Printing-Induced Alignment Network Design of Polymer Matrix for Stretchable Perovskite Solar Cells with Over 20% Efficiency

Polymer matrix is felicitously applied into the active layer and transporting layer of perovskite solar cells (PSCs) to enable a stretchable function. However, the chaotic deposition of polymer chains is the main cause for the inferior photoelectric performance. When the stretchable PSCs are in a working state, the stress cannot be removed effectively due to the random polymer chain deposition. The stress accumulation will cause irreversible damage to the stretchable PSCs. Herein, the structural bionics and patterned-meniscus coating technology are combined to print the polymer chain-oriented deposition in the stretchable PSCs. Based on this approach, the conducting polymer electrode is printed with both significant mechanical stability and conductivity. More importantly, the oriented polyurethane with self-healing property can enhance the crystal quality of perovskite films and repair perovskite cracks caused by stress destruction. Thus, the corresponding stretchable PSCs achieve a stabilized power conversion efficiency (PCE) of 20.04% (1.0 cm²) and 16.47% (9 cm²) with minor efficiency discrepancy. Notably, the stretchable PSCs can maintain 86% of the primitive PCE after 1000 cycles of bending with a stretch ratio of 30%. This directional growth of polymer chain strategy provides guidance for printing prominent-performance stretchable PSCs.     

Co-Evaporated MAPbI3 with Graded Fermi Levels Enables Highly Performing,Scalable, and Flexible p-i-n Perovskite Solar Cells

Recent progress of vapor-deposited perovskite solar cells (PSCs) has proved the feasibility of this deposition method in achieving promising photovoltaic devices. For the first time, it is probed the versatility of the co-evaporation process in creating perovskite layers customizable for different device architectures. A gradient of composition is created within the perovskite films by tuning the background chamber pressure during the growth process. This method leads to co-evaporated MAPbI₃ film with graded Fermi levels across the thickness. Here it is proved that this growth process is beneficial for p-i-n PSCs as it can guarantee a favorable energy alignment at the charge selective interfaces. Co-evaporated p-i-n PSCs, with different hole transporting layers, consistently achieve power conversion efficiency (PCE) over 20% with a champion value of 20.6%, one of the highest reported to date. The scaled-up p-i-n PSCs, with active areas of 1 and 1.96 cm², achieved the record PCEs of 19.1% and 17.2%, respectively, while the flexible PSCs reached a PCE of 19.3%. Unencapsulated PSCs demonstrate remarkable long-term stability, retaining ≈90% of their initial PCE when stored in ambient for 1000 h. These PSCs also preserve over 80% of their initial PCE after 500 h of thermal aging at 85 °C.     

Synergetic Excess PbI2 and Reduced Pb Leakage Management Strategy for 24.28% Efficient,Stable and Eco-Friendly Perovskite Solar Cells

Introducing excess PbI₂ has proven to be an effective in situ passivation strategy for enhancing efficiency of perovskite solar cells (PSCs). Nevertheless, the photoinstability and hysteresis are still tough issues owing to the photolysis nature of PbI₂. Moreover, the humidity-related degradation of perovskite films is also a difficult territory to cover in such an in situ passivation strategy. Herein, a synergistic strategy is reported via initiatively inducing vertical graded PbI₂ distribution (GPD) in the whole perovskite film and capping a cis-Ru(H₂dcbpy)(dnbpy)(NCS)₂ (Z907) internal encapsulation (IE) layer on the surface to ameliorate the above issues. The GPD design can enhance luminescence, prolong carrier lifetimes, ascertaining the improvement of efficiency and elimination of photoinstability in the PSCs. Besides, the introduced IE layer not only can promote the moisture and thermal resistance, but also inhibit Pb leakage and ion migration in the PSCs. Through the synergetic regulations, the resultant PSCs exhibit an impressive open circuit voltage (V_OC) of 1.253 V, fill factor of 81.25%, and power conversion efficiency (PCE) of 24.28%. Moreover, the PSCs maintain 91% of its initial PCE at relative humidity of 85% after 500 h aging and 94% under continuous heating at 85 °C after 750 h aging.     

