Power Conversion Efficiency Values Research Articles

Extrapolative Machine Learning for Accurate Efficiency Prediction in Non‐Fullerene Ternary Organic Solar Cells: Leveraging Computable Molecular Descriptors in High‐Throughput Virtual Screening

Adding a third component to binary organic solar cells (OSCs) enhances ternary OSCs, boosting power conversion efficiency (PCE). However, developing and optimizing appropriate donors, acceptors, and ternary materials remains a complex and demanding task. This study presents four machine‐learning (ML) predictive models using XGBoost and ANN approaches, utilizing both experimental and DFT‐derived HOMO and LUMO levels for efficient high‐throughput virtual screening (HTVS) of top candidates based on PCE. Two distinct latent databases were employed for HTVS: one consisting of 429 413 uniquely recombined ternary OSC systems from experimentally available data, and another comprising ≈2.3 million unique donor molecules from the Harvard Clean Energy Project database (CEPDB). The four ML models demonstrated notable predictive accuracy for PCE on a test dataset containing molecules closely aligned with the training set (interpolation). However, the XGBoost model showed constrained extrapolative ability for molecules significantly divergent from those in the training dataset. In contrast, the ANN models displayed a robust extrapolative capacity in HTVS, successfully predicting new potential ternary OSC systems and leading donors with PCE values exceeding 20%. Our ML models use HOMO and LUMO inputs for donors, acceptors, and ternaries, facilitating efficient optimization via rapid HTVS of high‐performance ternary materials.

A novel optical management layer with flexible color tunability and high transmittance in organic solar cells

The evaluation of colored semi-transparent organic solar cells (ST-OSCs) relies on the power conversion efficiency (PCE) and peak transmittance across the visible light spectrum. However, it is a significant challenge to enhance both parameters simultaneously. In this study, we investigate the impact of different film systems for the Ag electrode on transmittance enhancement using an optical interference formula derived for anti-reflective films. As a result, a novel ZnS/WO3 double-layer anti-reflective film is introduced as an optical management layer. The ZnS/WO3/Ag structure achieves a peak transmittance exceeding 75 % across the visible light spectrum while also offering customizable color attributes. Upon electrical simulation, the power conversion efficiency (PCE) of organic solar cells with 15 nm Ag and 80 nm PM6:Y6 reached to 11.72 %, and an ideal PCE value of 14.53 % is achieved by reducing non-radiative recombination. Through optical simulations, it has been demonstrated that the integration of a ZnS/WO3 double-layer anti-reflective film with organic solar cells enables the generation of OSCs in vibrant purple, blue, cyan, and green hues. Notably, these OSCs exhibit their highest peak transmittance at blue light (452.5 nm), reaching an impressive value of 50.49 %. These remarkable findings not only showcase exceptional performance but also highlight significant potential in applications involving colored OSCs utilizing the new optical management layer composed of ZnS/WO3 double-layer anti-reflective films.

Enhanced optical and electrochemical properties of FeBTC MOF modified TiO2 photoanode for DSSCs application

In this work, iron based 1, 3, 5-tricarboxylic acid (FeBTC) was prepared via microwave-assisted method and incorporated into TiO2 via ultrasonic assisted method. The TiO2–FeBTC nanocomposites were characterized by XRD, FTIR, Raman, BET, FESEM, HRTEM, TGA, UV‒vis DRS and PL to understand their crystallographic, surface morphology, and optical characteristics. The Raman spectra showed a blue shift of Eg, A1g, and B1g peaks upon incorporation of FeBTC MOF onto TiO2. HRTEM and XRD analysis confirmed a mixture of TiO2 nanospheres and hexagonal FeBTC MOF morphologies with high crystallinity. The incorporation of FeBTC onto TiO2 improved the surface area as confirmed by BET results, which resulted in improved absorption in the visible region as a results of reduced bandgap energy from 3.2 to 2.84 eV. The PL results showed a reduced intensity for TiO2–FeBTC (6%) sample, indicating improved separation of electron hole pairs and reduced recombination rate. After fabrication of the TiO2–FeBTC MOF photoanode, the charge transfer kinetics were enhanced at TiO2–FeBTC MOF (6%) with Rp value of 966 Ω, as given by EIS studies. This led to high performance due to low charge resistance. Hence, high power conversion efficiency (PCE) value of 0.538% for TiO2–FeBTC (6%) was achieved, in comparison with other loadings. This was attributed to a relatively high surface area which allowed more charge shuttling and thus better electrical response. Conversely, upon increasing the FeBTC MOF loading to 8%, significant reduction in efficiency (0.478%) was obtained, which was attributed to sluggish charge transfer and fast electron–hole pair recombination rate. The TiO2–FeBTC (6%) may be a good candidate for use in DSSCs as a photoanode materials for improved efficiency.

