Improvement Of Photovoltaic Performance Research Articles

The impact of quantum-sized nickel nanoparticles on TiO2 in photovoltaic and photocatalytic systems

The study examines the impact of the incorporation of quantum-sized nickel (Ni) nanoparticles in TiO2 (titanium dioxide) matrix at 1%, 3%, and 5% weight percentages by straightforward, easy, and potentially effective synthesis strategy of direct doping. The structural, morphological, optical, and electrical characterization studies of synthesized films are systematically done and the photovoltaic, photocatalytic applications are evaluated. The integration of nickel into TiO2 influences its photovoltaic properties by enhancing the open-circuit voltage (Voc). However, higher concentrations lead to increased recombination and defects, decreasing efficiency. On conducting photocatalytic studies, TiO2 doped with 1 wt. % nickel exhibits superior photocatalytic efficiency, surpassing that of undoped TiO2. This improvement in photovoltaic and photocatalytic performance is attributed to better charge separation and reduced recombination. However, optimizing nickel levels is crucial for maximizing benefits for the applications using the performed synthesis strategy.

Photon Sensitizer by Amalgamation of SrTiO3 and Dyes from Cnidoscolus Aconitifolius with Different pH Values for the Extensive Sustainability of the Dye Sensitized Solar Cell

By using the co-sensitization process, which involves combining dyes with perovskite materials, improvements in panchromatic light-harvesting and photovoltaic performance are reported for DSSC. This study aims to explore the effect of natural extract of Chaya tree spinach mixed with undoped SrTiO3 perovskite. Dyes were extracted from the leaves of Chaya tree spinach (Cnidoscolus Aconitifolius) leaves. An undoped SrTiO3 is synthesized via solid state method and mixed with TiO2 and dyes of Chaya spinach in order to fabricate solar cells. The prepared samples were characterized by structural properties by XRD and also optical properties by UV (DRS) for SrTiO3, UV-Vis and FTIR studies for the extracted dyes. The effect of the natural dye’s extracts containing chlorophyll a from Chaya tree spinach along with SrTiO3 was investigated for the performance of J-V characterization in which the cell made with SrTiO3 + natural dyes of pH maintained at 10 had shown better efficiency of about 1.691% in light with 3.4939 mA/cm2 of Jsc and 0.6023 Voc.

Interface properties study of black silicon solar cells with front surface a-Si:H/c-Si heterojunction

Abstract The exceptionally low reflectance of black silicon across a broad wavelength range makes it an intriguing surface texture for solar cell applications. Silicon heterojunction (SHJ) solar cells fabricated on black silicon (Si) formed by dry reactive ion etching (RIE) using inductive coupled plasma (ICP) on n-type Si are explored. The study is focused on the properties of the a-Si:H/c-Si interface, being a key issue for the photovoltaic performance of SHJ. Deep-level transient spectroscopy (DLTS) detected no radiation defect in Si after the etching. The surface of black Si was passivated with an intrinsic a-Si:H layer, followed by the deposition of p-type and n-type a-Si:H on the front and back sides, respectively. The SHJ solar cell photovoltaic performance based on black Si is strongly influenced by defect density at the a-Si:H/Si interface. Admittance spectroscopy and effective charge carrier lifetime measurements demonstrate that interface defect density decreases with the increase of (i)a-Si:H thickness. The value of 0.75 ms effective charge carrier lifetime was reached for single (i) a-Si:H layer passivation and 0.25 ms when (p)a-Si:H was deposited over the intrinsic a-Si:H layer. The measured open circuit voltage (VOC) values for the SHJ solar cells increase with the (i)a-Si:H layer thickness reaching 658 mV. However, the fill factor decreases with increasing (i) a-Si:H layer thickness, limiting the efficiency at the maximum value below 14% due to the thickness uniformity of the a-Si:H layer. The development of conformal growth of a-Si:H is a key issue for further improvement of black Si heterojunction solar cell photovoltaic performance. 

Enhancing Extraction and Suppressing Cooling of Hot Electrons in Lead Halide Perovskites by Dipolar Surface Passivation.

