Microscopic Charge Transport and Recombination Processes behind the Photoelectric Hysteresis in Perovskite Solar Cells

The microscopic charge transport and recombination processes behind the widely concerned photoelectric hysteresis in the perovskite solar cell have been investigated with both in situ transient photovoltage/photocurrent measurements and the semiconductor device simulation. Time‐dependent behaviors of intensity and direction of the photocurrent and photovoltage are observed under the steady‐state bias voltages and open‐circuit conditions. These charge processes reveal the electric properties of the cell, demonstrating evolutions of both strength and direction of the internal electric field during the hysteresis. Further calculation indicates that this behavior is mainly attributed to both the interfacial doping and defect effects induced by the ion accumulation, which may be the origins for the general hysteresis in this cell.     

Interfaces in Perovskite Solar Cells

The interfacial atomic and electronic structures, charge transfer processes, and interface engineering in perovskite solar cells are discussed in this review. An effective heterojunction is found to exist at the window/perovskite absorber interface, contributing to the relatively fast extraction of free electrons. Moreover, the high photovoltage in this cell can be attributed to slow interfacial charge recombination due to the outstanding material and interfacial electronic properties. However, some fundamental questions including the interfacial atomic and electronic structures and the interface stability need to be further clarified. Designing and engineering the interfaces are also important for the next‐stage development of this cell.     

Reliable Measurement of Perovskite Solar Cells

Perovskite solar cells (PSCs) have undergone an incredibly fast development and attracted intense attention worldwide owing to their high efficiency and low‐cost fabrication. However, it is challenging to make a reliable measurement of PSCs, which creates great difficulty for researchers to compare and reproduce published results. Herein, the major measurement methods and key factors affecting evaluation of PSCs are summarized, such as hysteresis in current–voltage measurement, calibration of solar simulators for less mismatch in spectra and light intensity, and the area for the calculation of current density and power conversion efficiency. PSCs are also compared with n–i–p or p–i–n structures that exhibit different feedback under the same measurement methods. Finally, a measurement proposal is provided to help researchers obtain reliable measurement results close to those certified by public test centers.     

Pb–Sn–Cu Ternary Organometallic Halide Perovskite Solar Cells

Exploiting organic/inorganic hybrid perovskite solar cells (PSCs) with reduced Pb content is very important for developing environment‐friendly photovoltaics. Utilizing of Pb–Sn alloying perovskite is considered as an efficient route to reduce the risk of ecosystem pollution. However, the trade‐off between device performance and Sn substitution ratio due to the instability of Sn²⁺ is a current dilemma. Here, for the first time, the highly efficient Pb–Sn–Cu ternary PSCs are reported by partial replacing of PbI₂ with SnI₂ and CuBr₂. Sn²⁺ substitution results in a redshift of the absorption onset, whereas worsens the film quality. Interestingly, Cu²⁺ introduction can passivate the trap sites at the crystal boundaries of Pb–Sn perovskites effectively. Consequently, a power conversion efficiency as high as 21.08% in inverted planar Pb–Sn–Cu ternary PSCs is approached. The finding opens a new route toward the fabrication of high efficiency Pb–Sn alloying perovskite solar cells by Cu²⁺ passivation.     

Planar‐Structure Perovskite Solar Cells with Efficiency beyond 21%

Low temperature solution processed planar‐structure perovskite solar cells gain great attention recently, while their power conversions are still lower than that of high temperature mesoporous counterpart. Previous reports are mainly focused on perovskite morphology control and interface engineering to improve performance. Here, this study systematically investigates the effect of precise stoichiometry, especially the PbI₂ contents on device performance including efficiency, hysteresis and stability. This study finds that a moderate residual of PbI₂ can deliver stable and high efficiency of solar cells without hysteresis, while too much residual PbI₂ will lead to serious hysteresis and poor transit stability. Solar cells with the efficiencies of 21.6% in small size (0.0737 cm²) and 20.1% in large size (1 cm²) with moderate residual PbI₂ in perovskite layer are obtained. The certificated efficiency for small size shows the efficiency of 20.9%, which is the highest efficiency ever recorded in planar‐structure perovskite solar cells, showing the planar‐structure perovskite solar cells are very promising.     