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.

Side‐chain symmetry‐breaking strategy on porphyrin donors enables high‐efficiency binary all‐small‐molecule organic solar cells

AbstractSide‐chain symmetry‐breaking strategy plays an important role in developing photovoltaic materials for high‐efficiency all‐small‐molecule organic solar cells (ASM OSCs). However, the power conversion efficiencies (PCEs) of ASM OSCs still lag behind their polymer‐based counterparts, which can be attributed to the difficulties in achieving favorable morphology. Herein, two asymmetric porphyrin‐based donors named DAPor‐DPP and DDPor‐DPP were synthesized, presenting stronger intermolecular interaction and closer molecular stacking compared to the symmetric ZnP‐TEH. The DAPor‐DPP:6TIC blend afforded a favorable morphology with nanoscale phase separation and more ordered molecular packing, thus achieving more efficient charge transportation and suppressed charge recombination. Consequently, the DAPor‐DPP:6TIC‐based device exhibited superior photovoltaic parameters, yielding a champion PCE of 16.62% higher than that of the DDPor‐DPP‐based device (14.96%). To our knowledge, 16.62% can be ranked as one of the highest PCE values among the binary ASM OSC filed. This work provides a prospective approach to address the challenge of ASM OSCs in improving film morphology and further achieving high efficiency via side‐chain symmetry‐breaking strategy, exhibiting great potential in constructing efficient ASM OSCs.

Formation of a potential barrier by a ZnSXSe1−X electron-blocking layer to improve the efficiency of CdSe0.3S0.7/CdSe quantum dot sensitized solar cells

We designed and fabricated multilayer quantum dots sensitized solar cells (QDSCs) with TiO2 NPs/CdSe0.3S0.7/CdSe/ZnSXSe1−X, X = S/S + Se = 0, 0.7, 0.8, 0.9, and 1 photoelectrodes to achieve optimum power conversion efficiency (PCE). In the corresponding structure, incoming light is absorbed by the CdSe0.3S0.7 and CdSe quantum dots (QDs), while the ZnSXSe1−X QDs act as an electron blocking layer or passivation layer, forming an energy barrier that restricts electron mobility from the light absorbers to the polysulfide electrolyte. The beneficial effect of the alloyed ZnSXSe1−X layer is the adjustability of its nanoparticle size/bandgap energy proportional to variations in the concentration of anionic precursors X, according to optical results. The PCE value of the reference cell with the TiO2 NPs/CdSe0.3S0.7/CdSe photoanode is 4.15 %. Following the coating of ZnSe, ZnS0.7Se0.3, ZnS0.8Se0.2, ZnS0.9Se0.1, and ZnS QDs via two successive ionic layer adsorption and reaction (SILAR) cycles (2Sc) on the CdSe0.3S0.7/CdSe co-sensitized photoelectrode increasing stability and improving the PCE value to 4.9 %, 5.40 %, 5.70, 5.25 %, and 5.05 %, respectively. Next, by modifying the thickness of the champion cell's passivation layer, the QDSCs with TiO2 NPs/CdSe0.3S0.7/CdSe/ZnS0.8Se0.2 (3Sc) photoelectrode exhibit maximum photovoltaic performance parameters of short circuit current density (JSC) = 26.25 mA/cm2, open circuit voltage (VOC) = 560 mV, fill factor (FF) = 0.42 % and PCE = 6.15 %. This improvement in performance is the result of decreased internal energy loss and recombination of charge carriers at the interface between the electrolyte and photoelectrode, which increases electron collection efficiency and electron injection efficiency in the visible region according to the external and internal quantum efficiency curves.

