High Absorption Coefficient Research Articles

Enhanced photocatalytic hydrogen and oxygen evolution activity by two-dimensional van der Waals AlSb/ZnO heterostructure: A first-principles study

Photocatalytic water splitting facilitates the generation of green hydrogen energy by transforming renewable solar energy into chemical energy. This paper investigated the electronic, optical, and photocatalytic properties of AlSb/ZnO van der Waals (vDW) heterostructure using density functional theory. AlSb/ZnO, a semiconductor heterostructure with an indirect bandgap, was energetically stable with a formation energy of −0.4 eV as well as dynamically and thermally stable. The band edges of the 2D heterostructure maintained the essential redox energy levels for complete water splitting, allowing hydrogen and oxygen generation. Moreover, the heterostructure exhibited a high absorption coefficient in the visible region of the solar spectrum compared to the individual AlSb and ZnO monolayers. We revealed low barrier potential at neutral pH conditions for oxygen and hydrogen evolution reactions from the Gibbs free energy calculation without any external potential. Our study additionally showed the solar-to-hydrogen efficiency of 27.93% and a carrier utilization efficiency of 42.83%, indicating the AlSb/ZnO heterostructure as an excellent water splitting photocatalyst with remarkable potential for fuel cells and energy storage applications.

Advancements in halide perovskite photonics

Halide perovskites have emerged as a new class of materials for photoelectric conversion, attracting an ever-increasing level of attention within the scientific community. These materials are characterized by expansive compositional choices, ease of synthesis, an impressively high light absorption coefficient, and extended carrier recombination lifetimes. These attributes make halide perovskites an ideal candidate for future optoelectronic and photonic applications, including solar energy conversion, photodetection, electroluminescence, coherent light generation, and nonlinear optical interactions. In this review, we first introduce fundamental concepts of perovskites and categorize perovskite photonic devices by the nature of their fundamental mechanisms, i.e., photon-to-electron conversion devices, electron-to-photon conversion devices, and photon-to-photon devices. We then review the significant progress in each type of perovskite device, focusing on working principles and device performances. Finally, future challenges and outlook in halide perovskite photonics will be provided.

A DFT Study on the Structural, Electronic, Optical, and Elastic Properties of BLSFs XTi4Bi4O15 (X = Sr, Ba, Be, Mg) for Solar Energy Applications

For the first time, a theoretical investigation has been conducted into the structural, electrical, elastic, and optical properties of innovative bismuth-layered structure ferroelectric (BLSF) materials XTi4Bi4O15 (where X = Sr, Ba, Be, and Mg). For all of the calculations, PBE-GGA and the ultra-soft pseudopotential plane wave techniques have been implemented with the DFT-based CASTEP simulation tool. Based on the exchange correlation approximation, the calculations reveal that XTi4Bi4O15 (X = Sr, Ba, Be, and Mg) materials demonstrate direct band-gap semiconductor behavior with an estimated density functional fundamental gap in the range from 1.966 eV to 2.532 eV. The optical properties of these materials exhibit strong absorption and low reflection in the visible range. Moreover, the estimations of the elastic properties of the materials have shown mechanical stability and ductile behavior (due to B/G > 1.75), where G and B denote the shear modulus and the bulk modulus. Based on the above-mentioned highlights, it can be confidently stated that these materials are promising potential candidates for photovoltaic applications and solar cells due to their suitable direct band gap and high absorption coefficient.

