Perovskite Precursor Solution Research Articles

Application of PACz-Based Self-Assembled Monolayer Materials in Efficient Perovskite Solar Cells.

Due to the advantages of low interface resistance, high work function, and high stability, PACz family materials have developed rapidly in p-i-n structure perovskite solar cells (PSCs) in recent years. Numerous studies have shown that PSCs prepared on the basis of PACz family materials or their derivatives as hole transport layers (HTLs) generally exhibit superior performance compared to PSCs prepared on the basis of organic HTL PTAA and inorganic HTL NiOx, especially in terms of stability, demonstrating unparalleled charm. Since the application of PACz-like molecule V1036 as a HTL in PSCs in 2018, research reports on high-performance PSCs based on the PACz family HTL have been widely disseminated. Currently, PSCs based on the PACz HTL exhibit a world record value of 26.7% power conversion efficiency (PCE), breaking the long-standing world record held by n-i-p-structured PSCs, indicating its great potential for application in PSCs. The main problem with using PACz as a HTL is that it exhibits poor wettability toward perovskite precursor solutions, is sensitive to the thickness of the HTL and the roughness of the substrate, has poor thermal stability, and lacks preparation methods, making it difficult to achieve large-area device fabrication. This review summarizes the outstanding achievements of PACz to date, describes the mechanism and unique properties of PACz in PSCs, and looks forward to the future development prospects of PACz.

Extending Shelf‐Life of Two‐Step Method Precursor Solutions through Targeted Regulation for Highly Efficient and Reproducible Perovskite Solar Cells

AbstractPrecursor solution aging process can cause significant influence on the photovoltaic performance of perovskite solar cells (PVSCs). Notably, we first observe that the aging phenomenon is more severe in the precursor of two‐step sequential method compared to that in one‐step method due to that the protic solvent isopropanol facilitates amine‐cation side reaction and iodide ions oxidation. Herein, we report a novel approach for selectively stabilizing both organic amine salt and lead iodide (PbI2) precursor solutions in two‐step method. The introduction of benzene‐1,3‐dithiol into organic amine salt solution can mitigate amine‐cation side reactions due to the formation of an acidic and reducing environment. Simultaneously, decamethylferrocene (FcMe10/FcMe+10) pair can act as a redox shuttle in PbI2 solution to concurrently oxidize Pb0 and reduce I2 in cyclic manner. Consequently, the PVSCs device fabricated from ameliorative precursor solutions demonstrates superior power conversion efficiency of 25.31 %, retaining 95 % of its efficiency after 21 days of solution aging. Moreover, the unencapsulated devices maintain 85 % of primitive efficiency for 1500 h at maximum power point tracking under continuous illumination. This work establishes a fundamental guidance and scientific direction for the stabilization of two‐step perovskite precursor solutions.

Cation reactivity inhibits perovskite degradation in efficient and stable solar modules.

Perovskite solar modules (PSMs) show outstanding power conversion efficiencies (PCEs), but long-term operational stability remains problematic. We show that incorporating N,N-dimethylmethyleneiminium chloride into the perovskite precursor solution formed dimethylammonium cation and that previously unobserved methyl tetrahydrotriazinium ([MTTZ]+) cation effectively improved perovskite film. The in situ formation of [MTTZ]+ cation increased the formation energy of iodine vacancies and enhanced the migration energy barrier of iodide and cesium ions, which suppressed nonradiative recombination, thermal decomposition, and phase segregation processes. The optimized PSMs achieved a record (certified) PCE of 23.2% with an aperture area of 27.2 cm2, with a stabilized PCE of 23.0%. The encapsulated PSM retained 87.0% of its initial PCE after ~1900 hours of maximum power point tracking at 85°C and 85% relative humidity under 1.0-sun illumination.

Crystallization Control to Prepare Uniform CsPbI2Br Thin Films for High-Efficiency Perovskite Solar Cells.

All-inorganic perovskite solar cells (PSCs) face challenges related to film inhomogeneity, which arises from nonideal crystallization. This issue significantly impedes the advancement of all-inorganic PSCs. In this study, we observed that during the crystallization process of CsPbI2Br, the Br-rich intermediate phase is often preferentially deposited, leading to an uneven distribution in the out-of-plane direction of the perovskite film. To address this issue, crown ether molecules (dibenzo-18-crown-6) were introduced into the perovskite precursor solution. The complexation of crown ether with Cs cations and Br anions optimizes the crystallization sequence of the perovskite, ensuring that the intermediate phase closely conforms to the standard stoichiometric ratio. This adjustment significantly mitigates the problem of uneven halogen ion distribution along the out-of-plane direction. Furthermore, the crown ether thermally decomposes during the high-temperature annealing process, thereby not affecting the composition of the final perovskite film. Following crown ether treatment, the efficiency of the PSCs reached 14.08%, and the unpackaged devices maintained 80% of their initial efficiency after 1000 h of exposure to light in an atmospheric environment.

