Long-term stability remains a key issue impeding the commercialization of halide perovskite solar cells (HPVKSCs). The diffusion of molecules and ions causes irreversible degradation to photovoltaic device performance. Here, we demonstrate a facile strategy for producing highly stable HPVKSCs by using a thin but compact semimetal Bismuth interlayer. The Bismuth film acts as a robust permeation barrier that both insulates the perovskite from intrusion by undesirable external moisture and protects the metal electrode from iodine corrosion. The Bismuth-interlayer-based devices exhibit greatly improved stability when subjected to humidity, thermal and light stresses. The unencapsulated device retains 88% of its initial efficiency in ambient air in the dark for over 6000 h; the devices maintain 95% and 97% of their initial efficiencies after 85 °C thermal aging and light soaking in nitrogen atmosphere for 500 h, respectively. These sound stability parameters are among the best for planar structured HPVKSCs reported to date.
Highly efficient and low-cost halide perovskite solar cells (HPVKSCs) are regarded as one of the most promising photovoltaic technologies to realize commercialization in the near future1,2,3,4,5. However, the long-term stability of HPVKSCs under real working conditions, involving stresses from moisture, heat, light, and the electric field, is still a challenge that must be addressed6.
The irreversible degradation of HPVKSCs can be mainly attributed to three phenomena: (1) volatilization of the organic components in organic–inorganic hybrid perovskites7, especially for the benchmark methylammonium lead triiodide (MAPbI3) under thermal aging conditions above 85 °C8, (2) permeation of external H2O/O2 and its induced degradation of perovskites, and (3) reactions between the normally used metal electrodes and halogens from the perovskites during prolonged operation9,10. For the last two issues, especially the third one, their resolutions are largely related to the essential properties of the interfacial layers (i.e., morphologic pin-hole free, chemical resistivity to H2O/O2 and halides), which could act as robust permeation barriers to block the undesired processes. If the interfacial layers are permeable or have pin-holes, sufficient separation between the perovskites and electrode metals cannot be achieved, and the corrosive reaction could be fast. For example, in regular-structured HPVKSCs, Grätzel et al. observed the inward diffusion of Au into the perovskite layer through Spiro-OMeTAD under thermal aging at 70 °C10, which may introduce broad tail states in the perovskite layer and thus increase the undesirable non-radiative recombination in the devices11. A similar case has been proven to exist in inverted-structured HPVKSCs. Wang et al. observed that I− ions could diffuse through the [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) layer and react with the Ag electrode under thermal aging at 85 °C in a N2 atmosphere. This reaction could facilitate the escape of I− ions from the perovskites and thus lead to an accelerated decomposition of the perovskite film, which results in an irreversible degradation of the device performance12.
Thus, a robust interfacial barrier is essential, and barrier design has been proven to be a feasible solution to the degradation of HPVKSCs that focuses on hindering the adverse diffusion of ions/molecules, such as the outward diffusion of perovskite species and inward diffusion of metal ions from the electrode or H2O/O2 from the atmosphere13,14,15,16. For example, multilayer interfacial layers made of PDCBT/Ta-WOx17, Spiro-OMeTAD/MoOx18, Spiro-OMeTAD/MoOx/CuPc19, EH44/MoOx20, and CuSCN/graphene21 were designed to strengthen the penetration barriers of regular-structured HPVKSCs and were considered essential for the largely enhanced long-term stability. In inverted-structured HPVKSCs, the electron transport layers (ETLs) are normally composed of fullerene derivatives such as PCBM or C60 and a buffer layer such as bathocuproine (BCP)22, LiF23, nano-carbon materials13, metal acetylacetonates24, and amorphous or nanocrystalline metal oxides23,25,26,27,28,29. Many bilayer-structured ETLs have also been found to be essential for selective charge extraction and enhancing the device’s power conversion efficiency (PCE) and long-term stability. In particular, Riedl et al.15 reported an impermeable triple-layered ETL composed of PCBM/Al-doped ZnO (AZO)/SnOx, in which the SnOx layer deposited by atomic layer deposition (ALD) technique possesses an extremely low water vapor transmission rate of approximately 7 × 10−5 g m−2 day−1. Their unencapsulated MAPbI3-based devices (MA-HPVKSCs) exhibited no degradation under thermal aging at 60 °C for 1000 h. Recently, McGehee et al. even found that their MA-HPVKSCs did not decay after 1000 h at 85 °C in the dark when a similar ALD-deposited SnO2 barrier with a chemically inert ITO electrode was implemented14. More impressively, Park et al.16 recently reported that Cs0.05MA0.95PbI3-based HPVKSCs with ALD-AZO barrier layers retained 86.7% of their initial efficiency after 500 h of maximum power point (MPP) tracking under continuous 1 Sun illumination at 85 °C in ambient air.