Advancing the Commercialization of Perovskite‐Based Radiation Detectors for High‐Resolution Imaging

AbstractRadiation detectors play an indispensable role in medical diagnostics, industrial non‐destructive inspection and national security. Recently, halide perovskites are considered as the new generation of radiation active materials due to excellent optoelectronic properties such as adjustable bandgap, high absorption coefficient, high carrier mobility and low cost. The radiation detectors based on perovskite show high sensitivity and low detection limit, contributing to excellent spatial resolution for imaging. However, the commercialization of perovskite radiation detectors for high quality imaging still faces many challenges, including ion migration in perovskite, fermi level pinning and electrochemical reaction at the interface of perovskite/electrode, and difficulties of integration with readout circuit. All the issues hinder the further improvement of device performance. This review summarizes the material forms and the optimized growth methods of perovskite for radiation imaging detectors. Further, this work focuses on challenges and improvements of the interface between perovskites and electrodes. Meanwhile, this work outlines the technical routes used to realize array detectors for radiation imaging. The comprehensive review would guide the commercialization of perovskite radiation detectors for high‐quality imaging.

Zinc phthalocyanine-bridged periodic mesoporous organosilica nanoparticle as biodegradable photosensitizer for photodynamic therapy

The development of efficient photosensitizers is vital for advancing photodynamic therapy (PDT), a non-invasive cancer treatment. Although zinc phthalocyanine (ZnPc) has garnered significant attention as a photosensitizer in preclinical studies, its clinical application is hindered by poor solubility and a tendency to aggregate, despite its high absorption coefficient and low dark toxicity. To address these challenges, we developed a novel ZnPc-conjugated periodic mesoporous organosilica (PMO) nanoparticle, which enhances the photosensitizer's solubility, photostability, and biodegradability. The PMO nanoparticles retained the characteristic mesoporous structure, exhibited strong fluorescence emission, and effectively generated singlet oxygen. In vitro studies using 4T1 cells, along with in vivo experiments on a tumor-bearing mouse model, demonstrated that under 675 nm laser irradiation, the ZnPc-PMO nanophotosensitizer induced reactive oxygen species, leading to significant inhibition of tumor growth. This ZnPc-bridged PMO nanophotosensitizer holds great promise for enhancing PDT efficacy and biocompatibility, offering a potential platform for multimodal phototherapeutic strategies.

Synthesis, characterization, and study of linear and non-linear optical properties of some newly thieno[2,3-b]thiophene analogs

Abstract Newly 3,4-Diaminothieno[2,3-b]thiophene derivatives were synthesized by attaching with different aromatic have rich electron. The resulted compounds have been investigated by FT-IR, NMR, elemental analysis, and optical absorption spectra. Comparison between these resulted compounds revealed oxoindolin-3-ylidene)amino)thieno[2,3-b]thiophene has the highest absorption peak intensity at ~ 696nm, thin films have been prepared by thermal evaporation technique and characterized by UV-Visible-NIR spectroscopy as well as the allied absorption, dielectric and dispersion parameters have been investigated and compared with other reported results. Obtained results indicated diethyl 3,4-bis(((E)-2-oxoindolin-3-ylidene)amino)thieno[2,3-b]thiophene-2,5-dicarboxylate and 3,4-bis(((E)-2-oxoindolin-3-ylidene)amino)thieno[2,3-b]thiophene-2,5-dicarbonitrile have manifested small band energy gap energy 1.95, 1.66 eV; respectively as a result of increasing conjugation and high absorption coefficient, make these compounds ideal for use in solar cell. The high nonlinear parameters such as refractive index and third-order nonlinear susceptibility of these organic compound thin films are significantly asymptotic compared with chalcogenide and oxide materials, making them suitable for nonlinear optical devices.

Investigation of optoelectronic, mechanical and thermodynamic properties of cubic perovskite FrBCl3 (B = Zn, Cd) in approach of density functional theory

Lead-free cubic metallic halide perovskite (MHP) compounds, FrBCl3 (where B = Zn, Cd), have been evaluated using first-principles density-functional theory (DFT). Both FrZnCl3 and FrCdCl3 satisfy the stability conditions determined by their tolerance and octahedral factors. These materials demonstrate the characteristics of indirect band gap semiconductors, and their high optical absorption coefficients create promising opportunities for the advancement of optoelectronic devices. The elastic properties of both perovskites indicate robust mechanical stability, while their ductility, flexibility, and stiffness suggest potential for thin film fabrication. Furthermore, the Debye temperature profile underscores the thermal stability of these compounds. This computational study reveals coherent relationships among their structural, electronic, optical, mechanical, and thermodynamic properties. Consequently, these materials may offer exciting applications in nuclear medicine, X-ray imaging, and a variety of optoelectronic devices.

