Efficient Tandem Cells Research Articles

Sn-Pb Perovskite with Strong Light and Oxygen Stability for All-Perovskite Tandem Solar Cells.

Research on mixed Sn-Pb perovskite solar cells (PSCs) is gaining significant attention due to their potential for high efficiency in all-perovskite tandem solar cells. However, Sn2+ in Sn-Pb perovskite is susceptible to oxidation, leading to a high defect density. The oxidation primarily occurs through two pathways: one involving a reaction with oxygen, and the other related to iodine defects, which generate I2 and further accelerate the oxidation of Sn2⁺, greatly reducing stability. First, to tackle the photo-stability issues caused by iodine defects, amber acid (AA) is screened as the additive. The Carboxyl group on AA can strongly coordinate with Sn2+, reinforcing the Sn─I bond and electrostatically interacting with negatively charged defects. This interaction inhibits the photoinduced formation of I2 and the subsequent oxidation of Sn2+, thereby enhancing the stability of Sn─Pb PSCs under continuous illumination. Building on the foundation of AA, a reductive sulfhydryl group is introduced to synthesize thiomalic acid (TA). It inhibits the formation of Sn4+ in both the perovskite precursor and the perovskite film, thereby improving air stability while maintaining strong photostability. Consequently, single PSCs achieved a champion efficiency of 22.7%. The best-performing two-terminal all-perovskite tandem solar cell achieved a power conversion efficiency of 28.6% with improved operational stability.

Perovskite/Silicon Tandem Solar Cells Above 30% Conversion Efficiency on Submicron-Sized Textured Czochralski-Silicon Bottom Cells with Improved Hole-Transport Layers.

In perovskite/silicon tandem solar cells, the utilization of silicon heterojunction (SHJ) solar cells as bottom cells is one of the most promising concepts. Here, we present optimization strategies for the top cell processing and their integration into SHJ bottom cells based on industrial Czochralski (Cz)-Si wafers of 140 μm thickness. We show that combining the self-assembled monolayer [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) with an additional phosphonic acid (PA) with different functional groups, can improve film formation when used as a hole transport layer improving wettability, minimizing shunt fraction and reducing nonradiative losses at the buried interface. Transient surface photovoltage and transient photoluminescence measurements confirm that the combined Me-4PACz/PA layer has similar charge transport properties to Me-4PACz alone. Moreover, this work demonstrates the potential for thin, double-side submicron-sized textured industry-relevant silicon bottom cells yielding a high accumulated short-circuit current density of 40.2 mA/cm2 and reaching a stabilized power conversion efficiency of >30%. This work paves the way toward industry-compatible, highly efficient tandem cells based on a production-compatible SHJ bottom cell.

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.

Homogenized contact in all-perovskite tandems using tailored 2D perovskite.

The fabrication of scalable all-perovskite tandem solar cells is considered an attractive route to commercialize perovskite photovoltaic modules1. However, The certified efficiency of 1-cm2 scale all-perovskite tandem solar cells lags behind their small-area (~0.1 cm2) counterparts2,3. This performance deficit originates from inhomogeneity in wide-bandgap (WBG) perovskite solar cells (PSCs) at a large scale. The inhomogeneity is known to be introduced at the bottom interface and within the perovskite bulk itself4,5. Here we uncover another crucial source for the inhomogeneity - the top interface formed during the deposition of the electron transport layer (ETL, C60). Meanwhile, the poor ETL interface is also a significant limitation of device performance. We address this issue by introducing a mixture of 4-fluorophenethylamine (F-PEA) and 4-trifluoromethyl-phenylammonium (CF3-PA) to create a tailored two-dimensional perovskite layer (TTDL), in which F-PEA forms a two-dimensional perovskite at the surface reducing contact losses and inhomogeneity, CF3-PA enhances charge extraction and transport. As a result, we demonstrate a high open-circuit voltage of 1.35 V and an efficiency of 20.5% in 1.77-eV WBG PSCs at a square centimeter scale. By stacking with a narrow-bandgap perovskite sub-cell, we report 1.05 cm2 all-perovskite tandem cells delivering 28.5% (certified 28.2%) efficiency, the highest among all reported so far. Our work showcases the importance of treating the top perovskite/ETL contact for upscaling perovskite solar cells.