To date, all of the reported barrier layers have been made of non-metals, such as carbon-based materials (such as graphene, nano-carbon materials) or metal oxides. The use of metallic materials in stable perovskite-based devices is challenging because of the “metals–halides perovskites” reaction. McGehee et al. even recommended replacing the metal electrodes with transparent conducting oxides, such as ITO, for stable perovskite-based devices30. In view of the above, when examining the periodic table of elements, we still find potential in the region between the metals and non-metals, i.e., bismuth (Bi) and antimony (Sb), which are referred to as semimetals.
Bi was chosen mainly because it prevents corrosion of halide perovskites, which is in contrast to most of the currently used metal electrodes, such as Ag, Au, Al, and Cu9,10,31,32,33. The tendency of the corrosion reaction can be predicted by theory, as discussed later. Previous experimental results indicated that Bi required a temperature of at least 150 °C to trigger a chemical reaction with gaseous iodine to form bismuth (III) iodide34. Furthermore, the rhombohedral lattice of Bi has crystal unit parameters of |a| = |b| ≈ 4.5 Å and trigonal axis |c| ≈ 11.8 Å35,36,37,38, resulting in anisotropic film growth and leading to a flaky structure with limited grain boundaries, which is essential for the as-formed Bi interlayer to act as a robust penetration barrier. Additionally, Bi can be easily deposited by conventional thermal evaporation, unlike other anti-corrosive metals such as molybdenum (Mo). To achieve a vapor pressure of 10−4 Torr for thin film deposition, the required temperature for Bi is 517 °C, which is lower than that required for Ag (832 °C) and much lower than that for tungsten (W, 2757 °C) and Mo (2717 °C)39. Mo and W films typically must be deposited by magnetron sputtering or e-beam evaporation. These high-energy processes may easily damage the perovskite layers underneath the electrodes. In addition, Bi is cost-effective, whose cost is approximately 1/10 that of Ag40.
Here, we demonstrate a facile processing strategy for highly stable HPVKSCs with the structure FTO/Li+-doped NixMg1−xO (NiMgLiO)/Perovskite (PVK)/PCBM/BCP/Bi/Ag by introducing the compact Bi interlayer. The devices and films were characterized by photoluminescence (PL), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), time of flight secondary ion mass spectrometry (ToF-SIMS), etc., which demonstrate that the Bi interlayer acts as a robust penetration barrier that blocks the unfavorable external molecules from diffusing into the devices and suppresses the diffusion of ions between the metal electrode and the perovskites. As a result, our unencapsulated MA-HPVKSCs retain 88% of their initial efficiency after being maintained in the dark in ambient air without humidity control for 6000 h. During long-term light soaking or thermal aging at 85 °C in the dark, the devices with Bi interlayers are considerably more stable than devices without Bi. This Bi-interlayer strategy is easily scalable and highly repeatable and may pave the way to the future practical application of large-area and highly stable HPVKSCs.
Chemically inert characteristic of Bi film
Here, regarding the chemically inert characteristic of Bi, we primarily focus on its anti-corrosivity to halide perovskites. To demonstrate this key characteristic, MAPbI3/metal samples were prepared by evaporating 5-nm-thick Bi, Cu, Au, or Ag films (which should have island-like morphology) directly onto MAPbI3 films, and XPS characterization was performed on both the fresh and aged samples (aging conditions: in the dark and N2 atmosphere, at 85 °C for 100 h). As shown in the Pb 4f XPS spectra (Fig. 1a), peaks at 138.40 and 143.25 eV can be attributed to the Pb–I bonds in perovskite, and peaks at 136.90 and 141.75 eV are from metallic Pb0 32. The figure shows there is no metallic Pb0 found in the purely MAPbI3 film samples even after thermal aging, indicating that MAPbI3 may remain stable when it is not attacked by the active metal films. However, when Cu or Ag was evaporated onto MAPbI3, the metallic Pb0 appeared, combined with the dominant Ag+ and Cu+ peaks in Ag 3d and Cu 2p spectra (Supplementary Figure 1), which demonstrate the corrosion reaction between Cu/Ag and MAPbI3. For MAPbI3/Au, although there are no peaks corresponding to metallic Pb0 or Au+, shoulders are observed at 137.2 and 142.2 eV. These were suggested to be attributed to partial charge transfer at the MAPbI3/Au interface in other work, which also gave rise to stability problem for Au electrode-based HPVKSCs31,32,41. In contrast, for MAPbI3/Bi, neither additional Pb 4f peaks nor Bi3+ peaks were observed, indicating Bi is chemically stable on the MAPbI3. This feature is unique in comparison to most of the metal electrodes reported to date.