Structural, electronic, optical, mechanical, and phononic bulk properties of tetragonal trirutile antimonate MSb2O6 (M = Fe, Co, Ni, or Zn): a first-principles prediction for optoelectronic applications

Abstract This work does an extensive analysis of the optoelectronic and mechanical properties of the tri rutile structure type 3d transition metal Antimonate MSb2O6 (M = Fe, Co, Ni, or Zn), for the first time, utilizing the pseudo-potential plane wave approach within the density functional theory framework. When calculating the structural, optical, and mechanical properties, the exchange–correlation interactions were studied using the GGA-PBE functional, whereas when computing electronic, it is analyzed using the HSE06 hybrid functional. The equilibrium lattice parameters exhibit good agreement with the available experimental results. The electronic properties were estimated using the GGA-PBE and HSE06 functionals. Based on the calculated electronic properties with the GGA-PBE functional, the FeSb2O6, CoSb2O6, and NiSb2O6 materials exhibit metallic behavior with energy gap values of 0 eV, while ZnSb2O6 is a semiconductor with a narrow direct band gap (Γ–Γ) of 0.5 eV. Furthermore, the computed band gaps using the HSE06 functional are 0 eV, 0 eV, 1 eV (Γ–Γ), and 4 eV (Γ–Γ) for FeSb2O6, CoSb2O6, NiSb2O6, and ZnSb2O6, respectively. Density of states diagrams were used to gain deeper insights into the characteristics of the energy bands. The optical properties of these compounds, such as the dielectric function, energy loss function, conductivity, reflectivity, refractive index, and absorption coefficient were investigated over the energy range of 0 to 40 eV. The materials exhibited a high absorption coefficient and a significantly low reflectivity within the UV–vis energy spectrum. The negative cohesive energy Ecoh implies the chemical (thermodynamic) stability of the trirutile MSb2O6 (M = Fe, Co, Ni, or Zn). Mechanical stability is confirmed by applying the Born stability criteria using elastic constants (Cij). The absence of imaginary frequencies in the phonon spectrum calculations confirms the dynamic stability of the studied compounds. These results are consistent with previous experimental research on these materials in photocatalysis and gas sensor applications. On the other hand, these compounds possess exceptional high and broad optical absorption UV range, making them suitable for use in next-generation ultraviolet photodetectors.

Giant Colloidal Quantum Dot/α-Ga2O3 Heterojunction for High Performance UV-Vis-IR Broadband Photodetector.

Broadband optoelectronics, which extend from the UV to IR regions, are crucial for imaging, autonomous driving, and object recognition. In particular, photon detection efficiency relies significantly on semiconductor properties, such as absorption coefficients and electron-hole pair generation rate, which can be optimized by designing a suitable p-n junction. In this study, we devise giant PbS colloidal quantum dots (G-PbS CQDs) that exhibit high absorption coefficients and broadband absorption. To leverage these exceptional optical properties, we combine G-PbS CQDs with an ultrawide-bandgap semiconductor, α-Ga2O3, and create an efficient G-PbS CQD/α-Ga2O3 heterojunction photodetector that exhibits high performance across the UVC-vis-NIR spectrum range. The resultant heterojunction facilitates efficient electron-hole pair separation at the G-PbS CQD/α-Ga2O3 heterojunction. Furthermore, we utilize transparent graphene electrodes to overcome the limitations of conventional transistor-type device structures and the substantial optical losses induced by opaque metal electrodes. This strategy maximizes the light-collection area and results in an approximately 3-orders of magnitude higher responsivity (55.5 A/W) and specific detectivity (1.66 × 1013 Jones) compared to devices with opaque metal electrodes.

