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Cathode–electrolyte interphase (CEI) formation between the cathode and the electrolyte is a critical factor that determines the stability of lithium-ion batteries (LiBs). The CEI layer consists of various by-products (e.g., LiF, Li2CO3, ROLi, and ROCO2Li (R: alkyl group)) decomposed from redox reactions between the cathode and the electrolyte, which can lead to dramatic capacity fading and stability issues. Herein, we empirically identify the energy level band bending of a Ni-rich NMC cathode (i.e., Li(Ni0.5Mn0.3Co0.2)O2) with the visual evidence of Li+ transfer from the electrode to the CEI layer (adsorbate). Negatively charged elements tend to be present at the close surface of the cathode, while the positively charged Li+ migrates from the cathode to the CEI layer. Hence, a downward band bending could be depicted based on the work function and the energy level difference between the Fermi level (EF) and the valence band maximum (EVBM). Energy level alignment itself is likely to be the key process that leads to the active formation of unstable CEI layers on charge–discharge.

Perovskite solar cells (PSCs) have attracted much attention due to their low-cost fabrication and high power conversion efficiency (PCE). However, the long-term stability issues of PSCs remain a significant bottleneck impeding their commercialization. Inverted PSCs with a p-i-n architecture are being actively researched due to their concurrent good stability and decent efficiency. In particular, the PCE of inverted PSCs has improved significantly in recent years and is now almost approaching that of n-i-p PSCs. This review summarizes recent progress in the development of high-efficiency inverted PSCs, including the development of perovskite compositions, fabrication methods, and counter electrode materials (CEMs). Notably, we highlight the development of charge transport materials (CTMs) and the effects of defect passivation strategies on the performance of inverted PSCs. Finally, we discuss the remaining issues and perspectives of high-efficiency inverted PSCs.

Upscalable fabrication of efficient and stable perovskite solar modules is urgently needed for commercialization. Here we introduce methylammonium chloride additives in the co-solvent system of N-methyl-2-pyrrolidone/N,N-dimethylformamide to control the formation of intermediate phases during the growth of formamidinium–caesium lead triiodide perovskite films. We achieve high-quality films upon drying without the use of anti-solvent. By implementing bulk and surface passivation, champion efficiencies of 24.02% for a small-sized solar cell and 20.5% for a 5 cm × 5 cm solar mini-module on an aperture area of 22.4 cm2 (geometric fill factor ∼ 96%) are achieved by spin-coating. The fully blade-coated perovskite solar sub-module demonstrates a champion efficiency of 15.3% on an aperture area of 205 cm2. The solar mini-module exhibits impressive operational stability with a T80 lifetime of over 1,000 h at maximum power point tracking under continuous light illumination.

Effective distribution coefficients of 9 impurities in 1,2-Diphenylethane have been calculated by directional crystallization under different ambient frozen temperature. The effect of varied zone size, temperature difference between the melt and ambient frozen environment, number of zone on purity of 1,2-Diphenylethane have been also investigated during the process of zone refining. The results indicate that the product purity in the intermediate purified region with varied zone size is higher 0.04%−0.2% than that with constant zone size. The product purity increases with temperature difference between the melt and ambient frozen environment. The appropriate temperature difference is adopted 50℃.The product purity in the intermediate region of sample bar with 2 molten zones is higher 0.05%−0.43% than that with 1 molten zone. In addition, the change of enthalpy and entropy between impurities and 1,2-Diphenylethane have been determined.

Flexible perovskite solar cells (F-PSCs) hold promise for portable power sources for applications in various fields, such as wearable and portable electronics and lightweight power supply in stratosphere and space applications. To date, it is still a challenge to achieve efficient and stable F-PSCs. Herein, a pre-applied strain on a flexible substrate to release the residual strain of the perovskite layers of the F-PSCs is reported. As a result, the F-PSC based on this strategy yielded a power conversion efficiency (PCE) of up to 18.71%, approaching that of its counterpart based on a glass substrate (20.32%). And it retained 90% of its initial PCE after 300 h under AM 1.5G light illumination with an extrapolated T80 lifetime (the time over which the device efficiency reduces to 80% of its initial value) exceeding 700 h. Furthermore, the PCE remained above 80% of its initial value even after 1500 tension-only bending cycles. The result of this work paves a possible way toward fabricating efficient and stable F-PSCs.

