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Ayan A. Zhumekenov

Publications and source records attributed to Ayan A. Zhumekenov.

8 recordsLinked to original sources

Second-order Raman and anharmonic lattice dynamics in lead-halide perovskites

We explore the microscopic origin of THz-driven lattice dynamics in methylammonium lead bromide CH$_3$NH$_3$PbBr$_3$ using two-dimensional THz Kerr-effect spectroscopy. The analysis of the experiment enables discrimination between competing nonlinear excitation mechanisms and reveals that the dominant pathway is phonon-mediated rather than purely photonic. In particular, we argue that the commonly observed 1.15~THz Raman-active $A_g$ mode is not excited directly by the THz electric field. Instead, it emerges through cubic anharmonic coupling to an infrared-active phonon at 0.68~THz. Furthermore, a satellite feature at 1.36~THz is identified as a two-phonon Raman response of the same infrared-active mode. The observation of strong quadratic coupling involving the infrared-active phonon suggests an unconventional form of electron-phonon dressing present in lead-halide perovskites.

cond-mat.mtrl-sci↗

Alignment-free ultra-broadband parametric frequency conversion in lead-halide perovskites

Lead-halide perovskites were demonstrated to exhibit some of the largest known optical nonlinearities, yet their potential for frequency conversion remains largely untapped. Here we demonstrate ultra-broadband four-wave mixing of near- and mid-infrared femtosecond pulses in thick single-crystal LHPs, generating bright, coherent, and highly collimated emission across an exceptionally wide continuous tuning range without phase-matching engineering, angular alignment, or dispersion optimization. Time resolved measurements reveal that the emission originates near the crystal surfaces, where phase-matching constraints are relaxed, while the unusually large intrinsic $χ^{(3)}$ response preserves efficient and directional frequency conversion despite the strongly localized interaction volume. These results position LHPs as a powerful bulk platform for ultra-broadband nonlinear photonics, opening a pathway toward compact, alignment-free architectures for ultrafast frequency conversion.

cond-mat.mtrl-sci↗

Observation of Analogue Dynamic Schwinger Effect and Non-Perturbative Light Sensing in Lead Halide Perovskites

Dielectric breakdown of physical vacuum (Schwinger effect) is the textbook demonstration of compatibility of Relativity and Quantum theory. Although observing this effect is still practically unachievable, its analogue generalizations have been shown to be more readily attainable. This paper demonstrates that a gapped Dirac semiconductor, methylammonium lead-bromide perovskite (MAPbBr$_3$), exhibits analogue dynamical Schwinger effect. Tunneling ionization under deep sub-gap mid-infrared irradiation leads to intense photoluminescence in the visible range, in full agreement with quasi-adiabatic theory. In addition to revealing a gapped extended system suitable for studying the analogue Schwinger effect, this observation holds great potential for non-perturbative field sensing, i.e., sensing electric fields through non-perturbative light-matter interactions. First, this paper illustrates this by measuring the local deviation from the nominally cubic phase of a perovskite single crystal, which can be interpreted in terms of frozen-in fields. Next, it is shown that analogue dynamic Schwinger effect can be used for nonperturbative amplification of non-parametric upconversion process in perovskites driven simultaneously by multiple optical fields. This discovery demonstrates the potential for material response beyond perturbation theory in the Schwinger regime, offering extremely sensitive light detection and amplification across an ultrabroad spectral range not accessible by conventional devices.

cond-mat.mes-hall↗

Spontaneous flexoelectricity in cubic lead-halide perovskite MAPbBr$_3$

Lead-halide perovskites exhibit remarkable efficiency in photovoltaics, driven by exceptionally long carrier diffusion lengths and recombination times. Paradoxically, this performance persists even in defect-rich, solution-grown samples. Here, we use a suite of optical and charge transport measurements to reveal that key optoelectronic properties of perovskites arise from localized flexoelectric polarization confined to the interfaces between domains of spontaneous strain, present even in nominally cubic single crystals. This insight provides a microscopic link between structural composition and charge transport in these materials, reconciling conflicting prior observations and offering new design principles for perovskite-based solar cells.

cond-mat.mtrl-sci↗

Bond polarizability as a probe of local crystal fields in hybrid lead-halide perovskites

A rotating organic cation and a dynamically disordered soft inorganic cage are the hallmark features of hybrid organic-inorganic lead-halide perovskites. Understanding the interplay between these two subsystems is a challenging problem but it is this coupling that is widely conjectured to be responsible for the unique behavior of photo-carriers in these materials. In this work, we use the fact that the polarizability of the organic cation strongly depends on the ambient electrostatic environment to put the molecule forward as a sensitive probe of local crystal fields inside the lattice cell. We measure the average polarizability of the C/N--H bond stretching mode by means of infrared spectroscopy, which allows us to deduce the character of the motion of the cation molecule, find the magnitude of the local crystal field and place an estimate on the strength of the hydrogen bond between the hydrogen and halide atoms. Our results pave the way for understanding electric fields in lead-halide perovskites using infrared bond spectroscopy.

cond-mat.mes-hall↗

Effective model for studying optical properties of lead-halide perovskites

We use general symmetry-based arguments to construct an effective model suitable for studying optical properties of lead-halide perovskites. To build the model, we identify an atomic-level interaction between electromagnetic fields and the spin degree of freedom that should be added to a minimally-coupled $\mathbf{k\cdot p}$ Hamiltonian. As a first application, we study two basic optical characteristics of the material: the Verdet constant and the refractive index. Beyond these linear characteristics of the material the model is suitable for calculating non-linear effects such as the third-order optical susceptibility. Analysis of this quantity shows that the geometrical properties of the spin-electric term imply isotropic optical response of the system, and that optical anisotropy of lead-halide perovskites is a manifestation of hopping of charge carriers. To illustrate this, we discuss third-harmonic generation.

cond-mat.mes-hall↗

Spin-Electric Coupling in Lead Halide Perovskites

Lead-halide perovskites enjoy a number of remarkable optoelectronic properties. To explain their origin, it is necessary to study how electromagnetic fields interact with these systems. We address this problem here by studying two classical quantities: Faraday rotation and the complex refractive index in a paradigmatic perovskite CH$_3$NH$_3$PbBr$_3$ in a broad wavelength range. We find that the minimal coupling of electromagnetic fields to the k$\cdot$p Hamiltonian is insufficient to describe the observed data even on the qualitative level. To amend this, we demonstrate that there exists a relevant atomic-level coupling between electromagnetic fields and the spin degree of freedom. This spin-electric coupling allows for quantitative description of a number of previous as well as present experimental data. In particular, we use it here to show that the Faraday effect in lead-halide perovskites is dominated by the Zeeman splitting of the energy levels, and has a substantial beyond-Becquerel contribution. Finally, we present general symmetry-based phenomenological arguments that in the low-energy limit our effective model includes all basis coupling terms to the electromagnetic field in the linear order.

cond-mat.other↗

Visualizing buried local carrier diffusion in halide perovskite crystals via two-photon microscopy

Halide perovskites have shown great potential for light emission and photovoltaic applications due to their remarkable electronic properties and compatibility with cost-effective fabrication techniques. Although the device performances are promising, they are still limited by microscale heterogeneities in their photophysical properties. In particular, the relation between local heterogeneities and the diffusion of charge carriers at the surface and in the bulk, crucial for efficient collection of charges in a light harvesting device, is not well understood. Here, a photoluminescence tomography technique is developed in a confocal microscope using one- and two-photon excitation to distinguish between local surface and bulk diffusion of charge carriers in methylammonium lead bromide single crystals. The local temporal diffusion is probed at various excitation depths to build statistics of local electronic diffusion coefficients. The measured values range between 0.3 to 2 $cm^2.s^{-1}$ depending on the local trap density and the morphological environment - a distribution that would be missed from analogous macroscopic or surface-measurements. Tomographic images of carrier diffusion were reconstructed to reveal buried crystal defects that act as barriers to carrier transport. This work reveals a new framework to understand and homogenise diffusion pathways, which are extremely sensitive to local properties and buried defects.

cond-mat.mtrl-sci↗