Solar Cells Research Articles

Aerodynamic optimisation of flat-upper-surface wing

Purpose The paper aims to optimise several concepts of the flat-upper-surface wing that could install the largest possible number of photovoltaic cells and test them in flight. A wing ideal flat upper surface was necessary to provide the same lighting conditions for each tested cell. Design/methodology/approach The optimised wings were built based on a developed family of airfoils having 75% of their upper surface flat. Within the developed parametric model of the wings, the design parameters described the spanwise distribution of base airfoils. Maximisation of the endurance factor was assumed as the main objective. The aerodynamic properties of optimised wings were evaluated using a panel method coupled with boundary layer analysis. Findings The paper proves that it is possible to design wings with 75% of their upper surface perfectly flat, which are also characterised by good aerodynamic properties. Practical implications The research conducted will allow designing an experimental unmanned aerial vehicle dedicated to investigating the properties of electrical propulsion systems at various altitudes. Data obtained in these investigations will help in the development of future generations of electric-propulsion aircraft. Originality/value The innovative wings, developed within the research are unique due to their unusual geometric and aerodynamic properties. They have 75% of their upper surface perfectly flat. That makes them ideal for testing various photovoltaic cells in flight. The biggest challenge was to design the wings so that their specific geometric features did not impair their aerodynamic properties. The paper proves that this challenge has been fully overcome.

Functional Nano-Metallic Coatings for Solar Cells: Their Theoretical Background and Modeling

We have collected theoretical arguments supporting the functional role of nano-metallic coatings of solar cells, which enhance solar cell efficiency via by plasmon-strengthening the absorption of sun-light photons and reducing the binding energy of photoexcitons. The quantum character of the plasmonic effect related to the absorption of photons (called the optical plasmonic effect) is described in terms of the Fermi golden rule for the quantum transitions of semiconductor-band electrons induced by plasmons from a nano-metallic coating. The plasmonic effect related to the lowering of the exciton binding energy (called the electrical plasmonic effect) is of particular significance for metalized perovskite solar cells and is also characterized in quantum mechanics terms. The coupling between plasmons in nanoparticles from a coating with band electrons in a semiconductor substrate significantly modifies material properties (dielectric functions) both of the particles and the semiconductor, beyond the ability of the classical electrodynamics to describe.

Recent Advances in NIR-Switchable Multi-Redox Systems Based on Organic Molecules.

In recent years, near-infrared (NIR) dyes, exhibiting absorption in the NIR region (750-2500 nm), have been applied to various optical applications such as security marking, photovoltaic cells and chemotherapy of deep tissues in vivo. Electrochromic systems capable of switching NIR absorption are attractive from the viewpoint of applications for material and life science, and thus several examples have been reported to date. The development of organic-based materials is needed to reduce the environmental impact and improve biocompatibility, however, the switching of NIR absorption based on redox interconversion is still a challenging issue regarding reversibility and durability during interconversion. To overcome this potential instability, several studies on organic electrochromic systems that allow ON/OFF switching of NIR absorption have been developed in recent years. In this review, we focus on redox-active well-defined small molecules that enable ON/OFF switching of NIR absorption, and present recent studies on their intrinsic electrochemical and spectroscopic properties and/or structural characterization of their charged states. We also address more sophisticated electrochromic systems that can modulate their properties in response to external stimuli such as light, heat, and electric potential.

Sensitive Self-Driven Single-Component Organic Photodetector Based on Vapor-Deposited Small Molecules.

Typically, organic solar cells (OSCs) and photodetectors (OPDs) comprise an electron donating and accepting material to facilitate efficient charge carrier generation. This approach has proven successful in achieving high-performance devices but has several drawbacks for upscaling and stability. This study presents a fully vacuum-deposited single-component OPD, employing the neat oligothiophene derivative DCV2-5T in the photoactive layer. Free charge carriers are generated with an internal quantum efficiency of 20 % at zero bias. By optimizing the device structure, a very low dark current of 3.4 · 10-11Acm-2 at -0.1V is achieved, comparable to the dark current of state-of-the-art bulk heterojunction OPDs. This optimization results in specific detectivities of 1· 1013Jones (based on noise measurements), accompanied by a fast photoresponse (f-3dB = 200kHz) and a broad linear dynamic range (>150dB). Ultrafast transient absorption spectroscopy unveils that charge carriers are already formed at very short time scales (<1ps). The surprisingly efficient bulk charge generation mechanism is attributed to a strong electronic coupling of the molecular exciton and charge transfer states. This work demonstrates the very high performance of single-component OPDs and proves that this novel device design is a successful strategy for highly efficient, morphological stable and easily manufacturable devices.