Boosting Efficiency to 22.73%: Unraveling the Role of Solvent Environment in Low‐Dimensional Perovskites Through Competitive Bonding Interactions

AbstractIt is reported that the solvent environment exerts a significant influence on the property of perovskite precursor solution and resultant film, which is more pronounced in more complex low‐dimensional perovskites. Four solvent additives with varying basicity are introduced to instigate a tug‐of‐war among bonding interactions, thereby exploring the systematic effect of the solvent environment on the growth of quantum wells and the photoelectric properties of the resultant low‐dimensional perovskite films. A governing principle that diverges significantly from those previously documented for three‐dimensional perovskites is elucidated in low‐dimensional perovskites. When coordination interactions predominate in the solvent environment, the emergence of a two‐dimensional GA2PbI4 transitional phase is fostered to facilitate subsequent transformation into the desirable ACI phase, and the perovskite crystallization kinetics is retarded to improve the film quality. Hence, the highest power conversion efficiency (PCE) of 22.73% is obtained for GA(MA)nPbnI3n+1 (n = 5) based solar cells with a p‐i‐n structure. The PCE achieved in this work is a record among the reported low‐dimensional perovskite solar cells.

Cost-Effective Acetonitrile-Based Precursor Solution Mitigates Heterogeneous Nucleation for Efficient and Stable Perovskite Solar Cells.

Solution-processing is the primary method for fabricating high-efficiency perovskite solar cells (PSCs), where solvent choice critically influences film formation and quality. Although additives can optimize film formation dynamics by balancing nucleation and growth of perovskite, they can also induce heterogeneous nucleation due to competitive coordination and varying crystallization kinetics, leading to compositional heterogeneity and structural disorders. Herein, a perovskite precursor solution is developed using acetonitrile (ACN) as a weak coordination host solvent instead of the traditional N,N-dimethylformamide (DMF). The ACN-based perovskite precursor solution reduces heterogeneous nucleation typically caused by the competitive coordination effect of DMF, and cuts costs by half compared to DMF-based precursor solutions. This approach promotes a single crystallization pathway via a dimethyl sulfoxide-solvated intermediate phase to α-FAPbI3, which extends the anti-solvent operation window, and enhances the crystallinity of perovskite films, and reduces defect states. The power conversion efficiencies (PCE) of 23.62% and 20.13% is achieved for the PSC and minimodule, respectively. The PSC retains over 97% of its initial efficiency after 800h of continuous illumination under maximum power point tracking (MPPT). These findings provide valuable insights into solvent interactions in perovskite film formation and offer a cost-effective strategy for improving the device's performance and stability.

Targeted synergistic chemical bonding strategy for Efficient and stable CsPbI3-based perovskite solar cells

Regulating the crystallization process of perovskite film and suppressing iodine-related defects hold significant importance in improving the efficiency and stability of CsPbI3-based perovskite solar cells (PSCs), thereby endowing their more potential for commercial applications. Herein, we introduced 2-Aminoethyl methylsulfone hydrochloride (AMS) into the perovskite precursor solution to establish targeted synergistic chemical bonding involving Lewis acid-base interactions and hydrogen bonds with CsPbI3 perovskite. We emphasize the importance of the DMAPbI3 intermediate phase for the crystal quality of CsPbI3 perovskite, and reveal that diminishing the size of Pb-I framework colloids in precursor solution can facilitate the formation of DMAPbI3 and optimize the crystallization process of CsPbI3 perovskite. Simultaneously, we demonstrate the generation of high valence iodine defects due to the photoinduction, and prove that constructing N-H···I hydrogen bond can effectively passivate the iodine-related defects. Consequently, the CsPbI3-based PSCs display an impressive power conversion efficiency of 19.59% along with markedly improved stability. Our finding presents a feasible strategy for managing perovskite crystallization and mitigating the defects-induced perovskite degradation, thus promoting the commercialization of CsPbI3-based PSCs.

Enhanced Homogeneity in Perovskite Photovoltaic Films via Antisolvent Extraction of a Methylamine-Based Gel Precursor.

Solution-processed perovskite solar cells (PSCs) are at the forefront of next-generation photovoltaics, exhibiting outstanding photoelectric performance and cost-effective manufacturing. However, the prevalent use of polar aprotic solvents such as N,N-dimethylformamide and dimethyl sulfoxide in the preparation of perovskite precursor solution hinders complete solvent removal during film formation. Their high boiling points and strong coordinating abilities lead to solvated intermediates and heterogeneous perovskite crystal nucleation, particularly in the absence of the antisolvent-assisted crystallization. To address this, we developed a methylamine (MA)-based gel dispersion system that significantly improves the uniformity of perovskite films. By employing ethyl acetate (EA) antisolvent extraction, the gel precursor is extracted from a solution of MAI and PbI2 in MA ethanol, which is then diluted in pure acetonitrile (ACN) solvent to form a clear perovskite precursor solution. Benefiting from the highly volatile nature of the ACN-based gel perovskite precursor solution and its rich concentration of high-valent PbIn2-n coordination compounds, this approach enables the fabrication of high-quality MAPbI3 perovskite films, yielding PCEs of 21.34% for PSC and 19.77% for a 5 × 5 cm2 mini-module. This MA-based gel perovskite precursor strategy offers a promising avenue for potential applications in the scalable manufacture of PSCs.

Study on the enhancement of device performance by the action of carbonohydrazide at the buried bottom interface of inverted mesoporous perovskite solar cells

The interface of perovskite solar cells (PSCs) significantly influences their efficiency and stability. Researchers tend to pay more attention to the upper surface of the perovskite absorber layer and conduct relatively less research on the bottom buried interface, mainly because the bottom of the perovskite film is challenging to peel off, which increases the difficulty of the characterization of the observation and analysis. Defects at the bottom interface make it more challenging to optimize the treatment than the upper surface. For inverted PSCs, the interface located in direct contact between the light absorption layer of perovskite and the hole transport layer is the buried interface. The buried interface is the direct interface for transporting charge carriers of PSCs and is also the center of non-radiative compound enrichment. The defect density is higher than the defect density of perovskite film crystal. Due to the DMSO initially left in the commonly used perovskite precursor solution during the film formation process, evaporation during the annealing and crystallization process creates vacancy holes at the bottom of the perovskite layer film. These holes and crystal boundaries tend to produce many non-radiative recombinations. These holes are also the sites of photodecomposition, leading to reduced efficiency and stability in PSCs, ultimately impacting the overall performance of PSCs. The work adds an Al2O3 mesoporous layer on top of the hole transport layer (HTL), which reduces the direct contact area between PTAA and perovskite film. In the perovskite precursor solution, we incorporate a solid additive called Carbonohydrazide (CBH), this substance replaces some of the DMSO and fills in the voids at the bottom of the perovskite film that is left when the DMSO evaporates. This process helps to reduce non-radiative recombination and photodegradation caused by the voids at the bottom of the perovskite, leading to an improvement in the efficiency and stability of the cell. The optimization of the buried bottom interface has improved the cell’s average efficiency from 17.6 % to 19.7 %, an 11.9 % increase. The aperture area of the devices in this work is 0.048 cm2, and the photoelectric conversion efficiency of our device still reaches 80.64 % of the initial efficiency after 600 h of continuous heating in a glove box with a nitrogen atmosphere, maintaining a test temperature of 60 °C.

Regulation of nucleation and crystallization for blade-coating large-area CsPbBr3 perovskite light-emitting diodes

Metal halide perovskite light-emitting diodes (PeLEDs) and large-area perovskite color conversion layers for liquid crystal display exhibit great potential in the field of illumination and display. Blade-coating method stands out as a highly suitable technique for fabricating large-scale films, albeit with challenges such as uneven nucleation coverage and non-uniformity crystallization process. In this work, we developed an in-situ characterization measurement system to monitor the perovskite nucleation, and crystallization process. By incorporating formamidine acetate (FAAc) into perovskite precursor solutions, the nucleation rate and nuclei density of perovskite were increased, leading to more uniform nucleation. In addition, we inserted a layer of [2-(9H-carbazol-9-yl)ethyl] phosphonic acid above the poly(9-vinylcarbazole) hole transport layer. This layer acts as an anchor for the perovskite nano-crystal nuclei formed in the precursor, enhancing the steric hindrance of the solute and subsequently slowing down the crystal growth rate, thereby improving crystal quality. Based on these improvements, large-area perovskite nano-polycrystalline films with significantly improved uniformity and enhanced photoluminescence quantum yield were obtained. A small-area PeLED (2 mm × 2 mm) with a maximum external quantum efficiency of 25.91% was realized, marking the highest record of PeLED prepared by blade-coating method to date. An ultra-large-area PeLED (5 cm × 7 cm) was also prepared, which is the largest PeLED prepared by the solution method reported so far.