Interfacial Energy Level Alignment and Defect Passivation by Using a Multifunctional Molecular for Efficient and Stable Perovskite Solar Cells

Tin oxide (SnO₂) is currently the dominating electron transport material (ETL) used in state-of-the-art perovskite solar cells (PSCs). However, there are amounts of defects distributed at the interface between ETL and perovskite to deteriorate PSC performance. Herein, a molecule bridging layer is built by incorporating 2,5-dichloroterephthalic acid (DCTPA) into the interface between the SnO₂ and perovskites to achieve better energy level alignment and superior interfacial contact. The multifunctional molecular bridging layer not only can passivate the trap states of Sn dangling bonds and oxygen vacancies resulting in improved conductivity and the electron extraction of SnO₂ but also can regulate the perovskite crystal growth and reduce defect-assisted nonradiative recombination due to its strong interaction with undercoordinated lead ions. As a result, the DCTPA-modified PSCs achieve champion power conversion efficiencies (PCEs) of 23.25% and 20.23% for an active area of 0.15 cm² device and 17.52 cm² mini-module, respectively. Moreover, the perovskite films and PSCs based on DCTPA modification show excellent long-term stability. The unencapsulated target device can maintain over 90% of the initial PCE after 1000 h under ambient air. This strategy guides design methods of molecule bridging layer at the interface between SnO₂ and perovskite to improve the performance of PSCs .     

Two-Dimensional Metal–Organic Frameworks-Based Grain Termination Strategy Enables High-Efficiency Perovskite Photovoltaics with Enhanced Moisture and Thermal Stability

Perovskite degradation induced by surface defects and imperfect grain boundaries of films seriously damages the performance of perovskite solar cells (PSCs). Meanwhile, conventional organic molecules cannot maintain the long-time passivation effects under the stimulation of external environmental factors. Here, efficient and stable grain passivation in perovskite films is realized by preparing formic acid-functionalized 2D metal–organic frameworks (MOFs) as the terminated agent. Through robust interactions between exposed active sites and PbI₂, the 2D MOFs tightly caps the surface of PbI₂-terminated perovskite grains to stabilize the perovskite phases and aids the adhesion of adjacent grains. The MOFs mainly distributed at the grain boundaries of the perovskite film is directly observed at the microscopic scale. The modified perovskite films have regular morphology, lower defect density, and superior optoelectronic properties. Benefiting from the suppressed charge recombination and faster charge extraction, a power conversion efficiency of 21.28% is achieved for the best-performing PSC device. The unencapsulated PSCs with the MOFs modification maintain 88% and 81% of their initial efficiency after 750 h heating at 85  ° C under N₂ atmosphere and more than 1000 h storage in ambient environment (25  ° C, RH  ≈  40%), respectively.     

Overcoming the PCBM/Ag Interface Issues in Inverted Perovskite Solar Cells by Rhodamine-Functionalized Dodecahydro-Closo-Dodecaborate Derivate Interlayer

Efficient modification of the interface between metal cathode and electron transport layer are critical for achieving high performance and stability of the inverted perovskite solar cells (PSCs). Herein, a new alcohol-soluble rhodamine-functionalized dodecahydro-closo-dodecaborate derivate, RBH, is developed and applied as an efficient cathode interlayer to overcome the (6,6)-phenyl-C₆₁ butyrie acid methyl ester (PCBM)/Ag interface issues. By introducing RBH cathode interlayer, the functions of the interface traps passivation, interfacial hydrophobicity enhancement, interface contact improvement as well as built-in potential enhancement are realized at the same time and thus correspondingly improve the device performance and stability. Consequently, a power conversion efficiency (PCE) of 21.08% and high fill factor of 83.37% are achieved, which is one of the highest values based on solution-processed MAPbI₃/PCBM heterojunction PSCs. Moreover, RBH can act as a shielding layer to slow down moisture erosion and self-corrosion. The PCE of the RBH devices still maintain 84% for 456 h (85 °C @ N₂), 87% for 360 h (23 °C @ relative humidity (RH) 35%) of its initial PCE value, while the control device can only maintain ≈23%, 58% of its initial PCE value under the same exposure conditions, respectively.     

Efficient Inverted Perovskite Solar Cells with a Fill Factor Over 86% via Surface Modification of the Nickel Oxide Hole Contact

The poor interface quality between nickel oxide (NiO_x) and halide perovskites limits the performance and stability of NiO_x-based perovskite solar cells (PSCs). Here a reactive surface modification approach based on the in situ decomposition of urea on the NiO_x surface is reported. The pyrolysis of urea can reduce the high-valence state of nickel and replace the adsorbed hydroxyl group with isocyanate. Combining theoretical and experimental analyses, the treated NiO_x films present suppressed surface states and improved transport energy level alignment with the halide perovskite absorber. With this strategy, NiO_x-based PSCs achieve a champion power conversion efficiency (PCE) of 23.61% and a fill factor of over 86%. The device's efficiency remains above 90% after 2000 h of thermal aging at 85 °C. Furthermore, perovskite solar modules achieve PCE values of 18.97% and 17.18% for areas of 16 and 196 cm², respectively.     

