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In recent years, the power conversion efficiencies of halide perovskite solar cells (PSCs) have reached 25.7%. Further commercialization puts forward higher requirements for the stability of PSCs under different stresses. Current research on the stability of PSCs predominantly focuses on investigating the effects of temperature, humidity, oxygen, ultraviolet light, and electrical bias stress, while stability under reverse bias has been poorly studied among the many factors. When large‐area application of PSCs panels occurs, the shading effect and local hot spots of PSCs modules in real scenarios all indicate that the research on reverse bias stability of PSCs is urgently needed. Within this review, a bird's‐eye view of the recent advances on the reverse bias stability issue and reverse bias behavior of PSCs is obtained, and the related mechanisms behind that have been proposed so far are reviewed and discussed. Furthermore, future directions are provided for further improving the reverse bias stability of PSCs via increasing the reverse breakdown voltage (VRB). This review aims to promote the establishment of well‐established reverse bias degradation and reverse breakdown mechanisms of PSCs as well as to establish standardized test procedures for reverse bias stability issues on the road to commercialization of PSCs. [ABSTRACT FROM AUTHOR]

Efficient electron transport layer–free perovskite solar cells (ETL‐free PSCs) with cost‐effective and simplified design can greatly promote the large area flexible application of PSCs. However, the absence of ETL usually leads to the mismatched indium tin oxide (ITO)/perovskite interface energy levels, which limits charge transfer and collection, and results in severe energy loss and poor device performance. To address this, a polar nonconjugated small‐molecule modifier is introduced to lower the work function of ITO and optimize interface energy level alignment by virtue of an inherent dipole, as verified by photoemission spectroscopy and Kelvin probe force microscopy measurements. The resultant barrier‐free ITO/perovskite contact favors efficient charge transfer and suppresses nonradiative recombination, endowing the device with enhanced open circuit voltage, short circuit current density, and fill factor, simultaneously. Accordingly, power conversion efficiency increases greatly from 12.81% to a record breaking 20.55%, comparable to state‐of‐the‐art PSCs with a sophisticated ETL. Also, the stability is enhanced with decreased hysteresis effect due to interface defect passivation and inhibited interface charge accumulation. This work facilitates the further development of highly efficient, flexible, and recyclable ETL‐free PSCs with simplified design and low cost by interface electronic structure engineering through facile electrode modification. [ABSTRACT FROM AUTHOR]

The pursuit of high power conversion efficiency (PCE) and cost‐effective perovskite solar cells (PSCs) has spawned many innovative device structure designs. Compared with the traditional NIP type PSCs, electron transport layer (ETL) free PSCs have attracted growing attention due to their enormous potential in large area, low‐cost flexible application. However, there is still a lack of in‐depth understanding of the energy level arrangement indium tin oxide (ITO)/perovskite interface, resulting in poor device performance. Here, a metal/insulator/n‐type perovskite/p‐type spiro‐MeOTAD (MINP) structure is proposed to elaborate on the influence of the apparent work function and contact barrier change of the metal–semiconductor (MS) and metal–insulator–semiconductor (MIS) junction on the carrier transfer and collection. Common and easily available 5‐amino‐valeric acid is inserted into the ITO/perovskite interface to form an insulating dipole layer and to ensure quasi‐ohmic contact at the front interface. Consequently, the device changes from Schottky/PN cascade heterojunction type to a single PN heterojunction device with its ideal factor decreasing from 3.35 to 2.05. Accordingly, the champion device achieves 19.37% PCE with significantly increased Voc and FF compared to the pristine device. This work provides a facile and effective method to improve the application potential of novel ETL‐free PSCs. [ABSTRACT FROM AUTHOR]

Quasi‐two‐dimensional (quasi‐2D) organic–inorganic hybrid perovskites have shown excellent ambient stability with decent photovoltaic performance. Further improvement of device level properties requires a comprehensive understanding of the performance‐limiting mechanisms such as phase segregation, ion/electron coupling conduction, and their effects on charge transport at both the micro‐ and macro‐scale. Here, space resolved investigations of Ruddlesden–Popper (RP) phases of the commonquasi‐2D perovskite are probed using two complementary methods, conducting atomic force microscopy (c‐AFM) and Kelvin probe force microscopy (KPFM). Bias‐driven photocurrent mappings obtained by c‐AFM measurements disclose local inhomogeneous conduction and hysteresis currents in quasi‐2D RP perovskites, while relatively uniform conductivity is observed on individual grains. Bias‐driven KPFM reveals that the surface average photovoltage sign is dominated by the band bending at the buried perovskite–substrate interface. The quasi‐2D RP film exhibits substantial variations in the spatial response of the photovoltage across grains and grain boundaries, which is direct evidence of the inherently benign nature of microstructures, and the final device performance. This research elucidates underlying space‐resolved photoresponse mechanisms behind the lower efficiency of quasi‐2D RP perovskites compared with the 3D perovskites, which is necessary for further development of efficient and stable 2D perovskite‐based devices. [ABSTRACT FROM AUTHOR]

We investigated the impact of annealing atmosphere on the properties of organic-inorganic perovskite films systematically, and the mechanism is elucidated in perspective of crystallization kinetics of perovskite. It is found that the kind of gas, the state of the gas and the existence of solvent during annealing can affect the crystallization process of perovskite films, which therefore influence the morphology of perovskite films. In addition, the perovskite-based thin-film field-effect transistors were fabricated in different heating environment. It was discovered that the effect of annealing atmosphere on the performance of transistors is consistent with that on the crystallization qualities of perovskite films, which further confirms the influence of annealing atmosphere on the electronic properties of perovskite films. We also found that the type of gas has impact on the electronic properties of perovskite thin films probably by influencing the defects in the surface of perovskite films. Furthermore, it is notable that we confirmed that perovskite based transistors, of which the active layer was completely fabricated in air, show better performance, which is beneficial for commercial production of perovskite based transistors with low cost. [ABSTRACT FROM AUTHOR]

A facile and low‐temperature solution processed UV/ozone process has been proposed for fabricating TiO2 layer, making it possible to fabricate planar perovskite solar cells at low temperature. UV/ozone photo‐annealing treatment could easily eliminate the organic components, resulting in high quality amorphous TiO2 films with high transparency, electrical conductivity, and hydrophilicity. In addition, perovskite solar cells with the UV/ozone‐treated TiO2 electron transport layer exhibiting the best power conversion efficiency of 11.58% for rigid substrate and 7.33% for flexible substrate, respectively. The results clearly indicate that UV/ozone photo‐annealing treatment is a simple and effective process of fabricating high performance flexible perovskite solar cells. Fully low‐temperature solution‐processed perovskite solar cells (PSCs) are fabricated using UV/ozone (UV/O3) treated TiO2 film as an electron transport layer. UV/O3 treatment increases the electrical conductivity and wettability of the TiO2 film, and therefore improves the performance of PSCs. By optimizing the processing time of UV/O3 treatment, the power conversion efficiency of the best rigid and flexible device is 11.58% and 7.33%, respectively. [ABSTRACT FROM AUTHOR]