Front Subcell Research Articles

High efficiency homojunction tandem organic solar cells with all solution processable interconnect layer

In the field of organic photovoltaics, the power conversion efficiency of single junction solar cells continues to improve. However, tandem organic solar cells are poised to push the efficiency limits even further and offer a promising avenue for improving the performance of organic photovoltaic devices. This study reports the development of an all-solution processed interconnecting layer (ICL) based on ZnO NPs:PEI/PEI/PEDOT:PSS/2PACz for tandem solar cells. The PM6:BTP-eC9 active layer material was adjusted for its donor-to-acceptor (D/A) ratio and film thickness as the front and back sub-cells. The ICL exhibits favorable mechanical, electrical and optical properties. Through multidimensional modulation, the front and rear sub-cells have been optimized to obtain highly efficient homojunction tandem solar cells. The tandem solar cell has a structure of indium tin oxide (ITO)/PEDOT:PSS/2PACz/active layer/ICL/active layer/PNDIT-F3N/Ag. This optimization resulted in a power conversion efficiency (PCE) of 19.9 %, which is the highest reported efficiency for homojunction tandem organic solar cells to date. Our research demonstrates that the PCE of homojunction tandem cells can be significantly improved by careful design of the interconnecting layers and optimization of the donor-to-acceptor (D/A) ratio. This strategy may provide guidance for further improvements in homojunction tandem cells.

Boosting the Efficiency of Perovskite/Organic Tandem Solar Cells via Enhanced Near-Infrared Absorption and Minimized Energy Losses.

The compatibility of perovskite and organic photovoltaic materials in solution processing provides a significant advantage in the fabrication of high-efficiency perovskite/organic tandem solar cells. However, additional recombination losses can occur during exciton dissociation in organic materials, leading to energy losses in the near-infrared region of tandem devices. Consequently, a ternary organic rear subcell is designed containing two narrow-bandgap non-fullerene acceptors to enhance the absorption of near-infrared light. Simultaneously, a unique diffusion-controlled growth technique is adopted to optimize the morphology of the ternary active layer, thereby improving exciton dissociation efficiency. This innovation not only broadens the absorption range of near-infrared light but also facilitates the generation and effective dissociation of excitons. Owing to these technological improvements, the power conversion efficiency (PCE) of organic solar cells increased to 19.2%. Furthermore, a wide-bandgap perovskite front subcell is integrated with a narrow-bandgap organic rear subcell to develop a perovskite/organic tandem solar cell. Owing to the reduction in near-infrared energy loss, the PCE of this tandem device significantly improved, reaching 24.5%.

Full optoelectronic simulation of all antimony chalcogenide thin film tandem solar cell: Design routes from 4-T to 2-T configuration

Antimony chalcogenide, as a newcomer to light harvesting materials, is regarded as an auspicious contender for incorporation as a photoactive layer in thin film tandem solar cells (TFTSCs). The current study introduces the design of all-antimony chalcogenide TFTSC comprised of an Sb2S3 (1.7 eV) front subcell and an Sb2Se3 (1.2 eV) rear subcell. The challenges to migrating from four-terminal (4-T) to two-terminal (2-T) designs are highlighted and possible solutions are proposed. To commence, a calibration procedure for the two subcells is conducted in alignment with experimental investigations. The benchmarked solar cells yield a power conversion efficiency (PCE) of 8.08 % for the upper subcell and 10.58 % for the lower subcell. Subsequently, upon integration of both subcells within the initial 4-T Sb2S3/Sb2Se3 TFTSC, the resultant PV cell attains a PCE of 12.27 %. Before transitioning it to a more efficient 2T tandem configuration, we explore alternative inorganic HTL materials to the Spiro-OMeTAD HTL to overcome its practical considerations. Cu2O is found to be the best HTL alternative to be included for both subcells. Upon stacking into the tandem structure, the combined cell exhibited an efficiency of 15.68 % and a notable Jsc of 16.23 mA/cm2. To further enhance the tandem performance, the device structure is optimized by engineering the CBO of two sub-cells and employing a double ETL design for the front sub-cell. At the considered current matching criterion, the tandem device PCE and Jsc are boosted to 27.86 % and 17.60 mA/cm2, respectively. Based on this full optoelectronic analysis, developed in the Silvaco TCAD environment, a 2-T all antimony chalcogenide tandem configuration can be realized and optimized, paving the way for future experimental endeavors.

