Conversion Efficiency Of Cells Research Articles

Slot‐Die Deposition of CuSCN Using Asymmetric Alkyl Sulfides as Cosolvent for Low‐Cost and Fully Scalable Perovskite Solar Cell Fabrication

The development of industrially relevant deposition processes for efficient, stable, and inexpensive charge extracting layers is crucial for the commercialization of perovskite solar cells (PSCs). This work demonstrates, for the first time, the deposition of copper thiocyanate (CuSCN) as a low‐cost and reliable hole‐transport layer using slot‐die coating. Methyl ethyl sulfide is thereby used as an asymmetric cosolvent to significantly increase the solubility of CuSCN in the utilized slot‐die ink compared to traditional pure diethyl sulfide‐based solutions. Optimized CuSCN inks allow for the deposition of CuSCN layers on 5 × 10 cm2 substrates with a wide range of thicknesses. Multidimensional imaging photoluminescence techniques are used to investigate the uniformity of the CuSCN thin films deposition as well as the influence of the solvent on charge losses. Finally, the CuSCN slot‐die deposition is integrated into a fully upscalable PSC fabrication process showing 19.1% power conversion efficiency for small laboratory cells and 14.7% for 9 cm2 minimodules. Furthermore, semitransparent minimodules retain 80% of their initial efficiency after 500 h of constant illumination.

The effects of periodic textured substrate to control diffusion angle on the conversion efficiency of dye-sensitized solar cells

We suggested improving the conversion efficiency of dye-sensitized solar cells (DSSCs) by the micro-nano periodic textures to control the diffusion angle of the incident light for certain absorbed wavelengths of the used dye. A periodic texture (Prd-Tx) was designed to enhance the light path of the wavelength of DSSCs’ dye absorption with a wide process window by optical simulation (pitch: 1400 nm, pillar diameter: 460–560 nm, pillar height: more than 500 nm). The Prd-Tx was fabricated by photolithography processes and nanoimprinting (pitch: 1400 nm, pillar diameter: 500 nm, pillar height: 1000 nm). The Prd-Tx increased the DSSCs’ conversion efficiency (η of 3.13%), surpassing our previous best result (refabricated W-Tx, η of 3.08%). It was considered that the ohmic loss was suppressed owing to the Prd-Tx enhanced electrical conductivity at the interface between the transparent electrode, F-doped tin oxide (FTO), and TiO2.

Lead-free perovskite solar cell based on methyl ammonium tin iodide: Possible power conversion efficiency enhancement by device simulation

Although solar cells have the potential to create an endless amount of electrical power, their comparatively low power conversion efficiency draws the curiosity of both academics and industry. The primary goal of this research is to examine the performance of lead-free perovskite solar cells that use methyl ammonium tin iodide (CH3NH3SnI3) as the active material. The SCAPS-1D programme is employed for the simulation and analysis of the solar cells. The solar cell structure was analyzed computationally, and the resulting output was examined by comparing the I-V characteristic curves across different combinations of parameters. Various materials and combinations of parameters were explored in an effort to enhance the power conversion efficiency of solar cells based on CH3NH3SnI3. A series of comprehensive evaluations were undertaken to examine the influence of technical factors, including absorber layer thickness, defect density, and acceptor density, on performance. The acceptor density that yielded the best results was selected in order to improve the performance of the solar cell. The simulation results were acquired across a temperature range spanning from 300K to 450K, revealing enhanced stability within the range of typical ambient temperatures. The study produced encouraging findings, which included a short circuit current density of 30.81mA/cm2, an open circuit voltage of 1.25V, a fill factor of 80.35%, and a power conversion efficiency of 31.11%. This study has the potential to facilitate the development of environmentally sustainable, highly efficient, and cost-effective thin film solar cells based on CH3NH3SnI3, which exhibit noteworthy physical characteristics as alternatives to lead-containing perovskite solar cells.