Defect‐Engineering‐Enabled High‐Efficiency All‐Inorganic Perovskite Solar Cells

The emergence of cesium lead iodide (CsPbI₃) perovskite solar cells (PSCs) has generated enormous interest in the photovoltaic research community. However, in general they exhibit low power conversion efficiencies (PCEs) because of the existence of defects. A new all‐inorganic perovskite material, CsPbI₃:Br:InI₃, is prepared by defect engineering of CsPbI₃. This new perovskite retains the same bandgap as CsPbI₃, while the intrinsic defect concentration is largely suppressed. Moreover, it can be prepared in an extremely high humidity atmosphere and thus a glovebox is not required. By completely eliminating the labile and expensive components in traditional PSCs, the all‐inorganic PSCs based on CsPbI₃:Br:InI₃ and carbon electrode exhibit PCE and open‐circuit voltage as high as 12.04% and 1.20 V, respectively. More importantly, they demonstrate excellent stability in air for more than two months, while those based on CsPbI₃ can survive only a few days in air. The progress reported represents a major leap for all‐inorganic PSCs and paves the way for their further exploration in order to achieve higher performance.     

钙钛矿太阳能电池技术发展历史与现状

简要回顾了钙钛矿太阳能电池的发展历史,解释了钙钛矿太阳能电池本质上是固态染料敏化太阳能电池。介绍了钙钛矿太阳能电池的微观发电机理,结合钙钛矿太阳能电池的能级图分析讨论了钙钛矿与电子传输层和空穴传输层的能级匹配。分析总结了钙钛矿太阳能电池的光伏技术参数,包括光生电流密度、开路电压、填充因子、能量转换效率以及光伏性能的稳定性。钙钛矿太阳能电池的能量转换效率、短路电流密度和开路电压均已超过非晶硅薄膜太阳能电池,填充因子与非晶硅薄膜太阳能电池很接近。钙钛矿太阳能电池有希望实现产业化而成为下一代薄膜太阳能电池。指出了钙钛矿太阳能电池大规模市场应用在制造技术上的瓶颈即空穴传输层的造价昂贵,并综述了解决该瓶颈的最新研究工作。     

Origins of High Performance and Degradation in the Mixed Perovskite Solar Cells

The origins of the high device performance and degradation in the air are the greatest issues for commercialization of perovskite solar cells. Here this study investigates the possible origins of the mixed perovskite cells by monitoring defect states and compositional changes of the perovskite layer over the time. The results of deep‐level transient spectroscopy analysis reveal that a newly identified defect formed by Br atoms exists at deep levels of the mixed perovskite film, and its defect state shifts when the film is aged in the air. The change of the defect state is originated from loss of the methylammonium molecules of the perovskite layer, which results in decreased J_SC, deterioration of the power conversion efficiency and long‐term stability of perovskite solar cells. The results provide a powerful strategy to diagnose and manage the efficiency and stability of perovskite solar cells.     

Strategically Constructed Bilayer Tin (IV) Oxide as Electron Transport Layer Boosts Performance and Reduces Hysteresis in Perovskite Solar Cells

Nanostructured tin (IV) oxide (SnO₂) is emerging as an ideal inorganic electron transport layer in n–i–p perovskite devices, due to superior electronic and low‐temperature processing properties. However, significant differences in current–voltage performance and hysteresis phenomena arise as a result of the chosen fabrication technique. This indicates enormous scope to optimize the electron transport layer (ETL), however, to date the understanding of the origin of these phenomena is lacking. Reported here is a first comparison of two common SnO₂ ETLs with contrasting performance and hysteresis phenomena, with an experimental strategy to combine the beneficial properties in a bilayer ETL architecture. In doing so, this is demonstrated to eliminate room‐temperature hysteresis while simultaneously attaining impressive power conversion efficiency (PCE) greater than 20%. This approach highlights a new way to design custom ETLs using functional thin‐film coatings of nanomaterials with optimized characteristics for stable, efficient, perovskite solar cells.     