23.6 % Efficient perovskite-organic tandem photovoltaics enabled by recombination layer engineering

Recombination layers are crucial in achieving high power conversion efficiency (PCE) in tandem solar cells. Here, we report the development and optimization of recombination junctions for high PCE perovskite-organic tandem solar cells (PO-TSCs). We choose a wide bandgap perovskite (1.79 eV) for the front subcell and a narrow bandgap (1.36 eV) organic bulk heterojunction (BHJ) for the rear subcell. The optimal thicknesses of the perovskite and organic layers were determined to be 260 and 100 nm, respectively, based on the analysis of Transfer-Matrix optical simulations. Our results demonstrate that the optimal recombination layer consists of an ultrathin layer of indium zinc oxide IZO (∼ 2 nm) deposited on MoOx/2PACz, which delivers a PCE of 23.6 %. This high PCE is attributed to the high transparency of the recombination layer in the NIR spectra region and the low sheet resistance of IZO. Furthermore, we provide a theoretical analysis of the potential efficiency of PO-TSCs as a function of front and rear subcells and predict a maximum theoretical PCE value of more than 36 %. Our work highlights the importance of selecting the proper recombination layer design for achieving high-performance PO-TSCs.

Zirconium Doping to Enable High-Efficiency and Stable CsPbI2Br All-Inorganic Perovskite Solar Cells.

All-inorganic wide-bandgap perovskite CsPbI2Br has attracted much attention because of its inherent thermal stability and ideal bandgap for the front subcell of tandem solar cells (TSCs). However, the low power conversion efficiency (PCE) and poor moisture stability of CsPbI2Br still restrict its future commercialization. Herein, zirconium tetrachloride (ZrCl4) was doped into CsPbI2Br films to modulate the crystal growth and improve the film quality. The partial substitution of the B-site Pb2+ of CsPbI2Br with Zr4+ suppresses the unwanted phase conversion from the crystallized black α-phase to the δ-phase, resulting in improved phase stability. Consequently, the humidity and thermal stability of the film are greatly improved. Additionally, the incorporation of ZrCl4 suppresses nonradiative recombination and forms a matched energy-level alignment with the hole-transport layer (Spiro-OMeTAD). Benefiting from these features, the ZrCl4-doped CsPbI2Br perovskite solar cell (PSC) shows an outstanding efficiency of 16.60% with a high open-circuit voltage of 1.29 V. The unencapsulated devices simultaneously show excellent humidity and thermal stability, retaining over 91% of PCEinitial after 1000 h of aging in ambient air conditions and 92% PCEinitial after 500 h of continuous heating at 85 °C in a nitrogen environment, respectively. Furthermore, ZrCl4-doped CsPbI2Br was employed as the front subcell of perovskite/organic TSCs and achieved a remarkable PCE of 19.42%, showing great potential for highly efficient and stable TSCs.

Numerical Simulation and Design of All-Thin-Film Homojunction Perovskite/c-Si Tandem Solar Cells

Double-junction solar devices featuring wide-bandgap and narrow-bandgap sub-cells are capable of boosting performance and efficiency compared to single-junction photovoltaic (PV) technologies. To achieve the best performance of a double-junction device, careful selection and optimization of each sub-cell is crucial. This work presents the investigation of an all-thin-film two-terminal (2T) monolithic homojunction perovskite (PVK)/c-Si tandem cell using Silvaco TCAD simulation. The front sub-cell utilizes homojunction PVK that has a bandgap of 1.72 eV, whereas the rear sub-cell uses thin c-Si with a bandgap of 1.12 eV. Both cells are connected via a p++/n++ silicon tunnel diode. Experimental calibration of the heterojunction PVK and c-Si cells yields power conversion efficiencies (PCE) of 18.106% and 17.416%, respectively. When integrated into an initial PVK/c-Si tandem, the resulting cell achieves a PCE of 29.38%. To compare the performance, the heterojunction PVK layer is replaced with an n-p homojunction PVK layer, revealing the impact of the absence of a surplus built-in electric field in the perovskite film as a strong limiting factor. Further, a thorough investigation of four distinct structures for the n-p homojunction PVK cell is conducted. The four structures include a complete cell, electron transport layer (ETL)-free, hole transport layer (HTL)-free, and carrier transport layer (CTL)-free structures. The results show that the CTL-free structure has significant potential after applying certain optimization techniques that result in reducing surface recombination, enhancing the built-in electric field, and improving light absorption. With the current-matching condition achieved, the tandem efficiency reaches 36.37%.

Strategies toward Highly Efficient Monolithic Perovskite/Organic Tandem Solar Cells

Comprehensive SummaryConstructing monolithic tandem solar cells (TSCs) is an effective method to break the Shockley–Queisser (S–Q) radiative efficiency limit for single‐junction solar cells. Employing the wide bandgap perovskite materials and low bandgap organic materials as absorber layers for front and rear subcells, respectively, to construct perovskite/organic TSCs can complementarily absorb sunlight in ultraviolet‐visible (UV‐Vis) range by front perovskite and near‐infrared (NIR) range by rear organic molecules, thus reducing the thermalization energy losses. Besides the subcells, the interconnection layer (ICL), which physically and electrically connects the front and rear subcells, is also an important tunnel junction to recombine charges. In this review, we summarize the optimization strategies of wide bandgap perovskites for front subcell, narrow bandgap organic material for rear subcell, and the ICLs employed in monolithic perovskite/organic TSCs.

Oxidation-resistant all-perovskite tandem solar cells in substrate configuration

The commonly-used superstrate configuration (depositing front subcell first and then depositing back subcell) in all-perovskite tandem solar cells is disadvantageous for long-term stability due to oxidizable narrow-bandgap perovskite assembled last and easily exposable to air. Here we reverse the processing order and demonstrate all-perovskite tandems in a substrate configuration (depositing back subcell first and then depositing front subcell) to bury oxidizable narrow-bandgap perovskite deep in the device stack. By using guanidinium tetrafluoroborate additive in wide-bandgap perovskite subcell, we achieve an efficiency of 25.3% for the substrate-configured all-perovskite tandem cells. The unencapsulated devices exhibit no performance degradation after storage in dry air for 1000 hours. The substrate configuration also widens the choice of flexible substrates: we achieve 24.1% and 20.3% efficient flexible all-perovskite tandem solar cells on copper-coated polyethylene naphthalene and copper metal foil, respectively. Substrate configuration offers a promising route to unleash the commercial potential of all-perovskite tandem solar cells.

Full Optoelectronic Simulation of Lead-Free Perovskite/Organic Tandem Solar Cells.

Organic and perovskite semiconductor materials are considered an interesting combination thanks to their similar processing technologies and band gap tunability. Here, we present the design and analysis of perovskite/organic tandem solar cells (TSCs) by using a full optoelectronic simulator (SETFOS). A wide band gap lead-free ASnI2Br perovskite top subcell is utilized in conjunction with a narrow band gap DPPEZnP-TBO:PC61BM heterojunction organic bottom subcell to form the tandem configuration. The top and bottom cells were designed according to previous experimental work keeping the same materials and physical parameters. The calibration of the two cells regarding simulation and experimental data shows very good agreement, implying the validation of the simulation process. Accordingly, the two cells are combined to develop a 2T tandem cell. Further, upon optimizing the thickness of the front and rear subcells, a current matching condition is satisfied for which the proposed perovskite/organic TSC achieves an efficiency of 13.32%, Jsc of 13.74 mA/cm2, and Voc of 1.486 V. On the other hand, when optimizing the tandem by utilizing full optoelectronic simulation, the tandem shows a higher efficiency of about 14%, although it achieves a decreased Jsc of 12.27 mA/cm2. The study shows that the efficiency can be further improved when concurrently optimizing the various tandem layers by global optimization routines. Furthermore, the impact of defects is demonstrated to highlight other possible routes to improve efficiency. The current simulation study can provide a physical understanding and potential directions for further efficiency improvement for lead-free perovskite/organic TSC.

Regulating Charge Carrier Recombination in the Interconnecting Layer to Boost the Efficiency and Stability of Monolithic Perovskite/Organic Tandem Solar Cells.

The charge carriers of single-junction solar cells can be fluently extracted and then collected by electrodes, leading to weak charge carrier accumulation and low energy loss (Eloss ). However, in tandem solar cells (TSCs), it is a considerable challenge to obtain a balance between the densities of the holes and electrons extracted from the two respective subcells to facilitate an efficient recombination in the interconnecting layer (ICL). Herein, a charge-carrier-dynamic management strategy for inorganic perovskite/organic TSCs is proposed, centered on the simultaneous regulation of the defect states of CsPbI1.9 Br1.1 perovskite in the front subcell and hole transport ability from the perovskite to ICL. The target hole density on the perovskite surface and the hole loss before reaching the ICL are significantly improved. As a result, the hole/electron density offset in the ICL can be effectively narrowed, leading to a balanced charge carrier recombination, which reduces the Eloss in TSCs. The resulting inorganic perovskite/organic 0.062-cm2 TSC exhibits a remarkable power conversion efficiency (PCE) of 23.17% with an ultrahigh open-circuit voltage (Voc ) of 2.15V, and the PCE of the 1.004-cm2 device (21.69%) exhibited a weak size-dependence. This charge-carrier-dynamic management strategy can also effectively enhance the operational and ultraviolet-light stabilities of the TSCs.

