High Power Conversion Efficiency Research Articles

Impact of La doping on the optoelectronic and structural properties of CsPbIBr2 perovskite solar cell

Inorganic lead halide perovskite solar cells (IPSC) have high power conversion efficiency (PCE). Currently, heteroatom substitution is a promising method for enhancing the properties of perovskite materials and the performance of associated devices. This study outlines the production process of a perovskite solar cell made from inorganic CsPbIBr2 with a 4 % La doping. The cubic crystal structure with large grain size and small band gap energy is observed at 4 % La–CsPbIBr2. The optoelectronic and structural characteristics of CsPbIBr2 perovskite solar cells have been substantiated through various methodologies, such as the determination of space charge restricted current, examination of the photoluminescence decay profile, assessment of charge transfer resistance, and utilization of Mott Schottky analysis. The incorporation of lanthanum-doped cesium lead iodide bromide (La-doped CsPbIBr2) resulted in a notable enhancement in both the open circuit voltage (Voc), and the short circuit current density (Jsc), leading to a much higher overall efficiency of 9.89 % compared to the pristine counterpart, which exhibited an efficiency of 8.62 %.

Establishing Co‐Continuous Network of Conjugated Polymers and Elastomers for High‐Performance Polymer Solar Cells with Extreme Stretchability

AbstractHigh power conversion efficiency (PCE) and mechanical robustness are prerequisites for wearable applications of organic solar cells (OSCs). However, stretchability of present active systems (i.e., crack‐onset strain (COS) < 30%) should be improved. While introducing elastomers into active systems is considered a simple method for improving stretchability, the inclusion of elastomers typically results in a decrease in PCE of the OSC with a limited enhancement in the stretchability due to lack of interconnected electrical and mechanical pathways. In this study, it is developed efficient and intrinsically stretchable (IS)‐OSCs with exceptional mechanical robustness, by constructing co‐continuous networks of conjugated polymers (D18) and elastomers (SEBS) within active layers. It is demonstrated that the blend film with a specific ratio (40:60 w/w) of D18:SEBS is crucial for forming co‐continuous structures, establishing well‐connected mechanical and electrical channels. Consequently, D180.4:SEBS0.6/L8‐BO OSCs achieve 16‐times higher stretchability (COS = 126%) than the OSCs based on D18/L8‐BO (COS = 8%), while achieving 4‐times higher PCE (12.13%) compared to the OSCs based on SEBS‐rich active layers (D180.2:SEBS0.8/L8‐BO, PCE = 3.15%). Furthermore, D180.4:SEBS0.6‐based IS‐OSCs preserve 86 and 90% of original PCEs at 50% strain and after 200 stretching/releasing cycles with 15% strain, respectively, demonstrating the highest mechanical robustness among reported IS‐OSCs.

“Exploration of Photovoltaic Behavior of Bithiophene-functionalized Dispiro-oxepine based Hole-transporting Materials for Efficient Perovskite Solar Cells”

Abstract Perovskite solar cells (PSCs) have got great attention from researchers due to their superior photovoltaic properties, high efficiency, and low cost. In this study, bithiophene dispiro-oxepine based five hole-transporting materials (DDOF1, DDOF2, DDOF3, DDOF4, and DDOF5) are designed by the substitution of end-capped acceptors via thiophene-based bridge to enhance the photovoltaic properties of PSCs. The results showed that designed HTMs have deeper HOMO levels (-4.88 eV to -5.04 eV), high solubility, and compatible stability with low band gaps (2.04 eV to 2.59 eV) than the reference molecule (EHOMO = -4.55 eV, Eg = -3.49 eV), which improved hole extraction and the open-circuit voltage in the PSCs. Moreover, the binding energy (0.41 eV to 0.46 eV) and TDM analysis indicated that DDOF1-DDOF5 HTMs have high charge mobility compared to the reference molecule DDOF (0.61 eV). The DDOF1-DDOF5 HTMs indicated anticipated high power conversion efficiency and open-circuit voltage than the reference molecule. Overall, our findings proved that designed molecules are efficient HTMs for the manufacture of high-efficiency PSCs in the solar industry.