Herein, we report the use of pyridine anchoring group functionalized poly(triarylamine) (p-PY) as a hole transport layer at buried interfaces between the ITO and formamidinium–cesium perovskite layer to enhance the efficiency and stability of inverted PSCs.

Perovskite solar cells (PSCs) are a promising third-generation photovoltaic (PV) technology developed rapidly in recent years. Further improvement of their power conversion efficiency is focusing on reducing the non-radiative charge recombination induced by the defects in metal halide perovskites. So far, defect passivation by the organic small molecule has been considered as a promising approach for boosting the PSC performance owing to their large structure flexibility adapting to passivating variable kinds of defect states and perovskite compositions. Here, the recent progress of defect passivation toward efficient and stable PSCs was reviewed from the viewpoint of molecular structure design and device performance. To comprehensively reveal the structure-performance correlation of passivation molecules, it was separately discussed how the functional groups, organic frameworks, and side chains affect the corresponding PV parameters of PSCs. Finally, a guideline was provided for researchers to select more suitable passivation agents, and a perspective was given on future trends in development of passivation strategies.

Suppressing nucleation over large areas Although formamidinium-based lead iodide (PbI 2 ) perovskites have a favorable bandgap and good thermal stability, the difficulty in controlling nucleation makes it difficult to grow high-quality, large-area films compared with methylammonium counterparts. Bu et al. show that adding N -methyl-2-pyrrolidone to the perovskite precursors forms an adduct with PbI 2 that promotes the formation of the desired black α-phase at room temperature. The addition of potassium hexafluorophosphate eliminated hysteresis by passivating interfacial defects and promoted long-term thermal stability at 85°C in unencapsulated devices. Large-area modules (17 square centimeters) achieved power conversion efficiencies of 20.4%. Science , abh1035, this issue p. 1327

Two-dimensional Ruddlesden–Popper (RP) and Dion–Jacobson (DJ) phase perovskites are promising alternatives to fabricate blue perovskite light-emitting diodes (PeLEDs) due to their strong quantum/dielectric confinement. While the RP phase perovskites have been widely used as emitter layers in blue PeLEDs, the DJ phase perovskites, possessing better structural stability and charge transfer property, have received little attention. Here, we report the use of DJ phase perovskites for fabricating efficient sky-blue PeLEDs. Organic diamine propane-1,3-diammonium cations were first incorporated into CsPbBr3 to prepare DJ phase perovskites. RbBr was further incorporated as a passivation agent to eliminate traps. It is found that diamine cations and RbBr are interdependent in terms of increasing the utilization of charges. Radiative recombination was enhanced, effectively benefiting from the synergetic confinement and passivation effects. The photoluminescence quantum yield approached 70%. Finally, the fabricated PeLEDs achieved an external quantum efficiency of 8.5% with an emission peak at 490 nm.

Metal halide perovskite solar cells are an emerging photovoltaic technology already exhibiting great potential. The main challenges at present that hinder the application of perovskite solar cells include scalable fabrication, operational stability, and environmental impact of Pb in Pb-containing perovskite solar cells. Among various scalable coating techniques, modified chemical vapor deposition (CVD) is a promising technology to enable large-area and uniform coating of perovskite layers at a low cost. Modified CVD also offers many other advantages such as being solvent-free, high compatibility with industrial manufacturing, and easy integration with other solar technologies to form tandem cells (or perovskite–perovskite tandem cells). In this review, we present the recent development of perovskite solar cells and modules prepared by modified CVD. We first discuss the differences between modified CVD and solution coating processing. We then summarize the present results from the cost-performance analysis point of view to show the potential of modified CVD for scalable fabrication of perovskite solar cells and modules with low cost. At the end of this review, we outline several future research directions.