Analysis of lead free CsSnBr3 based perovskite solar cells utilizing numerical modeling

In this study, we propose several CsSnBr3-based PSC configurations using the Solar Cell Capacitance Simulator (SCAPS-1D), incorporating various efficient Electron transport layers (ETLs) such as TiO2, PCBM, WS2, SnO2, ZnO, IGZO, C60, and Hole transport layers (HTLs) like CBTS, CFTS, CuO, CuI, Spiro-OMeTAD, PEDOT:PSS, P3HT, CuSbS2, CuSCN, and Cu2O. Numerical simulation results reveal that the device structure ITO/WS2/CsSnBr3/Cu2O/Au exhibits outstanding power conversion efficiency (PCE), retaining the closest photovoltaic parameter values among 70 different configurations. In this configuration, WS2 served as the ETL, and Cu2O acted as the HTL. This device achieved an outstanding peak PCE of 20.02%. It also boasted a high open circuit voltage (Voc) of 1.23 V, a short circuit current density (Jsc) of 19.32 mA cm−2, and an impressive fill factor (FF) of 84.18%. In comparison, devices utilizing materials like TiO2, PCBM, SnO2, ZnO, IGZO, and C60 yielded PCE values of 19.72, 19.73, 19.72, 19.73, 19.72, and 15.60%, respectively. Furthermore, for the seven best-performing configurations, we investigated the effects of CsSnBr3 absorber thickness, absorber-acceptor doping density (NA), conduction band offset (CBO), ETL doping density (ND), Capacitance–Voltage (C-V), Mott–Schottky (M-S) characteristics, generation and recombination rates, series resistance (Rse), shunt resistance (Rsh), temperature, current–voltage characteristics (J-V), and quantum efficiency (QE) on performance metrics. Our findings indicate that all seven ETLs, when combined with Cu2O HTL, can serve as excellent materials for fabricating high-efficiency CsSnBr3-based PSCs with the ITO/ETL/CsSnBr3/Cu2O/Au structure. To validate our results, we compared the simulation outcomes obtained with SCAPS-1D for the best seven CsSnBr3-PSC configurations with previously published research works. This comprehensive simulation study opens a promising avenue for the cost-effective production of high-performance, lead-free CsSnBr3-based PSCs, contributing to a greener and pollution-free environment.

Design tungsten oxides hole transport layers (HTLs) to modify the back interface in all-inorganic carbon-based CsPbBr3 solar cells

To enhance the inferior photovoltaic performance of all-inorganic carbon-based perovskite solar cells (C-PSCs) caused by inefficient charge extraction and transport processes of the CsPbBr3/carbon back interface, three types of tungsten oxides (WO3, WO2.72, WO2) are synthesized as low cost and stable hole transport layers (HTLs) to modify the back interface by tunning the energy level alignment. Among the three kinds of tungsten oxides, WO3 shows the best hole extraction and transport capability and the C-PSCs using WO3 HTL generates a power conversion efficiency (PCE) of 7.90% with a high open circuit voltage (Voc) of 1.307 V, indicating a great PCE enhancement of 43.9%, as compared with the device without HTL (5.49%). Meanwhile, WO2.72 and WO2 also are also proved to be qualified HTLs and the devices show PCE values of 7.57% and 6.24%, respectively. Importantly, WO3 and WO2.72 based device show excellent stabilities with PCE retention over 90% of the initial PCE values under ambient conditions for 60 days.

Design highly effective B or N doped mesoporous carbon fibers catalysts for I3-/I- redox couple regeneration in carbon-based dye-sensitized solar cells

Construction of mesoporous structure and improving the conductivity of carbon counter electrode are feasible paths to enhance the catalytic activity in dye-sensitized solar cells (DSCs) toward the I3-/I- redox couple regenerating (IRR). Herein, mesoporous carbon fiber (PCf) has been first synthesized and the DSCs using PCf counter electrode results in a power conversion efficiency (PCE) of 7.12%, significantly surpassing the PCE of 6.01% generated by the DSCs with carbon fiber (Cf) counter electrode without mesoporous structure. Additionally, doping with heteroatoms B or N can further enhance the catalytic performance of PCf. Consequently, B or N doped Cf (BPCf or NPCf) counter electrode-based DSCs achieve high PCE values of 8.43% and 7.96%, respectively, demonstrating PCE improvements of 40.3% and 32.4%. This enhancement in catalytic activity for IRR in DSCs can be first attributed to the increased specific surface area of Cf which can provide more catalytic activated sites. Meanwhile, the enhanced conductivity of PCf by heteroatoms B or N doping is also an important factor for the improved catalytic activity. This work is expected to provide potential path to enhanced the catalytic activity of carbon counter electrode in DSCs toward IRR.