Study on Performance Optimization of Perovskite Solar Cells Based on MAPbI3

AbstractMethylammonium lead iodide (MAPbI3) is a kind of perovskite material, which can effectively absorb photons in sunlight, with an adjustable band gap and relatively stable performance. Aiming at the problem of photoelectric conversion efficiency of perovskite solar cells, this paper proposes a perovskite solar cell with MAPbI3 as an absorption layer. The device structure adopts a trans structure with good stability and low cost, and the hole transport layer adopts poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate(PEDOT:PSS) material, which has good electrical properties and interface properties, and has certain transparency. The electron transport layer adopts tin oxide (SnO2), and its energy band structure is beneficial to carrier transport, and it has excellent electron transport performance and chemical stability, which makes it a material for the electron transport layer. The top electrode and the bottom electrode are made of indium tin oxide (ITO) and aurum (Au) with high reliability respectively. The thickness, band gap, and defect concentration of the battery are simulated by solar cell capacitance simulator (SCAPS) software. The results show that the thickness and band gap of the absorption layer has great influence on the performance of the battery. The open‐circuit voltage, short‐circuit current density, filling factor and photoelectric conversion efficiency of the optimized perovskite solar cell reached 1.219 V, 30.1641 mA cm−2, 70.14%, and 25.78% respectively.

Exploring mc‐Silicon Wafers: Utilizing Machine Learning to Enhance Wafer Quality Through Etching Studies

AbstractThis paper provides a method for improving the photovoltaic conversion efficiency and optical attributes of silicon solar cells manufactured from as‐cut boron doped p‐type multi‐crystalline silicon wafers using acid‐based chemical texturization via machine learning. A decreased reflectance, which can be attained by the right chemical etching conditions, is one of the key elements for raising solar cell efficiency. In this work, the mc‐Silicon wafer surface reflectance is obtained under (<2%) after optimization of wet chemical etching. The HF + HNO3 + CH3COOH chemical etchant is used in the ratio 1:3:2 at different conditions of the etching duration of 1 min, 2 min, 3 min, and 4 min, respectively. The as‐cut boron doped p‐type mc‐silicon wafers are analysed with ultraviolet–visible spectroscopy, optical microscopy, Fourier transforms infrared spectroscopy, thickness profilometer, and scanning electron microscopy before and after etching. The chemical etching solution produces good results in 3 min etched wafer, with a reflectivity value of <2%.The reflectivity and optical images are inputs to the convolutional neural network model and the linear regression model to obtain the etching rate for better reflectivity. The classification model provides 99.6% accuracy and the regression model results in the minimum mean squared error (MSE) of 0.062.

Comparison of polycrystalline and epitaxial Cu(In, Ga)Se2 solar cells with conversion efficiencies of more than 21%

Polycrystalline Cu(In,Ga)Se2 (CIGS) solar cells are widely studied for their application in thin-film photovoltaics, but analysis of their crystalline properties is difficult owing to the presence of grain boundaries and defects. Epitaxial CIGS (epi-CIGS) solar cells can potentially address the issues of polycrystalline CIGS (poly-CIGS) solar cells, but their conversion efficiency has not been widely studied. We fabricated epi-CIGS layers using techniques developed for high-efficiency ploy-CIGS solar cells such as Ga grading, Na doping, and heat-light soaking. Here, scanning transmission electron microscopy and secondary ion mass spectrometry were used to compare the structural characteristics of poly- and epi-CIGS solar cells with conversion efficiencies of more than 21%. Both types of solar cells had similar Ga gradient profiles, and abrupt interfaces were observed between the CIGS and Mo, CIGS and GaAs, and CdS and CIGS layers. The poly-CIGS layer had a higher Na concentration than the epi-CIGS layer because the grain boundaries of the former included high concentrations of Na ions. Meanwhile, the Na ions in the epi-CIGS layer promoted the interdiffusion of In and Ga. For both types of solar cells, heat-light soaking increased the carrier concentration by more than 1 × 1017 cm−3. These observations suggest that grain boundaries are not the main factor limiting the conversion efficiency of poly-CIGS solar cells.

Strain Regulation of Mixed-Halide Perovskites Enables High-Performance Wide-Bandgap Photovoltaics.

Wide-bandgap mixed-halogen perovskite materials are widely used as top cells in tandem solar cells. However, serious open-circuit voltage (Voc ) loss restricts the power conversion efficiency (PCE) of wide-bandgap perovskite solar cells (PSCs). Herein, it is shown that the resulting methylammonium vacancies induce lattice distortion in methylammonium chloride-assisted perovskite film, resulting in an inhomogeneous halogen distribution and low Voc . Thus, a lattice strain regulation strategy is reported to fabricate high-performance wide-bandgap PSCs. Rubidium (Rb) cations are introduced to fill the A-site vacancy caused by the methylammonium volatilization, which alleviates shrinkage strain of the perovskite crystal. The reduced lattice distortion and increased halide ion migration barrier result in a homogeneous mixed-halide perovskite film. Due to improved carrier transport and suppressed nonradiative recombination, the Rb-treated wide-bandgap PSC (1.68eV) achieves an excellent PCE of 21.72%, accompanied by a high Voc of 1.22V. The resulting device maintains more than 90% of its initial PCE after 1500h under 1-sun illumination conditions.

Enhanced Indoor Conversion Efficiency of Dye-Sensitized Solar Cells by Optimizing Ball-Milling Process of TiO2 Paste

The rapid spread of the Internet of Things (IoT) along with the development of innovative low-power electronic devices has also driven the development of indoor photovoltaics. In this paper, we propose a simple and economically feasible solution that can improve the efficiency of dye-sensitized solar cells (DSSCs) under indoor light conditions by ~112%, without requiring a complex TiO2 photoanode architecture or the design of new dyes. The ball milling process of the TiO2 paste was optimized for indoor light conditions for the first time, both in terms of efficiency and production costs, by developing a rapid preparation method that can be used industrially for the application of DSSCs. A simple use of 12 mm diameter balls caused beneficial structural modifications, decreasing the size of the crystallites, and leading to a high OH generation on the TiO2 surface responsible for the improvement of energy conversion efficiency.

Polymorphs of Copper Zinc Tin Sulfide: Optoelectronic Properties and Detection Using Raman

Despite its growing popularity as a solar material, there is no comprehensive reference to aid with determining various polymorphs of copper zinc tin sulfide (CZTS) in the lab. Understanding the diverse electronic, optical and vibrational properties of these polymorphs is crucial to further enhance the conversion efficiency of CZTS solar cells. Here, findings are presented that suggest the effective hole mass in a monoclinic polymorph, that is likely to form along with the more commonly reported tetragonal variations, is about 10 times heavier than that of its tetragonal counterparts, thereby affecting key attributes such as carrier transport and concentration. Among tetragonal polymorphs, the so‐called primitive mixed CuAu (PMCA) arrangement is likely to undergo a direct‐indirect gap transition due to internal strains. Optical absorption between different polymorphs could also vary by up to 90% in the visible spectrum. Finally, accurate Raman footprint of each polymorph is predicted to help establish a definitive method for their detection. From a modeling perspective, Becke‐Lee‐Yang‐Parr with spin‐orbit coupling is shown to be a superior yet 100X faster alternative to hybrid functionals when applied to studying electronic structure of CZTS.

Dark Current Reduction and Performance Improvements in Graphene/Silicon Heterojunction Photodetectors Obtained Using a Non-Stoichiometric HfOx Thin Oxide Layer.

