Damp Heat Conditions Research Articles

Mitigating UV-Induced Degradation in Solar Panels through ZnO Nanocomposite Coatings

This study explores the enhancement of silicon-based solar cell performance and durability through the application of zinc oxide (ZnO) nanocomposite film coatings. Utilizing the sol–gel method, ZnO nanorods were synthesized and dispersed within a polyvinyl butyral (PVB) matrix, resulting in uniform nanocomposite films. Comprehensive characterization using X-ray Diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), UV-Visible spectroscopy, and contact angle measurements confirmed the effective integration and desirable properties of ZnO within the PVB matrix. The ZnO coatings demonstrated superior UV absorptivity, significantly blocking UV radiation at 355 nm while maintaining high transparency in the visible range. This led to improvements in key photovoltaic parameters, including short circuit current (Jsc), open-circuit voltage (Voc), efficiency (η), and fill factor (FF). Although a minor reduction in Isc was observed due to the ZnO layer’s influence on the light absorption spectrum, the overall efficiency and fill factor experienced notable enhancements. Furthermore, the thermal load on the solar cells was effectively reduced, mitigating UV-induced degradation and thereby prolonging the operational lifespan of the solar panels. Under damp heat conditions, the coated solar panels exhibited remarkable durability compared to their uncoated counterparts, underscoring the protective advantages of ZnO films. These findings highlight the potential of ZnO nanocomposite coatings to significantly boost the efficiency, reliability, and longevity of silicon-based solar panels, making them more viable for long-term deployment in diverse environmental conditions.

Epoxy resin multimode optical waveguide fabricated by non-contact photolithography

Multimode polymer waveguides were created using epoxy resin materials. The fabrication process used non-contact photolithography, which is a simple and cost-effective method. During the experiments, a reliable and efficient developer was obtained. The samples were analyzed using scanning electron microscopy and the results showed that the ridge waveguides had a smooth surface and vertical sidewalls. The cross-section size was approximately 50 × 55 μm2. The waveguides had a transmission loss was about 0.08 dB/cm at a wavelength of 850 nm, which was measured using the cut-back method. Additionally, the waveguides were found to be stable in thermal and damp heat conditions.

Inhibiting perovskite decomposition by a creeper-inspired strategy enables efficient and stable perovskite solar cells

The commercialization of perovskite solar cells is badly limited by stability, an issue determined mainly by perovskite. Herein, inspired by a natural creeper that can cover the walls through suckers, we adopt polyhexamethyleneguanidine hydrochloride as a molecular creeper on perovskite to inhibit its decomposition starting from the annealing process. The molecule possesses a long-line molecular structure where the guanidinium groups can serve as suckers that strongly anchor cations through multiple hydrogen bonds. These features make the molecular creeper can cover perovskite grains and inhibit perovskite decomposition by suppressing cations’ escape. The resulting planar perovskite solar cells achieve an efficiency of 25.42% (certificated 25.36%). Moreover, the perovskite film and device exhibit enhanced stability even under harsh damp-heat conditions. The devices can maintain >96% of their initial efficiency after 1300 hours of operation under 1-sun illumination and 1000 hours of storage under 85% RH, respectively.

Chiral-structured heterointerfaces enable durable perovskite solar cells.

Mechanical failure and chemical degradation of device heterointerfaces can strongly influence the long-term stability of perovskite solar cells (PSCs) under thermal cycling and damp heat conditions. We report chirality-mediated interfaces based on R-/S-methylbenzyl-ammonium between the perovskite absorber and electron-transport layer to create an elastic yet strong heterointerface with increased mechanical reliability. This interface harnesses enantiomer-controlled entropy to enhance tolerance to thermal cycling-induced fatigue and material degradation, and a heterochiral arrangement of organic cations leads to closer packing of benzene rings, which enhances chemical stability and charge transfer. The encapsulated PSCs showed retentions of 92% of power-conversion efficiency under a thermal cycling test (-40°C to 85°C; 200 cycles over 1200 hours) and 92% under a damp heat test (85% relative humidity; 85°C; 600 hours).

Triple Cross-Linking Engineering Strategies for Efficient and Stable Inverted Flexible Perovskite Solar Cells.

