Low Power Conversion Efficiency Research Articles

Development and Challenges of Large‐Area All‐Perovskite Tandem Solar Cells and Modules

The efficiency of all‐perovskite tandem solar cells has recently surpassed that of single‐junction perovskite solar cells, showing great potential as a future photovoltaic technology due to its low manufacturing cost and high power conversion efficiency potential, yet the size of these cells is still at the laboratory level. It is highly required to develop scalable preparation methods to fabricate large‐area all‐perovskite tandem solar modules for commercial applications. Herein, the key challenges encountered in the laboratory of all‐perovskite tandem solar cells and the existing solutions are summarized and some views on the preparation of large areas and modules are given.

Regulating the Quantum Dots Integration to Improve the Performance of Tin–Lead Perovskite Solar Cells

AbstractDespite their advantageous attributes, such as a narrow bandgap and reduced toxicity, tin–lead halide perovskites (TLHPs) have received limited attention due to their lower power conversion efficiency (PCE) relative to lead‐only variants. In this study, a transformative approach is introduced that leverages perovskite quantum dots (PQDs) to optimize TLHP solar cells. While conventional oleyl‐capped PQDs enhance the open circuit voltage (VOC), the long‐chain ligands hinder charge transport. To overcome this limitation, a post‐treatment with isopropyl alcohol effectively dissociates these ligands and PQD crystals, resulting in reduced defect density, improved charge transfer, and elevated quasi‐Fermi level splitting in the TLHP device. Consequently, the PCE of the device is notably increased from 19.0% to 23.74% and elevated the VOC from 0.78 to 0.87 V, without compromising the photocurrent or fill factor. The findings highlight PQD modification as a compelling avenue for TLHP solar cell enhancement, particularly in boosting VOC.

Mitigation of Exciton Quenching Sites in All‐Metal‐Oxide‐Based Transparent Photovoltaic

Transparent photovoltaic (TPV) devices offer the potential to generate power without being visible to the human eye, making them ideal for use in building integrated photovoltaic applications. TPV devices based on inorganic materials offer eco‐friendly frameworks with stable performances. However, their low power conversion efficiency and incapacity to produce onsite power for real‐time practical applications limit their widespread deployment. Mitigation of exciton quenching by reducing the interface and bulk recombination can significantly improve the performance of TPVs. To address this, the present study investigates the effect of passivation layers (PLs) in all‐metal‐oxide TiO2/Cu2O TPV. The TiO2/Cu2O TPV interface is passivated by depositing thin Al2O3 and Ga2O3 films. The study comprehensively analyzes how passivation controls the interfacial and bulk defects. Electrochemical impedance spectroscopy and X‐ray photoelectron spectroscopy are used to elucidate exciton quenching mechanisms. The results show that the insertion of a thin PL on top of TiO2 effectively mitigates exciton quenching by suppressing hydroxyl ions, Ti2+, and Ti3+ bulk states. Ga2O3 PL, in particular, leads to a substantial enhancement in short‐circuit current density (12.4 mA cm−2) and open‐circuit voltage (669 mV). The study also demonstrates the real‐time onsite energy production and its utilization through the operation of an electric fan.

Comprehensive Insight into the Structure Contribution of A2‐A1‐D‐A1‐A2 Acceptor to Performance of P3HT Solar Cells

AbstractPoly(3‐hexylthiophene) (P3HT) acting as one of the most popular and low‐cost polymers is quite suitable for commercialization of organic solar cells but suffers from low power conversion efficiency (PCE) because of the limited matching non‐fullerene acceptors (NFAs). One important reason that restricts the enhancement but remains unresolved is the undisclosed contributions of the subtle structure modification to the obvious performance change. In combination with the previous reports and this work, herein A2‐A1‐D‐A1‐A2 type NFAs with single, dual, and triple modifications based on parent BTA3 is designed, including benzyl‐substitution on A2 group (namely Bn modification), fluorine‐substitution on A1 group (namely F modification), and thieno[3,2‐b]thiophene‐substitution on D group (namely TT modification). It is finally found that the binary devices of P3HT with these NFAs underwent unexpected variations in the aspect of molecular optoelectronic property, blend morphological feature and charge generation process. The triple modification (including Bn, F, and TT) gives full play to their unique advantages and consequently increases PCE by 60%. To the knowledge, the obtained optimal PCE is one of the highest values for A2‐A1‐D‐A1‐A2 type NFAs. This study provides clearer insights into the rational substitutions on the A2‐A1‐D‐A1‐A2 acceptors matched with P3HT for high‐performance organic photovoltaics.

