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Jacek J. Jasieniak

Publications and source records attributed to Jacek J. Jasieniak.

6 recordsLinked to original sources

Harnessing Linear and Nonlinear Optical Responses in Ferroelectric LaMoN$_3$ for Enhanced Photovoltaic Efficiency

Nitride perovskites are an emerging class of materials predicted to exhibit diverse functional properties, yet remain underexplored due to synthesis challenges of oxygen-free nitrides. Recently, LaMoN$_3$ has been reported as an oxygen-free nitride perovskite with polar symmetry, exhibiting excellent dynamic stability and ferroelectric properties under moderate pressure. However, its phase stability, linear and non-linear optical response, excitonic and polaronic behavior, and efficiency under high pressure remain unexplored. Applying pressure enables systematic tuning of the electronic structure properties, thereby facilitating the identification of phases optimized for either linear or nonlinear optical responses. Therefore, in this work, we systematically investigate these properties of LaMoN$_3$ up to 40 GPa using first-principles methods, including density functional theory, density functional perturbation theory, many-body perturbation theory (namely G$_0$W$_0$ and BSE), and tight binding approximation model. Our study shows that LaMoN$_3$ remains dynamically stable and retains its single-phase structure up to 40 GPa. The compound exhibits an indirect bandgap that decreases from 2.17 eV (0 GPa) to 1.45 eV (40 GPa) at the G$_0$W$_0$@PBE level. Using the BSE, we find that pressure enhances the SLME while lowering the exciton binding energy, both favorable for photovoltaic applications. The bulk photovoltaic efficiency trend with pressure mimics the behavior of the shift current density J$_SC$ , peaking near 15 GPa before declining at higher pressures due to a diminished nonlinear shift current response. These results highlight pressure-tuned regimes to enhance photovoltaic performance. We thereby propose multi-junction device, combining absorber layers optimized for linear and nonlinear optical currents, together boosting solar energy conversion through complementary mechanisms.

cond-mat.mtrl-sci↗

Hybrid Improper Ferroelectricity and Moiré Superlattices-induced Exciton Quantization in Layered 2D Halide Perovskite

2D Ruddlesden-Popper perovskites are compelling platforms for quantum-confined optoelectronics. However, polar order in iodide composition remains rare under ambient conditions, and the mechanistic origin of anomalous photoluminescence in this class of perovskite is still speculative. Here, we demonstrate that solution-grown $(PA)_2FAPb_2I_7$ single crystals develop an inadvertent moiré superlattice through pseudo-merohedral twinning, driven by hybrid improper ferroelectricity in which trilinear mode coupling between two primary zone-boundary modes ($X_2^+$ and $X_3^-$) and a secondary $Γ_4^-$ polar displacement simultaneously breaks inversion symmetry and imposes a ca. 5.17° rotational misalignment between adjacent layers. This symmetry breaking activates one of the highest piezoelectric coefficients $d_{33}$ (ca. 20 pm/V) reported among 2D perovskites. This misalignment generates a moiré superlattice that undergoes a thermally driven commensurate-incommensurate transition, switching between a periodic confinement potential that quantizes excitons into an equidistant photoluminescence ladder at 123 K and a disordered incommensurate phase with broadened emission at 298 K. These emissions are attributed to moiré-confined excitons, resolving a longstanding debate on anomalous secondary photoluminescence in layered 2D perovskites and opening pathways to twistronics, photoferroelectrics and piezo-optoelectronic devices.

cond-mat.mtrl-sci↗

Lead-free Magnetic Double Perovskites for Photovoltaic and Photocatalysis Applications