Slowing hot carrier (HC) cooling and improving HC extraction are considered two pivotal factors for enhancing power conversion efficiency in emerging HC photovoltaic applications of perovskites and other materials. Employing ab initio quantum dynamics simulations, we demonstrate the simultaneous slow cooling and efficient extraction of hot electrons at the C60/CsPbI3 interface through dipolar surface passivation with phenethylammonium and 4-fluorophenethylammonium ligands. The passivation effectively suppresses I-Pb lattice vibrations, weakens the hot electron-phonon interaction in CsPbI3, and thus slows down the HC cooling. At the same time, the dipolar surface passivation elevates the LUMO + 1 state in C60 and reduces the energy gap for HC extraction. Concurrently, higher-frequency vibrations of the dipolar layer enhance the coupling between C60 and CsPbI3, promoting efficient HC extraction further. These phenomena are intensified with increased polarity of the dipolar layer. Furthermore, we find that dipolar passivation has the opposite influence on cold electron collection at the band edge, underscoring the fact that the observed improvement in photovoltaic performance stems preferentially from the effective utilization of HCs rather than cold electrons. The work provides a new strategy for achieving high-performance HC perovskite solar cells.

Synthesis, spectral analysis, and DFT studies of the novel pyrano[3,2-c] quinoline-based 1,3,4-thiadiazole for enhanced solar cell performance

In this study, we synthesized a novel compound, 3-(5-amino-1,3,4-thiadiazol-2-yl)-6-ethyl-4-hydroxy-2H-pyrano[3,2-c]quinoline-2,5(6H)-dione (ATEHPQ), through a condensation reaction between 6-ethyl-4-hydroxy-2,5-dioxo-5,6-dihydro-2H-pyrano [3,2-c]quinoline-3-carboxaldehyde and thiosemicarbazide, followed by oxidative cyclization. We characterized ATEHPQ using elemental analysis, IR, 1H and 13C NMR spectroscopy, and mass spectrometry. Density Functional Theory (DFT) calculations with the B3LYP/6–311++G(d,p) basis set were employed to optimize the molecular geometry and analyze global reactivity descriptors, including HOMO-LUMO energies. The Molecular Electrostatic Potential (MEP) map was used to identify reactive sites, and drug-likeness studies indicated potential pharmaceutical applications. Notably, ATEHPQ showed a higher first hyperpolarizability (βtot) compared to urea, suggesting its suitability for nonlinear optical applications. We also determined the Miller indices for ATEHPQ's preferred orientations using a specialized program. Williamson–Hall analysis revealed an average crystal size of 26.08 nm and a lattice strain of 6.3 × 10−3. The thin films exhibited three distinct absorption peaks at 2.8, 3.41, and 4.21 eV, with a direct energy gap of 2.43 eV. Dispersion parameters from the single oscillator model provided oscillator and dispersion energies of 3.12 eV and 14.21 eV, respectively, with a high-frequency dielectric constant of 4.71. The ATEHPQ thin films, when combined with n-Si, demonstrated significant improvements in photovoltaic performance: the open-circuit voltage (Voc) rose from 0.13 V to 0.521 V, the short-circuit current (Isc) increased from 0.253 mA to 2.94 mA, the fill factor (FF) improved from 0.238 to 0.33, and the efficiency (η) grew from 0.71 % to 4.64 % with increased illumination intensity. These results highlight the excellent photovoltaic and photodetection capabilities of ATEHPQ thin films, underscoring their potential for advanced optoelectronic and solar cell applications.

Numerical investigation of photovoltaic performance improvement using Al2O3 nanofluid

To further elucidate the impact of fluctuations in environmental temperature and radiation intensity within a day on the temperature and performance of photovoltaic systems with and without nanofluid cooling, this study established a photovoltaic panel temperature and efficiency calculation model based on a nanofluid cooling system that considers the dynamic changes of photovoltaic panel temperature and air temperature over time. An empirical formula for predicting photovoltaic panel efficiency has been derived based on experimental data. Then a PV panel temperature and efficiency calculation model is established and validated. The simulation results show that using nanofluids to cool the PV panel can significantly reduce the temperature and improve the PV efficiency. Compared to the bare PV panel, the average PV panel temperature decreases by 7.99 ℃, 8.48 ℃, and 8.92 ℃ respectively when nanofluid volume fraction is 1 vol%, 3 vol%, and 5 vol%, and it decreases by 8.48 ℃, 9.27 ℃, and 9.94 ℃ respectively when nanofluid mass flow rate is 0.08 m3/h, 0.10 m3/h, and 0.12 m3/h. As the nanofluids' concentration increases, nanofluids' cooling ability in the high temperature range also increases.

Rational Strategies to Improve the Efficiency of 2D Perovskite Solar Cells.