Graphene/silicon heterojunction photodetectors suffer from a high dark current due to the high surface states and low barrier height at the interface, which limits their application. In this study, we introduce an HfOx interfacial layer via magnetron sputtering to address this issue. With this new structure, the dark current is reduced by six times under a bias voltage of -2 V. Under 460 nm illumination, the responsivity is 0.228A/W, the detectivity is 1.15 × 1011 cmHz1/2W-1, and the noise equivalent power is 8.75 × 10-5 pW/Hz1/2, demonstrating an excellent weak light detection capability. Additionally, the oxygen vacancies in the HfOx interfacial layer provide a conductive channel for charge carriers, resulting in a 2.03-fold increase in photocurrent and an external quantum efficiency of 76.5%. The photodetector maintains good photoresponse ability at a low bias voltage. This work showcases the outstanding performance of HfOx films as interfacial layer materials and provides a new solution for high-performance photodetectors, as well as a new path to improve the photovoltaic conversion efficiency of solar cells.

Absorber texture and the efficiency of polycrystalline thin film CdTe solar cells

A range of microstructural changes occur during the deposition and activation of CdTe based thin film solar cells. In particular, the cadmium chloride (CdCl2) activation treatment results in wholesale recrystallisation which transforms the conversion efficiency of the solar cell. One of the noticeable effects is the change of preferred orientation of the CdTe absorber. Highly orientated [111] texture is observed in as deposited or under-treated CdTe based devices. Optimized activation results in a more randomized texture and the [111] preferred texture component is significantly weakened. In this paper we use Electron Backscatter Diffraction to characterise absorber cross-sections. The focus is on how randomization of the absorber texture reflects device performance. We have had access to a range of CdTe devices using a variety of deposition techniques. We have observed a clear pattern that shows that devices with a highly orientated [111] texture have poor efficiency. Devices with a randomized texture have much higher efficiency. Here we illustrate this empirical correlation using devices deposited by Metal Organic Chemical Vapour Deposition with a range of efficiencies from 13.1 % to 17 %. We have also included the analysis of an absorber from a 18.7 % high efficiency CdSeTe/CdTe device to show that texture is similarly important in these advanced devices. We have been able to quantify the effect of texture by using multiples of uniform density or (MUD) values from the inverse pole figures. MUD figures close to 1 correlate with highest efficiency. Although the random texture of the absorber microstructure is only one of several important process factors, it appears to be a necessary feature for highest efficiency CdTe-based polycrystalline solar cells.

Non-Covalent Interaction Enhancement on Active/Interfacial Layers via Two-Dimensional Vermiculite Doping for Efficient Organic Solar Cells.

Interface modification plays an important role in improving the power conversion efficiency (PCE) of organic solar cells (OSCs). However, the low non-covalent interaction between the cathode interface layer (CIL) and nonfullerene acceptor (NFA) directly affects the charge collection of OSCs. Here, the non-covalent interaction between the CIL and NFA is enhanced by introducing the 2D vermiculite (VML) in the poly(9,9-bis(3'-(N,N-dimethyl)-Nethylammonium-propyl-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)) dibromide (PFN-Br) interface layer to form an efficient electron transport channel. As a result, the electron extraction efficiency from the active layer to the CIL is increased, and the PCE of OSCs based on PBDB-T:ITIC is boosted from 10.87% to 12.89%. In addition, the strategy of CIL doping VML is proven to be universal in different CIL materials, for which the PCE is boosted from 10.21% to 11.57% for OSCs based on PDINN and from 9.82% to 11.27% for OSCs based on PNDIT-F3N. The results provide a viable option for designing efficient CIL for high-performance non-fullerene OSCs, which may promote the commercialization of OSCs.

Broadband Sensitized Near‐Infrared Quantum Cutting Materials for Silicon Solar Cells: Progress, Challenges, and Perspectives

Silicon solar cells are currently the most widely used type, accounting for more than 90% of the commercial market. However, the spectral mismatch between the solar spectrum and the absorption spectra of the cells is the main cause restricting their conversion efficiency, which cannot exceed the Shockley–Queisser limit. Quantum cutting can convert one high‐energy photon into two or more low‐energy photons and reduce the energy loss of the high‐energy photons, providing a way to improve the photoelectric conversion efficiency (PCE) of silicon solar cells. The unique electronic configuration of rare‐earth elements gives them excellent optical properties and makes them good candidates for the luminescent centers of quantum cutting materials. This article reviews their luminescence mechanism, energy transfer (ET) mechanism, and application in silicon solar cells and outlines the potential problems of broadband‐sensitized near‐infrared (NIR) quantum cutting materials. Some key issues and future directions are also discussed.