The incorporation of a certain amount of Cl ions into methylammonium lead iodide (MAPbI3) perovskite films and how these incorporated Cl ions affect the structural and electronic properties of these films have been an intensively studied topic. In this study, we comprehensively investigated Cl incorporation in MAPbI3 at the atomic scale by a combined study of scanning tunneling microscopy, X-ray photoelectron spectroscopy, ultraviolet and inverse photoemission spectroscopy, density functional theory and molecular dynamics calculations. At a Cl concentration of 14.8 ± 0.6%, scanning tunneling microscopy images confirm the incorporation of Cl ions on the MAPbI3 surface, which also corresponds to the highest surface stability of MAPbI3 found from the viewpoint of both thermodynamics and kinetics by density functional theory and molecular dynamics calculations. Our results show that the Cl concentration is crucial to the surface bandgap and stability of MAPbI3.

Flexible solar cells, which are compatible with low cost and high throughput roll-to-roll manufacturing, are specifically attractive for applications in wearable/portable electronic devices, building-integrated photovoltaics (BIPV), drones and satellites, etc. Integration of the narrow bandgap flexible solar cells, e.g., Cu(In, Ga)(S, Se)2 solar cells, organic solar cells, or the new class of lead-tin mixed perovskite solar cells (PSCs) with wide bandgap NIR-transparent PSCs allows two sub-cells to utilize solar light with different photon energies more efficiently and therefore minimizes thermalization loss to overcome the theoretical Shockley–Queisser single-junction limit (33%). In this review, we provide an overview of the recent progress of flexible perovskite-based tandem solar cells from the perspective of the narrow bandgap bottom cell and the near-infrared (NIR) transparent top cell. In addition, we discuss the key limitations related to energy losses in the recombination layer in two-terminal (2-T) tandems and the optical losses in four-terminal (4-T) tandems. Then we outline several strategies to overcome these limitations. Finally, we provide an outlook on roll-to-roll manufacturing and device encapsulation.

We present an efficient and easy synthesis method for incorporating organocatalytic moieties into Zr-metal organic frameworks (Zr-MOFs). The catalytic activity and selectivity of the new chiral catalysts were improved by adjusting the aperture of the MOF cavities. The hole size of the Zr-MOF was modulated by adding acid and replacing bridge ligands during synthesis. The difunctional chiral units of amino acid-thiourea are anchored onto the Zr-MOF by a mild synthesis method from an isothiocyanate intermediate which could effectively avoid the racemization of chiral moieties in the synthesis process. By means of specific surface area measurement (BET), scanning electron microscopy (SEM) and powder X-ray Diffraction (PXRD), it was confirmed that Zr-MOFs with different pore sizes were synthesized without breaking the basic octahedral structure of the MOF. Finally, good yields (up to 83%) and ee values (up to 73%) were achieved with the new heterogeneous catalysts in 48 hours for the aldol reaction of 4-nitrobenzaldehyde with acetone. By contrast, using the catalyst support without modulating the synthesis, the yield (30%) and the ee-value (26%) were both low. Experiments have confirmed the important influence on the reaction selectivity of providing a suitable reaction environment by controlling the aperture of MOF cavities.

The booming growth of organic-inorganic hybrid lead halide perovskite solar cells have made this promising photovoltaic technology to leap towards commercialization. One of the most important issues for the evolution from research to practical application of this technology is to achieve high-throughput manufacturing of large-scale perovskite solar modules. In particular, realization of scalable fabrication of large-area perovskite films is one of the essential steps. During the past ten years, a great number of approaches have been developed to deposit high quality perovskite films, to which additives are introduced during the fabrication process of perovskite layers in terms of the perovskite grain growth control, defect reduction, stability enhancement, etc. Herein, we first review the recent progress on additives during the fabrication of large area perovskite films for large scale perovskite solar cells and modules. We then focus on a comprehensive and in-depth understanding of the roles of additives for perovskite grain growth control, defects reduction, and stability enhancement. Further advancement of the scalable fabrication of high-quality perovskite films and solar cells using additives to further develop large area, stable perovskite solar cells are discussed.