In the quest for durable photovoltaic devices, 2D halide perovskites have emerged as a focus of extensive research. However, the reduced dimension in structure is accompanied by inferior optical-electrical properties, such as widened band gap, enhanced exciton binding energy, and obstructed charge transport. As a result, the efficiency of 2D perovskite solar cells (PSCs) lags significantly behind their 3D counterparts. To overcome these constraints, extensive investigations into materials and processing techniques are pursued rigorously to augment the efficiency of 2D PSCs. Herein, The cutting-edge delve into developments in 2D PSCs, with a focus on chemical and material engineering, as well as their structure and photovoltaic properties. The review starts with an introduction of the crystal structure, followed by the key evaluation criteria of 2D PSCs. Then, the strategies around solution chemical engineering, processing technique, and interface optimization, to simultaneously boost efficiency and stability are systematically discussed. Finally, the challenges and perspectives associated with 2D perovskites to provide insights into potential improvements in photovoltaic performance will be outlined.

Ordered porous carbon nitride embedded with truncated carbon nanotubes for boosting photocatalytic degradation

Limited light absorption and low charge separation rates are the main obstacles for graphitic carbon nitride-based photocatalysts. In terms of these defects, an ordered-porous graphitic carbon nitride composites (PCN@CNT) modified with truncated carbon nanotubes (CNTs) were composited through hydrothermal-calcination method in this work. Due to their electron trapping ability, the CNTs can enhance visible light absorption, narrow the bandgap, and act as electron concentrators, achieving that spatial separation of photogenerated carriers can inhibit electron-hole pair recombination efficiently. In addition, a controllable ordered-porous structure was constructed to provide abundant active sites and mass transfer channels, shortening the carrier migration path. These two modifications acted synergistically to enhance the catalysts' performance. The top-performing sample in this work, PCN@CNT-1, showed significant improvement in photovoltaic performance and achieved a 97.7 % degradation of rhodamine B, with a photocatalytic degradation rate constant (k-value) more than three times that of PCN. This work demonstrates the potential for modification by coupling CNTs to design carbon-nitride-based photocatalysts with excellent catalytic performance, which can be used as catalysts for wastewater purification.

Study and Optimization of a New Perovskite Solar Cell Structure Based on the Two Absorber Materials Cs2TiBr6 and MASnBr3 Using SCAPS 1D

The main objective of this study is to optimize the photovoltaic parameters of a new perovskite solar cell structure (PSC) suggested, using the simulator solar cell capacitance simulator-one dimension (SCAPS-1D) which aims to improve its performance by adjusting different key variables. This new suggested cell which consists of six materials represents the major innovation point of our research, it is distinguished by a double active layer, composed of the two-cesium titanium hexabromide (Cs2TiBr6) and methylammonium tin tribromide (MASnBr3) perovskites. Using the SCAPS 1D software, the simulation allows to determine the optimal values of the various parameters to maximize the efficiency of the PSC. First, the effect of the thickness and defect densities of both Cs2TiBr6 and MASnBr3 materials on the output parameters was studied as well as the defect density in the interfaces. Subsequently, the doping density in Cs2TiBr6 and MASnBr3 was also optimized. Finally, the impact of temperature, series resistance and shunt resistance were evidenced. The results indicate that precise adjustments of these parameters can lead to significant improvements in photovoltaic performance, such as open circuit voltage of 1.105 V, short-circuit current density of 33.90 mA cm−2, fill factor of 88.01% and power conversion efficiency (PCE) 32.96%. These performances were obtained for a thickness of 700 nm for Cs2TiBr6 and 900 nm for MASnBr3, a defect density of 1014 cm−3 for each absorber layer, a defect density of 1014 cm−2 for each interface and a doping density of the order of 1018 cm−3 for each absorbent layer.

Collaborative Fabrication of High-Quality Perovskite Films for Efficient Solar Modules through Solvent Engineering and Vacuum Flash System.

The vacuum flash solution method has gained widespread recognition in the preparation of perovskite thin films, laying the foundation for the industrialization of perovskite solar cells. However, the low volatility of dimethyl sulfoxide and its weak interaction with formamidine-based perovskites significantly hinder the preparation of cell modules and the further improvement of photovoltaic performance. In this study, we describe an efficient and reproducible method for preparing large-scale, highly uniform formamidinium lead triiodide (FAPbI3) perovskite films. This is achieved by accelerating the vacuum flash rate and leveraging the complex synergism. Specifically, we designed a dual pump system to accelerate the depressurization rate of the vacuum system and compared the quality of perovskite film formed at different depressurization rates. Further, to overcome the limitations posed by DMSO, we substituted N-methylpyrrolidone as the ligand solvent, creating a stable intermediate complex phase. After annealing, it can be transformed into a uniform and pinhole-free FAPbI3 film. Due to the superior quality of these films, the large area perovskite solar module achieved a power conversion efficiency of 22.7% with an active area of 21.4 cm2. Additionally, it obtained an official certified efficiency of 22.1% with an aperture area of 22 cm2, and it demonstrated long-term stability.

Simultaneous Improvement in Photovoltaic Performance and Air Stability of Perovskite Solar Cells by Controlling Molecular Orientation of Spiro-OMeTAD

Simultaneous Improvement in Photovoltaic Performance and Air Stability of Perovskite Solar Cells by Controlling Molecular Orientation of Spiro-OMeTAD

Synergistic Co-sensitization: Unlocking the potential of carbohydrazide chromophores and metal complexes for high-performance dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs) have emerged as a promising alternative to traditional silicon-based photovoltaic devices due to their low-cost fabrication and tunable optical properties. One effective strategy to improve the light-harvesting capabilities of DSSCs is co-sensitization, which involves combining multiple dyes with complementary absorption properties. In this study, we report the co-sensitization of carbohydrazide-based organic chromophores, namely MRK-1–2, with a benchmark metal-complex dye (black dye) to enhance the photovoltaic performance of DSSCs. The synthesis of MRK-1–2 sensitizers is described, and their photophysical properties are thoroughly analyzed. The absorption spectra of the co-sensitizers revealed distinct absorption bands associated with intramolecular charge transfer and localized aromatic π-π* transitions. Sensitization by MRK-1–2 resulted in photovoltaic efficiencies ranging between 5.02–5.88 %. The ternary co-sensitization system of carbohydrazide-based chromophores (MRK-1–2 + black dye) showed promising potential for enhancing the short-circuit current density (JSC) (20.32–21.45 mA/cm2), open-circuit voltage VOC (691–729 mV), and overall power conversion efficiency (PCE) (9.52–9.90 %). This significant improvement in photovoltaic performance is attributed to the complementary light-harvesting abilities of the co-sensitizers, leading to enhanced light absorption and efficient charge separation and injection processes. The superior performance, with a (PCE) of up to 9.90 %, can be attributed to complementary light absorption, efficient charge injection facilitated by the carboxylic acid moiety in MRK-2, and suppressed charge recombination within the co-sensitized system. The findings of this study will contribute to the advancement of DSSC technologies and bring us closer to sustainable and renewable energy solutions.

Providing a Photovoltaic Performance Enhancement Relationship from Binary to Ternary Polymer Solar Cells via Machine Learning.

Ternary polymer solar cells (PSCs) are currently the simplest and most efficient way to further improve the device performance in PSCs. To find high-performance organic photovoltaic materials, the established connection between the material structure and device performance before fabrication is of great significance. Herein, firstly, a database of the photovoltaic performance in 874 experimental PSCs reported in the literature is established, and three different fingerprint expressions of a molecular structure are explored as input features; the results show that long fingerprints of 2D atom pairs can contain more effective information and improve the accuracy of the models. Through supervised learning, five machine learning (ML) models were trained to build a mapping of the photovoltaic performance improvement relationship from binary to ternary PSCs. The GBDT model had the best predictive ability and generalization. Eighteen key structural features from a non-fullerene acceptor and the third components that affect the device's PCE were screened based on this model, including a nitrile group with lone-pair electron, a halogen atom, an oxygen atom, etc. Interestingly, the structural features for the enhanced device's PCE were essentially increased by the Jsc or FF. More importantly, the reliability of the ML model was further verified by preparing the highly efficient PSCs. Taking the PM6:BTP-eC9:PY-IT ternary PSC as an example, the PCE prediction (18.03%) by the model was in good agreement with the experimental results (17.78%), the relative prediction error was 1.41%, and the relative error between all experimental results and predicted results was less than 5%. These results indicate that ML is a useful tool for exploring the photovoltaic performance improvement of PSCs and accelerating the design and application with highly efficient non-fullerene materials.

