arXiv subjects

Eduard Danilovskiy

Publications and source records attributed to Eduard Danilovskiy.

3 recordsLinked to original sources

arXiv2025

Separation of Hoke and Schottky effects for improvement of mixed halide perovskite solar cell stability

Ion migration in halide perovskites is a key factor limiting the operational stability of solar cells due to formation of halogen ion enriched domains and accumulation layers. The present work demonstrates the manifestation of ion migration in two ways via Hoke and Schottky effects. Both effects are induced by external exposure but have its peculiar way of solar cell performance degradation. We demonstrate the effects of ion migration on the device performance by measuring time dependent short-circuit current and different impedance characteristics that allow to see how charge-carrier separation property degrades. The Schottky effect leads to the rapid decrease of charge-carrier separation characteristic of solar cell while Hoke effect leads to the slow defect accumulation in the perovskite layer leading to the enhanced Shockley-Read-Hall recombination. Separation of these two effects can be realized by simple increase of transport layer thickness. A thick transport layer blocks losses of charge-carrier selectivity in a solar cell and leads to an enormous increase of T80 time, from 15 seconds up to 60 minutes.

cond-mat.mtrl-sci↗

arXiv2019

Dipolar cation accumulation at interfaces of perovskite light emitting solar cells

Ionic migration in organo-halide perovskites plays an important role in operation of perovskite based solar cells and light emitting diodes. Despite the ionic migration being a reversible process, it often leads to worsening of perovskite based device performance, hysteresis in current-voltage characteristics, and phase segregation in mixed halide perovskites being as the most harmful effect. The reason is in dynamical band structure changes, which controllable engineering would solve one of the biggest challenges for development of light-emitting solar cells. Here we demonstrate controllable band bending due to migration of both cation and anion ions in mixed halide perovskite devices. The band structure rearrangement is demonstrated in light emitting solar cells based on the perovskite with organic cations methylammonium (MA+) and formamidinium (FA+), possessing non-zero dipole momentum of 2.29 and 0.21 Debye, respectively, and with PEDOT:PSS and C60 transport layers having a high barrier of 0.8 eV for charge injection. Under applied external voltage MA+ and FA+ cations move towards the electron transport layer and form a dipole layer at the perovskite/electron transport interface, which lowers threshold voltage for electroluminescence down to 1.7 V for MAPbBr2I and 2.6 V for FAPbBr2I, whereas monohalide perovskite MAPbBr3 does not demonstrate such behavior. This ability to in-situ change the device band structure paves the way developing of dual-functional devices based on simple design. It also makes mixed halide perovskites more flexible than mono halides ones for developing different optoelectronic devices without the use of special types of work function modifying transport materials.

physics.app-ph↗

arXiv2018

Mixed Halide Perovskite Light Emitting Solar Cell

Organic-inorganic halide perovskites recently have emerged as a promising material for highly effective light-emitting diodes (LEDs) and solar cells (SCs). Despite efficiencies of both perovskite SCs and LEDs are already among the best, the development of a perovskite dual functional device that is capable of working in these two regimes with high efficiencies is still challenging. Here we demonstrate that the dual functional device based on mixed halide perovskite CH3NH3PbBr2I can be switched from SC to LED with low threshold voltage Vth < 2 V by exposing to Sun at open circuit Voc or at small bias voltage of Vpol ~ 1 - 2 V. Such photo-poling creates in-situ p-i-n junction via methylammonium (CH3NH3+, MA+) and I-/Br- ions migration to interfaces, lowering charge injection barriers, and self-balancing injection currents in perovskite LED. We show that before the photo-poling, the electroluminescence (EL) is highly unstable in LED regime, whereas after the photo-poling, stabilized EL exhibits unusual dynamics, increasing with time and poling cycle number, while Vth and injection current decrease with cycling runs. Additionally, photo-induced and current-induced halide segregation accumulates with cycling, that is found beneficial for LED, increasing its efficiency and brightness, but reversibly degrading photovoltaic (PV) performance, which can be easily recovered.

physics.app-ph↗