violet band states could be ruled out, our results point toward fundamental differences between excitons and atoms.

cond-mat.mtrl-sci↗

arXiv2025

Confined acoustic phonons in CsPbI3 nanocrystals explored by resonant Raman scattering on excitons

Optical properties of the lead halide perovskites nanocrystals are controlled by confined excitons and rich spectrum of confined acoustic and optical phonons. We study experimentally and theoretically the exciton-phonon interaction in CsPbI3 perovskite nanocrystals embedded in a glass matrix. Energies of phonon modes allowed by selection rules are detected by resonant Raman scattering for nanocrystals with sizes of 4-13 nm, covering exciton energies of 1.72-2.25 eV. While optical phonon energies remain size-independent, the energies of confined acoustic phonons increase in smaller nanocrystals. Acoustic phonons are modeled within the continuum approximation using elastic constants computed by density functional theory. The model provides the energy spectra of confined phonons for nanocrystals of various shapes (cube, sphere, spheroid), crystal symmetries (orthorhombic and tetragonal), and sizes. Exciton confinement restricts efficient coupling to only few phonon modes observable in Raman spectra. By comparing experimental data with model predictions, we conclude that the nanocrystals in our samples predominantly have spherical or spheroidal shapes.

cond-mat.mtrl-sci↗

arXiv2025

Efficient launch of shear phonons in photostrictive halide perovskites

Optical generation of transverse coherent phonons by femtosecond light pulses is appealing for high-speed sub-THz active control of material properties. Lead-free double perovskite semiconductors, such as Cs2AgBiBr6, attract particular interest due to their cubic to tetragonal phase transition below room temperature and strong polaron effects from carrier-lattice coupling. Here, we reveal that the anisotropic photostriction in halide perovskites with tetragonal crystal structure represents an efficient non-thermal tool for generating transverse coherent phonons. In particular, we demonstrate that along with compressive strain, optical generation of photoexcited carriers leads to strong shear strain in Cs2AgBiBr6 below the phase transition temperature of 122 K. Using time-domain Brillouin spectroscopy, we observe coherent transverse and longitudinal acoustic phonons with comparable amplitudes in the tetragonal phase, while in the cubic phase only longitudinal phonons are generated. The polarization of the photoinduced transverse phonons is dictated by the projection of the c-axis on the surface plane, which leads to a prominent anisotropic polarization response in the detection. The generated strain pulses correspond to transverse acoustic soft eigenmodes with a strong temperature dependence of dispersion, which provides an additional degree of freedom for active hypersonic control.

cond-mat.mtrl-sci↗