Edge passivation: Considerable improvement in photovoltaic performance of perovskite/silicon tandem solar cells

Edge recombination is considered hard to avoid entirely in silicon (Si) solar cells as well as Si-base solar devices, hindering their future commercialization. However, such an important issue in perovskite/silicon (PK/Si) tandem solar cells has not attracted much attention. Herein, a low-temperature, non-vacuum liquid-based edge passivation strategy (LEPS) to improve the power conversion efficiency (PCE) of PK/Si tandem solar cells is proposed. The minority carrier lifetime (τeff) of the PK/Si tandem sample with 495.8 μs significantly enhances to 739.7 μs after passivating the Si sub-cell edge recombination. The open circuit voltage (VOC) of the PK/Si tandem solar cell increases by up to +3.8%abs from the initial state after LEPS treatment due to edge passivation, leading to the PCE of the PK/Si tandem solar cell increases by up to +1.2%abs. Finally, a monolithic PK/Si tandem cell with a PCE of 29.48% was achieved by further utilizing the LEPS, which opened up a simple and effective avenue for enhancing the PCE of PK/Si tandem solar cells and further promoting a higher photovoltaic output power of tandem modules.

Improvement of photovoltaic performance on inverted chalcostibite CuSbS2 solar cells using Sr-doped TiO2 window layers

Improvement of photovoltaic performance on inverted chalcostibite CuSbS2 solar cells using Sr-doped TiO2 window layers

Maximizing photovoltaic performance of all-inorganic perovskite CsSnI3-xBrx solar cells through bandgap grading and material design

In the modern era of technology, worldwide paradigms have been shifted toward the utilization of green energy. Sun energy is the most astonishing eco-friendly resource of energy and can be harnessed with the help of photovoltaic cells. Hybrid (Organic-Inorganic) perovskite solar cells (PSCs) are emerged with incredible photovoltaic (PV) performance. Nevertheless, a significant challenge lies in their lower stability under diverse environmental conditions. To deal with this challenge, all inorganic cesium-based PSC has been studied and analyzed, results improved stability in comparison to hybrid PSC. However, the noxious nature of lead is deleterious to the environment. So, this work primarily aimed, to study lead-free all inorganic tin-based perovskite compound CsSnI3-xBrx, as the main light absorber layer. Further, to elevate the PV performance of PSC, bandgap grading is performed on CsSnI3-xBrx by varying bromide concentration x from 0 to 3. Bandgap grading encourages the absorption of a wide range of the light spectrum, by modulating bandgap (Eg) / affinity(χ) through the distance of the CsSnI3-xBrx layer. Additionally, it enhances light-generated charge carrier separation and collection by end electrodes. In this work, two different strategies have been adopted, linear and parabolic. During linear grading, the impact of variation in x (0 to 3) has been analyzed over the thickness 50–––500 nm in 10 linear steps for CsSnI3-xBrx. The highest PCE fetched from linearly graded layered FTO / CeO2 / CsSnI3-xBrx / CFTS / Gold PSC is 21.68 %. Similarly, in the parabolic graded absorber layer, the influence of change in the bowing factor (0 to 1), has been analyzed relative to different values of x (0 to 3). With improvement in PV performance, the maximum PCE delivered by parabolic-graded PSC is 23.61 %. Additionally, this work extends to check the compatibility of distinct electron transport layers (ETLs) and hole transport layers (HTLs). Upon analysis, it has been found that the best PV performance was obtained while selecting SnO2 / PEDOT as ETL / HTL respectively.

Multifunctional buried interface modification of SnO2-based planar perovskite solar cells via phosphorus hetero-phenanthrene flame retardants

Tin dioxide (SnO2) is widely utilized for the cost-effective electron transport layer (ETL) in perovskite solar cells (PSCs) owing to its excellent optoelectronic properties. However, the surface defect states present in SnO2 ETL prepared by conventional solution methods seriously hinder the further improvement of device photovoltaic performance. It is urgently essential to develop a facile strategy to effectively minimize the adverse effects of SnO2 ETL on PSCs. Herein, a phosphorus hetero-phenanthrene flame retardant, DOPO, is introduced as a multifunctional surface modifier to improve the interfacial properties between SnO2 ETL and perovskite. Through systematic characterization analysis, the PO group in DOPO not only passivates the defective states on the surface of SnO2 ETL, but also provides chemical chelation sites for the uncoordinated Pb2+ ions in the upper perovskite structure to improve the film crystalline quality. Eventually, the photoelectric conversion efficiency (PCE) of the optimized device is improved from an initial 19.74 %–22.57 %, along with significantly improved device stability. This work provides an important reference for the development of new multifunctional interface modification materials required for SnO2-based planar PSCs with excellent properties.