Novel Tl2SnX6 (X=Cl,Br) Double Perovskites for Photovoltaic Applications: A DFT Insight

New double perovskites Tl2SnCl6 and Tl2SnBr6 have been computationally investigated for the first time to determine their structural, mechanical, and optoelectronic properties. The calculations were carried out using Density Functional Theory (DFT), implemented in the Quantum Espresso and Thermo_pw codes. DFT is a theoretical framework used to accurately predict the ground state properties of quantum many-body systems ranging from atoms to condensed matter systems. The results indicated that Tl2SnCl6 and Tl2SnBr6 possess equilibrium lattice parameters of 10.28 Å and 10.77 Å, respectively. Their negative formation energy ensures chemical stability while their positive elastic tensors imply mechanical stability, which is also confirmed by the fulfillment of the Born-Huang stability criteria. Analysis of their Poisson’s and Pugh’s ratio suggested that the materials are brittle but Tl2SnCl6 was estimated to be ductile in some directions. The materials were found to possess semiconducting behavior with bandgap of 1.19 eV (1.48 eV) and 2.48 eV (2.84 eV) for Tl2SnBr6 and Tl2SnCl6, respectively, using the PBE (SCAN) functionals. The calculated optical characteristics indicated that both Tl2SnCl6 and Tl2SnBr6 exhibit remarkable optical properties including significantly high absorption coefficient and low reflectivity, rendering their potential as light absorbers. In particular, with an ideal band gap of 1.48 eV and strong absorption in the visible region of the solar spectra, Tl2SnBr6 is predicted to be an excellent absorber for perovskite solar cells.

Performance optimization of MA0.5FA0.5PbI3/CsPbI3 based hybrid perovskite solar cell emphasizing on double absorber layer

Abstract The utilization of cesium-based lead halide (CsPbI3) PSC has considerable potential in the photovoltaic industry due to their high efficiency, underpinned by features such as a high absorption coefficient, thermal stability, and commendable efficiency. Nevertheless, the bandgap of CsPbI3, standing at 1.7 eV, poses a challenge as it is relatively high for a single-junction device. To overcome this limitation, we introduced a dual absorber layer structure by interleaving CsPbI3 with a lead-based hybrid perovskite material, denoted as MA0.5FA0.5PbI3. This investigation focused on the MA0.5FA0.5PbI3/CsPbI3 hetero-junction structure to ascertain the maximum possible efficiency. Therefore, this study proposed a PSC with the configuration of Ag/MoO3/MA0.5FA0.5PbI3/CsPbI3/IGZO/Au. In this setup, MoO3 (Molybdenum Trioxide) is used as the HTL and IGZO (Indium Gallium Zinc Oxide) as the ETL. Silver (Ag) serves as the back contact and gold (Au) is the front contact. This device demonstrated remarkable characteristics with Voc = 1.307 V, Jsc = 22.71 mA cm−2, FF = 86.58%, and η = 26.21%, showcasing a substantial improvement compared to previously reported CsPbI3-based homojunction PSCs. Furthermore, this study delved into the effects of absorber doping, absorber material thickness, bulk defect, and interfacial defects on solar cell parameters to obtain high-performance solar cells.

Nonhalogenated Solvent-Processed Efficient Ternary All-Polymer Solar Cells Enabled by the Introduction of a Naphthyloxy Group into the Side Chain of Polymer Donors.

Conjugated polymer donors are crucial for enhancing the power conversion efficiencies (PCEs) in all-polymer solar cells (All-PSCs) in nonhalogenated solvents. In this work, three wide-band-gap polymer donors (Sil-D1, Ph-Sil-D1, and Nap-Sil-D1) based on dithienobenzothiadiazole (DTBT) and benzodithiophene (BDT) donor moieties optimized by side chain engineering were designed and synthesized. Alkyl (Sil-D1), phenyloxy (Ph-Sil-D1), and naphthyloxy (Nap-Sil-D1) alkyl siloxane side chain units were incorporated into these polymer donors, respectively. Notably, the Nap-Sil-D1 polymer donor had a greater conjugation length, π-electron delocalization, and improved dipole moment. The deepest highest occupied molecular orbital level of Nap-Sil-D1, with a high absorption coefficient, showed better aggregation properties. In addition, reduced bimolecular recombination and trap-state density generated a high charge transfer to cause a significant enhancement of open-circuit voltage, current density, and fill factor values of 0.94 V, 25.5 mA/cm2, and 70.4%, respectively, for the Nap-Sil-D1-blended All-PSC ternary device (PM6:Nap-Sil-D1:PY-IT), with the highest PCE of 16.8% in the o-xylene solvent, compared to other polymers (Sil-D1 and Ph-Sil-D1) with PCEs of 15.5 and 16.2%. As a result, this optimized device architecture was found to be the most promising as a nonhalogenated solvent processed in additive-free ternary All-PSCs with good stability.

Enhanced Singlet Oxygen Generation in Aggregates of Naphthalene-Fused BODIPY and Its Application in Photodynamic Therapy.

Several reports are available on aggregation-induced emission and its applications in biomedical imaging and other material sciences. However, enhancement of singlet oxygen generation in nanoaggregates is rarely reported. Here, we report the synthesis of Naph-BODIPY Br2, which absorbs at 661 nm (monomer) with a high molar absorption coefficient. The presence of bromine promotes intersystem crossing, thereby enhancing the singlet oxygen quantum yield (ΦΔ ∼ 0.50 in methanol). In order to increase hydrophilicity, we developed Naph-BODIPY Br2 nanoaggregates (∼100 nm), which demonstrated aggregation-induced properties and exhibited a bathochromic shift with an absorption maximum at 757 nm. The bathochromic shift in the UV-vis spectra due to aggregation is corroborated by TD-DFT analysis. The computational data also confirm the presence of a low-lying triplet state, which enhances the generation of singlet oxygen, making it effective for photodynamic therapy. These aggregates showed excellent singlet oxygen generation in aqueous media, compared to their monomeric form and standard methylene blue. Their hydrophilic nature and high singlet oxygen generation enabled significant phototoxicity against human carcinoma cells with IC50 values of 4.06 ± 0.01 and 4.09 ± 0.1 μM, respectively, for MCF-7 and A549 cells upon 5 min exposure to light. Moreover, their phototoxicity further increases with an increasing exposure time of light for both cell lines. Notably, Naph-BODIPY Br2 nanoaggregates exhibited nearly zero dark cell toxicity and effectively induced apoptosis in cancer cells upon light activation, highlighting their potential as powerful photosensitizers for photodynamic cancer therapy.

Next-Generation Self-Powered Photodetectors using 2D Bismuth Oxide Selenide Crystals.

The concept of self-powered photodetectors has attracted significant attention due to their versatile applications in areas such as intelligent systems and hazardous substance detection. Among these, p-n junction and Schottky junction photodetectors are the most widely studied types; however, their fabrication processes are often complex and costly. To overcome these challenges, we focused on the emerging self-powered, ultrasensitive photodetector platform based on photoelectrochemical (PEC) principles. This platform leverages the unique properties of the emerging material bismuth oxide selenide (Bi2O2Se), which features a wide bandgap (∼2 eV) and a high absorption coefficient. We utilized chemical exfoliation to obtain thin layers of Bi2O2Se, enabling highly efficient photodetection. The device characterization demonstrated impressive performance metrics, including a responsivity of 97.1 μA W-1 and a specific detectivity of 2 × 108 cm Hz 1/2 W-1. The PEC photodetector also exhibits broad-spectrum sensitivity, from blue to infrared wavelengths, and features an ultrafast response time of ∼82 ms and a recovery time of ∼86 ms, highlighting its practical potential. Moreover, these self-powered photodetectors show excellent stability in electrochemical environments, positioning them promising candidates for integration into future high-efficiency devices.