Structural, Mechanical, and Optoelectronic Properties of CH3NH3PbI3 as a Photoactive Layer in Perovskite Solar Cell

The structural, electronic, mechanical, and optical properties of pseudo-cubic CH3NH3PbI3 perovskite have been studied within the framework of density functional theory, in line with solar cell applications. The computed values of lattice and elastic constants concurred with the available theoretical and experimental data. This compound has a semi-conducting behavior, with a direct band gap of about 1.49 eV. Note that the solar radiation spectrum has a maximum energy intensity value of approximately 1.50 eV. Thus, semiconductors with such gaps are preferred for photovoltaic applications. Its elastic parameters reveal that it is a ductile material that is mechanically stable. Optical descriptors such as refractive index, reflectivity, extinction, energy loss, and absorption have been explored with the aim of establishing the optical features of the material. Our findings demonstrate that this perovskite is suitable for solar cell applications based on the size and nature of the band gap, as also supported by the obtained upper limit value of simulated power conversion efficiency via the spectroscopic limited maximum efficiency mathematical model.

Synergistic strategies to unveil the dual influence of additive and annealing treatment on the morphology of isatin-derived low bandgap small molecule donor in solution-processed organic solar cells

A novel organic small molecule, 5-(4-(diphenylamino)phenyl)-1-octylindoline-2,3-dione (TPI) containing an alkyl chain substituted electron accepting isatin (indoline-2,3-dione) and strong electron withdrawing N, N-diphenylaniline units have been synthesized through Suzuki coupling reaction. The molecular structure of TPI is confirmed by NMR, FT-IR, and Mass spectroscopy techniques. The TPI molecule exhibits a low band gap of approximately ∼ 2.03 eV which is also supported by the DFT results. The influence of additive and heat treatment on the electronic, morphological, and photovoltaic performance of organic solar cells was investigated meticulously. The TPI donor exhibits complementary light absorption with fullerene acceptor in combination with DIO and TA which efficiently absorb the photon in the 300–730 nm range. The TPI was later used as an electron donor material for the fabrication of organic solar cells. Remarkably, the morphology-dependent optimized TPI:PC71BM (1:3.0) exposed excellent power conversion efficiency (PCE) of about ∼ 5.56 % with enhanced VOC of ∼ 0.811 V, JSC of 11.81 mA cm−2 and FF of 55.3 % fabricated in addition with DIO and thermal annealing treatment. Most importantly, the unencapsulated devices maintained > 96 % of the initial PCE value after 240 h under ambient temperature. Our findings indicate that isatin-derived small molecules with simple architecture propose great potential for promising BHJ-OSCs material.

The strain regulated physical properties of PbI2/g-C3N4 for potential optoelectronic device

The van der Waals (vdW) heterostructures of Z-scheme PbI2/g-C3N4 with an indirect bandgap have gained much attention in recent years due to their unique properties and potential applications in various fields. However, the optoelectronic characteristics and strain-modulated effects are not yet fully understood. By considering this, six stacking models of PbI2/g-C3N4 are proposed and the stablest structure is selected for further investigation. The uniaxial and biaxial strains (−10%–10%) regulated band arrangement, charge distribution, optical absorption in the framework of density functional theory are systematically explored. The compressive uniaxial strain of −8.55% changes the band type from II→I, and the biaxial strains of −7.12%, −5.25%, 8.91% change the band type in a way of II→I→II→I, acting like the ‘band-pass filter’. The uniaxial strains except −10% compressive strain, and the −6%, −4%, 2%, 4%, 10% biaxial strains will enhance the light absorption of PbI2/g-C3N4. The exerted strains on PbI2/g-C3N4 generate different power conversion efficiency ( ηPCE ) values ranging from 3.64% to 25.61%, and the maximum ηPCE is generated by −6% biaxial strain. The results of this study will pave the way for the development of new electronic and optoelectronic materials with customized properties in photocatalytic field and optoelectronic devices.

Effect of modified titanium dioxide photoanode and agarose gel electrolyte on electrochemical studies of dye-sensitized solar cell

Recently, the study of new DSSC structures such as photoanodes, electrolytes, and counter electrodes (CE) have gained the attention of researchers. Combining these features allows DSSC to have a flexible and versatile way of working. Titanium dioxide-graphene (TiO2-G) nanocomposite containing 3 wt % graphene (G) was successfully fabricated and employed as the photoanode for the fabrication of a dye-sensitized solar cell (DSSC). Agarose (3 wt %) together with potassium iodide (KI) were prepared as gel electrolytes and polyaniline-graphene oxide (PANI-GO) served as the counter electrode (CE). In UV–visible spectroscopy, doping of graphene on TiO2 led to a remarkable reduction of the band gap energy from 3.0 eV (TiO2) to 2.4 eV (TiO2-G). The presence of agarose in the KI solution facilitated the creation of fine channels, promoting ionic transfer in electrolytes, as revealed by field emission scanning electron microscopy (FESEM). Moreover, the current-voltage (I–V) curve for TiO2-G/3 wt % agarose gel electrolyte/PANI-GO demonstrated a power conversion efficiency (PCE) value of 1.1324% with optimal values for short circuit current density (JSC), open circuit voltage (VOC), and fill factor (FF) of 34.48 mA/cm2, 0.1105 V, and 0.2972, respectively. Cyclic voltammetry (CV) illustrated redox potential occurrences at −0.2 V and +0.2 V, corresponding to oxidation and reduction processes, confirming the chemical stability of DSSC. The system demonstrated stability after 10 cycles, maintaining consistent current (μA) and voltage (V) patterns even after 20 cycles. These results demonstrate the efficient and cost-effective DSSC system's capacity to maintain stability and guarantee consistent energy conversion.

Enhancing predictive modeling of photovoltaic materials’ solar power conversion efficiency using explainable AI

We present a study on Explainable AI-based prediction of power conversion efficiency (PCE) of organic solar cells, conducted on a dataset of 566 small-molecule organic solar cell materials samples with varying donor and acceptor species combinations. This research uncovers an interesting phenomenon, the first of its kind to be reported, of PCE quantization, where the PCE values increase in steps with the increase in feature values. Our findings have significant implications for the development of efficient organic solar cells, as they provide a better understanding of the factors that influence PCE, and highlight the feature value ranges for which more efficient PCE would be achieved. Our study demonstrates the power of XAI techniques in uncovering hidden patterns in scientific datasets and highlights the importance of interdisciplinary research in the field of materials science.

Enhanced Photovoltaic Performance of Asymmetrical Benzo Dithiophene Homopolymer Donor Materials in Nonfullerene Acceptor-Based Organic Photovoltaics.

Although much promising synthetic progress in conjugated polymer-based organic solar cells (OSCs) has resulted in significant improvement in power conversion efficiencies (PCEs) of from over 15 to >19.0% in the last five years, the sophisticated and complex reactions from at least two families' monomers with remarkably different electron push-pull effects could still pose an unavoidable material burden for the commercialization of OSCs in the coming future. Therefore, the method of preparing a homopolymer from a sole monomer would significantly reduce the synthetic steps and costs in order to pave the way for the large-scale production of OSC materials. Therefore, alkylthio-thiophenyl-substituted benzo[1,2-b;4,5-b']dithiophene (BDTTS) as the sole and key structural moiety with dihalogen and distannyl functional groups was designed and synthesized, respectively, in this study, for facile monomer syntheses and polymerizations to achieve three wide-bandgap homopolymer donors of BDTTS-alt-BDTT-Cl (P13), BDTTS-alt-BDTT (P15), and BDTTS (P14), respectively. The structural symmetry dependency on their physical, electrochemical, and optical properties, thin-film morphologies, and photovoltaic (PV) performance was investigated in detail. As a result, OSCs based on the asymmetric polymer P15, paired with BTP-eC9 as the electron acceptor, presented the best PV performance, with a PCE of 11.5%, a fill factor (FF) of 65.87%, and a short-circuit current (JSC) of 22.04 mA·cm-2, respectively. This PCE value is among the highest ones reported for BDT-type homopolymer donor-based OPVs, providing us with knowledge for obtaining promising PV performance from devices made of P15-like materials.

FABRIKASI SEL SURYA BERBASIS MATERIAL PEROVSKIT MAPbI3 SEBAGAI SUMBER ENERGI TERBARUKAN

The increasing for energy need encourages all parties to develop alternative energy sources with the concept of renewable energy, which utilizes resources that are always available in nature, such as sunlight energy. The device that can convert sunlight into electrical energy is a solar cell. In this research, solar cells were made based on the MAPbI3 perovskite material as an active material which functions as an absorber to absorb photons of sunlight. The solar cell device was fabricated with the FTO/c-TiO2/mp-TiO2/MAPbI3/PTAA/Au device structure using the OSPD-FDC (one step precursor deposition-fast deposition crystallization) method. The UV-Vis characterization results show that the absorption area of MAPbI3 starts from the wavelength range of 325 nm to 800 nm and shows the presence of an absorption band edge which is a special characteristic of perovskite materials. Meanwhile, characterization of photovoltaic properties produces a power conversion efficiency value of 13% with Jsc, Voc and FF values of 23 mA/cm2, 1.1 V, and 54% respectively

Experimental investigation of spin coating acceleration effect on the DSSC performance

The optimization of the TiO2 mesoporous structure plays significant role in dye-sensitized solar cell (DSSC) to produce efficient devices. In this study, the TiO2 mesoporous layer was coated by using a spin coating equipment with different spin accelerations. As a consequence of this investigation, the impacts of the spin coating acceleration on the optoelectronic and electrical performance characteristics of the DSSC were investigated. It has been shown that altering the spin coating acceleration has a direct impact on the mesoporous layer, which in turn influences the absorption ability of dye. The light absorbance of the sample A5 (coated at 2000 rpm s−1) ascended drastically in accordance to other samples. Thanks to this augmentation in absorbance, the current density (J SC ) and power conversion efficiency (PCE) values also improved. According to electrochemical impedance spectroscopy analysis, it was attained that recombination resistance values increases with the rising spin coating acceleration rates after 500 rpm s−1 and reaches up to highest value at 2000 rpm s−1. A relatively longer electron lifetime of 40.36 ms and recombination resistance of 12.22 Ω were obtained for the device coated at the rate of 2000 rpm s−1. The device coated at a rate of 2000 rpm s−1 had a PCE (5.51%) that was superior than other devices because of its improved light collecting ability, quick electron transport, suppressed electron recombination, and having longer electron life time. As a starting point for future investigations and applications, results of present study provide an insight into the optimal spin coating parameters for DSSC applications.

Improved Performance and Stability of Quasi-Two-Dimensional Perovskite Solar Cells by Post-treatment with Acetaminophen.

Recently, perovskite solar cells (PSCs) based on quasi-two-dimensional (quasi-2D) perovskites have drawn more attention due to their excellent stability, although their efficiencies are still lower than those of 3D ones. Here we applied post-treatment of 2D perovskite GAMA5Pb5I16 (GA = guanidinium, MA = methylammonium) films with acetaminophen (AMP) to improve their performance. The efficiency of the solar cells with 2 mg/mL AMP post-treatment increased to 18.01% from 16.72% for those without post-treatment. The efficiency improvement results from the enlarged grain size, reduced trap state density, and better energy level matching after AMP post-treatment. In addition, the stability of the solar cells is improved. The solar cells with AMP post-treatment maintain 91% of the original power conversion efficiency value after aging for 30 days in the atmosphere. This work opens a new approach for the efficiency and stability enhancement of quasi-2D PSCs.

Enhanced efficiency and stability of inorganic CsPbBr3 perovskite solar cells based on carbon counter electrode by applying PbTiO3-coated TiO2 nanorod films as scaffold layers

The CsPbBr3 perovskite solar cells (PSCs) based on carbon counter electrode (CCE) are promising because of the advantages including fabrication simplicity and excellent stability, but their power conversion efficiencies (PCE) are low due to interfacial carrier recombination as the direct contact of the CsPbBr3 with electron transport materials (ETM). In this paper, PbTiO3 shells were grown onto TiO2 nanorods to form PbTiO3-coated TiO2 scaffold layer via a two-step method. The presence of PbTiO3 could promote crystallinity of the CsPbBr3 perovskite film and inhibits interface recombination at the CsPbBr3/TiO2 interface. Consequently, the carbon-based CsPbBr3 solar cells with PbTiO3/TiO2 scaffold layer achieves a high PCE of 7.28%, demonstrating an increase by 19.9% compared with the devices based on TiO2 NRs. Moreover, the champion devices exhibited excellent stability in ambient air, with the PCE value remaining at 93% over 28 days.

Zwitterion Dual-Modification Strategy for High-Quality NiOx and Perovskite Films for Solar Cells.

Nickel oxide (NiOx ) has been limited in use as a hole transport layer for its low conduction, surface defects, and redox reactions with the perovskite layer. To address these issues, the incorporation of zwitterion L-tryptophan (Trp) is proposed at the NiOx /Trp interface. The carboxyl group of Trp effectively passivates the surface positive defects of NiOx , thereby improving its optical and electrical properties. The ammonium group of Trp not only passivates negative defects but modulates the growth of the perovskite layer, resulting in an improved perovskite film quality. Furthermore, the Trp layer acts as a buffer layer, suppressing adverse interfacial reactions between the perovskite and NiOx . Consequently, perovskite solar cells with 1.56 and 1.68eV absorbers achieve the champion power conversion efficiency(PCE) of 23.79% and 20.41%, respectively. Moreover, the unencapsulated devices demonstrate excellent long-term stability, retaining above 80% of the initial PCE value after 1600 h of storage in the air with a humidity of 50-60%.