arXiv subjects

Sridhar Sahu

Publications and source records attributed to Sridhar Sahu.

15 recordsLinked to original sources

arXiv2026

Strain-Driven Electronic and Catalytic Modulation of g-C3N4/GeS van der Waals heterostructure for Photocatalytic Water Splitting

Photocatalytic water splitting offers a viable pathway for sustainable hydrogen production. In this study, first-principles density functional theory calculations were performed to explore the strain-dependent photocatalytic behaviour of a two-dimensional g-C3N4/GeS heterostructure. The heterostructure shows type-II band alignment with an indirect band gap of 2.17 eV, smaller than those of the individual g-C3N4 (2.81 eV) and GeS (3.31 eV) monolayers. Biaxial tensile strain up to 3% effectively modulates the band gap and band edge positions, allowing suitable alignment with water redox potentials. The calculated Gibbs free energy for the hydrogen evolution reaction ({\Delta}GHER) is 0.2 eV for the pristine heterostructure and approaches near-thermoneutral values (-/+ 0.1 eV) under +1% and +2% strain. Meanwhile, the OER overpotential decreases from 2.17 V to 0.97 V with increasing strain. AIMD simulations and optical absorption in the visible region confirm the thermodynamic stability and promising photocatalytic potential of the heterostructure for hydrogen generation.

cond-mat.mtrl-sci↗

arXiv2026

First-Principles Investigation of 2D Copper Boride as a High-Performance Anode for Lithium-Ion Batteries

In this study, we investigate the two-dimensional copper boride, Cu$_8$B$_{14}$, as a possible anode material for lithium-ion batteries using first-principles calculations. We found that the structural integrity of the monolayer was preserved even at elevated temperatures, while electronic calculations confirm the metallic character of the pristine and Li-loaded systems. On systematic lithiation on Cu$_8$B$_{14}$ a specific capacity of 430mAhg$^{-1}$ was obtained. A Li diffusion barrier of 0.32eV for the most favourable path, along with a diffusivity of approximately $2.26 \times 10^{-5}$cm$^2$s$^{-1}$ was obtained. The open-circuit voltage of 0.53 V falls within the optimal anode range of 0.1--1.0 V. These combined characteristics point to Cu$_8$B$_{14}$ as a compelling candidate for advanced battery anodes. Furthermore, to understand the defect and its effect on different parameters, we investigated an experimentally identified line-defect configuration of copper boride. The line defect monolayer retains a theoretical capacity of about 385mAhg$^{-1}$, while the introduced line defect further reduces the Li migration barrier to 0.21eV, yielding an enhanced macroscopic diffusivity of $\sim$5.6$\times$10$^{-4}$cm$^{2}$s$^{-1}$ and confirming that structural defects accelerate Li-ion transport kinetics in this material.

cond-mat.mtrl-sci↗

arXiv2025

First Principles study of Photocatalytic Water Splitting in BO Monolayer: Effect of Strain and Surface Functionalization

Light element based two dimensional (2D) materials are promising photocatalysts for hydrogen production via water splitting. Boron oxide (BO) is a recently synthesized 2D monolayer which has yet to be thoroughly explored for its potential applications. In this article, using first principles calculations, we report, for the first time, the visible-light photocatalytic activity of a BO monolayer for water splitting under mechanical strain and surface modification with single- and double-atom decorations (C, N, Si, Ge, P, As). The pristine BO monolayer exhibits an indirect band gap of 3.8 eV with band edges spanning the water redox potentials, but its optical absorption lies in the UV region (~ 4.5 eV). Strain engineering tunes the band gap and band alignment with a minimal shifting in the optical absorption (~0.5 eV). Single atom decoration produces a metallic state for elements like N, P, As, and an insulating state for single C, Si, Ge with a partial shifting in optical absorption. In contrast, double atom decoration produces substantial band gap reduction, improved band alignment, a pronounced red-shift in optical absorption into the visible range (1.6 to 3.2 eV) thus satisfying the criteria for water splitting. The stability of all the adsorbed configurations was confirmed by negative formation energy and ab-initio molecular dynamics simulations. These findings suggest BO monolayer functionalization can improve photocatalytic efficiency, providing hydrogen generation insights.