Guanidinium-assisted crystallization modulation and reduction of open-circuit voltage deficit for efficient planar FAPbBr3 perovskite solar cells

The bromide-based perovskites with wide bandgap have attracted particular interests for the potential ability to serve as front sub-cells of monolithic all-perovskite triple junction tandem solar cells. However, non-radiative recombination induced by crystal defects could cause the massive open-circuit voltage (VOC) losses, which severely disserves the performance of bromide-based perovskite solar cells. Hence, we incorporated guanidinium bromide (GABr) to modulate crystallization and heal charged defects of FAPbBr3-based solar cells. The introduction of GABr provides a non-wetting surface and suppresses heterogeneous nucleation, leading to larger grain size. Notably, nitrogen (N) atoms from GA+ cations are in two differently charged environments, which are ionized ammonium group (–NH3+) and unsaturated N atoms in form of amine or imine group (–NH2 or = NH). Thus, GA+ cations simultaneously heal both positively and negatively charged defects through multi-reactive sites with perovskite. Consequently, introduction of GABr releases microstrain and strengthens lattice structure, further transforms the perovskite from charge-rich to charge-natural region, which comprehensively leads to suppress non-radiative recombination. As a result, the high-quality planar FAPbBr3-based device yielded a PCE of 8.92% with a champion VOC of 1.639 V, which is the highest value among FAPbBr3 solar cells up to date.

Constructing Monolithic Perovskite/Organic Tandem Solar Cell with Efficiency of 22.0% via Reduced Open-Circuit Voltage Loss and Broadened Absorption Spectra.

Combining the high stability under UV light of the wide bandgap (WBG) perovskite solar cells (pero-SCs) and the broad near-infrared absorption spectra of the narrow bandgap (NBG) organic solar cells (OSCs), the perovskite/organic tandem solar cells (TSCs) with the WBG pero-SC as front cell and the NBG OSC as rear cell have attracted attention . However, the photovoltaic performance of the perovskite/organic TSCs needs to be further improved. Herein, nonradiative charge recombination loss is reduced through bulk defect passivation in the WBG pero-SC front subcell and broadening the range of absorption spectra of the NBG OSC rear cell. For the WBG pero-SCs, an organic cation chloro-formamidinium is introduced into FA0.6 MA0.4 Pb(I0.6 Br0.4 )3 to passivate the bulk defects in the perovskite film and the WBG pero-SC displays high open-circuit voltage of 1.25V and high fill factor of 83.0%. For the NBG OSCs, a new infrared-absorbing organic small molecule acceptor BTPV-4Cl-eC9 is designed and synthesized. Then, a monolithic perovskite/organic TSC is fabricated with the WBG pero-SC as the front cell and the NBG OSC as the rear cell, and the TSC demonstrates high power conversion efficiency up to 22.0%. The results indicate that the perovskite/organic TSC is promising for future commercialization.

Recent Advances of Monolithic All‐Perovskite Tandem Solar Cells: From Materials to Devices

Comprehensive SummaryOrganic–inorganic metal‐halide perovskite solar cells (PerSCs) have achieved significant progresses due to their outstanding optoelectronic characteristics, and the power conversion efficiency (PCE) of single‐junction PerSCs has been boosted from 3.8% to a certified 25.2%. However, the efficiency of single‐junction cells is governed by the Shockley–Queisser (S–Q) radiative limit, and fabricating all‐perovskite tandem solar cells is a particularly attractive method to break the S–Q limit. Since the bandgap of lead (Pb)–based mixed halide perovskite can be tuned from 1.55 eV to 2.3 eV, and the mixed tin (Sn)–Pb perovskites have bandgap of ~1.2 eV, these perovskites become the best candidates for the front and rear subcells of all‐perovskite tandem device, respectively. In this review, we firstly summarize the current development progresses of two‐terminal (2‐T) all‐perovskite tandem solar cells. For further optimizing the device performance, the wide bandgap mixed halide perovskites for front subcell, mixed Sn–Pb narrow bandgap perovskites for rear subcell, and the interconnection layer (ICL) of 2‐T tandem device are then discussed. This review aims to open a pathway to realize highly efficient all‐perovskite tandem solar cells.