Ligand-Induced In Situ Epitaxial Growth of PbI2 Nanosheets/MAPbI3 Heterojunction Realizes High-Performance HTM-Free Carbon-Based MAPbI3 Solar Cells.

Hole-transporting layer-free carbon-based perovskite solar cells (HTL-free C-PSCs) hold great promise for photovoltaic applications due to their low cost and outstanding stability. However, the low power conversion efficiency (PCE) of HTL-free C-PSCs mainly results from grain boundaries (GBs). Here, epitaxial growth is proposed to rationally design a hybrid nanostructure of PbI2 nanosheets/perovskite with the desired photovoltaic properties. A post-treatment technique using tri(2,2,2-trifluoromethyl) phosphate (TFEP) to induce in situ epitaxial growth of PbI2 nanosheets at the GBs of perovskite films realizes high-performance HTL-free C-PSCs. The structure model and high-resolution transmission electron microscope unravel the epitaxial growth mechanism. The epitaxial growth of oriented PbI2 nanosheets generates the PbI2 /perovskite heterojunction, which not only passivates defects but forms type-I band alignment, avoiding carrier loss. Additionally, Fourier-transform infrared spectroscopy, 31 P NMR, and 1 H NMR spectra reveal the passivation effect and hydrogen bonding interaction between TFEP and perovskite. As a result, the VOC is remarkably boosted from 1.04 to 1.10V, leading to a substantial gain in PCE from 14.97% to 17.78%. In addition, the unencapsulated PSC maintains the initial PCE of 80.1% for 1440h under air ambient of 40% RH. The work offers a fresh perspective on the rational design of high-performance HTL-free C-PSCs.

Fully solution-processed n-i-p type perovskite solar cells with efficiency over 19% enabled by a hydrophobic PEDOT:F interlayer and silver nanowire top electrode

Solution-processed top electrode is the key technology for the realization of fully solution-processed perovskite solar cells (PSCs). In this paper, we reported the preparation of fully-solution processed n-i-p type PSCs with spray-coated silver nanowires (AgNWs) top electrode. Experiment results demonstrated that low power conversion efficiency (PCE) of 16.00% with a low fill factor of 67.41% was obtained for the reference cell, when the AgNWs is directly coated on the 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (Spiro-OMeTAD) layer. This result indicates a charge extraction barrier at the Spiro-OMeTAD/AgNWs interface, which could be attributed to the poor compatibility between Spiro-OMeTAD and AgNWs layers. By inserting a thin layer of poly(3,4-ethylenedioxythiophene):perfluorinated sulfonic acid ionomers (PEDOT:F), a modified PEDOT with lower surface energy, the interface connection between Spiro-OMeTAD/PEDOT:F and AgNWs was improved, leading to an enhanced PCE of up to 19.11%. In addition, the PEDOT:F-based cells retained 64% of the initial PCE after operating at the maximum power point for 1800 h, whereas the reference cells retained only 30% of the initial PCE. The current work proved that PEDOT:F/AgNWs could be an excellent option for fully-solution processed n-i-p type PSCs.

A Comprehensive Review on Defects-Induced Voltage Losses and Strategies toward Highly Efficient and Stable Perovskite Solar Cells

The power conversion efficiency (PCE) of single-junction perovskite solar cells (PSCs) has reached 26.1% in small-scale devices. However, defects at the bulk, surface, grain boundaries, and interfaces act as non-radiative recombination centers for photogenerated electron-hole pairs, limiting the open-circuit voltage and PCE below the Shockley–Queisser limit. These defect states also induce ion migration towards interfaces and contribute to intrinsic instability in PSCs, reducing the quasi-Fermi level splitting and causing anomalous hysteresis in the device. The influence of defects becomes more prominent in large-area devices, demonstrating much lower PCE than the lab-scale devices. Therefore, commercializing PSCs faces a big challenge in terms of rapid decline in working performance due to these intrinsic structural defects. This paper provides a comprehensive review of recent advances in understanding the nature and the classification of defects, their impact on voltage losses, device parameters, intrinsic stability, and defect quantification and characterization techniques. Novel defect passivation techniques such as compositional engineering, additive engineering, post-treatments, dimensionality engineering, and interlayer engineering are also reviewed, along with the improvements in PCE and stability based on these techniques for both small-area devices and large-area roll-to-roll coated devices.

Density Functional Theory Simulation of Dithienothiophen[3,2-b]-pyrrolobenzothiadiazole-Based Organic Solar Cells

We have simulated the effect of changing the end groups in BTP core with five organic units of 1,3-Indandione (IN), 2-thioxothiazolidin-4-one (Rhodanine), propanedinitrile (Malononitrile), (2-(6-oxo-5,6-dihydro-4H-cyclopenta[c]thiophen-4-ylidene)malononitrile) (CPTCN) and 2-(3-oxo-2,3-dihydroinden-1-ylidene (IC), and two halogenated units of (4F) IC and (4Cl) IC on the optical and photovoltaic properties of the BTP DA’D core molecular unit. Thus modified, seven molecular structures are considered and their optical properties, including HOMO and LUMO energies and absorption spectra are simulated in this paper. On the basis of HOMO and LUMO energies, it is found that two of the seven molecules, BTP-IN and BTP-Rhodanine, can act as donors and the other four, BTP-(4F) IC, BTP-(4Cl) IC, BTP-CPTCN and BTP-IC, as acceptors in designing bulk heterojunction (BHJ) organic solar cells (OSCs). Using these combinations of donors and acceptors in the active layer, eight BHJ OSCs, such as BTP-IN: BTP-(4F) IC, BTP-IN: BTP-(4Cl) IC, BTP-IN: BTP-CPTCN, BTP-IN: BTP-IC, BTP-Rhodanine: BTP-(4F) IC, BTP-Rhodanine: BTP-(4Cl) IC, BTP-Rhodanine: BTP-CPTCN and BTP-Rhodanine: BTP-IC, are designed, and their photovoltaic performance is simulated. The photovoltaic parameters Jsc, Voc and FF for all eight BHJ OSCs and their power conversion efficiency (PCE) are simulated. It is found that the BHJ OSC of the BTP-IN: BTP-CPTCN donor–acceptor blend gives the highest PCE (14.73%) and that of BTP-Rhodanine: BTP-(4F) IC gives the lowest PCE (12.07%). These results offer promising prospects for the fabrication of high-efficiency BHJ OSCs with the blend of both donor and acceptor based on the same core structure.

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.

Thiophene-based Solar Cell. A Review

Abstract: In recent years, perovskite solar cells, which use a hybrid inorganic-organic material, have also made remarkable progress and achieved a rapid increase in efficiency. The organic materials used are usually small conductive molecules, polymers or oligomers. The fused thiophenes, polythiophenes and olithiophenes used for this purpose are presented. The condensed thiophene-based small molecule for DSSCs shows important properties such as simplicity of synthesis and purification methods, well-defined and reproducible structures, but low power conversion efficiencies. Polymers of thiophene for DSSCs show high power conversion efficiencies, especially in ternary systems, even >19%; however, they have poor long-term stability because of the molecular size and packing properties of the polymer chains. Oligomers of thiophene for DSSCs have good long-term stability but low power conversion efficiencies.

Crystallization control of wide-bandgap perovskites for efficient solar cells via adding an anti-solvent into the perovskite precursor.