cond-mat.mtrl-sci↗

arXiv2025

Unraveling the Surface Stability and Chemical Reactivity of Aza-Triphenylene Monolayer under O$_2$ and H$_2$O Exposure

Environmental oxidation has a great impact in tuning the physical, chemical and electronic properties of two-dimensional (2D) monolayers which can affect their practical applications in nanoscale engineering devices under ambient conditions. aza-triphenylene is a recently synthesized 2D materials whose practcal applications have not been systematically studied yet. In this study, we report for the first time, the adsorption and dissociation of O$_2$ and H$_2$O molecules on the surface of 2D aza-triphenylene monolayer through first principles calculations in combination with climbing image nudged elastic band (CINEB) method. The results indicates that both the O$_2$ and H$_2$O molecules weakly interact over the monolayer surface with an adsorption energy -0.16 eV and -0.37 eV respectively. In contrast, both the molecules exhibit resistance for dissociation due to the formation of energy barriers. The transition path indicates that molecular oxygen experience two energy barriers (0.16 ev and 1.22 eV) before getting dissociated atomic oxygen. However, the dissociation of H$_2$O requires larger energy barrier (2.3 eV and 0.86 eV) due to breaking of covalent bonds and transfer of hydrogen. The strong chemical adsorption of atomic oxygen and H$^+$/OH$^-$ ions is due to the significant charge transfer from monolayer to the adsorbate as evidenced from the charge density difference and Bader charge analysis. Moreover, the dissociated configuration exhibit a larger band gap as compared to the pristine aza-triphenylene due to the strong hybridization between the p states of carbon and oxygen. our work predicts the robustness of azatriphylene monolayer against oxygen/water exposer thus ensuring their stability for device applications using these materials.

cond-mat.mtrl-sci↗

arXiv2024

Feasibility of Li decorated Si6C14 and Si8C12 nanocages as promising hydrogen storage media: A computational study

This article presents the reversible hydrogen storage capacities of Li-decorated Si6C14 and Si8C12 using Density Functional Theory (DFT). The chemical stabilities of the designed Si6C14Li6 and Si8C12Li4 nanocages are investigated using HOMO-LUMO gaps and various global reactivity descriptors such as chemical hardness and electrophilicity index. Our study reveals that each Li atom decorated over the designed Si6C14 and Si8C12 nanocages can hold up to 5H2 molecules with adsorption energy lying in the optimum range of 0.14-0.085 eV, thereby yielding an overall gravimetric density of 13.8% and 9.2% respectively. The interaction between adsorbed H2 molecules and the Li metal sites is found to occur via non-covalent and closed shell type of interaction. The H2 molecules are adsorbed in a quasi-molecular fashion with elongated bond length. The molecular dynamics study reveals that most of the H2 molecules get desorbed from the designed host nanocages at 300K without causing any significant structural changes, which confirms their reversibility. When the adsorption and desorption conditions are set at 100K/60bar and 240K/1bar respectively, the practical storage gravimetric densities of Si6C14Li6 and Si8C12Li4 cages are estimated to be 13.73 wt% and 9.08 wt%, which are relatively high in comparison to the US-DOE target of 5.5 wt% by the year 2020. Hence, the computationally designed Si6C14Li6 and Si8C12Li4 nanocages can be regarded as prospective systems for hydrogen storage applications.

cond-mat.mtrl-sci↗

arXiv2023

Hydrogen storage in Li functionalized [2,2,2]paracyclophane at cryogenic to room temperatures: A computational quest