Alder-Ene Reaction-Mediated Suppression of Tin(II) Oxidation for Efficient Tin-Lead Perovskite Solar Cells.

Despite numerous studies have reported the inhibition of tin (II) oxidation in mixed tin-lead halide perovskite, there remains a dearth of mechanistic information regarding how tin (II) undergoes oxidation in the precursor solution, particularly in terms of the involvement of DMSO. We here take advantage of density functional theory (DFT) to uncover that SnI2 can coordinate with DMSO and react with singlet oxygen, resulting in the generation of Sn (IV). Moreover, our DFT simulations reveal that benzaldehyde oxime (BZHO) competes with SnI2 in reacting with oxygen through the Alder-ene reaction, hence effectively restraining the oxidation of tin (II), which is further verified by several experimental characterizations. Besides, the introduction of BZHO has also regulated the crystallization of the perovskite film and modified the electronic structure of the perovskite surface. As a result, the perovskite solar cells with the addition of BZHO demonstrate superior performance and operational stability, retaining 82 % of the initial PCE under continuous 1-sun illumination for 800 hours. Furthermore, the efficiency of all-perovskite tandem solar cells treated with BZHO reached 26.76 %. Therefore, this work presents a promising strategy for designing high-performance and stable all-perovskite tandem solar cells.

Photosystem I enhanced perovskite–Organic tandem solar cell efficiency

Tandem solar cells (TSC) have been introduced to better absorb the spectrum of sunlight and reduce optical loss. Among these, perovskite–organic tandem solar cells (P-OTSC) have emerged as a prominent topic over the last decade due to their complementary absorption spectrum. Additionally, incorporating diverse pigmented protein complexes in TSC fabrication is becoming more common. Natural chlorophyll-containing photosystems have garnered significant attention for their naturally solar-tuned absorption spectra. Photosystem I protein (PSI), is the most robust component of oxygenic photosynthesis and contains over 100 Chl a molecules/complex with two sharp absorbance peaks at 430 and 665 nm. PSI offers a second and complementary active layer because P-OTSCs often have a low extinction coefficient in the red wavelength region. In this research, the performance of P-OTSCs was enhanced by improving the absorption spectrum by utilizing an isolated plant PSI complex. The circuit current density (Jsc) increased from 14.23 mA/cm² to 14.95 mA/cm², and the power conversion efficiency (PCE) of P-OTSCs increased from 19.32 % to 20.24 %. We also observed that the external quantum efficiency (EQE) shows an apparent increase in the long wavelength region, reflecting the absorbance of light by PSI. This work is the first to report the integration of PSI into perovskite–organic tandem solar cells, and it motivates new design considerations that can further boost efficiency and utilize natural, earth-abundant pigment proteins.

Formulation of optimized TCA using PDMS epoxy and Ag-coated PMMA for high-efficiency Si tandem solar cell applications

In this study, we aimed to develop and characterize Transparent Conductive Adhesive (TCA) materials for mechanically stacked tandem solar cell applications. The research objectives were to enhance the transparency, conductivity, and adhesive strength of TCAs to improve the efficiency and practicality of tandem solar cells. The TCA formulation comprises a combination of polymers and Ag-coated particles, with flexible poly-methyl methacrylate (PMMA) micro-spheres serving as conductive particles and SYLGARD 184 silicon elastomer poly-di-methyl-siloxane (PDMS), mixed in a 10:1 ratio of base to curing agent, serving as the transparent adhesive. We conducted systematic experiments with Ag-particle coverage areas ranging from 0.34 % to 21.61 % at temperatures of 80 °C and 100 °C, under 500 mb pressure. The optimal conductivity was achieved at 2 wt% Ag-particle coverage, measuring 5.26 × 10⁷ S/m, with over 93 % transparency. These key results indicate the significant potential of the optimized TCA in enhancing the performance of mechanically stacked tandem solar cells, thus contributing to the advancement of renewable energy technologies.