Illumination Enhanced Crystallization and Defect Passivation for High Performance CsPbI3 Perovskite Solar Cells by Sacrificing Dye

All-inorganic perovskite solar cells (PSCs) have been the research focus due to their high thermal stability and proper band gap for tandem solar cells. However, their power conversion efficiency (PCE) is still lower than that of organic-inorganic hybrid PSCs. Herein, a sacrificing dye (Rhodamine B isothiocyanate, RBITC) is developed to regulate the growth of perovskite film by in situ release of ethylammonium cations, isothiocyanate anions and benzoic acid molecules upon annealing and illumination. The ethylammonium cations can efficiently passivate surface defects. The isothiocyanate anions incorporate with uncoordinated Pb to regulate the crystallization process. The benzoic acid molecules facilitate the nucleation of the perovskite crystals. Especially, the illumination can accelerate the release of these beneficial ions/molecules to improve the quality of perovskite films further. After optimization with RBITC, a high open circuit voltage (V_OC) of 1.24 V and a champion PCE of 20.95% are obtained, which are among the highest Voc and PCE values of CsPbI₃ PSCs. Accordingly, the operational stability of the PSC devices is significantly improved. The results provide an efficient chemical strategy to regulate the formation of perovskite films in whole crystallization process for high performance all-inorganic PSCs.     

Concurrent Top and Buried Surface Optimization for Flexible Perovskite Solar Cells with High Efficiency and Stability

Although much progress is made toward enhancing the efficiency of perovskite solar cells (PSCs), their operational reliability, particularly their mechanical stability, which is a crucial factor for flexible PSCs (f-PCSs), has not attracted sufficient attention. The defects in the perovskite layer, especially on the top and the buried surface of the perovskite layer, can induce perovskite fracture, highly limiting the performance of f-PSCs. Herein, a novel multifunctional organic salt, metformin hydrochloride, which can passivate cationic and anionic defects, is incorporated on both the top and buried surfaces of perovskite layer to suppress defects. As a result, a power conversion efficiency (PCE) of 24.40% for rigid PSCs and a PCE of 22.04% for f-PSCs are achieved. Simultaneously, the device can retain 90% and 80% of the initial efficiency after 1000 h of light illumination and 10 000 bending cycles, respectively, showing excellent operational stability. This study may provide a global way to design a passivation strategy and fabricate flexible perovskite solar cells with high efficiency and stability.     

Managing Interfacial Hot-Carrier Cooling and Extraction Kinetics for Inverted Ma-Free Perovskite Solar Cells Over 23% Efficiency via Dion–Jacobson 2D Capping Layer

While quasi-2D perovskite is often used in inverted perovskite solar cells (PSCs) to improve the interfacial carrier transfer, the development of pure 2D perovskite with superior stability is rarely seen and the corresponding carrier-extraction kinetics remains unclear. Here, a variety of hexatomic ring cations including piperidine, pyridine, and cyclohexane are introduced to modify the perovskite/electron transport layer interface. The Dion–Jacobson phase 2D cladding (n = 1) based on 3-(aminomethyl) piperidinium is proved to form a coordinated energy landscape and homogeneous surface potential distribution, and effectively prolong the electron diffusion length (≈1.58 µm) and accelerate the hot-carrier extraction rate (2.5 times that of Control at 400 K). Furthermore, the quasi-2D treatment (n ≈ 3,4) demonstrated a slight escalation in short-circuit current, but failed to inhibit the interdiffusion of Ag, Pb, and I under illumination. Finally, one of the state-of-art power conversion efficiency (PCE) for MA-free inverted PSCs is achieved at 23.62% with increased open-circuit voltage (≈1.15 V) and fill factor (≈82.8%). Most importantly, 89% and 93.6% of initial PCE are retained after 720 h under 85 °C heating and 1000 h under maximum power point tracking, illustrating satisfactory thermal and operational stability with pure 2D perovskite capping layer.     