In this work, we have studied the hydrogen adsorption-desorption properties and storage capacities of Li functionalized [2,2,2]paracyclophane (PCP222) using dispersion-corrected density functional theory and molecular dynamic simulation. The Li atom was found to bond strongly with the benzene ring of PCP222 via Dewar interaction. Subsequently, the calculation of the diffusion energy barrier revealed a significantly high energy barrier of 1.38 eV, preventing the Li clustering on PCP222. The host material, PCP222-3Li adsorbed up to 15H2 molecules via a charge polarization mechanism with an average adsorption energy of 0.145 eV/5H2, suggesting a physisorption type of adsorption. The PCP222 functionalized with three Li atom showed maximum hydrogen uptake capacity up to 8.32 wt%, which was fairly above the US-DOE criterion. The practical storage estimation revealed that the PCP222-3Li desorbed 100% of adsorbed H2 molecules at the temperature range of 260 K-300 K and pressure range of 1-10 bar. The maximum H2 desorption temperature estimated by the Vant-Hoff relation was found to be 219 K and 266 K at 1 bar and 5 bar, respectively. The ADMP molecular dynamics simulations assured the reversibility of adsorbed H2 and the structural integrity of the host material at sufficiently above the desorption temperature (300K and 500K). Therefore, the Li-functionalized PCP222 can be considered as a thermodynamically viable and potentially reversible H2 storage material below room temperature.

physics.chem-ph↗

arXiv2023

Transition from chemisorption to physisorption of H2 on Ti functionalized [2,2,2]paracyclophane: A computational search for hydrogen storage

In this work, we studied the hydrogen adsorption-desorption properties and storage capacities of Ti functionalized [2,2,2]paracyclophane (PCP222) using density functional theory and molecular dynamic simulation. The Ti atom was bonded strongly with the benzene ring of PCP222 via Dewar interaction. Subsequently, the calculation of the diffusion energy barrier revealed a significantly high energy barrier of 5.97 eV preventing the Ti clustering over PCP222 surface. On adsorption of hydrogen, the first H2 molecule was chemisorbed over PCP222 with a binding energy of 1.79 eV with the Ti metals. Further addition of H2 molecules, however, exhibited their physisorption over PCP222-Ti through the Kubas type H2 interaction. The charge transfer mechanism during the hydrogen adsorption was explored by the Hirshfeld charge analysis and electrostatic potential map, and the PDOS, and Baders topological analysis revealed the nature of the interaction between Ti and H2. The PCP222 functionalized with three Ti atoms showed a maximum hydrogen uptake capacity of up to 7.37 wt%, which was fairly above the US-DOE criterion. The practical H2 storage estimation revealed that at ambient conditions, the gravimetric density of up to 6.06 wt% H2 molecules could be usable, and up to 1.31 wt% of adsorbed H2 molecules were retained with the host. The ADMP molecular dynamics simulations assured the reversibility by desorption of adsorbed H2 and the structural integrity of the host material at sufficiently above the desorption temperature (300K and 500K). Therefore, the Ti-functionalized PCP222 can be considered as a thermodynamically viable and potentially reversible H2 storage material.

physics.chem-ph↗

arXiv2022

Computational Design of Crescent Shaped Promising NonFullerene Acceptors with 2,3-quinoxaline,1,4-dihydro Core and Different Electron-withdrawing Terminal Units for Photovoltaic Applications

This study aims to design a series of non-fullerene acceptors (NFAs) for photovoltaic applications having 2,3-quinoxalinedione,1,4-dihydro fused thiophene derivative as the core unit and 1,1-dicyanomethylene-3-indanone (IC) derivatives and different π-conjugated molecules other than IC as terminal acceptor units. All the investigated NFAs are found air-stable as the computed highest occupied molecular orbitals (HOMOs) are below the air oxidation threshold (ca. -5.27 eV vs. saturated calomel electrode). The studied NFAs can act as potential non-fullerene acceptor candidates as they are found to have sufficient open-circuit voltage (Voc) and fill factor (FF) ranging from 0.62-1.41 eV and 83%-91%, respectively. From the anisotropic mobility analysis, it is noticed that the studied NFAs except dicyano-rhodanine terminal unit containing NFA, exhibit better electron mobility than the hole mobility, and therefore, they can be more promising electron transporting acceptor materials in the active layer of an organic photovoltaic cell. From the optical absorption analysis, it is noted that all the designed NFAs have the maximum absorption spectra ranging from 597 nm-730 nm, which lies in the visible region and near infra-red (IR) region of the solar spectrum. The computed light-harvesting efficiencies for the PM6 (thiophene derivative donor selected in our study): NFA blends are found to lie in the range of 0.9589-0.9957, which indicates efficient light-harvesting by the PM6:NFA blends during photovoltaic device operation.