Perovskite materials with excellent optical and electrical properties are promising for light‐emitting diodes. In the field of perovskite light‐emitting diodes (PeLEDs), organic materials additive engineering has been proved to be an effective scheme for enhancing efficiency and stability in PeLEDs. Most impressively, the reported external quantum efficiency of PeLEDs based on perovskite‐organic composite has reached over 20%. Herein, we will review the important progress of the organic materials' additive‐modified PeLEDs and discuss the remaining problems and challenges and the key research direction in the near future.

In several photovoltaic (PV) technologies, the presence of electronic defects within the semiconductor band gap limit the efficiency, reproducibility, as well as lifetime. Metal halide perovskites (MHPs) have drawn great attention because of their excellent photovoltaic properties that can be achieved even without a very strict film‐growth control processing. Much has been done theoretically in describing the different point defects in MHPs. Herein, we discuss the experimental challenges in thoroughly characterizing the defects in MHPs such as, experimental assignment of the type of defects, defects densities, and the energy positions within the band gap induced by these defects. The second topic of this Review is passivation strategies. Based on a literature survey, the different types of defects that are important to consider and need to be minimized are examined. A complete fundamental understanding of defect nature in MHPs is needed to further improve their optoelectronic functionalities., Watching the defects: Defects play a pivotal role in the overall performance of perovskite solar cells. This Review focuses on central questions of “what defects exist in metal halide perovskites” and “how can one reduce detrimental defects towards high‐performance perovskite solar cells”.

All-inorganic halide perovskites are promising materials for optoelectronic applications. The surface or interface structure of the perovskites plays a crucial role in determining the optoelectronic conversion efficiency, as well as the material stability. A thorough understanding of surface atomic structures of the inorganic perovskites and their contributions to their optoelectronic properties and stability is lacking. Here we show a scanning tunneling microscopy investigation on the atomic and electronic structure of CsPbBr3 perovskite. Two different surface structures with a stripe and an armchair domain are identified, which originates from a complex interplay between Cs cations and Br anions. Our findings are further supported and correlated with density functional theory calculations and photoemission spectroscopy measurements. The stability evaluation of photovoltaic devices indicates a higher stability for CsPbBr3 in comparison with MAPbBr3, which is closely related to the low volatility of Cs from the perovskite surface.

Summary Tin-based perovskite solar cells (PSCs), with more consummate optical band gaps, lower exciton-binding energies, and higher charge-carrier mobility, have not attracted tremendous research efforts compared with the lead-based ones that have a record power conversion efficiency (PCE) of 24.2%. The major challenges for Sn-based research are significantly low open-circuit voltage, poor reproducibility, and environmental instability. It has been identified that the oxidation processes take place during the preparation of precursor solutions and fabrication of films, due to the low redox potential of the stannous absorption layer. Herein, we propose two strategies of crystal-resolving and recrystallization technology to reduce the oxidation process. As a result, PCEs of 8.9% (active area of 0.04 cm2) and 5.5% (active area = 1.01 cm2) are attained using the inverted p-i-n structure, which will lead to a revival of lead-free PSC research.