The Effect of Seeding Method on The Growth of Zinc Oxide Nanorods

The paper presents the investigation of the method of seeding process for the growth of zinc oxide (ZnO) nanorods (NRs) on the glass substrate as an electron transport layer (ETL) for solar cells. The ZnO NRs were grown by using the hydrothermal method. The seeding process was done via average deposition of zinc crystallite on the glass surface, and the process was compared between with and without spin coating technique. The effect of spin coating parameters during seeding phase on the growth of ZnO nanorods was also investigated in this study. It was found that the sample prepared using the unfiltered solution without spin coating in the seeding phase exhibited the densest ZnO NRs layer with the highest absorption coefficient and high crystallinity.

Exploring the structural, electronic, optical, transport, and photovoltaic properties of Rb2LiGa(Br/I)6 using DFT and SCAPS-1D simulations

Lead-free double perovskite halides are attracting considerable interest in the optoelectronics sector due to their remarkable electronic, optical, and transport properties. These materials are not only stable and easy to synthesize but also present a wide range of potential applications. This study investigates the fascinating characteristics of Rb₂LiGa(Br/I)₆, focusing on its structural, electronic, optical, transport, and photovoltaic attributes. Our findings indicate that Rb₂LiGaBr₆ and Rb₂LiGaI₆ have band gaps of 1.19 eV and 1.13 eV, respectively, highlighting their versatility for various applications. Both compounds exhibit exceptional optical properties, featuring high absorption coefficients and optical conductivity, along with low reflectivity throughout the UV-visible spectrum, positioning them as excellent candidates for solar cell technologies. Moreover, Rb₂LiGa(Br/I)₆ demonstrates impressive thermoelectric performance, with high figure-of-merit (ZT) values between 200 K and 800 K, indicating their potential as effective thermoelectric materials. Consequently, this study offers valuable insights for the development of efficient double perovskite-based solar cells. Encouraged by the outstanding absorption and optical conductivity of Rb₂LiGa(Br/I)₆, we simulated an Au/Cu₂O/Rb₂LiGa(Br/I)₆/TiO₂/FTO solar cell. Our results reveal that the modeled solar cell, Au/Cu₂O/Rb₂LiGaI₆/TiO₂/FTO, achieves an efficiency of 26.48%, surpassing previous reports. This research sets a new benchmark for high-performance double perovskite-based solar cells and lays the foundation for future advancements in this exciting area.

Van der Waals ZnO/HfSn2N4 Heterojunction with Exceptional Photoresponse for Photodetectors.

Two-dimensional van der Waals heterojunctions represent a promising avenue for a spectrum of optoelectronic endeavors. Nonetheless, their deployment has been somewhat constrained by the suboptimal efficiency of the photocurrent generated. In this article, a ZnO/HfSn2N4 heterojunction is proposed to achieve high photoresponse efficiency. First-principles calculations are utilized to confirm that this heterojunction possesses thermal stability with a direct bandgap (1.36 eV). It exhibits a high light absorption coefficient and high carrier mobility (2.51 × 103 cm2 V-1 s-1), and biaxial strain has a significant effect on the modulation of the band structure. As the tensile strain increases, the bandgap changes nonlinearly, transitioning from a type-II to a type-I heterojunction. When compressive strain increases, the bandgap decreases. Quantum transport simulations are employed to calculate the density of states and transmission spectrum of the ZnO/HfSn2N4 model, verifying its excellent photoresponse (a photocurrent peak reaching 4.93 a02/photon and an extinction ratio peak of 75.1). It shows that the ZnO/HfSn2N4 heterojunction is a potentially efficient photodetector.