Organic-inorganic halide-based wide-bandgap perovskite solar cells (PSCs) have been researched extensively due to their potential application in tandem solar cells. In this study, we directly added an anti-solvent (diethyl ether, DE) into the perovskite precursor for controlling the crystallization process of perovskite layers with a wide bandgap (1.74 eV). The introduction of DE could facilitate the nucleation and accelerate the perovskite growth during the spin-coating process. Due to the improved crystallization of the perovskite, the wide-bandgap PSCs showed a high power-conversion efficiency (PCE) of 19.7% on average with improved current density and fill factor. In contrast, the control devices without using DE exhibited a low average PCE of 17.6%. Moreover, the ambient stability of the related PSCs was simultaneously enhanced with a remarkably decreased PCE degradation, from 31.3% to 16.8%, after 16 days of storage and measurement. The DE-assisted well-crystallized PSCs showed a highest PCE of 20.1%, with a stable current output and negligible hysteresis. Our research provides a simple and effective way for controlling the crystallization of wide-bandgap perovskite layers and hence improving the performance of wide-bandgap PSCs.

Unraveling the Structure-Property-Performance Relationships of Fused-Ring Nonfullerene Acceptors: Toward a C-Shaped ortho-Benzodipyrrole-Based Acceptor for Highly Efficient Organic Photovoltaics.

The high-performance Y6-based nonfullerene acceptors (NFAs) feature a C-shaped A-DA'D-A-type molecular architecture with a central electron-deficient thiadiazole (Tz) A' unit. In this work, we designed and synthesized a new A-D-A-type NFA, termed CB16, having a C-shaped ortho-benzodipyrrole-based skeleton of Y6 but with the Tz unit eliminated. When processed with nonhalogenated xylene without using any additives, the binary PM6:CB16 devices display a remarkable power conversion efficiency (PCE) of 18.32% with a high open-circuit voltage (Voc) of 0.92 V, surpassing the performance of the corresponding Y6-based devices. In contrast, similarly synthesized SB16, featuring an S-shaped para-benzodipyrrole-based skeleton, yields a low PCE of 0.15% due to the strong side-chain aggregation of SB16. The C-shaped A-DNBND-A skeleton in CB16 and the Y6-series NFAs constitutes the essential structural foundation for achieving exceptional device performance. The central Tz moiety or other A' units can be employed to finely adjust intermolecular interactions. The single-crystal X-ray structure reveals that ortho-benzodipyrrole-embedded A-DNBND-A plays an important role in the formation of a 3D elliptical network packing for efficient charge transport. Solution structures of the PM6:NFAs detected by small- and wide-angle X-ray scattering (SWAXS) indicate that removing the Tz unit in the C-shaped skeleton could reduce the self-packing of CB16, thereby enhancing the complexing and networking with PM6 in the spin-coating solution and the subsequent device film. Elucidating the structure-property-performance relationships of A-DA'D-A-type NFAs in this work paves the way for the future development of structurally simplified A-D-A-type NFAs.

Eu-Based Porphyrin MOF Enables High-Performance Carbon-Based Perovskite Solar Cells.

The low power conversion efficiency (PCE) of hole transport materials (HTM) - free carbon-based perovskite solar cells (C-PSCs) poses a challenge. Here, a novel 2D Eu-TCPP MOF (TCPP; [tetrakis (4-carboxyphenyl) porphyrin]) sandwiched between the perovskite layer and the carbon electrode is used to realize an effective and stable HTM-free C-PSCs. Relying on the synergistic effect of both the metal-free TCPP ligand with a unique absorption spectrum and hydrophobicity and the EuO4(OH)2 chain in the Eu-TCPP MOF, defects are remarkably suppressed and light-harvesting capability is significantly boosted. Energy band alignment is achieved after Eu-TCPP MOF treatment, promoting hole collection. Förster resonance energy transfer results in improved light utilization and protects the perovskite from decomposition. As a result, the HTM-free C-PSCs with Eu-TCPP MOF reach a champion PCE of 18.13%. In addition, the unencapsulated device demonstrates outstanding thermal stability and UV resistance and keeps 80.6% of its initial PCE after 5500h in a high-humidity environment (65%-85% RH).