A thermodynamic analysis provides insight into the mechanism of the reactions between the perovskite and the metals. It is known that the corrosion reaction between metals and halogens can be considered a process of breaking the elemental metal–metal bonds and forming the corresponding metal–halogen bonds. When the formation enthalpy of metal iodide is not negative or there is an energy barrier for the change of chemical bond (the barrier can be denoted as ∆E, equal to the energy difference between the metal–metal bond (EM–M) and the metal–halogen bond (EM–I), ΔE = EM–M − EM–I), the corrosion reaction of metal to metal iodide is difficult or impossible (Fig. 1b, and see the formation enthalpy and energy barrier in Supplementary Table 1). In this work, the formation enthalpy of AuI is not negative, thus there was no metallic Pb0 or Au+ in the MAPbI3/Au samples (more information about Au–I case in Supplementary Note 1). To the contrary, AgI (ΔfH = −61.8 kJ mole−1, ∆E = −71.1 kJ mole−1) and CuI (ΔfH = −68.7 kJ mole−1, ∆E = −88 kJ mole−1) can be formed easily and are stable, so Pb0 and Ag+/Cu+ were observed in their corresponding samples. For Ag and Cu samples, we speculate that the following corrosion reactions may occur:
Although Bi has a negative ΔfH, there is an energy barrier of 18.3 kJ mole−1 hindering the formation of BiI3. This is similar to the case of C (∆E = 365.2 kJ mole−1, ΔfH(CI4) = −392.9 kJ mole−1) and Mo (∆E = 168.6 kJ mole−1, ΔfH(MoI2) = −103.9 kJ mole−1), which have been proven to be stable in previous experiments and theory31,42,43.
Also, the corrosion reactions could proceed further during thermal aging (Fig. 1c). In the MAPbI3/Ag and MAPbI3/Cu samples, the Pb0/Pb2+ atomic ratios increased after 85 °C thermal aging for 100 h, from 0.090 to 0.126 for MAPbI3/Ag, and from 0.092 to 0.095 for MAPbI3/Cu. Furthermore, the thermal aging appears to have promoted the penetration of Ag, Cu, and Au ions into the MAPbI3 films, resulting in reduced atomic ratios at the sample surface (XPS detection depth of about 10 nm), from 0.786 to 0.708 for Ag/Pb, from 3.167 to 2.156 for Cu/Pb, and from 7.664 to 5.360 for Au/Pb. In fact, a recent density function theory (DFT)-based computation study also shows that Ag, Cu, and Au easily diffuse into perovskites because of their very low diffusion barriers31. In contrast to Ag, Cu, and Au, the atomic ratios of Bi/Pb in the fresh and aged MAPbI3/Bi samples almost remained unchanged at 8.580 and 8.579, respectively, indicating that there is very limited penetration of Bi into the MAPbI3 films during thermal aging.
The chemical inertness of Bi is also applicable to other perovskites. The thermal stability of perovskites/Bi (40 nm) was studied by XRD characterizations of different perovskites, including MAPbI3, (FAMA)Pb(IBr)3, (FACs)Pb(IBr)3, and (FAMACs)Pb(IBr)3, and taking Ag and Cu as the references. The resulting optical images (Supplementary Figure 2) and XRD patterns (Supplementary Figure 3) show that all fresh samples show metallic luster and strong perovskite characteristic peaks at approximately 14°, especially for Bi and Cu. After thermal aging (85 °C, ambient air, in the dark) for 48 h, only the Bi samples maintained their metallic luster, while the Ag samples and Cu samples lost their metallic luster, indicating severe degradation of the perovskites and corrosion of the metals. From the XRD results (Supplementary Figure 3), much weaker peaks of the perovskite phases and stronger peaks of PbI2 were observed for the aged Ag and Cu samples, and for some samples, the perovskite peaks disappeared completely. However, the XRD patterns of the Bi sample changed much less with aging. These results consistently indicate that Bi is chemically inert for these kinds of perovskites, even under harsh conditions.
Morphology and structural impermeability of the Bi film
Having demonstrated that Bi is chemically inert under these conditions, we prepared Bi films with different thicknesses on the surfaces of Glass/PCBM/BCP substrates by a simple thermal evaporation deposition. Figure 2a shows SEM images of the as-deposited Bi films on the Glass/PCBM/BCP substrates. The image shows that the 5-nm-thick sample is composed of many nanometer-scale islands, indicating poor coverage on the film surface. On the other hand, the 10-nm-thick sample is comprised of some flakes along with nanoparticles filling in the gaps between flakes. When the film thickness increased to 20 nm, a film with completely continuous coverage showing closely-packed flakes (with the average size of approximately 110 nm) was achieved. A further increase in the thickness results in a growth in the size of Bi flakes to approximately 190 nm. Next, we characterized the crystalline structures of the Bi films by XRD. The XRD patterns of Bi films on glass/PCBM/BCP substrates are shown in Fig. 2b. The three main peaks are attributed to (003), (006), and (009) planes of rhombohedral Bi (JCPDS 85-1331)37,38,39,40, and their intensities increase with increasing Bi thickness. This indicates an anisotropic growth of the Bi film with predominant orientation along the c-axis of the rhombohedral crystal unit, as shown in Fig. 2c. The strong and sharp peaks reveal high structural orientation and crystallinity of the Bi film, which is consistent with the film morphology (Fig. 2).
The high structural orientation gives the Bi layer a very compact morphology and perfect impermeability. To examine the impermeability of the Bi interlayer, we designed a qualitative experiment to test its water/oxygen vapor transmission rate, as shown in Supplementary Figure 4. Large-area Ca films (thickness = 60 nm, area = 3 × 3 cm2) on glass substrates covered by different interfacial layers including PCBM (60 nm)/BCP (5 nm), PCBM (60 nm)/BCP (5 nm)/Ag (20 nm), and PCBM (60 nm)/BCP (5 nm)/Bi (20 nm) were compared under controlled air conditions (25 °C and 30% relative humidity (%RH)). By monitoring the color change of the deposited Ca films, we could qualitatively judge the impact of different interfacial layers on the water/oxygen vapor transmission rates. From the optical images, the bare Ca film without interfacial layers quickly reacted with H2O/O2 from the air and turned into colorless CaO or Ca(OH)2, whereas the hydrophobic interfacial layer of PCBM (60 nm)/BCP (5 nm) retarded this process by about 1 h. Unlike the first two samples, an additional Ag electrode layer (20 nm) on top of the PCBM/BCP strengthened the penetration barrier against H2O/O2, however, the shielding capability was not sufficient. After 3 h, the Ca film was seriously damaged because the as-deposited Ag film was comprised of nanocrystals and rich in grain boundaries (having a disconnected nature) that allowed H2O/O2 to penetrate (Supplementary Figure 5a). On the contrary, a Bi layer (20 nm) on top of the PCBM/BCP (with a dense film morphology and limited grain boundaries (Supplementary Figure 5b)) presented a much more robust penetration barrier to H2O/O2. After 3 h, the PCBM (60 nm)/BCP (5 nm)/Bi (20 nm) sample maintained its initial color without any change across the entire film’s surface. Thus, as the penetration barrier for H2O/O2, Bi performs much better than Ag thanks to its highly orientated growth and crystal structure, which differed greatly from Ag (Supplementary Figure 5c-f). Furthermore, it should be noted that such a robust penetration barrier can be easily scaled up to a large area of more than the 3 × 3 cm2 used in this experiment.
Device fabrication and photovoltaic performances
HPVKSCs were fabricated with Bi interlayers in an inverted structure of FTO/NiMgLiO/PVK/PCBM/BCP/Bi/Ag (Fig. 3a). The studied HPVKSCs had large active areas (typically 1 cm2). The corresponding band energy diagram and the SEM cross-sectional image of a whole MA-HPVKSCs are portrayed in Fig. 3b, c, respectively. The corresponding band energy levels were obtained from the literature22,23. The benchmark MAPbI3 film was prepared with an average thickness of approximately 400 nm by using the classic anti-solvent extraction method, and this layer was sandwiched between 20-nm-thick p-NiMgLiO and 60-nm-thick n-PCBM charge extraction layers prepared according to our previous work23. An ultrathin (5 nm) BCP buffer layer was deposited by thermal evaporation and was inserted between the PCBM and the metal electrode to form a remarkable Ohmic contact to suppress the charge accumulation between them22. The Bi interlayer was deposited by adopting similar technology and sandwiched between the BCP and Ag (150 nm). Here, the Bi interlayer performs as a continuous blocking layer for the diffusion of unfavorable molecules/Ag ions, but at the same time it should not affect the transfer of photon-generated charges in the devices. The presence of the continuous Bi interlayer could be observed from the SEM cross-sectional image in Fig. 3c. In accordance with previous reports44, the work function of the Bi layer was estimated to be 4.25 eV, which is close to that of Ag (4.30 eV) (Supplementary Figure 6 and Supplementary Table 2). Therefore, the contact of the PCBM/BCP/Bi/Ag architecture should be as good as that of the PCBM/BCP/Ag architecture. The conductivity of Bi is roughly 80 times lower than that of Ag; however, it is comparable to those of transparent conductive oxides, such as indium tin oxide45. The well-matched energy level along with the good conductivity implies that the Bi interlayer with the optimized thickness will have a negligible negative impact on the charge transfer in HPVKSCs. Photocurrent density–voltage (J–V) curves were measured for devices with different thicknesses of Bi interlayers (see their J–V curves and IPCEs in Supplementary Figure 7, and their photovoltaic parameters in Supplementary Table 3). The devices with a Bi interlayer less than 20 nm show good photovoltaic performance; however, a thicker Bi interlayer (40 nm) is found to be harmful to the device’s efficiency. This is due to the increased series resistance (RS). From the AFM and cross-sectional SEM images (Supplementary Figure 8), it was found that the surface morphology of Bi significantly changed as its thickness increased from 10 to 80 nm. Some protuberant columnar crystals with heights greatly exceeding the designed film thickness were clearly observed in the 40-nm-thick and especially in the 80 nm-thick Bi films, corresponding to their increased surface roughness (Ra) from 3.652 to 37.672 nm, which may lead to increased contact resistance between the Bi and Ag46. The contact resistance may be the original reason for the unexpectedly larger RS for the HPVKSC with 40-nm-thick Bi. Figure 3d shows typical J–V curves of MA-HPVKSCs with an optimized Bi interlayer (20 nm thick). Under AM 1.5G simulated sunlight (100 mW cm−2), the fabricated device has a PCE over 18% (a PCE of 18.01%, with an open-circuit voltage (VOC) of 1.098 V, a short-circuit photocurrent density (JSC) of 21.78 mA cm−2, and a fill factor (FF) of 0.753 for the forward scan; a PCE of 18.06%, with a VOC of 1.102, a JSC of 21.62 mA cm−2, and a FF of 0.758 for the reverse scan; stabilized PCE measured at MPP of 0.872 V is 18.02%). The PCE of Bi-based devices can be promoted to approximately 19% by changing the benchmark MAPbI3 to the currently popular FA/MA/Cs triple cation perovskite ((FAMACs)Pb(IBr)3) (for details, see the J–V curves and stabilized PCEs in Supplementary Figure 9 and Supplementary Figure 13, the photovoltaic parameters in Supplementary Table 5, and the performance statistics in Supplementary Figure 17 and Supplementary Figure 20).