Improvement of Photovoltaic Performance of Perovskite Solar Cells by Synergistic Modulation of SnO2 and Perovskite via Interfacial Modification.

In the past decade, perovskite solar cell (PSC) photoelectric conversion efficiency has advanced significantly, and tin dioxide (SnO2) has been extensively used as the electron transport layer (ETL). Due to its high electron mobility, strong chemical stability, energy level matching with perovskite, and easy low-temperature fabrication, SnO2 is one of the most effective ETL materials. However, the SnO2 material as an ETL has its limitations. For example, SnO2 films prepared by low-temperature spin-coating contain a large number of oxygen vacancies, resulting in energy loss and high open-circuit voltage (VOC) loss. In addition, the crystal quality of perovskites is closely related to the substrate, and the disordered crystal orientation will lead to ion migration, resulting in a large number of uncoordinated Pb2+ defects. Therefore, interface optimization is essential to improve the efficiency and stability of the PSC. In this work, 2-(5-chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol (CBTBC) was introduced for ETL modification. On the one hand, the hydroxyl group of CBTBC forms a Lewis mixture with the Sn atom, which reduces the oxygen vacancy defect and prevents nonradiative recombination. On the other hand, the SnO2/CBTBC interface can effectively improve the crystal orientation of perovskite by influencing the crystallization kinetics of perovskite, and the nitrogen element in CBTBC can effectively passivate the uncoordinated Pb2+ defects at the SnO2/perovskite interface. Finally, the prevailing PCE of PSC (1.68 eV) modified by CBTBC was 20.34% (VOC = 1.214 V, JSC = 20.49 mA/cm2, FF = 82.49%).

Simultaneous Defect Passivation and Electric Level Regulation with Rubidium Fluoride for High-Efficiency CsPbI2Br Perovskite Solar Cells.

Due to the good balance of efficiency and stability, CsPbI2Br perovskite solar cells (PSCs) recently have attracted widespread attention. However, the improvement in photovoltaic performance for CsPbI2Br PSCs was mainly limited by massive defects and unmatched energy levels. Surface modification is the most convenient and effective strategy to decrease defect densities of perovskite films. Herein, we deposited rubidium fluoride (RbF) onto the surface of CsPbI2Br perovskite films by spin-coating. The numerous defects could be significantly passivated by RbF, resulting in suppressed nonradiative recombination. Furthermore, the CsPbI2Br perovskite film after RbF treatment exhibits a deeper Fermi level, and an additional built-in electric field forms to promote charge transport. Consequently, the champion device achieves a high efficiency of 10.82% with an improved VOC of 1.14 V, and it also exhibits excellent stability after long-term storage. This work offers a simple and effective approach to enhance the photovoltaic performance and stability of PSCs for broader applications in the future.

Unlocking the Myths of Molecular Bonding State in Modulating Oxidation and Anderson Localization for Inorganic Sn/Pb‐based Perovskite Solar Cells

AbstractThe improvement of photovoltaic and stability performance of tin (Sn)‐based halide perovskite solar cells is impeded by notorious oxidation issues and Anderson localization. Despite previous implements in antioxidation through the incorporation of Lewis base additives, there still exist ongoing uncertainties surrounding its complex interaction mechanisms. A perplexing phenomenon regarding accelerated oxidation in acrylic acid is discovered that deviates from conventional Lewis base–acid reaction. The underlying insights into the deprotonation of acrylic acid followed by the formation of a “tripod” ionic bonding form are provided, which results in amplifying the delocalization effect of electrons of Sn2+. Furthermore, with the assistance of acrylamide and acrolein, synergistic enhancement in terms of the antioxidation and suppression of Anderson localization can be achieved — a concept referred to as “Dual Synergistic Engineering”. This suppresses the oxidation of Sn2+ and reduces Sn4+ content by ≈76%. Meanwhile, the diffusion length is prolonged significantly from 195.9 to 458.9 nm. The optimized all‐inorganic Sn/Pb‐based perovskite solar cells exhibit a power conversion efficiency of above 14% with enhanced stability. These findings provide an alternative viewpoint for comprehending the impact of chemical interaction on oxidation and crystal growth in Sn/Pb‐based perovskites.