Low-temperature crosslinked hole transport material for high-performance inverted perovskite solar cells

Hole transport materials (HTMs) play a crucial role in the development of high-performance inverted perovskite solar cells (PSCs) by facilitating hole transport, passivating defects, and tuning crystallization. Achieving high efficiency and stability remains a key challenge for the PSCs. Crosslinked HTMs combine the efficiency of small molecules with enhanced environmental stability, however, a significant challenge in developing crosslinked HTMs for PSCs is the high temperature required for crosslinking. In this work, we synthesized a concise crosslinkable HTM, Tetrastyrenebiphenyldiamine (TPDA), based on a biphenyl core with four styrene groups, using a one-step method. TPDA can be crosslinked through an annealing process at 100℃ for 10 min without the need for any dopants or initiators. Interestingly, the compact films formed in the anneal process and the excellent spreadability for the perovskite precursor solution leading to the high-quality perovskite films, as a result, the inverted devices based on CL-TPDA achieve a champion power conversion efficiency (PCE) of 21.4%. Furthermore, the stability of the devices without encapsulation has notably improved. The PCE maintains over 85% of its initial value after 1000 h of storage in ambient air (25℃, relative humidity about 50%).

Reactive Passivation of Wide-Bandgap Organic-Inorganic Perovskites with Benzylamine.

While amines are widely used as additives in metal-halide perovskites, our understanding of the way amines in perovskite precursor solutions impact the resultant perovskite film is still limited. In this paper, we explore the multiple effects of benzylamine (BnAm), also referred to as phenylmethylamine, used to passivate both FA0.75Cs0.25Pb(I0.8Br0.2)3 and FA0.8Cs0.2PbI3 perovskite compositions. We show that, unlike benzylammonium (BnA+) halide salts, BnAm reacts rapidly with the formamidinium (FA+) cation, forming new chemical products in solution and these products passivate the perovskite crystal domains when processed into a thin film. In addition, when BnAm is used as a bulk additive, the average perovskite solar cell maximum power point tracked efficiency (for 30 s) increased to 19.3% compared to the control devices 16.8% for a 1.68 eV perovskite. Under combined full spectrum simulated sunlight and 65 °C temperature, the devices maintained a better T80 stability of close to 2500 h while the control devices have T80 stabilities of <100 h. We obtained similar results when presynthesizing the product BnFAI and adding it directly into the perovskite precursor solution. These findings highlight the mechanistic differences between amine and ammonium salt passivation, enabling the rational design of molecular strategies to improve the material quality and device performance of metal-halide perovskites.

Extending Shelf-Life of Two-Step Method Precursor Solutions through Targeted Regulation for Highly Efficient and Reproducible Perovskite Solar Cells.

Precursor solution aging process can cause significant influence on the photovoltaic performance of perovskite solar cells (PVSCs). Notably, we first observe that the aging phenomenon is more severe in the precursor of two-step sequential method compared to that in one-step method due to that the protic solvent isopropanol facilitates amine-cation side reaction and iodide ions oxidation. Herein, we report a novel approach for selectively stabilizing both organic amine salt and lead iodide (PbI2) precursor solutions in two-step method. The introduction of benzene-1,3-dithiol into organic amine salt solution can mitigate amine-cation side reactions due to the formation of an acidic and reducing environment. Simultaneously, decamethylferrocene (FcMe10/FcMe+ 10) pair can act as a redox shuttle in PbI2 solution to concurrently oxidize Pb0 and reduce I2 in cyclic manner. Consequently, the PVSCs device fabricated from ameliorative precursor solutions demonstrates superior power conversion efficiency of 25.31 %, retaining 95 % of its efficiency after 21 days of solution aging. Moreover, the unencapsulated devices maintain 85 % of primitive efficiency for 1500 h at maximum power point tracking under continuous illumination. This work establishes a fundamental guidance and scientific direction for the stabilization of two-step perovskite precursor solutions.

Controllable Iodoplumbate-Coordination of Hybrid Lead Iodide Perovskites via Additive Engineering for High-Performance Solar Cells.