The impenetrability of Bi to ions
The effect of Bi as the penetration barrier to ion diffusion has been studied. First, ToF-SIMS was used to monitor the changes in the elemental distribution for each layer before and after thermal aging at 85 °C for 100 h in the dark under N2 atmosphere. As shown in Fig. 4a, b, for the controlled MA-HPVKSCs without Bi interlayers, inward diffusion of Ag+ ions into the perovskite layer and outward diffusion of I− ions towards the Ag electrode layer were detected after aging. Thus, the PCBM/BCP interfacial layer is permeable for the diffusion of I− and Ag+ ions. For the devices with Bi interlayers (Fig. 4c, d), the inward diffusion of the Ag+ ions and outward diffusion of I− ions were effectively blocked. Thus, the inserted Bi interlayer has robust impenetrability as an ion diffusion barrier.
Second, the morphologies and photoelectronic properties of MAPbI3 films in the configurations Glass/MAPbI3/PCBM/BCP/Bi/Ag and Glass/MAPbI3/PCBM/BCP/Ag (i.e., with and without a Bi interlayer) after thermal aging (at 85 °C for 100 h in the dark and N2 atmosphere) were compared by SEM and time-resolved PL characterizations. The films were obtained by washing away the top PCBM/BCP/electrode layers with chlorobenzene. For the MAPbI3 film in the configuration without Bi, the crystal grains fused, and their size increased considerably from approximately 500 nm to approximately 1100 nm (Fig. 5a, b). The large grain size of the aged MAPbI3 film can be correlated with the penetrated Ag+ ions (similar to the case in the study of Chen et al.47, which found that a small amount of Ag-doping could considerably increase the resultant perovskite film’s grain size.) By contrast, the morphology of the MAPbI3 films in the configuration with the Bi interlayer changed only marginally after aging (Fig. 5c, d). This result indicates that the Bi interlayer is very important for maintaining the MAPbI3 film’s morphology; this is important because the morphology may significantly affect the electronic properties. The transient PL spectra shown in Fig. 5e indicate that with the Bi interlayer’s protection, the aged-MAPbI3 and aged-MAPbI3/fresh-PCBM samples exhibited carrier lifetimes similar to those of fresh-MAPbI3, which confirms that the electronic quality of the MAPbI3 was not changed by thermal aging. In contrast, for the devices without Bi interlayers, the aged MAPbI3 sample exhibited a considerably shorter carrier lifetime in comparison to the fresh one (72 ns versus 120 ns). Moreover, the MAPbI3/PCBM sample exhibited deteriorated charge extraction at the interface after aging (the PL lifetime increased from 10 to 17 ns). These results confirm that the photoelectronic properties of the perovskite films degraded in the configuration without the Bi interlayer. We also fabricated devices based on the two types of aged MAPbI3 films by depositing fresh PCBM/BCP/electrodes (Fig. 5f). The J–V curves are presented in Fig. 5g, h, and the corresponding stabilized PCEs were shown in Supplementary Figure 10, and the photovoltaic parameters are tabulated in Supplementary Table 4. For the device without the Bi interlayer, the thermal aging severely decreased the PCE from its initial value of 18.51% to 14.24% and increased the hysteresis (Forward Scan: aging changed VOC from 1.104 to 1.085 V, JSC from 22.06 to 20.09 mA cm−2, FF from 0.759 to 0.670, and PCE from 18.49% to 14.61%; Reverse Scan: VOC from 1.107 to 1.081 V, JSC from 22.04 to 18.97 mA cm−2, and FF from 0.759 to 0.676, and PCE from 18.52% to 13.86%). After renewing the PCBM/BCP/Ag layers, the PCE of the refreshed device partially recovered to 15.93% (Forward Scan: VOC of 1.086 V, JSC of 20.43 mA cm−2, FF of 0.730, and PCE of 16.18%; Reverse Scan: VOC of 1.085 V, JSC of 19.88 mA cm−2, FF of 0.726, and PCE of 15.67%). The recovery of PCE from 14.24% to 15.93% was likely related to the freshly deposited Ag electrode without corrosion (discussed later), whereas, the irreversible PCE loss from 18.51% to 15.93% was probably due to electronic contamination of the MAPbI3 film by the inward diffusion of Ag+ ions, which could not be reversed by renewing the PCBM/BCP/Ag films. In contrast, for the device with the Bi interlayer, thermal aging caused only a marginal PCE decline from 18.00% to 16.91%. The PCE decline could almost be recovered (17.50%) by renewing the PCBM/BCP/Bi/Ag layers. The results indicate that the photoelectronic properties of the MAPbI3 film can be kept almost unchanged during thermal aging under the protection of the Bi interlayer, which prevents Ag diffusion into the MAPbI3.