A High-Performance Nonfused Wide-Bandgap Acceptor for Versatile Photovoltaic Applications.

Wide-bandgap (WBG) nonfullerene acceptors (NFAs) with nonfused conjugated structures play a critical role in organic photovoltaic (OPV) cells. Here, NFAs named GS-OEH, GS-OC6, and GS-ISO, with optical bandgaps larger than 1.70eV, are synthesized without using the fused ring structures. Compared with GS-OEH and GS-OC6, GS-ISO exhibits much stronger crystallinity, leading to a smaller energetic disorder and a larger exciton diffusion coefficient. GS-ISO also possesses a higher electroluminescence external quantum efficiency of 1.0×10-2 . The OPV cell based on PBDB-TF:GS-ISO demonstrates a power conversion efficiency (PCE) of 11.62% under the standard one sun illumination. Besides, the PBDB-TF:GS-ISO-based cell with effective area of 1.0cm2 exhibits a PCE of 28.37% under 2700K illumination of 500lux. A tandem OPV cell using PBDB-TF:GS-ISO as the front subcell shows an outstanding efficiency of 19.10%. Importantly, the GS-ISO-based OPV cell exhibits promising stability under the continuous illumination of simulated sunlight. This study indicates that the molecular design strategy demonstrated in this work has great superiority in developing nonfused NFAs and also that GS-ISO is a promising WBG acceptor for versatile photovoltaic applications.

Limitations and solutions for achieving high-performance perovskite tandem photovoltaics

The large light absorption coefficient, long carrier diffusion length, and high defect tolerance enable organic-inorganic lead halide perovskites for excellent photovoltaic performance. The highest certified power conversion efficiency of single-junction perovskite solar cells (PSCs) has reported 25.5%. Besides, the bandgap of perovskites can be tuned by engineering their composition. These merits have made perovskites promising candidates for tandem photovoltaics, which can cross over the Shockley-Queisser limit of single-junction PSCs with economic costs. However, there are yet some hurdles in the wide-bandgap and narrow-bandgap subcells as well as interconnected layers (ICLs), which limit the commercial applications of perovskite tandem solar cells (PTSCs). In this review, we summarize the major scientific and technical limitations of PTSCs. We firstly demonstrate the configurations and working principles of PTSCs. Then, the developments of front subcells and rear subcells are discussed. Their main drawbacks, implemented technologies, and underlying mechanisms are analyzed in detail. Subsequently, the progress of ICLs which are responsible for guaranteeing continuous current in 2 T PTSCs are discussed. In addition, the stability of PTSCs is also summarized. The purpose of this review is to map and thrive the future development of PTSCs.

Efficient Organic Tandem Solar Cells Enabled by Solution‐Processed Interconnection Layer and Fine‐Tuned Active Layer

AbstractOrganic tandem solar cells (OTSCs) with the merits of overcoming the S‐Q limit of single‐junction, enhancing and expanding the sunlight harvesting, and minimizing the thermalization energy loss, provide a practical strategy to break through the power conversion efficiency (PCE). However, it is still challenge to realize the multilayered structure by all‐solution processing, especially shortage of interconnection layer (ICL), which physically and electronically connects front and rear subcells to accomplish the complicated tandem structure. Herein, all‐solution‐processed ICL of modified poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (m‐PEDOT) and titanium (diisopropoxide) bis(2,4‐pentanedionate) (TIPD) is invented for constructing inverted OTSCs, and by systematically managing the light and carriers within the stacked multilayers, highly efficient OTSCs are demonstrated. Compared with the traditional ICLs, it avoids the complicated vacuum evaporation and synthesis processes, guaranteeing low cost and high reproducibility. Furthermore, m‐PEDOT/TIPD ICL demonstrates excellent solvent resistance, high transmittance, and good conductivity. To enhance the light harvesting, absorption complementary donors and acceptors are selected as photoactive materials in front and rear subcells, and the transfer matrix formalism optical modeling is introduced to achieve the balanced short‐circuit current density of each subcell in OTSCs. By systematic device optimizations, the best PCE of 15.26% is achieved, among the best results reported for OTSCs.

High Performance Tandem Solar Cells with Inorganic Perovskite and Organic Conjugated Molecules to Realize Complementary Absorption.