The crystallization and growth of perovskite crystals are two crucial factors influencing the performance of perovskite solar cells (PSCs). Moreover, iodoplumbate complexes such as PbI2, PbI3-, and PbI42- in perovskite precursor solution dictate both the quality of perovskite crystals and the optoelectrical performance of PSCs. Here, we propose an iodoplumbate-coordination strategy that employs pentafluorophenylsulfonyl chloride (PTFC) as an additive to tailor the crystal quality. This strategy directly affects the thermodynamics and kinetics of perovskite crystal formation by regulating hydrogen bonds or coordination bonds with Pb2+ or I- ions. Subsequently, the synergistic effect of the PTFC and FA+ complex was beneficial for intermediate-to-perovskite phase transition, improving the crystalline quality and reducing the defect density in the perovskite film to suppress nonradiative recombination loss. Consequently, the treated PSCs achieved a power conversion efficiency (PCE) of 24.61%, demonstrating enhanced long-term stability under both light and thermal stress. The developed device retained 92.53% of its initial PCE after 1200 h of continuous illumination and 88.6% of its initial PCE after 600 h of 85 °C thermal stability tests, respectively, both conducted in N2 atmospheres.

Additive engineering for efficient wide-bandgap perovskite solar cells with low open-circuit voltage losses.

High-performance wide-bandgap (WBG) perovskite solar cells are used as top cells in perovskite/silicon or perovskite/perovskite tandem solar cells, which possess the potential to overcome the Shockley-Queisser limitation of single-junction perovskite solar cells (PSCs). However, WBG perovskites still suffer from severe nonradiative recombination and large open-circuit voltage (Voc) losses, which restrict the improvement of PSC performance. Herein, we introduce 3,3'-diethyl-oxacarbo-cyanine iodide (DiOC2(3)) and multifunctional groups (C=N, C=C, C-O-C, C-N) into perovskite precursor solutions to simultaneously passivate deep level defects and reduce recombination centers. The multifunctional groups in DiOC2(3) coordinate with free Pb2+ at symmetric sites, passivating Pb vacancy defects, effectively suppressing nonradiative recombination, and maintaining considerable stability. The results reveal that the power conversion efficiency (PCE) of the 1.68eV WBG perovskite solar cell with an inverted structure increases from 18.51% to 21.50%, and the Voc loss is only 0.487V. The unpackaged device maintains 95% of its initial PCE after 500h, in an N2 environment at 25°C.

Small molecule induced interfacial defect healing to construct inverted perovskite solar cells with high fill factor and stability

Chemical defects at the surface and grain boundaries of perovskite crystals cause deterioration of conversion efficiency and stability of perovskite solar cells (PSCs). In this study, a multifunctional additive, 5-fluoro-2-pyrimidine carbonitrile (FPDCN) molecule, is added into the perovskite precursor solution in order to passivate the uncoordinated Pb2+ by the cyanogen (–CN) group and pyrimidine N in FPDCN. Interestingly, fluorine (F) atoms interact with FA+ to form hydrogen bonds, which could regulate the perovskite crystallization process for the formation of high-quality perovskite crystals. Besides, the F atoms in FPDCN increase the water contact angle of perovskite films. As a result, the carrier extraction and transport in the perovskite film are significantly enhanced, and the non-radiative recombination is suppressed. The corresponding devices achieve a champion photovoltaic conversion efficiency (PCE) of 20.7 % and a fill factor (FF) of over 83 %. The device based on FPDCN shows long-term stability under a high-humidity atmospheric environment by maintaining 85 % of the initial efficiency after aging of 700 h in the glove box. This study provides a simple and convenient method to prepare stable and efficient PSCs by optimizing the perovskite precursor solution.

Synergistic effects of the physical modification and chemical passivation enabling efficient perovskite solar cells

Inverted perovskite solar cells (IPSCs) with poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA) as hole transport materials exhibit superior stability and low-temperature processibility. However, the hydrophobicity of PTAA renders it difficult to prepare high-quality perovskite films due to the low wettability of perovskite precursor solutions, resulting in poor crystallization of perovskites and undesirable interface properties of PTAA/perovskites. Herein, a porous layer of Al2O3 nanoparticles functionalized using 2-thenoylacetonitrile (2-T-OACN) molecules is incorporated into the PTAA/perovskite interface. The physical adhesion of Al2O3 nanoparticles on the PTAA layer could enhance the surface wettability for perovskite precursor solutions, resulting in uniform perovskite films being realized on the PTAA layer. Meanwhile, 2-T-OACN adsorbed on the Al2O3 nanoparticles could form C=O··· Pb2+ and C≡N ···Pb2+ coordination interactions with the bottom surface of perovskites, thus passivating the defects at the PTAA/perovskite interface. Moreover, the electron-rich thiophene groups in 2-T-OACN molecules further promote interfacial charge carrier transport and thus significantly lower the interfacial recombination. Consequently, the IPSCs show a high efficiency of 23.3 %, which is largely improved compared with that of 19.4 % efficiency for control IPSCs. The synergistic strategy of the physical modification and chemical passivation provides a feasible approach for modulating the crystallization of perovskites and buried interface properties for IPSCs.