In addition to prohibiting inward diffusion of ions from the Ag to the perovskite, the Bi interlayer blocks the outward diffusion of I− ions at the inner surface of the Bi interlayer (Fig. 4c, d). We adopted SEM and XRD characterizations to investigate the changes of the inner surface of the electrodes before and after aging the devices at 85 °C for 100 h in a N2 filled glovebox in the dark (see Supplementary Figure 11). The metal electrode samples were obtained by dissolving the PCBM/BCP in chlorobenzene. For the device without the Bi interlayer, the morphology of the Ag electrode inner surface was changed significantly by thermal aging. The surface became rough with many concave pits, and the XRD patterns in Supplementary Figure 11 confirm the formation of AgI. On the contrary, the results for the devices with Bi interlayers were completely different. As shown in the SEM images (Supplementary Figure 11), the morphology of the Bi/Ag electrode inner surfaces remained almost unchanged after thermal aging. The corresponding XRD patterns confirm that no AgI or BiI3 was formed. These observations clearly demonstrate the validity of the Bi interlayer’s protection of the Ag electrode from corrosion by the halide perovskite.
Stability test of the devices
The excellent anti-corrosive property and robust impermeability of the introduced Bi interlayer may largely improve the stability of the corresponding solar cells. The stability of HPVSKSCs should be assessed under specified aging conditions, which have been well discussed in recent review papers48,49,50. A storage stability test was conducted in the dark in ambient air at room temperature (RT) without humidity control (relative humidity of the local climate is normally 40–90%). Separately, we implemented a thermal aging test at 85 °C in N2 atmosphere in the dark for 500 h. 85 °C is specified for the aging temperature according to the standard IEC 61215-1:201651. As proposed by Snaith et al.49, the thermal aging atmosphere could be relaxed to an inert atmosphere (N2) for eliminating the interference from other stresses from the ambient, such as H2O and O2. All devices were open circuits during thermal aging. Also, we measured the operational stability of our devices at an elevated temperature of 45 °C with the external bias near their MPPs by referring to the standard IEC 61646: 200852. As Grätzel et al.50 advocated, to eliminate interference from ultraviolet light and stress from H2O, and O2, our light soaking test was performed in a N2 filled glovebox by using a white light LED array as the light source. The light intensity was calibrated to achieve the same JSC from the HPVKSCs as for 1 sun AM1.5G solar irradiation.
First, the storage stability of unencapsulated large-area (1 cm2) MA-HPVKSCs was assessed. As illustrated in the normalized PCE in Fig. 6a (the performance statistics in Supplementary Figure 12, the J–V curves in Supplementary Figure 13 and their corresponding photovoltaic parameters in Supplementary Table 5), the Bi-based device maintained approximately 88% of its initial PCE after 6000 h, whereas the pristine device without the Bi interlayer maintained only approximately 33% of its initial PCE after 1000 h. The VOC and JSC of the Bi-based device were highly stable, and FF degraded slowly with the aging time. In contrast, the photovoltaic parameters of the typical devices without Bi, including VOC, JSC, and FF, suffered marked declines. Repeated experiments suggested that the Bi strategy can effectively improve the stability with high reproducibility (see the performance statistics in Supplementary Figure 12). To the best of our knowledge, MA-HPVKSCs using the interlayer strategy have not achieved such high stability during ambient storage (see the comparison of storage stability for selected HPVKSCs in Supplementary Table 6). Thus, the inserted Bi interlayer plays an important role in “self-encapsulation”, which can prevent the penetration of ambient moisture. The optical images of the devices with different thicknesses of the Bi interlayer after aging for 6000 h are displayed in Supplementary Figure 14. A large region of the active film in the device without Bi turned yellow, which indicates decomposition of the perovskite. The active films in the devices with the Bi interlayer (especially for a thickness greater than 20 nm) were almost unchanged. The presence of the dense Bi interlayer can prevent or delay direct exposure to external moisture and thus increase the long-term survivability of the device in the ambient air.