A review on Natural dyes as a sensitizer in dye- dye-sensitized solar cell

A review on Natural dyes as a sensitizer in dye- dye-sensitized solar cell

Stereo-Hindrance Induced Conformal Self-Assembled Monolayer for High Efficiency Inverted Perovskite Solar Cells.

Self-assembled monolayers (SAMs) are employed as hole-selective contacts in inverted perovskite solar cells (PSCs) and have achieved record power conversion efficiency (PCE) over 26%. However, the tendency of extensively employed SAM [2-(3,6-Dimethoxy-9H-carbazol-9-yl)ethyl]phosphonic acid to aggregate leads to its uneven coverage to the transparent conducting oxide substrate, which subsequently compromises the photovoltaic performance. Herein, a novel tert-butyl functionalized phosphonic acid carbazole SAM is developed, i.e., (4-(3,6-di-tert-butyl-9H-carbazol-9-yl)butyl)phosphonic acid (tBu-4PACz), and introduced to a mixed SAM system as the hole-extraction layer in inverted PSCs. The stereo-hindrance of the bulky tert-butyl group prevents undesired aggregation and leads to better conformality, which facilitates more efficient hole-extraction and suppresses interfacial recombination losses. The tBu-4PACz SAM-based inverted PSC has achieved record level PCE of 26.25% (26.21%, certificated) with outstanding fill factors over 86%. Moreover, the mixed SAM based inverted PSC devices maintained over 94.7% of their initial efficiency after 500h continuous maximum power-point tracking under simulation 1-sun irradiation.

Simulation of a Silicon Solar Cell Using Triple-Layer Anti-Reflection Coatings (ARC)

Considering solar energy is being used more and more frequently in recent years, numerous studies have been conducted in order to improve the performance of the solar cell. The application of anti-reflective coating (ARC) in the solar cell is one of the most effective techniques. It has been said that although single and double ARC layers are adequate, applying triple ARC layers would render them significantly more effective across a broad spectrum. Henceforth, in this study, different materials were recently designed to produce triple layers of ARC, which are SiO2/Si3N4/TiO2, SiO2/ZnO/TiO2, ZnO/Si3N4/TiO2, SiO2/Si3N4/ZnS, and SiO2/ZnO/ZnS, which are then applied in silicon solar cells using PC1D simulation software. The outcomes of the simulation included the analysis of the I-V curve, efficiency (ŋ), and reflection, in addition to the results for short circuit current (Isc), maximum power output (Pmax), open circuit voltage (Voc), and fill factor (FF), which have been compared to numerous other theoretical findings from other investigations and research projects. By that, the simulation revealed that SiO2/ZnO/TiO2 is the most suitable triple-layer ARC to be applied to a silicon solar cell, which exhibits the highest efficiency of 22.63% with an Isc of 3.967A, Pmax of 2.489W, a Voc of 0.7389V, and a fill factor of 84.91 at a wavelength of 400 nm.

Downshifting Encapsulant: Optical Simulation Evaluation of the Solution to Ultraviolet‐Induced Degradation in Silicon Heterojunction Solar Cells

Ultraviolet (UV)‐induced degradation (UVID) poses a significant challenge for the prospective mass production of silicon heterojunction (SHJ) solar cells, known for their high efficiency. In this study, the magnified impact of UV radiation when employing a silicon carbide (SiC)‐based transparent passivating contact (TPC) on the front side of SHJ solar cells is reported. A reduction in open‐circuit voltage (VOC), short‐circuit current (JSC), and fill factor of 12%, 6%, and 11%, respectively, is observed after UV exposure. Conventional UVID mitigation measures, UV‐blocking encapsulation, are assessed through single‐cell TPC laminates, revealing an unavoidable tradeoff between current loss and UVID. Alternatively, the utilization of ultraviolet‐downshifting (UV‐DS) encapsulants is proposed to convert UV radiation into the visible light spectrum. An optical simulation method, conducted via OPAL2, is presented to evaluate UV‐DS encapsulants for diminishing UVID in SHJ solar cells with different front contacts. A simple methodology is proposed to mimic the optical property of UV‐DS encapsulants. In the simulation results, additional current gains of up to 0.33 mA cm−2 achievable with suitable UV‐DS encapsulants are highlighted. The factors related to the UV‐DS effects are evaluated and the optimization pathway for UV‐DS encapsulants is elucidated.

Enhanced UV-Visible Absorption of Silicon Solar Cells Utilizing YAG:Ce3+ and Ba5Si2O6Cl6: Eu2+ Based on Spectral Down-Shifting.