Efficient Perovskite Light‐Emitting Diodes Processed with Green Solvents Enabling a Wide Antisolvent Time Window

AbstractGreen solvent processing of perovskite light‐emitting diodes (PeLEDs) is a necessity for their future commercialization. However, the almost insoluble nature of perovskites in most green solvents strongly impedes the progress of green solvent‐processed PeLEDs. Here, a novel green solvent triethylene glycol (TEG) is used as the processing solvent for perovskites. TEG has better solubility for perovskite precursors than most reported green solvents. Moreover, it is found that the low vapor pressure of TEG solvent and stable precursor solution render a much wider time window for the so‐called antisolvent treatment than that of perovskite precursor solution in commonly dimethyl sulfoxide. High‐quality perovskite film can be readily synthesized with the antisolvent treatment at a time window of 70–100 s, and the resultant green PeLEDs demonstrate nearly identical light‐emitting efficiencies. Together with further interface modification, the optimized green PeLEDs processed with TEG exhibit an external quantum efficiency of 20.4% and a maximal luminance over 38000 cd m−2. It is the first successful attempt to fabricate high‐efficiency PeLEDs utilizing green solvent and is enlightening for the development of high‐performance PeLEDs prepared with eco‐friendly solvents.

Crown Ethers with Different Cavity Diameters Inhibit Ion Migration and Passivate Defects toward Efficient and Stable Lead Halide Perovskite Solar Cells.

Organic-inorganic hybrid metal halide perovskite solar cells have been considered as one of the most promising next-generation photovoltaic technologies. Nevertheless, perovskite defects and Li+ ionic migration will seriously affect the power conversion efficiency and stability of the formal device. Herein, we designed two crown ether derivatives (PC12 and PC15) with different cavity diameters, which selectively bind to different metal cations. It is found that PC15 in perovskite precursor solution can actively regulate the nucleation and crystallization processes and passivate the uncoordinated Pb2+ ions, while PC12 at the interface between the perovskite layer and hole-transporting layer can effectively inhibit the migration of Li+ ions and reduce nonradiative recombination losses. Therefore, PC12 and PC15 can act as "lubricant" and defect passivators, as well as inhibitors of ion migration, when they are synergistically applied at the surface and bulk of perovskite layer. Consequently, the optimized device achieved a champion efficiency of 24.8% with significantly improved humidity, thermal, and light stability.

Synergistic effects of MOF 545 and inorganic additives synchronously for enhanced performance of low-cost carbon-based perovskite solar cells

Perovskite solar cells (PSCs) hold significant promise for the future of renewable energy, with their commercial viability highly anticipated. However, their limited long-term stability, mainly due to degradation from moisture, humidity, elevated temperatures, and UV-A light exposure, remains a significant obstacle. This study addresses these challenges by employing a multifaceted approach involving additive engineering and surface passivation. A novel method was used to synthesize CZTS nanoparticles, which were incorporated as an additive within the perovskite precursor solution. Additionally, MOF 545 was successfully integrated into the perovskite precursor solution, and a CdS layer was deposited at the ETL/perovskite interface. XRD analysis revealed that the combined addition of MOF 545 and CZTS enhanced the perovskite's crystallinity and surface morphology, leading to an increase in grain size and a reduction in grain boundary defects. Furthermore, these additives effectively restricted Pb2+ ion migration within the perovskite absorber layer. The champion cell, incorporating all three additives, achieved a notable power conversion efficiency (PCE) of 10.32 %, representing a significant 70.58 % increase compared to the pristine PSC. The use of additive-treated cells demonstrated improved thermal stability compared to untreated cells, as confirmed through stress testing. These results highlight the potential of additive engineering to significantly enhance the performance and stability of PSCs. Further exploration and optimization of synergistic additive combinations to achieve even greater performance enhancements and long-term stability in PSCs can pave the way for their successful commercialization.