A Pyrazinyl Wide‐Bandgap Polymer Donor Yields 19.35% Efficiency in Tandem Organic Solar Cells

A Pyrazinyl Wide‐Bandgap Polymer Donor Yields 19.35% Efficiency in Tandem Organic Solar Cells

Impact of Temperature Optimization of ITO Thin Film on Tandem Solar Cell Efficiency.

This study examined the impact of temperature optimization on indium tin oxide (ITO) films in monolithic HJT/perovskite tandem solar cells. ITO films were deposited using magnetron sputtering at temperatures ranging from room temperature (25 °C) to 250 °C. The sputtering target was ITO, with a mass ratio of In2O3 to SnO2 of 90% to 10%. The effects of temperature on the ITO film were analyzed using X-ray diffraction (XRD), spectroscopic ellipsometry, and sheet resistance measurements. Results showed that all ITO films exhibited a polycrystalline morphology, with diffraction peaks corresponding to planes (211), (222), (400), (440), and (622), indicating a cubic bixbyite crystal structure. The light transmittance exceeded 80%, and the sheet resistance was 75.1 Ω/sq for ITO deposited at 200 °C. The optical bandgap of deposited ITO films ranged between 3.90 eV and 3.93 eV. Structural and morphological characterization of the perovskite solar cell was performed using XRD and FE-SEM. Tandem solar cell performance was evaluated by analyzing current density-voltage characteristics under simulated sunlight. By optimizing the ITO deposition temperature, the tandem cell achieved a power conversion efficiency (PCE) of 16.74%, resulting in enhanced tandem cell efficiency.

Comprehensive design and analysis of thin film Sb2S3/CIGS tandem solar cell: TCAD simulation approach

This research presents a design and analysis of a tandem solar cell, combining thin film wide bandgap Sb2S3 (1.72 eV) and narrow bandgap CIGS (1.15 eV) for the top and bottom sub-cells, respectively. The integration of all thin film layers enhances flexibility, rendering the tandem solar cell suitable for applications such as wearable electronics. To optimize the power conversion efficiency (PCE) of the tandem solar device, advanced technology computer-aided design (TCAD) simulation tools are employed to estimate loss mechanisms and fine-tune parameters for each layer. An experimentally validated optoelectronic model is introduced, calibrated and validated against fabricated reference solar cells for the individual top and bottom cells. The calibrated model is then utilized to propose optimization routines for the Sb2S3/CIGS tandem solar cell. The initial tandem cell exhibits a J SC of 15.72 mA cm−2 and a PCE of 15.36%. The efficiency drop in the tandem configuration is identified primarily in the top cell. A systematic optimization process for the top cell is initiated, exploring various configurations, including HTL-free and ETL-free setups. Moreover, an np homojunction structure for the top cell is proposed. Optimization routines are applied that involve determining optimal thickness and doping concentration of the n-layer, investigating the effect of p-layer doping concentration, and exploring the influence of the work function of the front contact. As a result, the tandem cell efficiency is significantly improved to 23.33% at the current matching point (CMP), with a J SC of 17.15 mA cm−2. The findings contribute to the advancement of thin-film tandem solar cell technology, showcasing its potential for efficient and flexible photovoltaic applications.

