arXiv subjects

Monojit Bag

Publications and source records attributed to Monojit Bag.

4 recordsLinked to original sources

arXiv2026

Unraveling the Roles of Shallow, Deep and Auger Trapping in Charge Carrier Recombination in Triple-Cation Perovskites

Understanding charge-carrier recombination in metal halide perovskites is essential for accurately identifying the factors limiting solar cell efficiency, yet it remains challenging due to the interplay of multiple competing processes. Here, we combine time-resolved photoluminescence and excitation dependent photoluminescence quantum yield measurements over a wide range of fluences and repetition rates to investigate recombination dynamics in triple-cation perovskite thin films. By jointly analyzing these multidimensional datasets, we develop a unified model that quantitatively reproduces both photoluminescence decays and absolute quantum yields across all excitation conditions. Our results reveal the coexistence of deep and shallow traps, as well as a second-order nonradiative recombination pathway attributed to Auger-assisted trapping. Importantly, this mechanism dominates under one-sun illumination, making it a critical limiting factor for photovoltaic performance. These findings provide a comprehensive framework for understanding recombination in perovskites and highlight the importance of higher-order defect-mediated processes in determining their efficiency.

cond-mat.mtrl-sci↗

arXiv2026

An Interfacial Balance Rule Governs Binder-Electrolyte Coupling in Lead-Free Perovskite Energy Storage

Electrode binders are conventionally regarded as inert structural components. Here, we show that in lead-free perovskite supercapacitors, the binder defines the optimal electrolyte composition. Across a factorial matrix of poly(vinylidene fluoride) (PVDF) loadings and LiTFSI concentrations in CsSnCl$_3$ electrodes, the capacitance optimum shifts systematically with binder content along a single linear relationship, described by the Interfacial Balance Rule ($\lambda+\theta=1$), where $\lambda$ and $\theta$ are the normalized lithium-supply and polymer contributions at the optimized interfacial state. The same relationship holds for hybrid MASnCl$_3$, showing that the optimum is governed by the polymer-electrolyte interface rather than the perovskite lattice chemistry. Simulations using a pre-trained MACE machine-learned interatomic potential show that PVDF adopts a planar configuration on CsSnCl$_3$ and simultaneously interacts with cationic and anionic sites. This configuration homogenizes lithium adsorption energetics, introduces fluorine-mediated coordination, and confines lithium to a two-dimensional interfacial region while preserving lateral mobility. Tuning polymer coverage through surface density and chain length reveals a finite interfacial lithium accommodation capacity that marks the onset of out-of-plane aggregation. The Interfacial Balance Rule provides a macroscopic descriptor of this finite interfacial resource, balancing polymer-mediated lithium stabilization against limited accommodation space. Binder loading is therefore an active design parameter for polymer-regulated energy-storage interfaces.

cond-mat.mtrl-sci↗

arXiv2022

Raveling the Role of Dopants on Charge Carrier Kinetics of TiO$_2$ Electrodes using Electrochemical Impedance Spectroscopy

We synthesized the pure and co-doped titanium dioxide (TiO$_2$) electrodes via spin coating. We examined the optical and electronic properties of as-prepared thin film electrodes with co-doping of transition metals and non-metals. The co-doping of Cu, Zn, and N increase the absorption of the radiation in the visible region. The doping leads to the formation of defect states in the electrodes. In this article, we have studied the carrier kinetics in pristine and co-doped TiO2 electrodes. To study the role of dopants in carrier transport of the synthesized TiO2 based electrodes, the electrochemical impedance spectroscopy measurement is performed in the frequency range of 10-1 Hz to 106 Hz. The study reveals the influence of dopants on electron-hole recombination in the defect sites present in bulk and the transport mechanism of the electrons and ions to the surface/interface of the electrodes.

physics.app-ph↗

arXiv2010

Universality in Intensity Modulated Photocurrent in Bulk-Heterojunction Polymer Solar Cells

We observe a universal feature in the frequency dependence of intensity modulated photocurrent Iph based on studies of a variety of efficient bulk-heterojunction polymer solar cells (BHJ-PSCs). This feature of Iph appears in the form of a local maximum in the 5 kHz < frequency < 10 kHz range and is observed to be largely independent of the external parameters such as modulated light intensity (Lac), wavelength, temperature (T), and external field (EF) over a wide range. Simplistic kinetic models involving carrier generation, recombination and extraction processes are used to interpret the overall essential features of Iph and correlate it to the device parameters.

cond-mat.mtrl-sci↗