Stabilizing Bottom Side of Perovskite via Preburying Cesium Formate toward Efficient and Stable Solar Cells

The fragile bottom side of perovskite films is demonstrated to be harmful to the efficiency and stability of perovskite solar cells (PSCs) because the carrier extraction and recombination can be significantly influenced by the easily formed strain, voids, and defects on the bottom side. Nevertheless, the bottom side of perovskite films is usually overlooked because it remains a challenge to directly characterize and modify the bottom side. Herein, a facile and effective strategy is reported to stabilize the bottom side via preburying cesium formate (CsFo) into the SnO₂ electron transport layer (ETL). It is found that the synergistic effect of cesium cation (Cs⁺) and formate anion (HCOO⁻) causes strain relaxation, void elimination, and defects’ reduction, which further facilitate the charge extraction. Consequently, the champion power conversion efficiency (PCE) of formamidinium (FA)-based PSCs is increased from 23.34% to 24.50%. Meanwhile, the ultraviolet (UV), thermal, and operational stability are also enhanced. Finally, formamidinium–cesium (FACs)-based PSCs are investigated to confirm the effectiveness of this preburied CsFo strategy, and the optimal device exhibits a champion PCE of 25.03% and a remarkably high fill factor (FF) of 85.65%.     

Multifunctional Organic Potassium Salt Additives as the Efficient Defect Passivator for High-Efficiency and Stable Perovskite Solar Cells

Despite the rapid developments are achieved for perovskite solar cells (PSCs), the existence of various defects in the devices still limits the further enhancement of the power conversion efficiency (PCE) and the long-term stability of devices. Herein, the efficient organic potassium salt (OPS) of para-halogenated phenyl trifluoroborates is presented as the precursor additives to improve the performance of PSCs. Studies have shown that the 4-chlorophenyltrifluoroborate potassium salt (4-ClPTFBK) exhibits the most effective interaction with the perovskite lattice. Strong coordination between  BF₃⁻/halogen in anion and uncoordinated Pb²⁺/halide vacancies, along with the hydrogen bond between F in  BF₃⁻ and H in FA⁺ are observed. Thus, due to the synergistic contribution of the potassium and anionic groups, the high-quality perovskite film with large grain size and low defect density is achieved. As a result, the optimal devices show an enhanced efficiency of 24.50%, much higher than that of the control device (22.63%). Furthermore, the unencapsulated devices present remarkable thermal and long-term stability, maintaining 86% of the initial PCE after thermal test at 80 °C for 1000 h and 95% after storage in the air for 2460 h.     

Dual-Phase Stabilized Perovskite Nanowires for Reduced Defects and Longer Carrier Lifetime

1D perovskite materials are of significant interest to build a new class of nanostructures for electronic and optoelectronic applications. However, the study of colloidal perovskite nanowires (PNWs) lags far behind those of other established perovskite materials such as perovskite quantum dots and perovskite thin films. Herein, a dual-phase passivation strategy to synthesize all-inorganic PNWs with minimized surface defects is reported. The local phase transition from CsPbBr₃ to CsPb₂Br₅ in PNWs increases the photoluminescence quantum yield, carrier lifetime, and water-resistivity, owing to the energetic and chemical passivation effect. In addition, these dual-phase PNWs are employed as an interfacial layer in perovskite solar cells (PSCs). The enhanced surface passivation results in an efficient carrier transfer in PSCs, which is a critical enabler to increase the power conversion efficiency (PCE) to 22.87%, while the device without PNWs exhibits a PCE of 20.74%. The proposed strategy provides a surface passivation platform in 1D perovskites, which can lead to the development of novel nanostructures for future optoelectronic devices.     

The Synergistic Effect of Pemirolast Potassium on Carrier Management and Strain Release for High-Performance Inverted Perovskite Solar Cells

The quality of the perovskite absorption layer is critical for the high efficiency and long-term stability of perovskite solar cells (PSCs). The inhomogeneity due to local lattice mismatch causes severe residual strain in low-quality perovskite films, which greatly limits the availability of high-performance PSCs. In this study, a multi-active-site potassium salt, pemirolast potassium (PP), is added to perovskite films to improve carrier dynamics and release residual stress. X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FTIR) measurements suggest that the proposed multifunctional additive bonds with uncoordinated Pb²⁺ through the carbonyl group/tetrazole N and passivated I atom defects. Moreover, the residual stress release is effective from the surface to the entire perovskite layer, and carrier extraction/transport is promoted in PP-modified perovskite films. As a result, a champion power conversion efficiency (PCE) of 23.06% with an ultra-high fill factor (FF) of 84.36% is achieved in the PP-modified device, which ranks among the best in formamidinium-cesium (FACs) PSCs. In addition, the PP-modified device exhibits excellent thermal stability due to the inhibited phase separation. This work provides a reliable way to improve the efficiency and stability of PSCs by releasing residual stress in perovskite films through additive engineering.     