Performance and optimization study of selected 4-terminal tandem solar cells

Tandem solar cells owing to their layered structure in which each sub-cell utilizes a certain part of the solar spectrum with reduced thermal losses, are promising applicants to promote the power conversion efficiency beyond the Shockley–Queisser limit of single-junction solar cells. This study delves into the performance and optimization of 4-terminal organic/silicon tandem solar cells through numerical simulations using SCAPS-1D software. The tandem architecture combining organic, perovskite, and silicon materials, shows potential in enhancing light absorption across the solar spectrum with complementary absorption spectra. Through innovative material exploration, optimization techniques are explored to advance the performance boundaries of organic/silicon tandem solar cells. The study employs the Beer–Lambert law to assess the impact of varied physical parameters on tandem solar cell efficiency, aiming to propose optimal configurations. Results indicate a maximum efficiency of 25.86% with P3HT:PC70BM organic active layer (150 nm thickness) and 36.8% with Cs2AgBi0.75Sb0.25Br6 active layer (400 nm thickness) in the studied 4-terminal tandem structures. These findings offer valuable insights into the complex physics of these tandem solar cells, for developing high-performance and commercially practical photovoltaic devices.

Sustainable thermal regulation improves stability and efficiency in all-perovskite tandem solar cells

Mixed Sn-Pb perovskites have emerged as promising photovoltaic materials for both single- and multi-junction solar cells. However, achieving their scale-up and practical application requires further enhancement in stability. We identify that their poor thermal conductivity results in insufficient thermal transfer, leading to heat accumulation within the absorber layer that accelerates thermal degradation. A thermal regulation strategy by incorporating carboranes into perovskites is developed; these are electron-delocalized carbon-boron molecules known for their efficient heat transfer capability. We specifically select ortho-carborane due to its low thermal hysteresis. We observe its existence through the perovskite layer showing a decreasing trend from the buried interface to the top surface, effectively transferring heat and lowering the surface temperature by around 5 °C under illumination. o-CB also facilitates hole extraction at the perovskite/PEDOT:PSS interface and reduces charge recombination. These enable mixed Sn-Pb cells to exhibit improved thermal stability, retaining 80% of their initial efficiencies after aging at 85 °C for 1080 hours. When integrated into monolithic all-perovskite tandems, we achieve efficiencies of over 27%. A tandem cell maintains 87% of its initial PCE after 704 h of continuous operation under illumination.

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.

Highly Transparent Oxygen‐Doped Poly‐Si with In‐situ N2O Oxidant for Poly‐Si Passivating Contacts in Perovskite/Silicon Tandem Solar Cells

Tunnel oxide passivated contact (TOPCon) silicon solar cells have been developed and transferred into industrial mass production, which is beneficial to the future production of perovskite/silicon tandem solar cells (TSCs) in a large scale. However, the doped polycrystalline silicon (poly‐Si) layer in the poly‐Si‐based passivating contact structure yields a profound optical loss from reflection and parasitic absorption, which obstacles the efficiency promotion of TSCs. In this work, the optical property of poly‐Si is improved by in‐situ oxygen incorporation using plasma enhanced chemical vapor deposition (PECVD) with nitrous oxide (N2O) as the oxygen source. The p‐type oxygen‐incorporated poly‐Si (poly‐SiOx) shows a reduced refractive index and extinction coefficient over 700–1200 nm wavelength, leading to a reduced reflection, a lower parasitic absorption and a higher transmission. After applying an optimized p‐type oxygen‐incorporated poly‐Si in the front‐side poly‐Si passivating contact structure of c‐Si bottom cell, the short‐circuit current density and efficiency of a perovskite/c‐Si tandem cell increases by ≈0.32 mA cm−2 and ≈0.8%, respectively, leading to 25.12% tandem cell efficiency.