Utilizing rubidium chloride as an effective andstable interface modification layer forhigh-efficiency solar cells.

The presence of interface defects between the perovskite layer and the underlying substrate has a significant impact on the power conversion efficiency (PCE) and stability of perovskite solar cells (PSCs). S n O 2 thin films are employed in PSCs as electron transport layers to achieve high PCE. However, the significant lattice mismatch between S n O 2 and the perovskite material leads to a large number of uncoordinated defects at the interface between perovskite and substrate, resulting in recombination losses at the interface. In this study, rubidium chloride (RbCl) was introduced as the interface modification layer between the perovskite layer and the S n O 2 electron transport layer to enhance the PCE of PSCs. The research showed that the RbCl interface modification layer effectively passivated the under-coordinated defects of Sn ions and optimized the energy level alignment between the perovskite layer and the S n O 2 film. Moreover, the fabricated PSCs exhibited an open-circuit voltage of 1.11V and a power conversion efficiency of 21.64%. Furthermore, the device maintained 80% of initial efficiency after storage for 30days in an inert gas environment and 60% of the value after storage for 30days in ambient air.

Star-shaped small donor molecules based on benzotriindole for efficient organic solar cells: a DFT study.

The purpose of the S01-S05 series of end-capped modified donor chromophores is to amplify the energy conversion efficiency of organic solar cells. Using quantum chemical modeling, the photophysical and photoelectric characteristics of the S01-S05 geometries are examined. The influence of side chain replacement on multiple parameters, including the density of states (DOS), molecular orbital analysis (FMOS), exciton-binding energy (Eb), molecular electrostatic potential analysis, dipole moment (μ), and photovoltaic characteristics including open circuit voltage (VOC), and PCE at minimal energy state geometries, has been investigated employing density functional theory along with TD-DFT analysis. The molar absorption coefficient (λmax) of all the proposed compounds (S01-S05) was efficiently enhanced by the terminal acceptor alteration technique, as demonstrated by their scaling up with the reference molecule (SR). Among all molecules, S04 has shown better absorption properties with a red shift in absorption having λmax at 845nm in CHCl3 solvent and narrow energy gap (EG) 1.83eV with least excitation energy (Ex) of 1.4657eV. All created donors exhibited improved FF and VOC than the SR, which significantly raised PCE and revealed their great efficiency as OSC. Consequently, the results recommended these star-shaped molecules as easily attainable candidates for constructing extremely efficient OSCs.

Kinetics Controlled Perovskite Crystallization for High Performance Solar Cells.

The power conversion efficiencies (PCEs) of perovskite solar cells have recently developed rapidly compared to crystalline silicon solar cells. To have an effective way to control the crystallization of perovskite thin films is the key for achieving good device performance. However, a paradox in perovskite crystallization is from the mismatch between nucleation and Oswald ripening. Usually, the large numbers of nucleation sites tend to weak Oswald ripening. Here, we proposed a new mechanism to promote the formation of nucleation sites by reducing surface energy from 44.9 mN/m to 36.1 mN/m, to spontaneously accelerate the later Oswald ripening process by improving the grain solubility through the elastic modulus regulation. The ripening rate is increased from 2.37 Åm ⋅ s-1 to 4.61 Åm ⋅ s-1 during annealing. Finally, the solar cells derived from the optimized films showed significantly improved PCE from 23.14 % to 25.32 %. The long-term stability tests show excellent thermal stability (the optimized device without encapsulation maintaining 82 % of its initial PCE after 800 h aging at 85 °C) and an improved light stability under illumination. This work provides a new method, the elastic modulus regulation, to enhance the ripening process.