Spacer Cation Tuning Enables Vertically Oriented and Graded Quasi-2D Perovskites for Efficient Solar Cells

Halide substitution in phenethylammonium spacer cations (X-PEA⁺, X  = F, Cl, Br) is a facile strategy to improve the performance of PEA based perovskite solar cells (PSCs). However, the power conversion efficiency (PCE) of X-PEA based quasi-2D (Q-2D) PSCs is still unsatisfactory and the underlying mechanisms are in debate. Here, the in-depth study on the impact of halide substitution on the crystal orientation and multi-phase distribution in PEA based perovskite films are reported. The halide substitution eliminates n  =  1 2D perovskite and thus leads to the perpendicular crystal orientation. Furthermore, nucleation competition exists between small-n and large-n phases in PEA and X-PEA based perovskites. This gives rise to the orderly distribution of different n-phases in the PEA and F-PEA based films, and random distribution in Cl-PEA and Br-PEA based films. As a result, (F-PEA)₂MA₃Pb₄I₁₂ (MA = CH₃NH₃⁺, n = 4) based PSCs achieve a PCE of 18.10%, significantly higher than those of PEA (12.23%), Cl-PEA (7.93%) and Br-PEA (6.08%) based PSCs. Moreover, the F-PEA based devices exhibit remarkably improved stability compared to their 3D counterparts.     

Tailoring Precursor Chemistry Enabled Room Temperature-Processed Perovskite Films in Ambient Air for Efficient and Stable Solar Cells with Improved Reproducibility

The perovskite solar cells (PSCs) are promising for commercialization and practical application. However, high-quality perovskite films are normally fabricated in inert gas-filled glovebox, followed by thermal annealing, which is energy-consuming and thus not cost-effective. In this study, a simple manufacturing strategy is demonstrated to fabricate the highly-crystalline perovskite films in ambient air (a relative humidity of over ≈50%) at room temperature via blade-coating without the subsequent thermal–annealing. The perovskite precursor chemistry is tailored by solvent engineering via employing 2-methoxyethanol, which can strongly coordinate with ammonium halide species, thus forming highly uniform small-sized colloids and facilitating the homogeneous nucleation and rapid crystallization of perovskite films even at room temperature. The resultant PSCs fabricated with ambient-processed, annealing-free MAPbI₃ perovskite films exhibit a champion efficiency up to 19.16% with negligible hysteresis and improved reproducibility, which is on par with the high-temperature annealed counterparts fabricated in N₂, and represented one of the highest reported efficiencies for the room-temperature processed PSCs in ambient air. The unencapsulated devices show extended lifespan over 1000 h with nearly no efficiency loss.     

Excellent Intrinsic Long-Term Thermal Stability of Co-Evaporated MAPbI3 Solar Cells at 85 °C

Thermal stability is a critical criterion for assessing the long-term stability of perovskite solar cells (PSCs). Here, it is shown that un-encapsulated co-evaporated MAPbI₃ (TE_MAPbI₃) PSCs demonstrate remarkable thermal stability even in an n-i-p structure that employs Spiro-OMeTAD as hole transport material (HTM). TE_MAPbI₃ PSCs maintain over ≈95% and ≈80% of their initial power conversion efficiency (PCE) after 1000 and 3600 h respectively under continuous thermal aging at 85 °C. TE_MAPbI₃ PSCs demonstrate remarkable structural robustness, absence of pinholes, or significant variation in grain sizes, and intact interfaces with the HTM, upon prolonged thermal aging. Here, the main factors driving TE_MAPbI₃ stability are assessed. It is demonstrated that the excellent TE_MAPbI₃ thermal stability is related to the perovskite growth process leading to a compact and almost strain-stress-free film. On the other hand, un-encapsulated PSCs with the same architecture, but incorporating solution-processed MAPbI₃ or Cs_0.05(MA_0.17FA_0.83)_0.95Pb(I_0.83Br_0.17)₃ as active layers, show a complete PCE degradation after 500 h under the same thermal aging condition. These results highlight that the control of the perovskite growth process can substantially enhance the PSCs thermal stability, besides the chemical composition. The TE_MAPbI₃ impressive long-term thermal stability features the potential for field-operating conditions.     