All-inorganic halide perovskite solar cells (PerSCs) have achieved rapid development in recent years. However, limited by narrow absorption bands, the power conversion efficiency (PCE) of all-inorganic halide PerSCs lag behind the organic-inorganic hybrid ones. In this contribution, to expand their absorption spectra and enhance the PCE, tandem solar cells (TSCs) with inorganic perovskite and organic conjugated molecules are constructed, utilizing CsPbI2Br as an ultraviolet-visible light absorber and a PTB7-Th:IEICO-4F bulk-heterojunction (BHJ) active layer as a near-infrared light absorber. To physically and electronically connect the front and rear subcells, P3HT/MoO3/Ag/PFN-Br is introduced as an interconnecting junction. Finally, the TSCs exhibit a remarkably higher PCE of 17.24% compared to that of the single junction PerSCs (12.09%) and organic solar cells (OSCs) (10.89%). These results indicate that the combination of all-inorganic perovskite and a low bandgap organic active layer for TSCs is a feasible approach to realize broad spectra utilization and efficiency enhancement.

Enabling High-Performance Tandem Organic Photovoltaic Cells by Balancing the Front and Rear Subcells.

In tandem organic photovoltaics, the front subcell is based on large-bandgap materials, whereas the case of the rear subcell is more complicated. The rear subcell is generally composed of a narrow-bandgap acceptor for infrared absorption but a large-bandgap donor to realize a high open-circuit voltage. Unfortunately, most of the ultraviolet-visible part of the photons are absorbed by the front subcell; as a result, in the rear subcell, the number of excitons generated on large-bandgap donors will be reduced significantly. This reduces the (photo) conductivity and finally limits the hole-transporting property of the rear subcell. In this work, a simple and effective way is proposed to resolve this critical issue. To ensure sufficient photogenerated holes in the rear subcell, a small amount of an infrared-absorbing polymer donor as a third component is introduced, which provides a second hole-generation and transporting mechanism to minimize the aforementioned detrimental effects. Finally, the short-circuit current density of the two-terminal tandem organic photovoltaic is significantly enhanced from 10.3 to 11.7mAcm-2 (while retaining the open-circuit voltage and fill factor) to result in an enhanced power conversion efficiency of 15.1%.

High Efficiency Non-fullerene Organic Tandem Photovoltaics Based on Ternary Blend Subcells.

The application of tandem structure that integrates multiple subcells into one device is a promising way to realize high efficiency organic solar cells. However, current-matching among different subcells remains as the main challenge for organic tandem photovoltaics. Here, we provide a facile approach to achieve a good current matching via engineering the chemical composition of non-fullerene ternary blend subcells. For the front subcell, a ternary blend of PDBT-T1:TPH-Se:ITIC is selected due to its good thermal stability. The amorphous nature of TPH-Se can sufficiently suppress the unfavorable phase separation of blends during the heat treatment, enabling a sintering in the fabrication of high quality interconnecting layer. A double-junction tandem device is fabricated with a rear subcell consisting of PBDB-T:ITIC. After the optimization of the chemical composition of the front subcell, the power conversion efficiency (PCE) of double-junction tandem device increased from 10.6% using PDBT-T1:TPH-Se binary front subcell to 11.5% using PDBT-T1:TPH-Se:ITIC (1:0.9:0.1) ternary front subcell due to better current matching. In order to further enhance the light absorption in the near-infrared region, a third junction PBDTTT-EFT:IEICO-4F is introduced. The champion cell of triple-junction non-fullerene tandem solar cell achieves a PCE of 13.0% with a high open circuit voltage of 2.52 V.

A Nonfullerene Semitransparent Tandem Organic Solar Cell with 10.5% Power Conversion Efficiency

AbstractSemitransparent organic solar cells have great potential for building integrated photovoltaics and power‐generating windows owing to their advantages of light weight, mechanical flexibility, and color tunability. However, the performance of previous semitransparent organic solar cells have been limited by their relatively weak optical absorptions. In this paper, an efficient nonfullerene semitransparent tandem organic solar cell that exhibits a broad absorption from 300 to 1000 nm is reported. The rear subcell is based on a narrow‐bandgap nonfullerene acceptor named IEICS‐4F that exhibits a strong crystallinity and high electron mobility. As a result, the IEICS‐4F‐based single‐junction opaque and semitransparent organic solar cells yield high efficiencies of 10.3% and 7.5%, respectively. To further enhance light harvesting of the single‐junction semitransparent organic solar cells while maintaining a decent transmittance, a semitransparent tandem organic solar cell is fabricated by incorporating a medium‐bandgap P3TEA:FTTB‐PDI4 blend as the front subcell. A high efficiency of 10.5% is recorded with an average transmittance of 20%.