Spectral down-shifting materials can convert the less utilized photons in the solar spectrum into the portion that solar cells can fully utilize, providing an effective means of improving the efficiency of solar cells. In this work, the spectral down-shifting material Ba5Si2O6Cl6: Eu2+ (BSOC) was prepared by a high-temperature solid-state method. The fluorescence spectra indicate that the absorption spectrum of BSOC can cover the range of 210-500nm, and has a strong emission spectrum with a broadband of 410-650nm. The wider spectral characteristics make it convenient to utilize the solar spectrum efficiently. Additionally, the BSOC phosphors precisely compensate for the weak absorption of YAG: Ce3+ (YAG) phosphors below 425nm. The YAG and BSOC phosphors were mixed, and the hybrid material has a wider absorption range (200-540nm) compared to YAG or BSOC alone. Finally, the electrical properties of the packaged cells were tested, and the results showed that the packaged cells with hybrid materials had higher short-circuit current density and photoelectric conversion efficiency compared to YAG or BSOC alone. In addition, the efficiency of the packaged cells with hybrid materials increased from 19.54 to 20.08% compared with the bare cells, a relative increase of 2.760%.

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.

Device optimization of all-perovskite triple-junction solar cells for realistic irradiation conditions

All-perovskite two-terminal tandem solar cells, comprising two or more junctions, offer high power conversion efficiencies (PCEs) that exceed the limits of single-junction photovoltaics. Realizing high-efficiency SCs requires carefully optimizing the photoactive layer, front electrodes, and functional layers. Here, we first aim to determine the optimal device architecture, i.e., the perovskites bandgaps and optimum layer thicknesses, for standard test conditions (STCs). We then optimize the energy yield (EY) under realistic outdoor conditions (ROCs), i.e., the overall electrical energy to be expected in one year at a specific location. In the first step, we reference our simulation with two terminal all-perovskite triple-junction SCs (2T3J-PSCs) to previously experimentally realized PSC with a PCE of 20.1% as a benchmark to derive the underlying diode parameters and use our in-house energy yield code combined with a hybrid particle swarm optimization and gravitational search algorithm (PSOGSA) to find the optimal bandgap combination and perovskite layer thicknesses. The optimized SCs with the optimal bandgap combination offer a PCE of 25.1% with a current density of 10.1 mA/cm2. Furthermore, the effect of the other functional layers, such as transparent conductive oxide (TCO), hole transport layer (HTL), and recombination junctions (RJs), is also investigated to enhance the cell performance further. The SCs with optimized layers exhibit improved parameters: PCE of 27.1%, with a relative improvement of 34.8% in the PCE compared with the fabricated cell, and a high current matching a of 10.8 mA/cm2. The numerical results showed that the reported cell can potentially achieve a PCE of 36% at an eVoc/EG ratio of 0.72. However, the optimal parameters may vary in real-world operating conditions due to variations in temperature, humidity, and light exposure. As a result, the optimal energy yield (EY) parameters may differ. Therefore, the energy yield optimizing process is also carried out by considering ROCs in Phoenix, AZ, USA, to find the best parameters under these conditions. We found that the optimum top layer bandgap under ROCs is lower than under STCs due to a bluer, more shifted spectrum in ROCs. After that, the optimized cell under ROCs is tested in several locations exhibiting different climatic conditions (Seattle, Honolulu, Los Angeles, Miami, and Milwaukee). The numerical results show that the optimized cell under ROCs offers an increase in energy yield in several locations compared to conventional single-junction crystalline Si-SCs (PCE = 23.6%) with a high energy yield of 648.2 kWh/m2 in Phoenix, with an improvement of 39.9% in the EY compared to the Si-SC counterpart. Our results provide design guidelines for fabricating a highly efficient triple-junction perovskite SC in the lab and outdoor applications and improve the efficiency of 2T3J-PSCs beyond the 30% limit.

High-Quality Thiophene-Based Two-Dimensional Perovskite Films Prepared with Dual Additives and Their Application in Solar Cells

High-Quality Thiophene-Based Two-Dimensional Perovskite Films Prepared with Dual Additives and Their Application in Solar Cells

Progress in MXenes and Their Composites as Electrode Materials for Electrochemical Sensing and Dye-Sensitized Solar Cells

In the present mini-review article, we have compiled the previously reported literature on the fabrication of MXenes and their hybrid composite materials based electrochemical sensors for the determination of phenolic compounds and counter electrodes for platinum (Pt)-free dye-sensitized solar cells (DSSCs). MXenes are two-dimensional (2D) materials with excellent optoelectronic and physicochemical properties. MXenes and their composite materials have been extensively used in the construction of electrochemical sensors and solar cell applications. In this paper, we have reviewed and compiled the progress in the construction of phenolic sensors based on MXenes and their composite materials. In addition, co1.unter electrodes based on MXenes and their composites have been reviewed for the development of Pt-free DSSCs. We believe that the present review article will be beneficial for the researchers working towards the development of phenolic sensors and DSSCs using MXenes and their composites as electrode materials.

Towards highly efficient thin-film solar cells with a graded-bandgap CZTSSe layer. Part II: piecewise-homogeneous bandgap grading

Abstract In Part I, we optoelectronically optimized a thin-film solar cell with a graded-bandgap CZTSSe photon-absorbing layer and&amp;#xD;a periodically corrugated backreflector, using the hybridizable discontinuous&amp;#xD;Galerkin (HDG) scheme to solve the drift-diffusion equations.&amp;#xD;The efficiency increase due&amp;#xD;to periodic corrugation was minimal, but significant improvement was achieved&amp;#xD;with a nonlinearly graded bandgap. Due to occasional failures of the HDG&amp;#xD;scheme from negative carrier densities, we developed a new computational scheme using the finite-difference&amp;#xD;method, which also reduced the overall computational cost of optimization. Later, a normalization error&amp;#xD;was discovered in the electrical submodel in Part I, but it did not alter the overall conclusions. We have&amp;#xD;now re-optimized the solar cells with (i) a homogeneous bandgap, (ii) a linearly graded bandgap, or (iii)&amp;#xD;a nonlinearly graded bandgap, and (iv) piecewise-homogeneous bandgap which is easier to implement than a&amp;#xD;continuously graded bandgap.&amp;#xD;An efficiency of 13.53\% is predicted with a three-layered piecewise-homogeneous CZTSSe &amp;#xD;layer. Furthermore, concentrating sunlight by a factor of one hundred can boost the efficiency to 16.70\%&amp;#xD; with the&amp;#xD;piecewise-homogeneous bandgap.

A Comprehensive Approach to Optimization of Silicon-Based Solar Cells

In this work, we report a detailed scheme of computational optimization of solar cell structures and parameters using PC1D and AFORS-HET codes. Each parameter’s influence on the properties of the components of heterojunction silicon-based solar cells (HIT) has been thoroughly examined. The proposed approach follows a stringent sequence of steps to optimize various parameters of the studied HITs. Furthermore, we have revealed the effects of the metal-semiconductor contact, and a model of a photocell with an ohmic contact and a Schottky contact has been simulated. The optimal model of HIT for available materials has been proposed and fabricated based on the results of these simulations. A comparison of predicted and measured performance unequivocally demonstrates the efficiency of the proposed scheme in developing silicon-based HITs, providing reassurance about its practical application.

Surface n-Doped Metal Halide Perovskite for Efficient and Stable Solar Cells through Organic Chelation.

Perovskite solar cells (PSCs) have emerged as a leading photovoltaic technology due to their high efficiency and low cost. Even though they have developed rapidly since their inception, with efficiencies of over 26%, inverted PSCs face challenges such as nonradiative recombination and ion migration. Surface treatment, especially the utilization of organic compounds, has improved efficiency and stability by optimizing the perovskite-charge transport layer interface. Herein, we report a facile and effective strategy by introducing 2,2'-bipyridyl to modify the surface of perovskite, achieving a power conversion efficiency of 24.43% with increasing open-circuit voltage and fill factor and good repeatability on multiple devices. We reveal that the 2,2'-bipyridyl molecule can chelate lead ions on the surface of perovskite, effectively suppressing nonradiative recombination. Furthermore, this modification can induce surficial n-doping to refine the energy level alignment, thereby minimizing charge transport losses. Additionally, the device maintained over 92% of the initial efficiency after 1000 h of operation at the maximum power point under continuous illumination. This surface chelation and defect passivation strategy employing 2,2'-bipyridyl offers a promising avenue for exploring the details of potential long-term degradation mechanisms and the development of commercially viable high-performance p-i-n PSCs.