Kinetics Controlled Perovskite Crystallization for High Performance Solar Cells

AbstractThe power conversion efficiencies (PCEs) of perovskite solar cells have recently developed rapidly compared to crystalline silicon solar cells. To have an effective way to control the crystallization of perovskite thin films is the key for achieving good device performance. However, a paradox in perovskite crystallization is from the mismatch between nucleation and Oswald ripening. Usually, the large numbers of nucleation sites tend to weak Oswald ripening. Here, we proposed a new mechanism to promote the formation of nucleation sites by reducing surface energy from 44.9 mN/m to 36.1 mN/m, to spontaneously accelerate the later Oswald ripening process by improving the grain solubility through the elastic modulus regulation. The ripening rate is increased from 2.37 Åm ⋅ s−1 to 4.61 Åm ⋅ s−1 during annealing. Finally, the solar cells derived from the optimized films showed significantly improved PCE from 23.14 % to 25.32 %. The long‐term stability tests show excellent thermal stability (the optimized device without encapsulation maintaining 82 % of its initial PCE after 800 h aging at 85 °C) and an improved light stability under illumination. This work provides a new method, the elastic modulus regulation, to enhance the ripening process.

Remarkable enhancement of power conversion efficiency of silicon photovoltaic cell overlaying with novel metallic-polymer nanocomposites utilising immersion technique

Remarkable enhancement of power conversion efficiency of silicon photovoltaic cell overlaying with novel metallic-polymer nanocomposites utilising immersion technique

Hot-Antisolvent Assisted Morphological Regulation of Perovskites for Semitransparent Photovoltaics Employing Hot-Pressing Approach

The processing of halide perovskites in the air significantly influences their morphology and surface coverage, often leading to the presence of numerous trap densities that adversely affect device performance. In this study, we explored the development of perovskite films using a solvent extraction method, where the temperature of the anisole antisolvent was varied. Our findings demonstrate that the hot-antisolvent strategy effectively controls nucleation, resulting in the formation of highly dense, pinhole-free, and crack-free perovskite films with reduced surface roughness. Films fabricated using this hot-antisolvent approach exhibited enhanced photoluminescence, indicating lower trap density and increased recombination resistance. They also showed slower charge carrier recombination rates and efficient charge extraction, suggesting the suppression of nonradiative recombination. Furthermore, the superior quality of perovskite films obtained through the hot-antisolvent strategy significantly enhanced the power conversion efficiency (PCE) of hot-pressed semitransparent perovskite solar cells. The PCE remarkably increased from 0.13% to an impressive 12.65% while maintaining an average visible transmittance of 26.55% and exceptional air stability for 2000 hours with no significant degradation in initial PCE. This study achieves a record-breaking light utilization efficiency of 3.36% in the realm of research on hot-press processes.

Efficient Dual Mechanisms Boost the Efficiency of Ternary Solar Cells with Two Compatible Polymer Donors to Exceed 19.

Ternary strategyopens a simple avenue to improve the power conversion efficiency (PCE) of organic solar cells (OSCs). The introduction of wide bandgap polymer donors (PDs) as third component canbetter utilize sunlight andimprove the mechanical and thermal stability of active layer. However, efficient ternary OSCs (TOSCs) with two PDs are rarely reported due to inferior compatibility and shortage of efficient PDs match with acceptors. Herein, two PDs-(PBB-F and PBB-Cl) are adopted in the dual-PDs ternary systems to explore the underlying mechanisms and improve their photovoltaic performance. The findings demonstrate that the third components exhibit excellent miscibility with PM6 and are embedded in the host donor to form alloy-like phase. A more profound mechanism for enhancing efficiency through dual mechanisms, that are the guest energy transfer to PM6 and charge transport at the donor/acceptor interface, has been proposed. Consequently, the PM6:PBB-Cl:BTP-eC9 TOSCs achieve PCE of over 19%. Furthermore, the TOSCs exhibit better thermal stability than that of binary OSCs due to the reduction in spatial site resistance resulting from a more tightly entangled long-chain structure. This work not only provides an effective approach to fabricate high-performance TOSCs, but also demonstrates the importance of developing dual compatible PD materials.