Enhanced efficiency in two-terminal all-perovskite tandem solar cells via binary functional high polymer doping strategy

An enhanced power conversion efficiency (PCE) of 26.1 % has been achieved in two-terminal (2T) all-perovskite tandem perovskite solar cells (TPSCs) via a binary functional high polymer doping strategy. By incorporating methylene diphenyl diisocyanate polyurethane (MDI-PU) and PJ71 into the wide bandgap (WBG) and narrow bandgap (NBG) perovskite layers, respectively, the perovskite crystalline quality of them was significantly improved. The optimized PCE of the WBG top cell and the NBG bottom cell achieved 17.6 % and 20.9 %, respectively. After continuous dark storage of 150 days in nitrogen-filled glovebox, the PCE of optimized TPSC remained 94.2 % of initial. TPSCs on flexible substrates of polyethylene naphthalate (PEN) and silk-derived substrate (SDS) were also studied. With the binary polymer doping strategy, the PEN-based TPSC achieved a champion PCE of 22.2 %, and exhibited excellent anti-bending ability compared with control. The champion SDS-based TPSC achieved the PCE of 11.6 %, and showed enhanced anti-stretching ability. We demonstrate that strong coordinate bonding formed between the O atom in the carbonyl group of MDI-PU and the Pb2+ ions at the grain boundaries (GBs) in WBG perovskite. For the NBG layer, the S atoms in the thiophene structure of PJ71 interact with the Pb2+ and Sn2+ ions in the NBG perovskite and effectively passivate the GB defects. The study suggests the potential for developing new generation multi-functional optoelectronic high polymers to further boost the performance of 2T all-perovskite TPSCs.

Octahedral Tilt Enables Efficient and Stable Fully Vapor‐Deposited Perovskite/Silicon Tandem Cells

AbstractThermal evaporation can significantly facilitate scalable, uniform, and conformal perovskite film, particularly well‐suited for the preparation of perovskite/silicon (Si) tandem solar cells . However, the perovskite material easily induces a phase transition from a photoactive phase to a photoinactive phase, limiting the development of the stability and efficiency of tandem cells. Introducing lead chloride (PbCl2) into wide‐bandgap perovskite materials is beneficial for the fabrication of efficient and stable light‐absorbing materials, but the microscopic mechanism of the effect of PbCl2 on perovskite is still unclear. The study here reports evidences that the addition of PbCl2 to improve perovskite film stability and optoelectronic performance is due to the minor octahedral tilting of the perovskite structure are reported. It also demonstrates that this strategy accelerates interfacial charge transfer and carrier diffusion in the perovskite bulk and heterojunction interfaces. Therefore, the wide‐bandgap perovskite solar cells (PSCs) prepared by adding PbCl2 exhibit a champion power conversion efficiency (PCE) of 17.80%. The PSCs retain 97% of their performance following 200 h of operation at the maximum power point under full 1‐sun illumination. Finally, monolithic perovskite/Si tandem cells with record PCEs of 27.43% and an open‐circuit voltage of 1.817 V are fabricated.

Versatile implied open‐circuit voltage imaging method and its application in monolithic tandem solar cells

AbstractAs the efficiency of perovskite silicon tandem solar cells is increasing, the upscaling for industrial production is coming into focus. Spatially resolved, quantitative, fast, and reliable contactless measurement techniques are demanded for quality assurance and to pinpoint the cause of performance losses in perovskite silicon tandem solar cells. In this publication, we present a measurement method based on spectrally integrated photoluminescence (PL) imaging to extract subcell‐selective implied open‐circuit ( ) images from monolithic perovskite silicon tandem solar cells. We validate the approach using spectrally resolved absolute PL measurements based on an integrating sphere for the perovskite top cell and PL‐calibrated carrier lifetime images for the silicon bottom cell. Additionally, measurements of solar cells with low contact losses are used to validate the new measurement technique. We find a good agreement of the images with the validating measurements with a maximum deviation of well below 1% compared to the validation measurements.