Understanding the Dominant Physics Mechanisms on the p‐i‐n Perovskite Solar Cells Fabricated by Scalable Slot‐Die Coating Process in Ambient Air

Perovskite solar cells (PSC) are emerging technologies that have shown continuous improvement in power conversion efficiency (PCE) and stability. However, a very important aspect that has been seldom considered is the reproducibility of PCE of PSC devices. It is possible to achieve PCE from 10.21% to 17.05% using scalable slot‐die‐coating technique. However, a spatial distribution of performance is clearly observed for device samples on a 4 × 4 cm substrate. The relatively low PCE is mainly coming from the losses of electrical mechanism. To have in‐depth understanding of the losses, the dominant loss analysis techniques including numerical simulations are used to explore the mechanism. In the results, it is indicated that a part of efficiency decrease is due to the increase of bulk defect density which linearly changes with the quality of the perovskite layer and related to recombination process. However, extremely high‐charge‐carrier transportation losses are found at the HTL/perovskite interface that are related to the Fermi‐level pinning mechanism for low‐efficiency device. The result of physics insight of perovskite solar cells leads to a strategy, where chemical passivation technique is used to achieve the PCE from 13.81% to 18.07% for the batch of devices with good reproducibility.

Machine Learning for Ultra High Throughput Screening of Organic Solar Cells: Solving the Needle in the Haystack Problem

AbstractOver the last two decades the organic solar cell community has synthesized tens of thousands of novel polymers and small molecules in the search for an optimum light harvesting material. These materials are often crudely evaluated simply by measuring the current–voltage (JV) curves in the light to obtain power conversion efficiencies (PCEs). Materials with low PCEs are quickly disregarded in the search for higher efficiencies. More complex measurements such as frequency/time domain characterization that could explain why the material performed as it is often not performed as they are too time consuming/complex. This limited feedback forced the field to advance using a more or less random walk of material development and has significantly slowed progress. Herein, a simple technique based on machine learning that can quickly and accurately extract recombination time constants and charge carrier mobilities as a function of light intensity simply from light/dark JV curves alone. This technique reduces the time to fully analyze a working cell from weeks to seconds and opens up the possibility of not only fully characterizing new devices as they are fabricated, but also data mining historical data sets for promising materials the community has overlooked.

Achieving More Insight on the Dynamic Process from Conventional/Inverted Layer‐by‐Layer All‐Polymer Solar Cells with 17.24% or 12.41% Efficiency

Series of bulk heterojunction (BHJ) and layer‐by‐layer (LbL) all‐polymer solar cells (APSCs) were prepared with polymer PM6 as donor and polymer PY‐DT as acceptor based on conventional and inverted configuration. Benefiting from the sequential deposition strategy, the good vertical phase separation and more ordered molecular arrangement can be formed in the LbL APSCs. The conventional LbL APSCs exhibit an optimized power conversion efficiency (PCE) of 17.24% with a relatively large short circuit current density of 23.83 mA cm−2 and fill factor of 74.60%, photogenerated excitons near the indium tin oxide electrode can be efficiently utilized through energy transfer from PM6 to PY‐DT and the self‐absorption effect of PM6 for its long exciton diffuse distance. The 17.24% PCE of conventional LbL APSCs is higher than 16.72% of conventional BHJ APSCs, 14.59% of inverted BHJ APSCs and 12.41% of inverted LbL APSCs. The rather low PCE of 12.41% for the inverted LbL APSCs further indicates that the energy transfer from donor to acceptor and self‐absorption effect of donor should play a vital role in determining the performance of LbL APSCs. This work provides more insights on the exciton and carrier dynamic process in sequentially deposited active layer, providing more guidance for preparing efficient LbL APSCs.

Numerical Study on Overcoming the Light-Harvesting Limitation of Lead-Free Cs2AgBiBr6 Double Perovskite Solar Cell Using Moth-Eye Broadband Antireflection Layer

Lead-free Cs2AgBiBr6 double perovskite has emerged as a promising new-generation photovoltaic, due to its non-toxicity, long carrier lifetime, and low exciton binding energies. However, the low power conversion efficiency, due to the high indirect bandgap (≈2 eV), is a challenge that must be overcome and acts as an obstacle to commercialization. Herein, to overcome the limitations through the light trapping strategy, we analyzed the performance evaluation via FDTD simulation when applying the moth-eye broadband antireflection (AR) layer on top of a Cs2AgBiBr6 double perovskite cell. A parabola cone structure was used as a moth-eye AR layer, and an Al2O3 (n: 1.77), MgF2 (n: 1.38), SiO2 (n: 1.46), and ZnO (n: 1.9) were selected as investigation targets. The simulation was performed assuming that the IQE was 100% and when the heights of Al2O3, MgF2, SiO2, and ZnO were 500, 350, 250, and 450 nm, which are the optimal conditions, respectively, the maximum short-circuit current density improved 41, 46, 11.7, and 15%, respectively, compared to the reference cell. This study is meaningful and innovative in analyzing how the refractive index of a moth-eye antireflection layer affects the light trapping within the cell under broadband illumination until the NIR region.

Suppressing Oxidation at Perovskite-NiOx Interface for Efficient and Stable Tin Perovskite Solar Cells.

Inorganic nickel oxide (NiOx) is an ideal hole transport material (HTM) for the fabrication of high-efficiency, stable, and large-area perovskite photovoltaic devices because of its low cost, stability, and ease of solution processing. However, it delivers low power conversion efficiency (PCE) in tin perovskite solar cells (TPSCs) compared to other organic HTMs. Here, the origin of hole transport barriers at the perovskite-NiOx interface is identified and a self-assembled monolayer interface modification is developed, through introducing (4-(7H-dibenzo[c,g]carbazol-7-yl)ethyl)phosphonic acid (2PADBC) into the perovskite-NiOx interface. The 2PADBC anchors undercoordinated Ni cations through phosphonic acid groups, suppressing the reaction of highly active Ni≥3+ defects with perovskites, while increasing the electron density and oxidation activation energy of Sn at the perovskite interface, reducing the interface nonradiative recombination caused by tetravalent Sn defects. The devices deliver significantly increased open-circuit voltage from 0.712 to 0.825V, boosting the PCE to 14.19% for the small-area device and 12.05% for the large-area (1 cm2) device. In addition, the 2PADBC modification enhances the operational stability of NiOx-based TPSCs, maintaining more than 93% of their initial efficiency after 1000 h.

Green-based modifiable CaZnBr4 for solar cells application

Future revolution in photovoltaics will be hinged mainly on cost, health implication, and material stability and performance. Based on these criteria, lead-based inorganic photovoltaics, organic–inorganic hybrid, and silicon photovoltaics are screened-out. According to the literature, the lead-free inorganic perovskite solar cell is favorably disposed to cost and safe-health. However, the simultaneous solution to material stability, high defect density, and low power conversion efficiency (PCE) still remains a mystery that has not been solved. This research proposed the green-based modifiable CaZnBr4 as a potential candidate for lead-free solar cell application based on the principle of A-site cation with green-based additive incorporation. The green-based additive was obtained from Kola Nitida, Carica Papaya, Ficus Exasperata, and Musa paradisiaca. The elemental characterization of the green-based additives was performed using X-ray fluorescence spectroscopy (XRF). The optical, crystalline, and electronic properties were characterized using ultraviolet–visible (UV–Vis) spectroscopy, X-ray diffractometry, Quantum Espresso, scanning electron microscopy and SCAPS-1D. The green-base-modified CaZnBr4 showed significant PCE improvement by 3% with significant film and crystallinity formation. The stressed state of the parent compound CaZnBr4 shows that it may be better suited for thermovoltaics application. It is recommended that better results could be obtained when different synthetic routes and green-based additives are used to initiate the defect passivation protocols.

Bimolecularly passivated interface enables efficient and stable inverted perovskite solar cells

Compared with the n-i-p structure, inverted (p-i-n) perovskite solar cells (PSCs) promise increased operating stability, but these photovoltaic cells often exhibit lower power conversion efficiencies (PCEs) because of nonradiative recombination losses, particularly at the perovskite/C 60 interface. We passivated surface defects and enabled reflection of minority carriers from the interface into the bulk using two types of functional molecules. We used sulfur-modified methylthio molecules to passivate surface defects and suppress recombination through strong coordination and hydrogen bonding, along with diammonium molecules to repel minority carriers and reduce contact-induced interface recombination achieved through field-effect passivation. This approach led to a fivefold longer carrier lifetime and one-third the photoluminescence quantum yield loss and enabled a certified quasi-steady-state PCE of 25.1% for inverted PSCs with stable operation at 65°C for >2000 hours in ambient air. We also fabricated monolithic all-perovskite tandem solar cells with 28.1% PCE.