Lead-free double perovskite materials have attracted much interest for optoelectronic applications due to their nontoxicity and high stability. In this work, centimetre-sized Cs2AgBiBr6 single crystals were successfully grown using methylammonium bromide (MABr) as the flux by a top-seeded solution growth (TSSG) method. The low-temperature crystal structure of Cs2AgBiBr6 single crystals was determined and refined. To investigate the interface problems between Cs2AgBiBr6 single crystals and electrodes, the optical band gap, X-ray photoelectron spectroscopy (XPS), and ultraviolet photoemission spectroscopy (UPS) measurements were performed on Cs2AgBiBr6 single crystals. More importantly, we investigated the photodetectors based on Cs2AgBiBr6 single crystals with different contact electrodes (Au, Ag, and Al). It is found that a good Ohmic contact with Ag electrodes enables excellent photo-response behaviors. Furthermore, we studied the photodetectors based on Cs2AgBiBr6 single crystals using Ag electrodes under room and low temperature conditions, which underwent phase transition. Cs2AgBiBr6 single crystal photodetectors show clear differences at room and low temperatures, which is caused by the work function changes of Cs2AgBiBr6 single crystals induced by the reversible phase transition. These attractive properties may enable opportunities to apply emerging double perovskite single-crystalline materials for high-performance optoelectronic devices.

Hybrid chemical vapor deposition (HCVD) has been employed in the fabrication of perovskite solar cells (PSCs) and modules (PSMs), and it shows strong promise for upscalable fabrication. The conventional HCVD process needs a relatively long processing time (e.g., several hours) and the fabricated PSCs often exhibit salient hysteresis, which impedes utilization of this technology for mass production. Herein, we demonstrate a rapid HCVD (RHCVD) fabrication process for PSCs using a rapid thermal process, which not only significantly reduces the deposition time to less than 10 min, but also effectively suppresses hysteresis. This markedly reduced deposition time is comparable to that of solution-coating processes. Furthermore, the shorter processing time inside the furnace reduces the exposure time of the glass/ITO/SnO2 substrates under vacuum, which helps maintain the high quality of the SnO2 electron-transport layer and results in a lower density of gap states. Finally, PSMs with a designated area of 22.4 cm2 fabricated via RHCVD achieved an efficiency of 12.3%, and maintained 90% of the initial value after operation under continuous light illumination for over 800 h.

Lead-free tin perovskite solar cells (PSCs) have undergone rapid development in recent years and are regarded as a promising eco-friendly photovoltaic technology. However, a strategy to suppress charge recombination via a built-in electric field inside a tin perovskite crystal is still lacking. In the present study, a formamidinium tin iodide (FASnI

The spectral instability issue is a challenge in blue perovskite light-emitting diodes (PeLEDs). Dion–Jacobson (DJ) phase perovskites are promising alternatives to achieve high-quality blue PeLEDs. However, the current exploration of DJ phase perovskites is focused on symmetric divalent cations, and the corresponding efficiency of blue PeLEDs is still inferior to that of green and red ones. In this work, we report a new type of DJ phase CsPb(Br/Cl)3 perovskite via introduction of an asymmetric molecular configuration as the organic spacer cation in perovskites. The primary and tertiary ammonium groups on the asymmetric cations bridge with the lead halide octahedra forming the DJ phase structures. Stable photoluminescence spectra were demonstrated in perovskite films owing to the suppressed halide segregation. Meanwhile, the radiative recombination efficiency of charges is improved significantly as a result of the confinement effects and passivation of charge traps. Finally, we achieved an external quantum efficiency of 2.65% in blue PeLEDs with stable spectra emission under applied bias voltages. To our best knowledge, this is the first report of asymmetric cations used in PeLEDs, which provides a facile solution to the halide segregation issue in PeLEDs.

Metal halide perovskite materials (MHPMs) have attracted significant attention because of their superior optoelectronic properties and versatile applications. The power conversion efficiency of MHPM solar cells (PSCs) has skyrocketed to 25.5 %. Although the performance of PSCs is already competitive, several important challenges still need to be solved to realize commercial applications. A thorough understanding of surface atomic structures and structure–property relationships is at the heart of these remaining issues. Scanning tunneling microscopy (STM) and spectroscopy (STS) can be used to characterize the surface properties of MHPMs, which can offer crucial insights into MHPMs at the atomic scale. This Review summarizes recent progress in STM and STS studies on MHPMs, with a focus on the surface properties. We provide understanding from the comparative perspective of several different MHPMs. We also highlight a series of novel phenomena observed by STM and STS. Finally, we outline a few research topics of primary importance for future studies.

It has been slightly over a decade since metal halide perovskite materials were first used in solar cells. Nowadays it has become one of the most active research fields and continues to progress rapidly on various fronts. My group at OIST is making efforts to use surface science and advanced material characterization techniques to obtain in-depth understanding about perovskite materials and devices. In this talk, I will present our research progress on surface science understanding of perovskite materials and stability.

Metal halide perovskites (MHPs) have become a major topic of research in thin film photovoltaics due to their advantageous optoelectronic properties. These devices typically have the MHP absorber layer sandwiched between two charge selective layers (CSLs). The interfaces between the perovskite layer and these CSLs are potential areas of higher charge recombination. Understanding the nature of these interfaces is key for device improvement. Additionally, non-stoichiometric perovskite films are expected to strongly impact the interfacial properties. In this study, the interface between CH

Atomistic characterization of surface termination and the corresponding mechanical properties of single-crystal methylammonium lead tribromide (MAPbBr3) are performed using combined atomic force microscopy (AFM) measurements and density functional theory (DFT) calculations. A clean MAPbBr3 surface is obtained by in situ cleavage in ultrahigh vacuum at room temperature, and the subsequent AFM measurements of the as-cleaved MAPbBr3 exhibit the coexistence of two different surface terrace types with step height differences corresponding to about half the thickness of a PbI6 octahedron layer. Concurrent friction force microscopy measurements show that the two surfaces result in two distinct friction values. Based on DFT calculations, we attribute the higher-friction and lower-friction surfaces to MABr-terminated flat and PbBr2-terminated vacant surface terminations, respectively. The calculated electronic band structures of the various MABr- and PbBr2-terminated surfaces show that the midgap states are absent, revealing the defect-tolerant nature of the ideal single-crystal MAPbBr3 surfaces.

A series of challenging issues such as field-driven spectral drift for the CsPbClxBr3–x system and mixed phases in quasi-two-dimensional structures still exist when devising blue-emitting perovskites. In this Letter, the CsPbBr3 quantum-dot (QD) system is proposed to overcome these challenges. However, to date, the CsPbBr3 QD films with tunable colors from green to blue still cannot be achieved using existing methods. Herein, a simple one-step spin-coating route incorporated with efficient ligand passivation is developed to realize this goal. The size restriction of CsPbBr3 QDs is enabled by a diammonium ligand, propane-1,3-diammonium bromide (PDAB). A mixed-ligand system of phenethylammonium bromide (PEAB) with PDAB is further explored to enhance their optical performance. The CsPbBr3 QDs experience a second growth process upon controlled air exposure, which is utilized to realize their size control and emission wavelength tunability. The CsPbBr3 QD-based devices exhibit no spectral drift in electroluminescence under voltage bias.

Metal halide-based perovskite solar cells (PSCs) have developed rapidly due to exceptional optoelectronic properties of perovskite materials (such as high optical absorption coefficient, long charge carrier lifetime, long diffusion length, high carrier mobility and tunable bandgaps) and low-cost fabrication processes. The record power conversion efficiency has exceeded 24%, demonstrating the great potential for photovoltaic application. However, the lead toxicity and instability still present as major obstacles for commercialization. In principle, Pb can be replaced with other less-toxic as well as environmentally benign metals, such as Ag, Na, Sn, Ge, Bi, Sb and Ti, to solve the toxicity issue. Replacing methylammonium (MA(+)) or formamidinium (FA(+)) with cesium (Cs+) represents a promising direction to address the instability issue. Herein, we review the recent progress of all-inorganic cesium lead-free halide PSCs. At the end, we outline challenges and future directions.