Inverted flexible perovskite solar cells (fPSCs) are promising for commercialization due to their low cost, lightweight, and excellent stability. However, enhancing fPSCs' power conversion efficiency and stability remains challenging. Here, an unprecedented triple cross-linking engineering strategy is innovatively exhibit for efficient and stable inverted fPSCs. First, a carefully designed cross-linker, 4-fluorophenyl 5-(1,2-dithiolan-3-yl) pentanoate (FB-TA), is added to the perovskite precursor solution. During the perovskite film's crystallization at a low temperature, the cross-linking product of FB-TA can passivate the grain boundaries and reduce the film's residual strain and Young's module. Then, FB-TA is also introduced for the bottom- and top-interface modification of the perovskite film. The interfacial treating strategy protects the perovskite from water invasion and strengthens the interfaces. The combination of triple strategies affords highly efficient inverted fPSCs with a champion efficiency of 21.42% among the state-of-the-art inverted fPSCs based on nickel oxides. More importantly, the flexible devices also exhibit superior stabilities with T90 >4000 bending cycles, photostability with T90 >568h, and ambient stability with T90 >2000h, especially the stability with T80 >1120h under harsh damp-heat conditions (i.e., 85°C and 85% RH). The strategy provides new insights into the industrialization of high-performance and stable fPSCs.

Potential‐induced degradation in bifacial silicon heterojunction solar modules: Insights and mitigation strategies

AbstractPotential‐induced degradation (PID) may be a serious concern in photovoltaic (PV) modules and plants, particularly when approaching high system voltages (1500+ V). Here, we investigate PID occurring in bifacial rear‐emitter silicon heterojunction (SHJ) solar cells encapsulated in a glass/glass (G/G) module configuration with ethylene vinyl acetate (EVA) as an encapsulant. PID testing was performed at 85°C in 85% relative humidity (RH), and the solar cells were subjected to −1 kV and +1 kV for up to 800 h. SHJ cells were found to degrade when subjected to −1 kV, and to a lesser extent when left unbiased in damp heat (DH) conditions, while the application of +1 kV prevented degradation. Although prone to PID after extended test durations, the SHJ mini‐modules investigated in this study noticeably passed the industry standard (IEC 61215:2021) PID test of 96 h. The degradation was primarily characterized by losses in short‐circuit current (ISC) at the front side, followed by fill factor (FF) and open‐circuit voltage (VOC). A cross‐sectional transmission electronic microscopy analysis of the laminates subjected to −1 kV highlighted a transport of sodium (Na) through the transparent conductive oxide (TCO), reaching the amorphous Si/TCO interface. The samples tested in DH conditions and with positive PID test conditions did not exhibit such a migration of Na. To account for these observations, we updated a previously proposed model describing the sensitivity of SHJ cells to water. In our degradation model, moisture in the module corrodes the glass, creating sodium hydroxide (NaOH) that then percolate through the EVA before reaching the SHJ cell. The application of a high negative bias amplifies the previous mechanism by increasing the availability of Na+ and also enhances the drift of Na+ through the EVA to the cell. Finally, we demonstrate that PID can be mitigated or suppressed at the module level by using a high‐volume resistivity encapsulant with a low water vapor transmission rate (WVTR) or by encapsulating SHJ solar cells in a configuration impermeable to water (e.g., using an edge sealant).

Functional-Group-Induced Single Quantum Well Dion-Jacobson 2D Perovskite for Efficient and Stable Inverted Perovskite Solar Cells.

In two-dimensional/three-dimensional (2D/3D) perovskite heterostructure, randomly distributed multiple quantum wells (QW) 2D perovskites are frequently generated, which are detrimental to carrier transport and structural stability. Here, the high quality 2D/3D perovskite heterostructure is constructed by fabricating functional-group-induced single QW Dion-Jacobson (DJ) 2D perovskites. The utilization of ─OCH3 in the precursor solution facilitates the formation of colloidal particles with uniform size, resulting in the production of a pure 2D DJ perovskite with an n value of 3. This strategy facilitates the improvement of 3D structural stability and expedites carrier transport. The resultant devices accomplish a power conversion efficiency of 25.26% (certified 25.04%) and 23.56% at a larger area (1 cm2 ) with negligible hysteresis. The devices maintain >96% and >89% of their initial efficiency after continuous maximum power point tracking under simulated AM1.5 illumination for 1300h and under damp-heat conditions (85°C and 85% RH) for 1010h, respectively.

Effect of global damp heat ageing on debonding of crosslinked EVA- and POE-glass laminates

Polyolefin elastomers (POE) have been established as a promising alternative to commonly used peroxide crosslinked ethylene vinyl acetate copolymer (EVA) photovoltaic encapsulation materials. The main objective of this work was to assess the long-term ageing behavior of double-glass laminates based on UV-transparent EVA and POE under damp heat (85 °C, 85 %rh) conditions for up to 10,000h. Ageing induced changes were characterized by microscopy, UV–visible–near infrared (UVVISNIR) spectroscopy, compressive shear testing (CST), differential scanning calorimetry (DSC), macro- and microscopic Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS). Within the laminates, the formation of birefringent spheric microdomains (maltese-crosses) was confirmed after an exposure time of more than 2,000h. The compressive shear behavior of EVA laminates was not significantly affected by damp heat ageing. Interestingly, the POE laminates revealed an even improved compressive shear performance. Whereas the tested EVA laminates failed in an interfacial manner independent on damp heat ageing time, POE laminates exhibited a failure mode transition from interfacial (unaged) to combined interfacial and cohesive (10,000h). On the interfacially fractured surfaces of EVA and POE laminates, carboxylic acid groups were ascertained. Deprotonated silanol and water bands were discernible on the opposite glass sides. Damp heat exposure of POE laminates for 10,000h resulted in pronounced glass ageing close to the interface associated with a partly cohesive failure within glass. This phenomenon was quite different to EVA and was attributed to the alkaline characteristics of the hindered amine light (HALS) stabilized, less-polar, UV-transparent POE encapsulant.

Addressing sodium ion-related degradation in SHJ cells by the application of nano-scale barrier layers

Silicon heterojunction (SHJ) solar cells are renowned for their high efficiency. However, SHJ solar cells are susceptible to various contaminants, leading to significant performance degradation when exposed to damp-heat conditions (e.g., 85 °C and 85% relative humidity). Sodium (Na) has been identified as one of the main contributors to degradation in silicon solar modules subjected to damp-heat conditions. This work investigates the role of an ultra-thin AlOx capping layer (∼10 nm) in preventing the failure in SHJ cells caused by Na-related contaminants. NaCl is applied directly to the solar cell, and the unencapsulated cell undergoes a damp heat test at 85 °C and 85% relative humidity (DH85). It is found that without the AlOx barrier layer, the SHJ cells experience a relative reduction in power of ∼30%rel after only 20 h at DH85. Both the front and rear sides of the cell degrade when exposed to NaCl. This is primarily due to a deterioration of the Ag contact resulting in increased series resistance (Rs), and decrease in fill factor (FF), and an increase in recombination, leading to a significant drop in open-circuit voltage (Voc), particularly when NaCl is applied on the rear side. However, when an AlOx barrier layer is applied to the SHJ cells, the performance losses caused by NaCl are significantly reduced to only ∼3.3%rel. The loss in Voc on the rear side is completely suppressed, and there is only a slight increase in Rs of ∼50%rel compared to ∼300%rel increase in Rs for cells without the AlOx barrier layer. These findings indicate that the ultra-thin AlOx barrier layer provides effective protection for SHJ cells against Na ions, mitigating both Rs and recombination losses. This AlOx barrier layer depositing method is compatible with existing industrial mass-production ALD tools and thus presents a viable solution at the cell level for SHJ cells.

Aging effect on copper stabilizers in second-generation high-temperature superconducting tapes

Copper stabilizers play an essential role in second-generation high-temperature superconducting (2G-HTS) tapes. Corrosion or aging of the copper stabilizer is unavoidable and affects the tape performance. In this study, aging tests were performed on fresh copper-plated 2G-HTS tapes under steady-state damp heat conditions, in accordance with the IEC 60068–2-78:2012 regulations. To accelerate the aging, the conditions were set as 40 °C, a relative humidity of 93%, and test durations of up to 48 h. The surface contact resistivity (ρc) in liquid nitrogen was measured for fresh and aged specimens under normal pressure of up to 160 MPa. The results indicated that ρc increased with the test duration and tended to become saturated. After 48 h aging tests, the ρc of the specimens was three times higher that of the fresh 2G-HTS tapes. Moreover, the microstructure of the copper stabilizer was characterized. Height fluctuations were observed on all the specimen surfaces, which might be the reason for the ρc scattering. X-ray photoelectron spectroscopy elemental analysis revealed higher amounts of carbon and oxygen on the surfaces of the specimens after aging, which significantly reduced the purity of the copper stabilizer. It was also found that Cu2O was the main product on the tape surface during the reaction with oxygen and, water vapor and so on. This study provides a reference for the design of non-insulated coils and the preservation of 2G-HTS tapes.

Stable passivation of cut edges in encapsulated n-type silicon solar cells using Nafion polymer

In this study, the edge passivation effectiveness and long-term stability of Nafion polymer in n-type interdigitated back contact (IBC) solar cells are investigated. For new module technologies such as half-cut, triple-cut, or shingled modules, cutting of the cells introduces unpassivated edges with a high recombination rate and this limits the module power. These cut edges can be “repassivated” after cutting and in this work Nafion polymer is used to achieve this. First, different edge types, namely emitter edges (n+/n/p+) and back surface field (BSF) edges (n+/n/n+), as well as different cutting techniques such as laser cut and cleave (L&C), thermal laser separation (TLS), and mechanical cleaving are evaluated. It is found that TLS and mechanical cleaving enable good repassivation on both BSF and emitter edges. Second, industrial-size IBC solar cells are made to assess the effect of the edge repassivation on performance. On 1/4-cut M2 size IBC cells with two emitter edges, efficiency is improved by over 0.3%abs. However, an efficiency improvement was not observed for similar cells with BSF edges, due to an insufficient passivation at the bulk edges. Last, the real-world stability of the Nafion repassivation is evaluated in industrially relevant module stacks by laminating the repassivated wafers with ethylvinylacetate (EVA) or polyolefin elastomer (POE) encapsulants and then exposing them to industry standard testing of 1000 h under damp heat conditions (85 °C, 85% relative humidity). The tests reveal that the repassivation is stable in EVA encapsulants but not in POE.

Aerosol‐Jet‐Printed Encapsulation of Organic Photovoltaics

Organic electronic devices (OEDs) are prone to oxygen‐ and water‐induced degradation and therefore need to be encapsulated with barrier materials. In this work, an aerosol jet (AJ)‐printing process is developed to coat perhydropolysilazane (PHPS) directly onto OEDs by adapting the print setup and systematically optimizing the process parameters. Furthermore, a novel curing process that converts PHPS to silica barrier layers is developed by combining damp heat (DH) exposure with subsequent vacuum–UV irradiation. This two‐step treatment is shown to be considerably faster and gentler than the state‐of‐the‐art curing processes and also yields a quantitatively higher conversion. Both the printing and the conversion process are fully compatible with OED devices, which is demonstrated by a damage‐free direct encapsulation of organic solar cells. The encapsulated cells show a significant reduction of degradation in DH conditions (65 °C/85% r.h.), maintaining >95% of their initial performance for >100 h. Complementary electroluminescence measurements reveal that the AJ‐printed barrier layers effectively prevent lateral water ingress into the devices. Herein, the proof of principle is provided that AJ printing can be used to print barrier layers directly onto OEDs and is thus an industrially highly relevant technology to precisely encapsulate such devices even on 3D objects.

Rationally Designed Eco-Friendly Solvent System for High-Performance, Large-Area Perovskite Solar Cells and Modules.

The important but remained issue to be addressed to achieve the mass production of perovskite solar modules include a large-area fabrication of high-quality perovskite film with eco-friendly, viable production methods. Although several efforts are made to achieve large-area fabrication of perovskite, the development of eco-friendly solvent system, which is precisely designed to be fit to scale-up methods are still challenging. Herein, this work develops the eco-friendly solvent/co-solvent system to produce a high-quality perovskite layer with a bathing in eco-friendly antisolvent. The new co-solvent/additive, methylsulfonylmethane (MSM), efficiently improves the overall solubility and has a suitable binding strength to the perovskite precursor, resulting in a high-quality perovskite film with antisolvent bathing method in large area. The resultant perovskite solar cells showed high power conversion efficiency of over 24% (in reverse scan), with a good long-term stability under continuous light illumination or damp-heat condition. MSM is also beneficial to produce a perovskite layer at low-temperature or high-humidity. MSM-based solvent system is finally applied to large-area, resulting in highly efficiency perovskite solar modules with PCE of 19.9% (by aperture) or 21.2% (by active area) in reverse scan. These findings contribute to step forward to a mass production of perovskite solar modules with eco-friendly way.

High photoactive black phase stability of CsPbI3nanocrystals under damp-heat conditions of 85 °C and 85% relative humidity

High damp-heat stability of CsPbI3nanocrystals is demonstrated by B-site ion doping engineering. The black phase stability time of these nickel ion doped nanocrystals reaches a record 54 hours under the conditions of 85 °C and 85% relative humidity.

Improved Stability of MAPbI3 Perovskite Solar Cells Using Two-Dimensional Transition-Metal Dichalcogenide Interlayers.

Perovskite solar cells (PSCs) have been receiving considerable attention as next-generation solar cells. However, their short lifetime is a major obstacle to their commercialization. In addition to the properties of the materials used in PSCs, their interfaces play an important role in device stability by maintaining their initial design. In this study, we developed a transition-metal dichalcogenide (TMD) as a stable and efficient interlayer. MoS2 and WSe2 were applied to both the hole and electron transport sides of the PSCs with general FTO/TiO2/MAPbI3/Spiro-OMeTAD/Au structures, respectively. Owing to efficient charge transfer by TMD interlayers, our PSCs achieved a 19.24% efficiency, which is higher than the efficiency of the control devices (18.22%). Furthermore, the device stability was markedly improved by the passivation and strain-release effects of the TMD interlayers. Thus, the PSCs with TMD interlayers demonstrated a stable performance over 1000 h under damp heat (85 °C and 85% relative humidity) conditions.

Optically and Mechanically Engineered Anti‐Reflective Film for Highly Efficient Rigid and Flexible Perovskite Solar Cells

AbstractSticker‐type anti‐reflective (AR) film is a powerful route to achieve the highest efficiency and commercialization of perovskite solar cells (PSCs) by improving the light transition efficiency (LTE). However, conventionally used AR film has high flexural rigidity owing to its limitation of material and thickness, thereby hindering its application to high‐efficiency flexible devices. This paper proposes a sticker‐type ultra‐thin perfluoropolyether (PFPE) AR film (SUPA) made of PFPE (n = 1.34) that is fabricated through a well‐designed two‐step peeling propagation method. The proposed SUPA demonstrates superior properties in terms of LTE (≈98.3%) and film thickness (≈20 µm), exhibiting the best performance among the existing AR films for PSCs. The SUPA‐assisted rigid and flexible PSC guarantees high short‐circuit current density (rigid ≈26.63 mA cm−2, flexible ≈23.05 mA cm−2) and power conversion efficiency (rigid ≈24.31%, flexible ≈20.05%). The SUPA sustains over 97.5% of its initial transmittance under exposure to the light (168 h) and damp heat condition (1000 h), and devices with SUPA show remarkable flexibility maintaining their initial efficiency after 10 000 cycles of a bending test (2 mm radius).

Double Heterojunction Crystalline Silicon Solar Cells: From Doped Silicon to Dopant-Free Passivating Contacts

Carrier-selective passivating contacts for effective electron and hole extraction are crucial to the attainment of high efficiency in crystalline silicon (Si) solar cells. In this comprehensive review, the principle of carrier extraction and recombination mechanisms in conventional industrial Si solar cells are discussed first. Passivating contacts based on (i) amorphous hydrogenated Si and (ii) polysilicon/silicon oxide are next reviewed, with emphasis on carrier selectivity mechanisms including contact layer band alignment with silicon, and localized carrier transport in ultrathin oxides. More recent developments in dopant-free passivating contacts deposited by lower-cost fabrication processes with lower thermal budget are then described. This third category of non-Si based electron- and hole-selective passivating contacts include transition metal oxides, alkali/alkali earth metal fluorides and organic conjugated polymers. The photovoltaic performance of asymmetric double heterojunction Si solar cells fabricated using these non-Si passivating contacts and their stability in damp heat conditions are discussed and compared with Si based passivating contacts.