Second, unencapsulated large-area (1 cm2) MA-HPVKSCs were investigated under thermal aging (85 °C, dark, N2 atmosphere) and light soaking conditions (45 °C, white LED light, near MMP, N2 atmosphere) for 500 h in a N2 filled glovebox. The normalized PCEs of typical devices as a function of the aging time are shown in Fig. 6b, c. The devices with the Bi interlayer retained approximately 87% and approximately 91% of their initial PCEs after thermal aging and light soaking tests, respectively, whereas the pristine devices without Bi retained only approximately 42% and approximately 27% of their initial PCEs after the thermal aging and light soaking tests, respectively. The Bi-based MA-HPVKSCs showed more stable VOC, JSC, and FF than did the devices without Bi, especially JSC (see the typical J–V curves in Supplementary Figure 13, the performance statistics of thermal stability in Supplementary Figure 15, and the performance statistics of light-soaking stability in Supplementary Figure 16). The considerably improved thermal and light-soaking stabilities were due to the robust shielding capability of the Bi interlayer.
Third, we further changed the composition of the perovskite film in our devices from the early benchmark MAPbI3 to the currently popular FA/MA/Cs triple cation perovskite53. In this configuration, the Bi interlayer also had a positive effect on the devices’ long-term stability. Under the same thermal aging and light soaking conditions, the (FAMACs)Pb(IBr)3 based HPVKSCs (FAMACs-HPVKSCs) with Bi interlayers maintained approximately 95% and approximately 97% of their initial PCEs, respectively (Fig. 6b, c, see the typical J–V curves and stabilized PCEs in Supplementary Figure 13 and Supplementary Figure 17, and their photovoltaic parameters in Supplementary Table 5, the performance statistics of thermal stability in Supplementary Figure 18, the performance statistics of light-soaking stability in Supplementary Figure 19). By extrapolation, the time at which a typical FAMACs-HPVKSC with Bi interlayers would have degraded to 80% of its initial efficiency under light soaking was determined to be 11,800 h. Furthermore, the statistical parameters reflect that FAMACs-HPVKSCs with Bi interlayers are highly stable and highly reproducible (see the performance statistics of thermal stability in Supplementary Figure 18, and the performance statistics of light-soaking stability in Supplementary Figure 19). The stability data of the FAMACs-HPVKSCs were superior to those of the MA-HPVKSCs and close to the international acceleration test standards for silicon solar cells (IEC 61215)51. Overall, our Bi interlayer strategy compares well to the recent reports regarding the improvement of long-term stability (see the comparison of storage stability for selected HPVKSCs in Supplementary Table 6, the comparison of thermal stability for selected HPVKSCs in Supplementary Table 7 and the comparison of operational stability for selected HPVKSCs in Supplementary Table 8). These results demonstrate the importance of using chemically inert barrier interlayers in the devices for achieving long-term stability and provide a promising strategy for the further application of perovskites in commercial-scale production.
We demonstrated Bi to be an intrinsically stable metal for halide perovskites even under harsh conditions. The XPS and XRD analyses indicate that no reaction occurred between the Bi and perovskites including MAPbI3, (FAMA)Pb(IBr)3, (FACs)Pb(IBr)3, and (FAMACs)Pb(IBr)3 at 85 °C over an extended period. Another notable feature of the Bi film is that it can grow into compact barrier layers with scalable device sizes via a facile thermal evaporation technique. Thus, the Bi metal was introduced conveniently into inverted-structured HPVKSCs as an interlayer before the thermal-deposition of the Ag electrode. The Bi interlayer acted as a penetration barrier that insulated against the undesirable intrusion of external moisture while also suppressing the diffusion of internal ions, including the inward diffusion of Ag+ ions into the perovskite layer and the outward diffusion of I− ions to the Ag electrode. As a result, the Bi-interlayer-based HPVKSCs exhibit greatly enhanced long-term stability under various humidity, thermal and light stresses. On average, the unencapsulated MAPbI3-HPVKSC devices retained approximately 88% of their initial efficiency in ambient air in the dark for over 6000 h; moreover, the FAMACs-HPVKSCs maintained approximately 95% and approximately 97% of their initial efficiencies after 85 °C thermal aging and light soaking in a N2 atmosphere for 500 h, respectively. These superior stability parameters are among the best for planar-structured HPVKSCs reported to date. Thanks to its low-cost, non-toxicity, and compatibility with scalable thermal evaporation processes, the Bi interlayer strategy is a commercially feasible means of resolving the problem caused by unsettled metal electrodes in practical HPVKSCs.
Methylammonium iodide (CH3NH3I (MAI), 99.99%), methylammonium bromide (CH3NH3Br (MABr), 99.99%) and formamidinium iodide (CH(NH2)2I (FAI), 99.99%), and formamidinium bromide (CH(NH2)2Br (FABr), 99.99%) were purchased from Hangzhou Perov Optoelectronic Technology Co., Ltd. Lead (II) iodide (99.99% metals basis), lead (II) bromide (>98%), cesium bromide (>99%), cesium iodide (>99%), and bathocuproine (>99%) were purchased from Tokyo Chemical Industry Co., Ltd. All other chemicals were purchased from Sigma-Aldrich and used as received.