Double internal magnetic fields significantly improve photocatalytic activity over Ba0.5Sr0.5TiO3/BaFe12O19/SrFe12O19 photocatalysts

The Z-scheme Ba0.5Sr0.5TiO3/BaFe12O19/SrFe12O19 (BST5/10 %BFO/SFO) magnetic photocatalysts with different SFO mass percents and bimagnetic components were successfully constructed using the multistep polyacrylamide gel method and heat treatment technology. The phase structure information, binding energy information, microstructure information, optical and magnetic properties and photocatalytic activity of BST5/10 %BFO/SFO photocatalysts were confirmed by various characterization methods. The photocatalyst composed of BST5, BFO, and SFO is completely free of impurities and creates a unique interface contact between its components. When the mass percentage of SFO was 20 wt%, the BST5/10 % BFO/SFO photocatalyst exhibited the highest saturation magnetization, remanent magnetization, high optical absorption coefficient and photocatalytic activity for the degradation of tetracycline hydrochloride (TC). When the optimal catalyst content is 1 g/L, the initial TC concentration is 100 mg/L and pH is 13, the degradation percentage of BST5/10 % BFO/SFO photocatalyst reaches 87 %. Through active species verification experiments, it was found that the holes, hydroxyl radicals, and superoxide radicals were the most dominant active species in the TC degradation process of BST5/10 % BFO/SFO photocatalysts. The transfer and separation efficiency of charge carriers is enhanced and the formation of Z-scheme heterojunctions is facilitated by the bimagnetic components in BST5/10 % BFO/SFO photocatalysts, which improve the photocatalytic activity of the system. A new technical reference and concept for designing new magnetic separation photocatalysts can be found in the construction method of Z-scheme heterojunction caused by bi-magnetic components.

Investigation on indium concentration in two-terminal tandem indium gallium nitride solar cells by SCAPS-1D

Indium gallium nitride (InGaN) thin-film solar cell is a promising photovoltaic (PV) device. InGaN’s bandgap is tunable from 0.7 to 3.4 eV and it exhibits a high absorption coefficient exceeding 105 cm−1. Besides, InGaN solar cells can be used in tandem configuration, to effectively absorb the solar spectrum. Previous works found that increased indium (In) concentration leads to inverse relationship between open-circuit voltage (Voc) and power conversion efficiency (PCE) of the solar cell. This leads to deleterious device performance. This study aims to assess the performance of two-terminal InGaN tandem solar cells using SCAPS-1D simulation software. The findings revealed maximum short-circuit current density (Jsc) of 26.19 mA cm−2, open-circuit voltage (Voc) of 2.13 V, fill factor (FF) of 89.68%, and PCE of 30.17% from the tandem device. The results indicate that higher In concentration enhances light absorption and the overall PCE, with tandem cells outperforming single-junction cells. This study makes a valuable contribution to the advancement of high-efficiency solar technology based on InGaN.

Design and Simulation for Minimizing Non-Radiative Recombination Losses in CsGeI2Br Perovskite Solar Cells.

CsGeI2Br-based perovskites, with their favorable band gap and high absorption coefficient, are promising candidates for the development of efficient lead-free perovskite solar cells (PSCs). However, bulk and interfacial carrier non-radiative recombination losses hinder the further improvement of power conversion efficiency and stability in PSCs. To overcome this challenge, the photovoltaic potential of the device is unlocked by optimizing the optical and electronic parameters through rigorous numerical simulation, which include tuning perovskite thickness, bulk defect density, and series and shunt resistance. Additionally, to make the simulation data as realistic as possible, recombination processes, such as Auger recombination, must be considered. In this simulation, when the Auger capture coefficient is increased to 10-29 cm6 s-1, the efficiency drops from 31.62% (without taking Auger recombination into account) to 29.10%. Since Auger recombination is unavoidable in experiments, carrier losses due to Auger recombination should be included in the analysis of the efficiency limit to avoid significantly overestimating the simulated device performance. Therefore, this paper provides valuable insights for designing realistic and efficient lead-free PSCs.