Perovskite photovoltaic (PV) technology toward commercialization relies on high power conversion efficiency (PCE), long lifetime, and low-toxicity in addition to development of scalable fabrication...

Carbon electrode-based perovskite solar cells (PSCs) with low-cost and long-term stability have been recognized as a competitive candidate toward future practical applications. However, energy leve...

The correct identification of all gases released during hybrid perovskite degradation is of great significance to develop strategies to extend the lifespan of any device based on this semiconductor. CH3X (X = Br/I) is a released degradation gas/low boiling point liquid arising from methylammonium (MA+) based perovskites, which has been largely overlooked in the literature focusing on stability of perovskite solar cells. Herein, we present an unambiguous identification of CH3I release using microwave (rotational) spectroscopy. An experimental back-reaction test demonstrates that the well-known CH3NH2/HX degradation route may not be the ultimate degradation pathway of MAPbX3 in thermodynamic closed systems. Meanwhile, the CH3X/NH3 route cannot back-react selectively to MAX formation as occurred for the former back-reaction. Metadynamics calculations uncover the X halide effect on energy barriers for both degradation reactions showing a better stability of Br based perovskite ascribed to two aspects: (i) lower Brönsted–Lowry acidity of HBr compared to HI and (ii) higher nucleophilic character of CH3NH2 compared to NH3. The latter property makes CH3NH2 molecules stay preferentially attached on the electrophilic perovskite surface (Pb2+) during the dynamic simulation instead of being detached as observed for the NH3 molecule.

Lithium-ion batteries (LIBs) continue to draw vast attention as a promising energy storage technology due to their high energy density, low self-discharge property, nearly zero-memory effect, high open circuit voltage, and long lifespan. In particular, high-energy density lithium-ion batteries are considered as the ideal power source for electric vehicles (EVs) and hybrid electric vehicles (HEVs) in the automotive industry, in recent years. This review discusses key aspects of the present and the future battery technologies on the basis of the working electrode. We then discuss how lithium-ion batteries evolve to meet the growing demand on high charge capacity and electrode stability. An account of a stand-alone energy device (off-grid system) that combines an energy harvesting technology with a lithium-ion battery is also provided. The main discussion is categorized into three perspectives such as the evolution from the conventional to the advanced LIBs (e.g., Li-rich transition metal oxide and Ni-rich transition metal oxide batteries), to the state-of-the-art LIBs (e.g., Li–air, Li–sulfur batteries, organic electrode batteries, solid-state batteries, and Li–CO2 batteries), and to the hybridized LIBs (e.g., metal halide perovskite batteries).

MXenes have been demonstrated as a potential candidate in the field of photovoltaics and energy storage owing to their high transmittance, metallic conductivity and tunable work function. In this work, we introduce a two-dimensional (2D) structure of Ti3C2-MXene nanosheets into all inorganic CsPbBr3 solar cells as an interlayer to realize a better interfacial energy level alignment, which helps to eliminate the energy level mismatch, accelerate the hole extraction and reduce the recombination at the interface of perovskite/carbon electrode. In addition, the functional groups such as O existing in the surface of Ti3C2-MXene nanosheets also provide strong interactions between the MXene and under-coordinated Pb atoms, which remarkably reduces the deep trap defects in the CsPbBr3 films. The device with the Ti3C2-MXene interlayer shows an impressive initial power conversion efficiency of 9.01% and long-term stability for over 1900 hours in a moisture environment and more than 600 hours under thermal conditions.