cond-mat.mtrl-sci↗

arXiv2022

High capacity H2 adsorption over Si4Lin (n=1-3) binary clusters: A DFT study

This paper presents a detailed study of the hydrogen adsorption properties of small silicon-lithium binary nanoclusters. The stabilities of H2 adsorbed binary clusters are assured by maximum hardness and minimum electrophilicity principle. Detail computational studies demonstrate that each Li in Si4Li, Si4Li2 and Si4Li3 binary clusters can adsorb a maximum of 5H2, 4H2 and 3H2 molecules respectively, resulting in a total gravimetric density of 7.8%, 11.3% and 12%. The adsorption energy is observed to be in the range of 0.12eV-0.17eV, indicating that the adsorption of H2 molecules occurs in a quasi-molecular fashion via physisorption. Hence, our study concludes that the studied silicon -lithium binary clusters can be considered as potential candidates for hydrogen storage systems.

physics.app-ph↗

arXiv2022

Reversible hydrogen storage capacity of Sc and Y functionalized [1,1]paracyclophane: Insights from density functional study

This work reports the hydrogen storage, and delivery capacities of Sc and Y functionalized [1,1]paracyclophane using dispersion corrected density functional theory calculations. The Sc and Y atoms are bind strongly with benzene rings of [1,1]paracyclophane. Each Sc and Y atom functionalized over [1,1]paracyclophane adsorb up to 6 H2 molecules via Kubas interaction achieving maximum gravimetric density up to 8.22 wt% and 6.33 wt%, respectively. The calculated average hydrogen adsorption energy (0.36 eV) is lower than the chemisorption but higher than the physisorption process. The kinetic stabilities are verified through the HOMO-LUMO gap and different global reactive descriptors. ADMP molecular dynamics simulations reveal the reversibility of adsorbed H2 molecules at sufficiently above the room temperature and the solidity of host material at 500 K. Average Van't Hoff desorption temperature for Sc and Y decorated system was calculated to be 439 K and 412 K respectively at 1 atm of pressure. The estimated thermodynamically usable hydrogen capacities are found to be 5.92 wt% and 5.87 wt% of hydrogen which fulfil the hydrogen energy criteria (by 2025) of US-DOE. Hence, we believe that Sc and Y functionalized [1,1]paracyclophane can be considered as a thermodynamically viable, and potential reversible hydrogen storage materials at ambient environment.

physics.chem-ph↗

arXiv2021

Tuning from unipolar (p-type or n-type) to ambipolar charge transport efficiency in bowl-shaped perylene-derivatives: a DFT study

A series of bowl-shaped dicyclopenta perylene (DCPP) derivatives have been theoretically constructed by indeno-substitution at the peri-positions of DCPP, and suitably functionalizing with aza-, fluoride and imide-groups to enhance the electron transport behavior in the materials. To further ensure the solubility and stability of these organic compounds, we incorporated triethylsilylethynyl (TES) groups in the designed structures. The factors such as degree of aromaticity, electronic structure, molecular packing motif, intermolecular charge coupling, and charge transfer rate are essential in determining the charge transporting ability. The low-lying LUMO-levels (< -4.0 eV) and high electron affinities (> 3.0 eV) of a few DCPPs ensure efficient electron injection from the metal electrodes. These molecules are arranged in bowl-in-bowl columnar packing, which is suitable for facilitating the intermolecular charge transport in the crystal. As a result, we observed enhanced hole-transport behavior in DCPP-9 (μh = 6.296 cm2V-1s-1), electron transport in DCPP-TES-6 (μe = 0.142 cm2V-1s-1) and ambipolar nature of DCPP-12 and DCPP-TES-12. The DCPP-derivatives are also optically active in the UV-visible region, which is confirmed from the TD-DFT analysis. Inspired from their non-centrosymmetric molecular geometry and optical activity, we also investigated their non-linear optical (NLO) responses, which may pave their way towards applications in photonics and optoelectronics.

cond-mat.mtrl-sci↗

arXiv2010

On the Nature of Optical Excitations in Hydrogenated Aluminium Cluster Al4H6: A Theoretical Study

In this paper, we present a theoretical investigation of photoabsorption spectrum of the newly synthesized hydrogenated cluster of aluminium, Al4H6. The calculations are performed within the wave-function-based semi-empirical method employing the complete neglect of differential overlap (CNDO) model, employing a large-scale configuration interaction (CI) methodology, and our results are found to be in very good agreement with the earlier ones obtained from the ab initio time-dependent density functional theory (TDDFT). We carefully analyse the many-particle wave functions of various excited states up to 8 eV, and find that they are dominated by single-particle band to band excitations. This is in sharp contrast to bare aluminium clusters, in general, and Al4, in particular, whose optical excitations are plasmonic in nature. We attribute this difference to be a consequence of hydrogenation.

physics.atm-clus↗

arXiv2009

Theory of Linear Optical Absorption in B_12 Clusters: Role of the geometry

Boron clusters have been widely studied theoretically for their geometrical properties and electronic structure using a variety of methodologies. An important cluster of boron is the B$_{12}$ cluster whose two main isomers have distinct geometries, namely, icosahedral ($I_{h}$) and quasi planar ($C_{3v}$). In this paper we investigate the linear optical absorption spectrum of these two B$_{12}$ structures with the aim of examining the role of geometry on the optical properties of clusters. The optical absorption calculations are performed using both the semi-empirical and the ab initio approaches. The semi-empirical approach uses a wave function methodology employing the INDO model Hamiltonian, coupled with large-scale configuration interaction (CI) calculations, to account for the electron-correlation effects. The \emph{ab initio} calculations are performed within a time-dependent-density-functional-theory (TDDFT) methodology. The results for the two approaches are in very good qualitative agreement with each other. Quantitatively speaking, results agree with each other in the lower energy region, while in the higher energy region, features predicted by the TDDFT approach are red-shifted as compared to the INDO-CI results. Both the approaches predict that the optical absorption begins at much lower energies in the icosahedral cluster as compared to the planar one, a fact which can be utilized in experiments to distinguish between the two geometries. At higher energies, both the isomers exhibit plasmon-like excitations. 73,1 4%

physics.atm-clus↗

arXiv2009

Probing Aromaticity of Borozene Through Optical and Dielectric Response: A Theoretical Study

In this work, we report electronic structure calculations aimed at computing the linear optical absorption spectrum, and static dipole polarizablity of a newly proposed boron-based planar aromatic compound borozene (B_12H_6$. For the purpose, we use the semiempirical INDO model Hamiltonian, accompanied by large-scale correlation calculations using the multi-reference singles-doubles configuration-interaction (MRSDCI) approach. We present detailed predictions about the energetics, polarization properties, and the nature of many-particle states contributing to various peaks in the linear absorption spectrum. Our results can be used to characterize this material in future optical absorption experiments. We also argue that one can deduce the aromaticity of the cluster from the optical absorption and static polarizability results.

physics.atm-clus↗

arXiv2008

Fortran 90 implementation of the Hartree-Fock approach within the CNDO/2 and INDO models

Despite the tremendous advances made by the ab initio theory of electronic structure of atoms and molecules, its applications are still not possible for very large systems. Therefore, semi-empirical model Hamiltonians based on the zero-differential overlap (ZDO) approach such as the Pariser-Parr-Pople, CNDO, INDO, etc. provide attractive, and computationally tractable, alternatives to the ab initio treatment of large systems. In this paper we describe a Fortran 90 computer program developed by us, that uses CNDO/2 and INDO methods to solve Hartree-Fock(HF) equation for molecular systems. The INDO method can be used for the molecules containing the first-row atoms, while the CNDO/2 method is applicable to those containing both the first-, and the second-row, atoms. We have paid particular attention to computational efficiency while developing the code, and, therefore, it allows us to perform calculations on large molecules such as C_60 on small computers within a matter of seconds. Besides being able to compute the molecular orbitals and total energies, our code is also able to compute properties such as the electric dipole moment, Mulliken population analysis, and linear optical absorption spectrum of the system. We also demonstrate how the program can be used to compute the total energy per unit cell of a polymer. The applications presented in this paper include small organic and inorganic molecules, fullerene C_60, and model polymeric systems, viz., chains containing alternating boron and nitrogen atoms (BN chain), and carbon atoms (C chain).

physics.atm-clus↗