Alleviating the Angular Dependence of Perovskite Solar Cells via Light Harvesting Nanostructure

Over the past decade, perovskite solar cells (PSCs) have witnessed a remarkable surge in power conversion efficiency (PCE). However, the electrical output performance of PSCs is dependent on the incident angle of solar radiation, and energy loss occurs during photovoltaic conversion when light impinges at angles. Here, a perovskite light absorbed layer with inverse opal structure was used to fabricate PSCs and reduce the angular dependence of the performance. The results demonstrate that ordered periodic perovskite inverse opal (PVSK‐IO) not only exhibits a remarkable slow‐photon effect for enhancing the absorption of sunlight near the photonic band gap (PBG), but also promotes the carrier transfer by expanding the contact area with hole transport layer. Moreover, the slow photon region of PBG could be intentionally tuned by changing the direction of sunlight illumination, thereby more intuitively delaying and storing light in the PVSK‐IO layer. As a consequence, the slow‐photon effect originated from the PVSK‐IO structure efficiently improved the short‐circuit current density (JSC), resulting in a higher PCE than that of planar devices under the irradiation from different incident angles. Our research offers a rational strategy for enhancing the performance of PSCs while alleviating their angular dependence.This article is protected by copyright. All rights reserved.

Stable Organic Solar Cells Enabled by Simultaneous Hole and Electron Interlayer Engineering

The development of high‐performance organic solar cells (OSCs) with high operational stability is essential to accelerate their commercialization. Unfortunately, our understanding of the origin of instabilities in state‐of‐the‐art OSCs based on bulk heterojunction (BHJ) featuring non‐fullerene acceptors (NFAs) remains limited. Herein, we developed NFA‐based OSCs using different charge extraction interlayer materials and studied their storage, thermal, and operational stabilities. Despite the high power conversion efficiency (PCE) of the OSCs (17.54%), we found that cells featuring self‐assembled monolayers (SAMs) as hole‐extraction interlayers exhibited poor stability. The time required for these OSCs to reach 80% of their initial performance (T80) was only 6 h under continuous thermal stress at 85 °C in a nitrogen atmosphere and 1 h under maximum power point tracking (MPPT) in a vacuum. Inserting MoOx between ITO and SAM enhanced the T80 to 50 and ~15 h after the thermal and operational stability tests, respectively, while maintaining a PCE of 16.9%. Replacing the organic PDINN electron transport layer with ZnO NPs further enhances the cells' thermal and operational stability, boosting the T80 to 1000 and 170 h, respectively. Our work reveals the synergistic roles of charge‐selective interlayers and device architecture in developing efficient and stable OSCs.

Filtered spectrum modeling of high-performance perovskite tandem solar cells: Tailoring absorber properties and electron/hole transport layers for 31.55 % efficiency

In this study, the perovskite tandem solar cell (TPSC) has been accomplished using SCAPS-1D. The present study focuses on comprehensive exploration and detailed optimization using various strategies constructing a tandem device. To calculate high photovoltaic power conversion efficiency (PCE), the numerical analysis has been carried out for a wide-bandgap halide (WBH) FA0.75Cs0·25Pb(I0·8Br0.2)3 of bandgap 1.67eV and a Pb–Sn based narrow-bandgap halide (NBH) FA0.7MA0.3Pb0·5Sn0·5I3 of bandgap 1.22eV as absorber layer in top-cell (TCELL) and bottom-cell (BCELL) respectively. The WBH has huge potential as a front light absorber and the NBH based BCELL provides stability and high performance by accepting high and low energy photons respectively. This method mitigates thermalization and non-absorbed photon loss which results in the growth in PCE. The proposed work demonstrates the impact of active-layer thickness along with defect density on the solar-cell parameters. It has been observed that defect density is low for the optimal performance. An investigation for various electron transport medium (ETMs) and hole transport medium (HTMs) has been done to secure an optimum performing TCELL as well as BCELL. Using filtered-spectrum study along with current-matching method, every PV metric parameter has been analyzed after their deployment into tandem configuration. The numerical investigation has shown promising photovoltaic parameters with aa high open circuit voltage (VOC) of 2.33 V, a short circuit current density (JSC) of 17.07 mA/cm2, a fill factor (FF) of 79.34 % and PCE of 31.55 % in tandem configuration.

Revealing the Roles of Guanidine Hydrochloride Ionic Liquid in Ion Inhibition and Defects Passivation for Efficient and Stable P erovskites Solar Cells.

As a result of full-scale ongoing global efforts, the power conversion efficiency (PCE) of the organic-inorganic metal halide perovskite has skyrocketed. Unfortunately, the long-term operational stability for commercialization standards is still lagging owing to intrinsic defects such as ion migration-induced degradation, undercoordinated Pb2+, and shallow defects initiated by disordered crystal growth. Herein, we employed multifunctional, non-volatile tetra-methyl guanidine hydrochloride [TMGHCL] ionic liquid (IL) as an additive to elucidate defects' passivation effects on organic-inorganic metal halide perovskite. More specifically, the formation of hydrogen bonds between H+ in GA+ and I- and coordinate bonding between Cl- and undercoordinated PbI2+could significantly passivate these defects. The hypothesis was confirmed by both experimental and DFT simulations displaying that the optimized ratio of IL integration restrains ion migration, improving grains' size, and significantly elongating the carrier lifetime. Remarkably, the modified cell achieved a peak efficiency of 22.00% with negligible hysteresis, compared to the control device's PCE of 20.12%. In addition, the TMGHCL-based device retains its 93.29% efficiency after 16 days of continuous exposure to air. This efficient approach of adding IL to perovskites absorber can produce high PCE and has strong commercialization potential.

Enhanced photovoltaic response in WSe2 photodetector with asymmetric two-dimensional contacts

Asymmetric contact pairs with different work functions provide an efficient method to extract photogenerated carriers in optoelectrical devices. Specifically, vertical optoelectrical devices based on two-dimensional (2D) materials utilize graphene layers as the bottom and top contacts. Whereas an additional terminal is required for electrostatic doping in either top or bottom graphene to enlarge the built-in electric field. Herein, we present an enhanced photovoltaic response in a vertical WSe2 photodetector utilizing asymmetric 2D contacts. A graphite layer and a degenerate SnSe2 are used as the top and bottom contacts, respectively, with a significant difference in their work functions. By establishing a large built-in electric field across the vertical WSe2 layer, a strong photovoltaic effect is achieved, resulting in an open-circuit voltage of 0.37 V and a short-circuit current of 0.42 μA under 532 nm illumination. The device shows high-performance photodetection characteristics, with a responsivity of 32.04 A W−1, external quantum efficiency of 7475%, and specific detectivity of 3.61 × 1012 Jones. Furthermore, the device can generate a maximum output electrical power of 70.9 nW, enabling a high-power conversion efficiency of 3.5%.

An Efficient Fiber Gel Dye‐Sensitized Solar Cell with Stable Interlaced Interfaces

AbstractFiber gel dye‐sensitized solar cells (FGDSCs) are recognized as an effective solution for high‐performance, durable and safe wearable power supply. However, poor and unstable interfaces between fiber electrodes and gel electrolytes are bottleneck problems that have restricted the photovoltaic performances of FGDSCs and their stabilities during deformations. Here, an FGDSC with stable interlaced interfaces is designed by incorporating polymerized gel electrolyte into the aligned channels in fiber electrodes and the gaps between photoanode and counter electrode in situ. The interlaced structure of gel electrolyte in FGDSC improves the interfacial stability and provided stable channels for rapid ion diffusions, offering efficient charge transports at interfaces. The resulting FGDSC thus produced a high power conversion efficiency of 7.95%, and it is further maintained by over 90% after bending for 5000 cycles. These FGDSCs can be integrated with fiber batteries as a self‐charging power system, demonstrating an effective power solution for wearables.

High Performance As-Cast Organic Solar Cells Enabled by a Refined Double-Fibril Network Morphology and Improved Dielectric Constant of Active Layer.

High performance organic solar cells (OSCs) are usually realized by using post-treatment and/or additive, which can induce the formation of metastable morphology, leading to unfavorable device stability. In terms of the industrial production, the development of high efficiency as-cast OSCs is crucially important, but it remains a great challenge to obtain appropriate active layer morphology and high power conversion efficiency (PCE). Here, efficient as-cast OSCs are constructed via introducing a new polymer acceptor PY-TPT with a high dielectric constant into the D18:L8-BO blend to form a double-fibril network morphology. Besides, the incorporation of PY-TPT enables an enhanced dielectric constant and lower exciton binding energy of active layer. Therefore, efficient exciton dissociation and charge transport are realized in D18:L8-BO:PY-TPT-based device, affording a record-high PCE of 18.60% and excellent photostability in absence of post-treatment. Moreover, green solvent-processed devices, thick-film (300nm) devices, and module (16.60 cm2) are fabricated, which show PCEs of 17.45%, 17.54%, and 13.84%, respectively. This work brings new insight into the construction of efficient as-cast devices, pushing forward the practical application of OSCs.

Correlating Aggregation Ability of Polymer Donors with Film Formation Kinetics for Organic Solar Cells with Improved Efficiency and Processability.

Film formation kinetics significantly impact the molecular processability and power conversion efficiency (PCE) of organic solar cells (OSCs). In this article, we report two kinds of ternary random copolymerization polymers, D18-N-p and D18-N-m, to modulate the aggregation ability of the conventional polymer donor D18 by introducing trifluoromethyl substituted pyridine unit at para- and meta-position, respectively. The introduction of the pyridine unit significantly reduced material aggregation ability and adjusted the interactions with acceptor L8-BO, thereby leading to largely changed film formation kinetics with earlier phase separation and longer film formation times, which enlarged fiber sizes in blend films and improved carrier generation and transport. As a result, D18-N-p with moderate aggregation ability delivered a high PCE of 18.82% by pairing with L8-BO, which was further improved to 19.45% via interface engineering. Despite the slightly inferior small area device performances, D18-N-m showed improved solubility, which inspired us to adjust the ratio of meta-trifluoromethyl pyridine carefully and obtain a polymer donor D18-N-m-10 with good solubility in non-halogenated solvent o-xylene. High PCEs of 13.07% and 12.43% in 1 cm2 device and 43 cm2 module fabricated with slot-die coating method were achieved based on D18-N-m-10: L8-BO blends. Our work emphasizes film formation kinetics optimization in device fabrication via aggregation ability modulation of polymer donors for efficient devices. This article is protected by copyright. All rights reserved.

All-Round Passivation Strategy Yield Flexible Perovskite/CuInGaSe2 Tandem Solar Cells with Efficiency Exceeding 26.5.

The perovskite/Cu(InGa)Se2 (CIGS) tandem solar cells (TSCs) presents a compelling technological combination poised for the next generation of flexible and lightweight photovoltaic (PV) tandem devices, featuring a tunable bandgap, high power conversion efficiency (PCE), lightweight flexibility, and enhanced stability and durability. Over the years, the imperative to enhance the performance of wide bandgap (WBG) perovskite solar cells (PSCs) has grown significantly, particularly in the context of a flexible tandem device. In this study, an all-round passivation strategy known as Dual Passivation at Grains and Interfaces (DPGI) is introduced for WBG PSCs in perovskite/CIGS tandem structures. The implementation of DPGI is tailored to improve film crystallinity and passivate defects across the solar cell structure, leading to a substantial performance enhancement for WBG PSCs. Subsequently, both rigid and flexible tandem devices are assembled. Impressively, a fully flexible 4T perovskite/CIGS TSCs is successfully fabricated with a PCE of 26.57%, making it the highest value in this field and highlighting its potential applications in the next generation of flexible lightweight PV tandem devices.

Enhancing CsSn0.5Ge0.5I3 Perovskite Solar Cell Performance via Cu2O Hole Transport Layer Integration

Perovskite solar cells (PSCs) have emerged as a promising alternative to traditional silicon solar cells due to their low cost of fabrication and high power conversion efficiency (PCE). The utilization of lead halide perovskites as absorber layers in perovskite solar cells has been impeded by two major issues: lead poisoning and stability concerns. These hindrances have greatly impeded the industrialization of this cutting-edge technology. In light of the harmful effects of lead in perovskite solar cells, researchers have shifted their attention to exploring lead-free metal halide perovskites. However, the present alternatives to lead-based perovskite exhibit poor performance, thus prompting further inquiry into this matter. The primary objective of this research is to investigate the use of Cu2O as a hole transport layer in combination with lead-free metal halide perovskite (CsSn0.5Ge0.5I3) to achieve superior performance. Through meticulous experimentation, the suggested model has achieved outstanding results by optimizing several key variables. These variables include the thickness of the absorber layer (CsSn0.5Ge0.5I3), defect density, and doping densities, as well as the back contact work function and the operating temperature associated with each layer. The proposed FTO/PC60BM/CsSn0.5Ge0.5I3/Cu2O/Au solar cell structure surpassed prior configurations by comprehensively examining key aspects such as absorber layer thickness and defect density, doping densities, and back contact work. The structure has been also compared with multiple electron transport elements and concluded that the proposed model functions superior due to the use of PC60BM as an electron transport layer and it has an improved electron extraction procedure. Finally, the proposed model has achieved the optimized values as Jsc of 31.56 mA/cm-2, Voc of 1.12 V, FF of 81.47%, and PCE of 27.72%. As a consequence of this research, the investigated structure may be an excellent contender for the eventual creation of lead-free solar power cells made from perovskite.

Manipulating Crystal Growth and Secondary Phase PbI2 to Enable Efficient and Stable Perovskite Solar Cells with Natural Additives

HighlightsThe novel ionic cellulose derivative with cyano-imidazolium cation and chloride anion, designed from natural cellulose, promotes the crystallization process, grain growth, and orientation of perovskite in perovskite solar cells (PSCs).The use of ionic cellulose leads to the suppression of defect formation, reduction of grain boundaries, enhancement of carrier extraction, and inhibition of non-radiative recombination, resulting in a high power conversion efficiency of 24.71% in PSCs.The biopolymer-based approach enables excellent stability of PSCs, which maintain over 91.3% of their initial efficiencies after 3000 h in conventional air atmosphere.

Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells.

Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long-term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non-radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO-based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect-mitigated PSCs showing enhanced performance and stability.

The Role of Solution Aggregation Property toward High-Efficiency Non-Fullerene Organic Photovoltaic Cells.

In organic photovoltaic cells, the solution-aggregation effect (SAE) is long considered a critical factor in achieving high power-conversion efficiencies for polymer donor (PD)/non-fullerene acceptor (NFA) blend systems. However, the underlying mechanism has yet to be fully understood. Herein, based on an extensive study of blends consisting of the representative 2D-benzodithiophene-based PDs and acceptor-donor-acceptor-type NFAs, it is demonstrated that SAE shows a strong correlation with the aggregation kinetics during solidification, and the aggregation competition between PD and NFA determines the phase separation of blend film and thus the photovoltaic performance. PDs with strong SAEs enable earlier aggregation evolutions than NFAs, resulting in well-known polymer-templated fibrillar network structures and superior PCEs. With the weakening of PDs' aggregation effects, NFAs, showing stronger tendencies to aggregate, tend to form oversized domains, leading to significantly reduced external quantum efficiencies and fill factors. These trends reveal the importance of matching SAE between PD and NFA. The aggregation abilities of various materials are further evaluated and the aggregation ability/photovoltaic parameter diagrams of 64 PD/NFA combinations are provided. This work proposes a guiding criteria and facile approach to match efficient PD/NFA systems.

DFT combined to Boltzmann transport theory for optoelectronic and thermoelectric properties investigations for Se (4 & 8 (at.%)) doped Li2SnS3

Cubic Li2SnS3 emerges as a noteworthy ionic conductor and a viable electrode material for lithium secondary batteries. Its application extends to solar cell technologies, owing to its commendable optoelectronic properties and high-power conversion efficiency. In this study, we present density functional theory (DFT)-based first principles calculations for Li2SnS3-xSex (x = 0, 4, and 8% (atomic percent (at.%)) utilizing the modified Becke Johnson (mBJ) approximations, proposing a compelling alternative. Our investigation reveals significant optical absorption in the ultraviolet region for Li2SnS3-xSex (x = 0, 4, and 8%), accompanied by modest effective mass and indirect band gaps of 2.18 eV for the pristine material. Conversely, doped materials exhibit direct band gaps, with values of 2.113 eV for 4% and 2.026 eV for 8%. Furthermore, the calculated thermoelectric power factor underscores the potential and efficacy of Li2SnS3-xSex in thermoelectric energy devices. The findings not only highlight the material’s promise for solar applications but also underscore its candidacy as a novel solid-state electrolyte for lithium-ion batteries. This stems from its robust thermal stability and notable lithium-ion conductivity, positioning Li2SnS3 as a compelling candidate for advanced energy storage technologies.

High efficiency and stability of perovskite solar cells prepared by alkali metal interfacial modification

Perovskite solar cells (PSCs) have attracted much attention at home and abroad due to their excellent photoelectric properties. Defects in the electron transport layer (ETL) and ETL/perovskite interface greatly affect the power conversion efficiency (PCE) and stability of PSCs. In the paper, the surface of tin dioxide (SnO2) ETL was modified by an alkali metal salt (NaBr, KBr, and RbBr) solution to optimize electron transport and passivate SnO2/perovskite. The results show that the photovoltaic performance of the PSCs is significantly improved after interfacial modification, especially the KBr-modified PSC has the highest PCE, which is 7.8% higher than that of the unmodified device, and the open-circuit voltage, short-circuit current density and fill factor are all greatly improved. This improvement is attributed to the fact that interfacial modification reduces the trap density of the SnO2 films, increases the mobility of the SnO2 films film, effectively passivates defects, and significantly inhibits the recombination at the SnO2/perovskite interface. This method aims to use simple and low-cost inorganic materials for effective interface modification.

Design and Optimization of High-Performance Novel RbPbBr3-Based Solar Cells with Wide-Band-Gap S-Chalcogenide Electron Transport Layers (ETLs).

Inorganic cubic rubidium-lead-halide perovskites have attracted considerable attention owing to their structural, electronic, and unique optical properties. In this study, novel rubidium-lead-bromide (RbPbBr3)-based hybrid perovskite solar cells (HPSCs) with several high-band-gap chalcogenide electron transport layers (ETLs) of In2S3, WS2, and SnS2 were studied by density functional theory (DFT) and using the SCAPS-1D simulator. Initially, the band gap and optical performance were computed using DFT, and these results were utilized for the first time in the SCAPS-1D simulator. Furthermore, the impact of different major influencing parameters, that is, the thickness of the layer, bulk defect density, doping concentration, and defect density of interfaces, including the working temperature, were also investigated and unveiled. Further, a study on an optimized device with the most potential ETL (SnS2) layer was performed systematically. Finally, a comparative study of different reported heterostructures was performed to explore the benchmark of the most recent efficient RbPbBr3-based photovoltaics. The highest power conversion efficiency (PCE) was 29.75% for the SnS2 ETL with Voc of 0.9789 V, Jsc of 34.57863 mA cm-2, and fill factor (FF) of 87.91%, while the PCEs of 21.15 and 24.57% were obtained for In2S3 and WS2 ETLs, respectively. The electron-hole generation, recombination rates, and quantum efficiency (QE) characteristics were also investigated in detail. Thus, the SnS2 ETL shows strong potential for use in RbPbBr3-based hybrid perovskite high-performance photovoltaic devices.

Development of natural dye photosensitizers for dye-sensitized solar cells: a review.

Dye-sensitized solar cell (DSSC) is a photovoltaic device that can be produced from natural source pigments or natural dyes. The selection of natural dyes for DSSC application is currently under research. The utilization of natural dye materials that are easy to obtain, cost-effective, and non-toxic can reduce waste during DSSC fabrication. Natural dyes can be extracted from plants through extraction and chromatography methods. The suitability and viability of utilizing natural dyes as photosensitizers in DSSCs can be predicted using appropriate software simulation by varying related parameters to produce high power conversion efficiency. In this context, the purpose of the review is to highlight the evolution of performance improvement in the development of DSSCs with consideration of natural dye extraction and software simulation. This review also focuses on the results of extracting natural dyes from herbal ingredients, which are still very limited in information, and several parts of herbal plants that can be used as natural dye sources in the future of solid-state DSSCs have been identified. Based on the results of this review, the highest efficiency was obtained for the DSSC that used chlorophyll pigments as natural dyes using Peltophorum pterocarpum leaves with 6.07%, followed by anthocyanin pigments as natural dyes using raspberries (black) fruits with 1.5%, flavonoid pigments as natural dyes using Curcuma longa herbs with 0.64%, and flavonoid pigments as natural dyes using Indigofera tinctoria flowers with 0.46%.