Enhancing Tandem Solar Cell's efficiency through convolutional neural network-based optimization of metasurfaces

Tandem Solar cells are composed of multiple layers with varying bandgap materials to facilitate the absorption of a wider range of solar energy. However, their performance is hampered by interface losses leading to current mismatching. To overcome these limitations, tandem solar cells often require the use of mirrors and lenses to concentrate and trap light to achieve optimal efficiency. Recently, the use of nanoscale 2D meta-materials has emerged as a promising alternative to traditional lenses. However, the optical optimization of these meta-materials can be both time-consuming, resources, and space-intensive, posing a challenge to their implementation. This study explores the use of deep learning to predict the optimal optical design for the top cell in tandem solar cells to maximize power conversion efficiency. Computational techniques are used to analyze the optical responses of metasurfaces. 2D-Convolutional Neural Networks (CNN) are used to train a dataset of 10,578 TiO2/CH3NH3PBr3/ZnO metasurfaces. Nine different CNN models were used with different architectures to identify the best hyperparameters that give the low mean square error. CNN displayed fast high prediction accuracy taking an average of 0.3 ± 0.05 seconds per prediction. The Deep SHapley Additive Explanations (SHAP) algorithm was used to gain insights into CNN's predictions and understand the behavior of complex metasurfaces integrated into a typical reference tandem solar cell architecture. The proposed metasurfaces can significantly enhance the efficiency of tandem solar cells. The active layer comprises of near 90% absorption of the solar spectrum. The average absorption of the top cell increased in the UV-vis region (650-800nm) up to 93.4%.

Transparent Recombination Electrode with Dual-Functional Transport and Protective Layer for Efficient and Stable Monolithic Perovskite/Organic Tandem Solar Cells.

Rational selection and design of recombination electrodes (RCEs) are crucial to enhancing the power conversion efficiency (PCE) and stability of monolithic tandem solar cells (TSCs). Sputtered indium tin oxide (ITO) with high conductivity and excellent transmittance is introduced as RCE in perovskite/organic TSCs. To prevent high-energy ITO particles destroy the underlying material during sputtering, dual-functional transport and protective layer (C1) is employed. The styryl group in C1 can be thermally crosslinked to serve as a sputtering protective layer. Meanwhile, the conjugated phenanthroline skeleton in C1 shows high electron mobility and hole blocking capability to promote the electron transport process at the interfaces and effectively reduce charge accumulation. Monolithic perovskite/organic TSC with high PCE of 24.07% and excellent stability is demonstrated by stacking a 1.77eV bandgap perovskite layer and a 1.35eV bandgap organic active layer. This strategy provides new insights for overcoming the fundamental efficiency limits of single-junction devices and promotes the further development of TSC devices.

Nanoscale Size Control of Si Pyramid Texture for Perovskite/Si Tandem Solar Cells Enabling Solution‐Based Perovskite Top‐Cell Fabrication and Improved Si Bottom‐Cell Response

AbstractA monolithic perovskite/silicon tandem solar cell architecture is employed to surpass the single‐junction efficiency limit. Recently, there is an increasing need for the double‐sided textures in the Si bottom cell to be compatible with the solution‐processed perovskite top cell from an industrial perspective. Herein, a silver‐assisted alkaline etching method is applied to fabricate nanoscale Si pyramid textures, and the influence of varying pyramid size (400–900 nm) on the interface morphology and the performance of perovskite/Si tandem cells is investigated. It is demonstrated that electrical shunting starts to increase, and the open‐circuit voltage (VOC) decreases when the texture size exceeds the perovskite thickness (~500nm) due to the non‐uniform top‐cell formation on a rough Si surface. However, when the texture size is reduced to 400–500 nm, all spin‐coated perovskite top‐cell component layers exhibit an even form over the nanopyramid Si, resulting in a high VOC and an enhanced Si bottom cell current (≈1.0 mA cm−2) due to the suppressed reflectance at the top/bottom cell interface without using optical couplers. The double‐sided nanopyramid Si texture offers opportunities to increase tandem cell efficiency while reducing its production cost compared with the commonly used single‐sided textured Si.