Electropolymerization of a New Diketopyrrollopyrrole Derivative into Inherent Chiral Polymer Films

Electropolymerization is a convenient way to obtain conducting polymers (CPs) directly adhered to an electrode surface. CPs are well-known for their various application fields in photovoltaic cells, chemical sensors, and electronics. By implementing chirality into a CP, the application possibilities will spread further onto chiral sensors or optoelectronics. In this work, we introduce a new inherently chiral polymer based on a macrocyclic 3,4-ethylenedioxythiophene-diketopyrrolopyrrole-3,4-ethylenedioxythiophene triad (EDOT-DPP-EDOT) fused by 1,4-phenylene groups, which was prepared via oxidative electropolymerization directly on the electrode surface. The investigation of the chiroptical properties was performed by circular dichroism spectroscopy in the solid state. The enantiomeric pure polymer films obtained showed dissymmetry factors of up to −2.71 × 10−4, whereby linear dichroism contributions can be widely excluded.

Asymmetric Alkyl Chain Engineering for Efficient and Eco-Friendly Organic Photovoltaic Cells.

Recent advancements in organic photovoltaic (OPV) cells have resulted in power conversion efficiencies (PCEs) surpassing 20%. However, the use of halogen solvents in the fabrication of OPV cells raises concerns due to their potential environmental and health impacts. In this work, a novel non-fullerene small molecule acceptor BO-AM-4F, featuring an asymmetric alkyl chain design that includes a 2-butyloctyl and a unique 6-(hexylamino)-6-oxohexyl chain is synthesized. This design significantly improves molecular packing, crystallinity, and electrostatic potential distribution compared to the controlled acceptor DBO-4F, which possesses symmetric 2-butyloctyl chains. When combined with the polymer donor PBDB-TF and processed using the non-halogen solvent o-xylene, the BO-AM-4F-based OPV cell achieves an impressive PCE of 18.0%, surpassing the 16.6% PCE observed in the PBDB-TF:DBO-4F device. Furthermore, the PBDB-TF:BO-AM-4F system demonstrates enhanced photostability and thermal stability compared to its DBO-4F counterpart. These findings emphasize asymmetric alkyl chain engineering as an effective strategy for developing high-performance, environmentally friendly OPV materials. This represents a significant step towards sustainable OPV technology.

Triphenylamine-Functionalized Metal Nanoclusters for Efficient and Stable Perovskite Solar Cells.

Reported herein is a ligand engineering strategy to develop photoelectric active metal nanoclusters (NCs) with atomic precision. Triphenylamine (TPA), a typical organic molecule in the photoelectric field, is introduced for the first time to prepare atomically precise metal NCs that prove effective in the fabrication of perovskite solar cells (PSCs). The scalable synthetic prototype, unique electronic strucuture, and atomically precise structure of the cluster ([(AgCu)37(PPh3)8(TPA-C≡C)24]5+) are illustrated in this work. When being employed as a buffer layer in the perovskite/HTL interface of PSCs, significantly enhanced performance is observed. The resultant n-i-p devices achieved a substantial power conversion efficiency as high as 25.1% and long-term stability. The findings offer valuable insights into preparing functionalized metal NCs that play multiple roles in improving the performance of the device: while the inorganic metal core enhances conductivity, the organic TPA shell promotes the "carrier transfer" between the perovskite and HTL layer and prevents the perovskite from corrosion.

Achieving Closed-Loop Recycling of a Semi-Conjugated Polymer Through the Incorporation of Ester Linkers Along the Backbone.

Design strategies to achieve degradation and ideally closed-loop recycling of organic semiconductors have attracted great interest in order to minimize the electronic waste (E-waste). In this work, three ester-incorporated monomers were synthesized by the names of Thiophene-Ester-Ethylene-Thiophene (TEET), Thiophene-Ester-Methylene-Thiophene (TEMT), and Thiophene-Ester-Thiophene (TET), which were co-polymerized via Stille polycondensation with a benzodithiophene (BnDT) π-conjugated unit to yield a series of ester-incorporated polymers: PBnDT-TEET, PBnDT-TEMT, and PBnDT-TET. While the ester-only linker can maintain some extended conjugation in PBnDT-TET, the other two ester linkers having conjugation breaking units result in isolated conjugated segments in PBnDT-TEET and PBnDT-TEMT, evidenced by UV-Vis and CV results. This yields an improved photovoltaic performance of PBnDT-TET compared to PBnDT-TEET. While all three polymers can depolymerize under methanolysis, the alternating co-polymer PBnDT-TEET demonstrates the highest recyclability potential with a single dimethyl ester-functionalized product with an excellent 92 % isolated yield, which can then be repolymerized to reobtain PBnDT-TEET with a 36 % yield. This work provides a framework towards achieving recyclable organic semiconductors to reduce E-waste. Although the incorporation of ester linkers allowed for closed-loop recycling, the low solar cell efficiency of PBnDT-TEET highlights the significant challenge in achieving both recycling and high device performance.