Synergistic Coassembly of Highly Wettable and Uniform Hole‐Extraction Monolayers for Scaling‐up Perovskite Solar Cells

All organic charge‐transporting layer (CTL)‐featured perovskite solar cells (PSCs) exhibit distinct advantages, but their scaling‐up remains a great challenge because the organic CTLs underneath the perovskite are too thin to achieve large‐area homogeneous layers by spin‐coating, and their hydrophobic nature further hinders the solution‐based fabrication of perovskite layer. Here, an unprecedented anchoring‐based coassembly (ACA) strategy is reported that involves a synergistic coadsorption of a hydrophilic ammonium salt CA‐Br with hole‐transporting triphenylamine derivatives to acquire scalable and wettable organic hole‐extraction monolayers for p–i–n structured PSCs. The ACA route not only enables ultrathin organic CTLs with high uniformity but also eliminates the nonwetting problem to facilitate large‐area perovskite films with 100% coverage. Moreover, incorporation of CA‐Br in the ACA strategy can distinctly guarantee a high quality of electronic connection via the cations' vacancy passivation. Consequently, a high power‐conversion‐efficiency (PCE) of 17.49% is achieved for p–i–n structured PSCs (1.02 cm²), and a module with an aperture area of 36 cm² shows PCE of 12.67%, one of the best scaling‐up results among all‐organic CTL‐based PSCs. This work demonstrates that the ACA strategy can be a promising route to large‐area uniform interfacial layers as well as scaling‐up of perovskite solar cells.     

Water‐Soluble Triazolium Ionic‐Liquid‐Induced Surface Self‐Assembly to Enhance the Stability and Efficiency of Perovskite Solar Cells

Despite being a promising candidate for next‐generation photovoltaics, perovskite solar cells (PSCs) exhibit limited stability that hinders their practical application. In order to improve the humidity stability of PSCs, herein, a series of ionic liquids (ILs) “1‐alkyl‐4‐amino‐1,2,4‐triazolium” (termed as RATZ; R represents alkyl chain, and ATZ represents 4‐amino‐1,2,4‐triazolium) as cations are designed and used as additives in methylammonium lead iodide (MAPbI₃) perovskite precursor solution, obtaining triazolium ILs‐modified PSCs for the first time (termed as MA/RATZ PSCs). As opposed to from traditional methods that seek to improve the stability of PSCs by functionalizing perovskite film with hydrophobic molecules, humidity‐stable perovskite films are prepared by exploiting the self‐assembled monolayer (SAM) formation of water‐soluble triazolium ILs on a hydrophilic perovskite surface. The mechanism is validated by experimental and theoretical calculation. This strategy means that the MA/RATZ devices exhibit good humidity stability, maintaining around 80% initial efficiency for 3500 h under 40 ± 5% relative humidity. Meanwhile, the MA/RATZ PSCs exhibit enhanced thermal stability and photostability. Tuning the molecule structure of the ILs additives achieves a maximum power conversion efficiency (PCE) of 20.03%. This work demonstrates the potential of using triazolium ILs as additives and SAM and molecular design to achieve high performance PSCs.     

基于氮气辅助一步溶液法的高质量钙钛矿太阳能电池光吸收层研制

有机无机杂化钙钛矿太阳能电池因其可调节的带隙、高吸收系数、宽吸收光谱、高载流子迁移率和长电荷扩散长度而被公认为是光伏领域的新希望。然而,采用一步溶液法所制备CH3 NH3 PbI3光吸收层薄膜为树枝状结晶,膜层覆盖率低,大大限制了光电转换效率的进一步提升。本文将氮气引入一步溶液法,通过发挥辅助结晶作用,获得了晶粒均匀且致密的钙钛矿薄膜,并显著提高了钙钛矿太阳能电池的光电转换效率。此外,系统研究了氮气起始时间、气体压强等因素对钙钛矿光吸收层表面形貌及太阳能电池光电转换效率的影响,实验证明氮气起始时间在2~5 s,氮气压强在0.4~0.8 MPa的宽操作窗口范围内,均可制备高质量CH3 NH3 PbI3光吸收层薄膜。