FTO glasses (TEC-8, Nippon Sheet Glass Co., Japan) were cleaned through sequential ultrasonication for 20 min in a detergent solution, distilled water, alcohol, and acetone. Then, a p-type NiMgLiO was deposited on top of the FTO glass: an mixture solution of acetonitrile and ethanol (with 95:5 volume ratio, 30 mL) of nickel acetylacetonate (with magnesium acetate tetrahydrate and lithium acetate, and the mole atomic ratios of Ni:Mg:Li is 80:15:5, the total metal ion concentration is 0.02 mol L−1) was sprayed by an air nozzle (with 0.2 mm caliber) onto the hot FTO glasses (500 °C). After spraying, the samples were further treated at 500 °C for another 20 min and then leave them to cool naturally. After cooling to RT, perovskite was then deposited by the anti-solvent method: a 80 μL 1.5 M MAPbI3 solution (a mixture of PbI2:MAI = 1.05:1 by molar ratio and DMF:DMSO = 4:1 by volume) was spin-coated at 5000 rpm for 30 s, followed by quickly drop-casting diethyl ether (1000 μL) as an anti-solvent within 10 s. The (FAMA)Pb(IBr)3 perovskite films were deposited by a precursor solution containing FAI (1 M), PbI2 (1.1 M), MABr (0.2 M) and PbBr2 (0.2 M) in DMF:DMSO = 4:1 by volume. The (FACs)Pb(IBr)3 perovskite films were deposited by a precursor solution containing FAI (1.275 M), PbI2 (1.52 M), and CsBr (0.225 M) in DMF:DMSO = 4:1 by volume. The (FAMACs)Pb(IBr)3 perovskite films were deposited by a mixture of 1 mL (FAMA)Pb(IBr)3 precursor solution and 0.05 mL CsI solution (1.5 M in DMSO). Then, the perovskite films were treated thermally at 100 °C for a period of time, 10 min for MAPbI3, 30 min for (FAMA)Pb(IBr)3, (FACs)Pb(IBr)3, and (FAMACs)Pb(IBr)3. The PCBM solution was prepared by dissolving 20 mg PCBM in 1 mL of chlorobenzene and was stirred vigorously at 45 °C overnight before spin-coating. A approximately 60-nm-thick PCBM was deposited on the perovskite/NiMgLiO/FTO substrate by spin-coating at 2000 rpm for 30 s at RT followed by a 70 °C thermal treatment for 10 min. In the final step, the BCP, Bi, and Ag were deposited at high vacuum (less than 5 × 10−4 Pa) while finely controlling the evaporation rate at 0.1, 0.1, and 0.1–0.5 Å s−1, respectively.
Characterization and measurement
SEM images were obtained using a Nova NanoSEM 450 scanning electron microscope (FEI Co., Netherlands). An XPS system (Thermo ESCALAB 250XI) was used to acquire the XPS spectra. The crystal structure of the films was characterized using XRD with an Empyrean X-ray diffractometer with Cu Kα radiation (PANalytical B.V. Co., Netherlands). ToF-SIMS depth profiles were carried out using an IonToF ToF-SIMS 5 instrument (IONTOF Co., Germany). The work functions of the samples were investigated using a KP Technology Ambient Kelvin probe system package. The time-resolved PL studies were performed using an Edinburgh FLS920 fluorescence spectrometer (Edinburgh Co., UK). The UV–vis spectra were recorded using a Lambda 950 spectrophotometer (PerkinElmer Co., USA). Photovoltaic measurements employed a black mask with an aperture area of 1 cm2 under standard AM1.5G simulated sunlight (Oriel, model 9119) and the simulated light intensity was calibrated with a silicon photodiode. Incident photon-to-electron conversion efficiency (IPCE) was measured using a Newport IPCE system (Newport, USA). The light-soaking stability was measured with a CHI1000c multichannel electrochemistry workstation (Chenhua, Co., China).
The data that support the findings of this study are available from the corresponding author upon request.
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This work was financially supported by the National Natural Science Foundation of China (51672094, 51861145404, and 51822203), the China Postdoctoral Science Foundation Grant (2016M602286), the Self-determined and Innovative Research Funds of HUST (2016JCTD111), Shenzhen Science and Technology Innovation Committee (JCYJ20170307165905513), and Natural Science Foundation of Guangdong Province (2017A030313342). The authors thank Analytical and Testing Center of Huazhong University Science and Technology for the sample measurements.
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks Thomas Riedl and the other anonymous reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Wu, S., Chen, R., Zhang, S. et al. A chemically inert bismuth interlayer enhances long-term stability of inverted perovskite solar cells. Nat Commun 10, 1161 (2019). https://doi.org/10.1038/s41467-019-09167-0
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