Semitransparent Perovskite Solar Cells: From Materials and Devices to Applications

Semitransparent solar cells (ST-SCs) have received great attention due to their promising application in many areas, such as building integrated photovoltaics (BIPVs), tandem devices, and wearable electronics. In the past decade, perovskite solar cells (PSCs) have revolutionized the field of photovoltaics (PVs) with their high efficiencies and facile preparation processes. Due to their large absorption coefficient and bandgap tunability, perovskites offer new opportunities to ST-SCs. Here, a general overview is provided on the recent advances in ST-PSCs from materials and devices to applications and some personal perspectives on the future development of ST-PSCs.     

基于对氯苄胺的2D/3D钙钛矿太阳能电池

三维(3D)有机–无机金属卤化物钙钛矿薄膜的表面和晶界处存在大量缺陷,容易导致载流子的非辐射复合并加快3D钙钛矿分解,进而影响钙钛矿太阳能电池(PSCs)能量转换效率(PCE)及稳定性.本研究通过引入对氯苄胺阳离子,与3D钙钛矿薄膜及其表面过剩的碘化铅反应后原位形成了二维(2D)钙钛矿,实现了对3D钙钛矿薄膜表面和晶界...     

钙钛矿太阳能电池的研究进展

作为一种新型清洁可再生能源,钙钛矿太阳能电池(Perovskite solar cells,PSC)从发展至今已取得了重大的突破,成为研究的热点。主要介绍了钙钛矿太阳能电池的基本结构和工作原理及电子传输层、钙钛矿层、空穴传输层的制备方法,以及在发展过程中所面临的技术问题,最后展望了钙钛矿太阳能电池未来的研究重点及发展前景。     

柔性染料敏化太阳能电池和柔性钙钛矿太阳能电池关键电极材料研究进展

柔性太阳能电池具有轻便、可弯曲的优点,可用于可穿戴设备等器件的即时充电,具有广阔的应用前景,受到持续广泛的关注。柔性太阳能电池制备中的关键在于基材以及与之相关的电极材料的制备。本文综述了柔性染料敏化太阳能电池和柔性钙钛矿太阳能电池近几年的发展情况,着重介绍了柔性染料敏化太阳能电池光阳极、对电极以及柔性钙钛矿太阳能电池的底电极和电子传输层。结果发现高温烧结目前仍是制备高效染料敏化太阳能电池光阳极不可避免的方法,而对电极则不受这一限制并且已经有多种材料的效率超过了高温烧结的铂。柔性钙钛矿太阳能电池的研究重点是用其他材料代替底电极中柔性较差的ITO以及高温烧结的电子传输材料TiO₂,并且都取得显著成效。在此基础上,展望了柔性染料敏化太阳能电池和柔性钙钛矿太阳能电池未来的发展方向。     

Efficient Bifacial Passivation with Crosslinked Thioctic Acid for High-Performance Methylammonium Lead Iodide Perovskite Solar Cells

Defects, inevitably produced within bulk and at perovskite-transport layer interfaces (PTLIs), are detrimental to power conversion efficiency (PCE) and stability of perovskite solar cells (PSCs). It is demonstrated that a crosslinkable organic small molecule thioctic acid (TA), which can simultaneously be chemically anchored to the surface of TiO₂ and methylammonium lead iodide (MAPbI₃) through coordination effects and then in situ crosslinked to form a robust continuous polymer (Poly(TA)) network after thermal treatment, can be introduced into PSCs as a new bifacial passivation agent for greatly passivating the defects. It is also discovered that Poly(TA) can additionally enhance the charge extraction efficiency and the water-resisting and light-resisting abilities of perovskite film. These newly discovered features of Poly(TA) make PSCs herein achieve among the best PCE of 20.4% ever reported for MAPbI₃ with negligible hysteresis, along with much enhanced ultraviolet, air, and operational stabilities. Density functional theory calculations reveal that the passivation of MAPbI₃ bulk and PTLIs by Poly(TA) occurs through the interaction of functional groups ( COOH,  C S) in Poly(TA) with under-coordinated Pb²⁺ in MAPbI₃ and Ti⁴⁺ in TiO₂, which is supported by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy.