Increase In Short-circuit Current Density Research Articles

Characterization of graphene–TiO2-deposited semi-organic solar cell

High energy supply is critical, particularly in developing countries, to maintain lifestyles as the world's population and technological-economic metropolis grow. Solar photovoltaic cells have been used as an alternative to generate renewable, sustainable, and green energy for the past two decades. In general, the materials employed in the photoanode part are critical to manufacturing high-efficiency solar cells with 14–18% efficiency. A simple and successful method has been discovered for creating a film composed of graphene sheets and 99.8% pure anatase titanium oxide (TiO2) nanoparticles. After sensitization, the films were tested as photoelectrodes for dye-sensitized solar cells. The experimental results show that using an optimized graphene material considerably improves the power conversion efficiency of the cells, resulting in a 45% increase in short-circuit current density ( JSC). This study uses capsician as a bonding agent to enhance the current density of a graphene–TiO2 based semi-organic solar cell. The mechanical and electrical properties of the cell are investigated using a scanning electron microscope, energy dispersive X-ray, and Corescan.

Polyvinyl Chloride-Based Luminescent Downshifting Film with High Flame Retardancy and Excellent UV Resistance for Silicon Solar Cells.

Solar power generation, as a clean energy source, has significant potential for development. This work reports the recent efforts to address the challenge of low power conversion efficiency in photovoltaic devices by proposing the fabrication of a luminescence downshifting layer using polyvinyl chloride (PVC) with added fluorescent dots to enhance light utilization. A photoluminescent microsphere (HCPAM) is synthesized by cross-linking hexachlorocyclotriphosphazene, 2-iminobenzimidazoline, and polyethyleneimine. Low addition of HCPAM can improve the fire safety of PVC films, raising the limiting oxygen index of PVC to 32.4% and reducing the total heat release and smoke production rate values by 14.5% and 42.9%, respectively. Additionally, modified PVC film remains a transparency of 88% and shows down-conversion light properties. When the PVC+1%HCPAM film is applied to the solar cell, the short-circuit current density increases from 42.3 to 43.8mAcm-2, resulting in a 7.0% enhancement in power conversion efficiency. HCPAM also effectively delays the photooxidative aging of PVC, particularly at a 3% content, maintaining the surface morphology and optical properties of PVC samples during ultraviolet aging. This study offers an innovative strategy to enhance the fire and UV-resistant performance of PVC films and expand their applications in protecting and efficiently utilizing photovoltaic devices.

Introduction of Co atoms into CdS thin films for improving photovoltaic properties

This paper represents a systematic work on the fabrication of chemical bath-grown CdS films with and without Co atoms and their photovoltaic performances in hybrid solar cells. Structural properties showed 1% Co-doping promoted crystal quality of CdS films. However, a poor crystal quality was developed above 3% Co concentrations. A reduction in sphere size of CdS samples was observed for 1% Co-doping which was ascribed to slow growth of film. Optical examination demonstrated CdS films with 1% Co-doping displayed the highest transparency of 85% in the visible and near-infrared regions, which were explained by the improvement of crystal quality. A maximum band gap of 2.43 eV was found for 1% Co-doped CdS films, whereas an increase in Co concentration to 7% led to a decline in the band gap of CdS that was attributed to sp-d exchange interaction. Photoluminescence data showed Co-doped CdS films had lower PL peak intensity than that of CdS, demonstrating a decrease in the number of intrinsic defects. Photovoltaic measurements displayed that the best efficiency of 0.488% was achieved for CdS-based device including 1% Co atoms, which were almost a seven-fold boost in overall efficiency compared to bare CdS-based device. The enhancement in power conversion efficiency originated from an increase in short-circuit current density of 1% Co-doped CdS-based photovoltaic cell.