While organic–inorganic hybrid perovskite solar cells are emerging as promising candidates for next-generation solar cells with fascinating power conversion efficiency, the instability of perovskites remains a significant bottleneck for their commercialization. An atomic scale understanding of the degradation of hybrid perovskites, however, is only in its beginning stages because of the difficulty in preparing well-defined surface conditions for characterization. Using atomic force microscopy at ultra-high vacuum and room temperature, we report the first direct observation of the degradation process of a cleaved methylammonium lead bromide, MAPbBr3 (MA: CH3NH3+), single crystal. Upon in situ cleavage, atomic force microscopy images show large flat terraces with monolayer height steps, which correspond to the surface of cubic MAPbBr3 with methylammonium ligand termination. While this surface can be prepared via the cleavage process and is energetically stable, we observe that after several weeks under dark and vacuum conditions it degrades and produces clusters surrounded by pits. Guided by density functional theory calculations, we propose a degradation pathway that initiates even at low humidity levels and leads to the formation of surface PbBr2 species. We finally identify the electronic structure of the MA-bromine-terminated flat surface and find that it is correlated with a strong field-induced degradation of the MAPbBr3 only at positive sample bias voltages.

Polycrystalline properties of perovskites can induce the growth of different nanostructures, thanks to their facile fabrication. In this work, the CsPb2Br5 perovskite grains were used as templates to induce the growth of the ring-like structures on a SiO2/Si substrate. Owing to the oxidation of the volatile PbBr2 originated from the decomposition of CsPb2Br5, the grain boundaries of perovskites are prone to reaction with SiO2, which leads to the formation of Pb-silicate glass at high temperatures. The quasi-circular grain structure of CsPb2Br5 defines the final dimension of the Pb-silicate glass ring-like structures. X-ray photoelectron spectroscopy (XPS) measurement results reveal the formation and composition of the Pb-silicate glass ring-like structures converting from the halide perovskite film on the SiO2/Si substrate. Furthermore, these ring-like structures can extend to the field of display and pulsed-laser by combining existing techniques.

Dynamic disorders, which possess a finite charge delocalization, play a critical role in the charge transport properties of high-mobility molecular organic semiconductors. The use of two-dimensional (2D) charge transport in crystalline organic semiconductors can effectively facilitate reducing the sensitivity of charge carriers to thermal energetic disorders existing in even single crystals to enhance the carrier mobility. An isotropic transfer integral among adjacent molecules enables a dimensional transition from quasi-one-dimensional to 2D for charge transport among molecules. Herein, a tuned molecular packing, especially molecular rotation, was achieved in highly crystalline organic thin films via a brush-coating method. This tuned molecular packing was favorable for approaching isotropic transfer integrals. Consequently, high-performance organic transistors with a carrier mobility up to $21.5\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{2}\phantom{\rule{0.16em}{0ex}}{\mathrm{V}}^{\ensuremath{-}1}\phantom{\rule{0.16em}{0ex}}{\mathrm{s}}^{\ensuremath{-}1}$ and low angle dependence were obtained. This work presents a unique modulation of molecular packing at the molecular scale to enable less sensitivity of the charge transport to dynamic disorders, providing an alternative route for enhancing the electrical performance of organic electronic devices.

Summary With the rapid developments in lead halide perovskite solar cell technology, record-high power conversion efficiencies have been achieved, and significant research efforts have been directed toward stability, which is still a major challenge facing the commercialization of perovskite solar cell technology. In this review article, we review the research progress that has been made on the stability of perovskite solar cells. We start with an analysis of recently reported operational stability profiles of perovskite solar cells. On the basis of the analysis, we determine the solar cell lifetime (i.e., T80 values) and the total amount of energy generated during the lifespan of a perovskite solar cell, from which several trends are inferred. In the subsequent sections, we further examine the instability issues associated with various constituents in a perovskite solar cell and the new methods/strategies that have been developed to solve these issues.

Summary In recent years, metal halide perovskite opens the new era of the photovoltaic field. The highest power conversion efficiency has exceeded 23%. Although most of reported perovskite solar cells (PSCs) were fabricated by solution methods, the vacuum thermal evaporation method has its unique advantages, such as easy controlling of film thickness, compatibility with tandem cell designs, flexibility to tune interfaces, free of solvent, etc. In this paper, we review the development and progress of the vacuum thermal evaporation method for fabricating PSCs.