Fully solution-processed, light-weight, and ultraflexible organic solar cells

Organic photovoltaic (OPV) devices have the potential to be superior to other PV technologies for the use in applications that require very high flexibility or maximum specific power (power-per-weight ratio), such as textile integration, wearable electronics, or outer space applications. However, OPV devices also require encapsulation by barrier films to reduce the degradation driven by extrinsic factors, which in turn limits their flexibility and leads to lower specific power values. In this work, fully solution-processed (including both electrodes) semitransparent organic solar cells (OSCs) with performance comparable with conventional indium tin oxide-based devices are processed directly onto different barrier films of varying thicknesses. Direct cell fabrication onto barrier films leads to the elimination of the additional polyethylene terephthalate substrate and one of the two adhesive layers in the final stack of an encapsulated OPV device by replacing the industrial state-of-the-art sandwich encapsulation with a top-only encapsulation process, which yields significantly thinner and lighter ‘product-relevant’ PV devices. In addition to the increase of the specific power to 0.38 W g−1, which is more than four times higher than sandwich-encapsulated devices, these novel OSCs exhibit better flexibility and survive 5000 bending cycles with 4.5 mm bending radius. Moreover, the devices show comparable stability as conventionally encapsulated devices under constant illumination (1 sun) in ambient air for 1000 h. Finally, degradation under damp heat conditions (65 °C, 85% rh) was investigated and found to be determined by a combination of different factors, namely (UV) light soaking, intrinsic barrier properties, and potential damaging of the barriers during (laser) processing.

Investigating the reliability of electrically conductive adhesives for shingled photovoltaic Si modules

This paper discusses the environmental stability of an electrically conductive adhesive (ECA) applied to shingled photovoltaic (PV) modules. This study aims to verify the degradation behavior of ECA joints when shingled PV modules are exposed to an accelerated aging test under hot and humid environmental conditions. To achieve this, we prepared shingled PV modules through an assembly process wherein five pre-cut crystalline silicon solar cells were bonded with a ECA paste cured by an infrared lamp, and then stored under damp heat (85 °C/85% RH) and high temperature (65 and 85 °C) conditions. To confirm the aging of the ECA, we determined the changes in the electrical resistance of the ECA and in the efficiencies of the shingled PV modules. Results suggest that the electrical properties of the ECA did not deteriorate under heat and moisture conditions, while the performance of the shingled modules degraded under the same conditions. It was confirmed that the degradation in performance was mainly due to a drop in the fill factor (FF) caused by current leakage. Physicochemical analyses of the samples revealed that Ag atoms, which diffused from the ECA joint to the Si wafer, acted as the shunt path for the solar cell. The bonding properties of the ECA joint to moisture were evaluated as well.

Methylammonium Compensation Effects in MAPbI3 Perovskite Solar Cells for High-Quality Inorganic CuSCN Hole Transport Layers.

Recent studies have demonstrated that copper (I) thiocyanate (CuSCN) has huge potential as a hole extraction material (HEM) for perovskite solar cells. Here, we used CuSCN as a HEM and analyzed its relationships with a methylammonium lead iodide (MAPbI3) perovskite layer. The CuSCN dissolved in diethyl sulfide (DES) was spin-coated on the MAPbI3 layer. For high-quality and dense CuSCN layers, post-annealing was carried out at various temperatures and times. However, the unwanted dissociation of MAPbI3 to PbI2 was observed due to the post-annealing for a long time at elevated temperatures. In addition, DES, which is used as a CuSCN solvent, is a polar solvent that damages the surface of MAPbI3 perovskites and causes poor interfacial properties between the perovskite layer and HEM. To solve this problem, the effect of the molar ratio of methylammonium iodide (MAI) and PbI2 in the MAPbI3 precursor solution was investigated. The excess MAI molar ratio in the MAPbI3 precursor solution reduced MAPbI3 surface damage despite using DES polar solvent for CuSCN solution. In addition, dissociation of MAPbI3 to PbI2 following an adequate post-annealing process was well suppressed. The excess MAI molar ratio in the MAPbI3 precursor could be compensated for the MA loss and effectively suppress phase separation from MAPbI3 to MAI + PbI2 during post-annealing. The efficiency based on the normal planar structure of CuSCN/MAPbI3 (using excess MAI)/TiO2 was approximately 17%. The CuSCN-based MAPbI3 device shows more optimized stability than the conventional spiro-OMeTAD under damp heat (85 °C and 85% relative humidity) conditions because of the robust inorganic HEM.