The magnetic spin degrees of freedom in magnetic materials serve as additional capability to tune materials properties, thereby invoking magneto-optical response. Herein, we report the magneto-optoelectronic properties of a family of lead-free magnetic double perovskites Cs_{2}AgTX_{6} (T = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu; X=Cl, Br, I). This turns out to provide an extremely fertile series, giving rise to potential candidate materials for photovoltaic(PV) applications. In conjunction with high absorption coefficient and high simulated power conversion efficiency for PV applications, few compounds in this series exhibit novel magnetic character useful for spintronic applications. The interaction between magnetism and light can have far-reaching results on the photovoltaic properties as a consequence of the shift in the defect energy levels due to Zeeman effect. This subsequently affects the recombination rate of minority carriers, and hence the photoconversion efficiency. Moreover, the distinct ferromagnetic and anti-ferromagnetic ordering driven by hybridization and super-exchange mechanism can play a significant role to break the time-reversal and/or inversion symmetry. Such a coalescence of magnetism and efficient optoelectronic response has the potential to trigger magnetic/spin anomalous photovoltaic (non-linear Optical) effect in this Cs$_{2}$AgTX$_{6}$ family. These insights can thus channelize the advancement of lead-free double perovskites in magnetic/spin anomalous photovoltaic field as well.

cond-mat.mtrl-sci↗

Clearly Discriminate the Continuum Band and Exciton State of the Hybrid Lead Bromide Perovskite

Electronic states of the hybrid perovskite enable their promising applications as distinctive optoelectronic materials. The understanding of their electronic structures and charge characters remains highly controversial. The electronic mechanism such as reabsorption, Urbach tail and indirect band for interpreting dual-peak emissions is one of the controversial focuses. Herein, we report that through heterojunction enhanced exciton dissociation and global tracing of multiple radiative electronic states across wide temperature regions, we have succeeded in directly observing free carrier emissions from the hybrid lead bromide perovskite and clearly discriminating the direct continuum band and exciton states. The widely-concerned dual-peak emissions are clarified to be excitonic, arising from two types of exciton states of the perovskite. These excitons possess giant binding energies and superior phase stability compared to conventional inorganic semiconductors, providing important implications for exploiting the excitonic mechanism for realizing novel optoelectronic applications.

physics.app-ph↗

Low-threshold Stimulated Emission of Hybrid Perovskites at Room Temperature through Defect-Mediated Bound Excitons

Excitonic stimulated emission provides a promising mechanism and route to achieve low-threshold semiconductor lasers for micro-nano optoelectronic integrations. However, excitonic stimulated emission from quantum structure-free semiconductors has rarely been realised at room temperature due to the phase transition between excitonic and electron-hole plasma states. Herein, we show that through trap-state and band-edge engineering, bound exciton states can be stabilised within the hybrid lead bromide perovskite. Under modest pumping conditions, these states enable stimulated emission behaviour that exhibits a low threshold carrier density of only 1.6*1017 cm-3, as well as a high peak gain coefficient of ~1300 cm-1. This is the first time that bound exciton stimulated emission has been realised at room temperature from a quantum structure-free semiconductor. Not only does this open up new research horizons for perovskite materials, but also it has important implications for semiconductor excitonic physics and the development of next-generation optoelectronic applications.

physics.app-ph↗

Identification of Free and Bound Exciton States and Their Phase-Dependent Trapping Behavior in Lead Halide Perovskites

In this work we probe the sub-gap energy states within polycrystalline and single crystal lead halide perovskites to better understand their intrinsic photophysics behaviors. Through combined temperature and intensity-dependent optical measurements, we reveal the existence of both free and bound exciton contributions within the sub-gap energy state manifold. The trapping and recombination dynamics of these excitons is shown to be strongly dependent on the structural phase of the perovskite. The orthorhombic phase exhibits ultrafast exciton trapping and distinct trap emission, while the tetragonal phase gives low monomolecular recombination velocity and capture cross-sections (~10-18 cm2). Within the multiphonon transition scenario, this suppression in charge trapping is caused by the increase in the charge capture activation energy due to the reduction in electron-lattice interactions, which can be the origin for the unexpected long carrier lifetime in these material systems.

cond-mat.mtrl-sci↗