Influence of Mg concentration in Zn1-xMgxO buffer layers for enhanced Cu2(Sn,Ge)S3 solar cells performance

This study is focused on the influence of band alignment at the buffer/absorber interface of Cu2(Sn,Ge)S3 (CTGS) thin film solar cells fabricated on soda-lime glass substrates with an Al/Ni/Zn0.92Mg0.08O:Al/Zn1-xMgxO − 2nd buffer/CdS − 1st buffer/CTGS/Mo/glass structure. Here, Zn1-xMgxO 2nd buffers are used to minimize the energy losses and prevent direct contact between the Zn0.92Mg0.08O:Al and CTGS absorber. The study found that the conduction band offset between Zn1-xMgxO and CTGS changed from −0.68 eV (i.e., cliff-like, negative band offset) to +0.60 eV (i.e., spike-like, positive band offset) as the Mg content x increased in Zn1-xMgxO from 0 (i.e., pure ZnO) to 0.52. Optimization of the conduction band offset via tuning the Mg content in Zn1-xMgxO 2nd buffer reduced carrier recombination in the CTGS devices, improving band bending and enhancing the power conversion efficiency up to 3.1%. This was primarily attributed to an increase in short-circuit current density and fill factor.

CdS/CdSe/PbS quantum dots sensitized TiO2 eggshell hollow microspheres photoanode to boost photocurrent and power conversion efficiency of QDSSC

Light harvesting plays crucial role for high photovoltaic performance of quantum dots sensitized solar cell (QDSSC). However, there are still issues need to be tackled, such as enlarging light response range and enhancing light scattering capability. In this work, TiO2 eggshell hollow microspheres (EHMS) were synthesized by carbonaceous microspheres (CMS) template method and co-sensitized by CdS/CdSe/PbS quantum dots (QDs) for application in QDSSC. Compared with QDSSC based on TiO2 nanoparticles (NP) and TiO2 hollow microspheres (HMS), the TiO2 EHMS based QDSSC showed a remarkable increase of short-circuit current density (Jsc) to 24.81 mA cm−2 with a power conversion efficiency (PCE) of 4.07 %. Photoelectrochemical analysis of QDSSC indicate that CdS/CdSe/PbS QDs can enlarge the light response range, and the TiO2 EHMS improve the light scattering, leading to the improvement of light harvesting efficiency. Charges dynamics tests results proved that a larger charges recombination resistance at photoanode/electrolyte interface and longer electron lifetime can be achieved with TiO2 EHMS, contributing to the boost of Jsc. The presented study introduces a simple strategy for researchers interested in designing photoanode for various photoelectrochemical applications.

Effect of Anode Interfacial Modification by Self-Assembled Monolayers on the Organic Solar Cell Performance.

A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5'-phenyl-2,2'-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5'-(4-fluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5'-(3,5-difluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (Jsc) was increased from 6.16 to 7.10 mA/cm2 and 6.94 mA/cm2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (Jsc) shows that the hole-transporting properties between ITO and MoO3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO3 electrode configuration. The open-circuit voltage (Voc) of the SAM-modified ITO-based devices was also improved compared with the Voc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I-V measurements.

Efficient Tin-Based Perovskite Solar Cell with a Cesium Acetate Pre-buried PEDOT:PSS Hole Transport Layer.

The strong Lewis acid tin halide leads to an excessively fast crystallization rate, resulting in more defects in the film and degraded device performance. In this work, a cesium acetate (CsAc) pre-buried poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hole transport layer acts as nucleation points during the crystallization of tin-based perovskite, which can induce preferential orientation growth of crystals and increase the grain size to improve the quality of crystallization. The addition of CsAc not only can increase the conductivity of PEDOT:PSS but also can improve the wettability of the perovskite precursor solution to enhance the interface contact between the hole transport layer and perovskite layer. Because of the incorporation of CsAc in PEDOT:PSS, the average short-circuit current density increases from 23.80 to 27.60 mA cm-2. Furthermore, a power conversion efficiency of 10.99% is achieved for a tin-based perovskite solar cell with CsAc-doped PEDOT:PSS as the hole transport layer.

Effects of alkali metals or Cu+ addition to α-FAPbI3 perovskite crystals on electronic structures and photovoltaic properties

A monovalent copper ion (Cu+) with the same valence as formamidinium is focused on the present work, and the effects of A-site inorganic cations on the electronic structures and device performance are discussed from the experiments and the first-principles calculations. The addition of inorganic cations increased the conversion efficiencies, and the copper-doped device showed the highest conversion efficiency. In particular, the hysteresis of current density–voltage characteristics was significantly suppressed by the addition of Cu+, which would be due to suppression of iodine ion (I−) diffusion by electrostatic interaction between Cu+ and I−. The addition of rubidium or cesium contributed to the increase in short-circuit current density by suppressing decomposition of perovskite crystals and formation of PbI2.

Light and triboelectrification management by nanostructure coupled with plasma-polymerized-fluorocarbon thin film for enhancing performance of energy harvestings

Nanostructures are pivotal in enlarging surface area, increasing transparency, and enhancing power generation. We presented a novel methodology that employs plasma from a linear ion beam source to fabricate irregular nanostructures on a colorless polyimide (CPI) surface. This innovative technique improves transparency, positioning it as an attractive choice for energy and optoelectronic applications. Furthermore, we enhanced the nanostructured CPI surface by applying a plasma-polymerized-fluorocarbon (PPFC). This coating, notable for its low refractive index and superior triboelectrification properties, enabled us to attain ultra-low reflectance (<1%) and a high surface charge density. Integrating PPFC with nanostructured CPI, we amplified the effective surface area of a triboelectric nanogenerator (TENG) by 14.8%, leading to a boost in TENG performance with outputs reaching 184.0 V and 72.8 μA. We also introduced a figure of merit (FOM) for transparent TENGs. The FOM for PPFC/nanostructured CPI exhibits an impressive value of 206.5. In flexible perovskite solar cells (f-PSCs) incorporating PPFC/nanostructured CPI, we observed an increase in short-circuit current density from 22.61 to 23.24 mA/cm2 and an enhancement in power conversion efficiency from 17.47% to 18.25%. Our results validate the efficacy of this approach in both transparent TENGs and f-PSCs, marking a substantial advancement in their performance.

High-Performance Self-Powered Quantum Dot Infrared Photodetector with Azide Ion Solution Treated Electron Transport Layer.

The demand for self-powered photodetectors (PDs) capable of NIR detection without external power is growing with the advancement of NIR technologies such as LIDAR and object recognition. Lead sulfide quantum dot-based photodetectors (PbS QPDs) excel in NIR detection; however, their self-powered operation is hindered by carrier traps induced by surface defects and unfavorable band alignment in the zinc oxide nanoparticle (ZnO NP) electron-transport layer (ETL). In this study, an effective azide-ion (N3 -) treatment is introduced on a ZnO NP ETL to reduce the number of traps and improve the band alignment in a PbS QPD. The ZnO NP ETL treated with azide ions exhibited notable improvements in carrier lifetime and mobility as well as an enhanced internal electric field within the thin-film heterojunction of the ZnO NPs and PbS QDs. The azide-ion-treated PbS QPD demonstrated a increase in short-circuit current density upon NIR illumination, marking a responsivity of 0.45 AW-1, specific detectivity of 4 × 1011 Jones at 950nm, response time of 8.2 µs, and linear dynamic range of 112dB.

Enhanced photoelectrochemical performance of mesoporous TiO2 photoanode prepared by multi-step evaporation-induced self-assembly method

Mesoporous TiO2 films are promising in photocatalysis and photoelectrochemistry for energy and environment applications, because of its high specific surface area and regular mesopore structure. However, the performances of mesoporous TiO2 films are still limited by low catalyst loading due to the damage during the preparation process. In this study, a multi-step evaporation-induced self-assembly method is proposed to develop a mesoporous TiO2 photoanode with high catalyst loading. The prepared mesoporous TiO2 photoanodes possess not only high catalyst loading without damage but also large specific surface area, which provides more active sites. Moreover, regular mesopore structure is remained to benefit mass transport. Because of these merits, the mesoporous TiO2 photoanode prepared by the multi-step evaporation-induced self-assembly method exhibits superior performance than does conventional nanoparticles-packed TiO2 photoanode. The superiority of the mesoporous TiO2 photoanode prepared by this multi-step evaporation-induced self-assembly method is also demonstrated by incorporating it into a photocatalytic fuel cell. The short circuit current density and maximum power density increase by 90.9% and 25.0%, respectively. The present work provides a new way to prepare high-performance mesoporous TiO2 films for various photocatalytic and photoelectrochemical applications.

Two-Dimensional Graphitic Carbon Nitride for Improving the Performance of Organic Solar Cells.

Organic solar cells (OSCs) have attracted lots of attention owing to their low cost, lightweight, and flexibility properties. Nowadays, the performance of OSCs is continuously improving with the development of active layer materials. However, the traditional hole transport layer (HTL) material Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) presents insufficient conductivity and rapid degradation, which decreases the efficiency and stability of OSCs. To conquer the challenge, the two-dimensional (2D) graphitic carbon nitride (g-C3N4) nanomaterials incorporated into the PEDOT:PSS as hybrid HTL are reported. The addition of g-C3N4 into PEDOT:PSS enables the thickness of the HTL to decrease for enhancing the transmittance of the film and increase the conductivity of PEDOT:PSS. Thus, the device exhibts improved charge transport and suppressed carrier recombination, leading to the increase in short-circuit current density and power conversion efficiency of the devices. This work demonstrates that the incorporation of 2D g-C3N4 into PEDOT:PSS for D18:Y6 and PM6:L8-BO-based OSCs can significantly improve the device efficiency to 17.48% and 18.47% with the enhancement of 7.04% and 8.46%, respectively.

The ultrathin PEALD-GaN surface/interface layer-modulated charge dynamics in quantum dot-sensitized solar cells

In this work, gallium nitride (GaN) is employed for the first time to modulate the charge dynamics of quantum dot-sensitized solar cells (QDSCs). An ultrathin GaN layer has been coated on the surface of both mesoporous TiO2 photoanode and quantum dots (QDs) at 240 °C by plasma-enhanced atomic layer deposition (PEALD) approach. It is revealed that there exists a stepped energy level alignment among the as-prepared TiO2 film, GaN layer and QDs, which accelerates the extraction and collection of photogenerated electrons. Meanwhile, a type-II core-shell QD/GaN structure is formed benefiting from the self-limiting reactions of PEALD, resulting in an enhanced light absorption and a redshift of absorption edge. In addition, the dense GaN layer can also effectively inhibit the reverse transfer of photogenerated electrons from TiO2 to QDs or electrolyte while improving the connection between TiO2 and QDs. Ultimately, the QDSCs with a 0.68 nm-thick GaN layer achieve a 29% increase of short-circuit current density and enhanced device efficiency, even with reduced fill factor. This work has shown the multi-functions of GaN in regulating the charge dynamics of QDSCs as well as the potential advantages in replacing TiO2 as photoanode for electronic extraction and transport.

Avoiding Shading Losses in Concentrator Photovoltaics Using a Soft-Imprinted Cloaking Geometry

Shading losses are a longstanding obstacle in photovoltaic devices, particularly in concentrator photovoltaics, where the tradeoff between shading and resistive losses limits the concentration at which the highest power conversion efficiency is achieved to values far below the capabilities of concentrator optics. Here, we demonstrate a simple and scalable fabrication method that enables large front metal coverage while keeping shading losses to a minimum. Soft-imprint lithography is used to create trenches in a transparent polymer above the metal contacts, enabling cloaking via refraction at a range of angles near normal incidence. Using optical characterization techniques, we first confirm that the metal contacts are indeed optically cloaked. We then demonstrate an increase in short-circuit current density from 29.95 to 39.12 mA/cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sup> for a Si solar cell with 25% front metal coverage before and after patterning, respectively. We investigate the angular performance of the trench pattern and further demonstrate how such a cloaking strategy could be implemented in concentrator photovoltaics to enable efficiency peaks at concentrations beyond 1000 suns.

Color-temperature dependence of indoor organic photovoltaic performance

Organic materials are uniquely suited for indoor light energy harvesting because they absorb mostly in the visible spectrum and the absence of ultraviolet light minimizes their degradation. However, the performance of photovoltaic devices under indoor lighting depends on the correlated color temperatures (CCTs) of the light sources but has not been examined previously. Here we study organic photovoltaics with different combinations of donor and acceptor materials under white light-emitting diode (LED) illumination. The current density – voltage (J - V) measurements were performed under illuminance of 1000 lx at nominal LED CCTs of 3000 K, 4000 K, and 6000 K. Absorption spectra of neat and blended films and device external quantum efficiency were measured. Our results show that active layer absorption in the blue LED emission region determines the short-circuit current density (J sc ) increase from 3000 K to 6000 K CCT; the more the active layer absorbs at 450 nm, the larger the J sc increase under higher CCTs. We find that the normalized fractional absorption of the active layer at 450 nm needs to be > 0.85 to eliminate a decrease in power conversion efficiency as the CCT is varied from 3000 K to 6000 K. This work highlights the unique tunability of organic absorbers that is difficult to achieve in inorganic materials and provides guidance on how to select organic absorbers for specific applications under different indoor illumination conditions. • Study color-temperature dependence of organic photovoltaic performance under white light-emitting diode illumination. • Active layer absorption at 450 nm determines the power conversion efficiency (PCE) under cool white light. • A threshold exists in the 450-nm absorption to eliminate PCE decrease as color-temperature increases. • Analyze color-temperature behavior of high-performance organic photovoltaics.

Effect of Polarization on Performance of Inverted Solar Cells Based on Molecular Ferroelectric 1,6-Hexanediamine Pentaiodide Bismuth with PCBM as Electron Transport Layer

The depolarization field of ferroelectric photovoltaic materials can enhance the separation and transport of photogenerated carriers, which will improve the performance of photovoltaic devices, thus attracting the attention of researchers. In this paper, a narrow bandgap molecular ferroelectric Hexane-1,6-diammonium pentaiodobismuth (HDA-BiI5) was selected as the photo absorption layer for the fabrication of solar cells. After optimizing the ferroelectric thin film by the antisolvent process, the effect of different polarization voltages on the performance of ferroelectric devices was studied. The results showed that there was a significant increase in short-circuit current density, and the photoelectric conversion efficiency showed an overall increasing trend. Finally, we analyzed the internal mechanism of the effect of polarization on the device.

A proposal to enhance SnS solar cell efficiency: the incorporation of SnSSe nanostructures

Tin sulfide (SnS) semiconductor has recently attracted a great deal of attention from the scientific community regarding its application in solar cells. However, SnS solar cell efficiencies are still limited to less than 5%. The incorporation of nanostructures into solar cells has been demonstrated to be a potential route to improve device performance. So far, there have been no reports on the incorporation of nanostructures into SnS solar cells. In this work, a theoretical study on the incorporation of tin sulfide selenide (SnSSe) nanostructures in the form of quantum wells (QWs) into SnS solar cells under the radiative limit is presented, for the first time. In particular, the impact of well number, well thickness, and Se/(S + Se) compositional ratio at the wells, on solar cell characteristics, is evaluated. An efficiency enhancement of 11.1% is found for a SnS/SnSSe QW solar cell, compared to the optimized device without nanostructures, for 50 wells of 54 nm width with a Se/(S + Se) well composition of 0.4 and considering barrier thicknesses of 5 nm, which is a result of the increase in short-circuit current density of 14.5%. The influence of defects at wells and barriers, as well as defects at interfaces, on solar cell behavior is also presented, demonstrating that the introduction of QWs can result in higher efficiencies than that of the device without nanostructures. In this sense, the addition of SnSSe nanostructures to SnS solar cells is introduced as a potential route to promote the absorption of photons with energy lower than the SnS band-gap, while keeping open-circuit voltage values similar to those of a SnS solar cell without nanostructures, thereby increasing solar cell efficiency.

Design investigation on 100 μm-thickness thin silicon PERC solar cells with assistance of machine learning

Thin crystalline silicon passivated emitter and rear cell (PERC) solar cells are a very prospective technology for next-phase photovoltaic development due to the potential of high cost effectiveness. The reduction of silicon wafer thickness can significantly save the costs, but there is a loss of cell efficiency if cell design is not conducted. For the thinned 100 μm-thickness PERC solar cells without design, the efficiency loss is pronounced from commercial 180 μm-thickness. In this paper, we have designed and optimized SiO2/SiNx/SiNx/SiOx thin films (here two SiNx layers have different refractive index) on the front surface and SiNx/SiOx thin films on the back surface for the standard front single-sided textured PERC cells. Based on this, we further design and investigate the case of double-sided textured PERC solar cells. Compared with the reference cell, the present designs can lead to the short-circuit current density increase by 0.6 mA/cm2 and the open-circuit voltage enhancement by 10 mV for the front textured case, which causes the efficiency gain of 0.7% from 21.6% to 22.3%. For the double-sided textured cells, the efficiency has an extra increase of 0.6% from 22.3% to 22.9%. Finally, we have constructed the efficiency prediction model by using the multilayer perceptron algorithm in machine learning. It is found from the SHAP values that a significant effect of the front SiNx thickness is observed to predict the performance of the PERC cells.

Solution processable transition metal oxide ultra-thin films as alternative electron transport and hole blocking layers in dye sensitized solar cells

An electron transporting and hole-blocking layer (ETL) between the fluorine-doped tin oxide (FTO) and mesoporous titanium dioxide interface of photoanode is essential in dye-sensitized solar cells (DSCs) for improving their photovoltaic performance. In the present work, we have examined the potential for further improving device performance by using alternative materials for ETLs. Accordingly, the effect of replacing TiO2 based ETLs with spin coated ultra-thin transition metal oxides (TMOs), molybdenum trioxide (MoO3) and tungsten trioxide (WO3) films has been studied. TMO films of 10 nm thickness have been found to be optimal for obtaining good transparency and charge transport properties, without compromising device performance. Further, devices fabricated with surfactant assisted (SA-) MoO3 ETLs have shown efficiency ∼4%, which is comparable with devices based on conventionally prepared TiO2 ETLs. In addition, a significant improvement in efficiency (15 %) has been observed for DSCs prepared using SA-WO3 films. The overall improvement in device efficiency is attributed to the increase in short-circuit current density without loss of open circuit potential and fill factor. Detailed analyses of results suggest that in addition to surface morphology, transparency and charge transport properties; oxygen vacancies in sub-stoichiometric TMOs also plays an important role in determining the device performance. The findings reveal that TMOs have significant potential to replace TiO2 ETL in DSCs and other third generation solar cell, viz. perovskite and polymer solar cells.

19% Efficient P3CT-Na Based MAPbI3 Solar Cells with a Simple Double-Filtering Process

A high-efficiency inverted-type CH3NH3PbI3 (MAPbI3) solar cell was fabricated by using a ultrathin poly[3-(4-carboxybutyl)thiophene-2,5-diyl]-Na (P3CT-Na) film as the hole transport layer. The averaged power conversion efficiency (PCE) can be largely increased from 11.72 to 18.92% with a double-filtering process of the P3CT-Na solution mainly due to the increase in short-circuit current density (JSC) from 19.43 to 23.88 mA/cm2, which means that the molecular packing structure of P3CT-Na thin film can influence the formation of the MAPbI3 thin film and the contact quality at the MAPbI3/P3CT-Na interface. Zeta potentials, atomic-force microscopic images, absorbance spectra, photoluminescence spectra, X-ray diffraction patterns, and Raman scattering spectra are used to understand the improvement in the JSC. Besides, the light intensity-dependent and wavelength-dependent photovoltaic performance of the MAPbI3 solar cells shows that the P3CT-Na thin film is not only used as the hole transport layer but also plays an important role during the formation of a high-quality MAPbI3 thin film. It is noted that the PCE values of the best P3CT-Na based MAPbI3 solar cell are higher than 30% in the yellow-to-near infrared wavelength range under low light intensities. On the other hand, it is predicted that the double-filtering method can be readily used to increase the PCE of polymer based solar cells.