Ziming Chen

Highly efficient fullerene/perovskite planar heterojunction solar cells via cathode modification with an amino-functionalized polymer interlayer

A new amino-functionalized polymer, PN4N, was developed and applied as an efficient interlayer to improve the cathode interface of fullerene/perovskite (CH3NH3PbIxCl3−x) planar heterojunction solar cells. The PN4N polymer is soluble in IPA and n-BuOH, which are orthogonal solvents to the metallohalide perovskite films, and therefore they can be spuncast on the heterojunction layer before the deposition of the metal cathode. This simple modification of the cathode interface showed a remarkable enhancement of power conversion efficiency (PCE) from 12.4% to 15.0% and also reduced the hysteresis of photocurrent. We also found that conventional water–methanol-soluble polymer interlayer, such as PFN, was incompatible with the perovskite films because of the small molecular size of aprotic solvent such as MeOH, which could decompose the perovskite films to PbI2, resulting in considerably lower solar cell performance. This study provides new design guidelines for efficient interfacial materials and also demonstrates that interface engineering could be a key strategy to improve perovskite solar cells.

Phosphonium Halides as Both Processing Additives and Interfacial Modifiers for High Performance Planar-Heterojunction Perovskite Solar Cells

Organic halide salts are successfully incorporated in perovskite-based planar-heterojunction solar cells as both the processing additive and interfacial modifier to improve the morphology of the perovskite light-absorbing layer and the charge collecting property of the cathode. As a result, perovskite solar cells exhibit a significant improvement in power conversion efficiency (PCE) from 10% of the reference device to 13% of the modified devices.

Metallohalide perovskite–polymer composite film for hybrid planar heterojunction solar cells

A polymer with tailored chemical functionality was introduced as a processing additive to control the film formation of the CH3NH3PbI3 perovskite structure, leading to enhanced photovoltaic performance in a PEDOT:PSS/perovskite/PCBM-based planar heterojunction solar cell under optimized conditions. By adjusting the polymer doping content and the processing solvent, the grain size, film coverage and the optical properties of the perovskite films can be effectively tuned. At optimized conditions, the planar heterojunction solar cell composed of a thin layer of perovskite–polymer film (∼50 nm) exhibits an average PCE of 6.16% with a Voc of 1.04 V, a Jsc of 8.85 mA cm−2 and a FF of 0.65, which are much higher than those of the control device with a pristine perovskite film. The higher performance was attributed to improved morphology and interfaces of the perovskite–polymer films, which reduced the undesired contact between PEDOT:PSS and PCBM and minimized the shunting paths in the device. In addition, since the fabrication process for the perovskite solar cells can be performed at low temperature, flexible cells built on plastic substrates can therefore be realized with a PCE of 4.35%.

High-Performance Color-Tunable Perovskite Light Emitting Devices through Structural Modulation from Bulk to Layered Film

Adding 2-phenoxyethylamine (POEA) into a CH3 NH3 PbBr3 precursor solution can modulate the organic-inorganic hybrid perovskite structure from bulk to layered, with a photoluminescence and electroluminescence shift from green to blue. Meanwhile, POEA can passivate the CH3 NH3 PbBr3 surface and help to obtain a pure CH3 NH3 PbBr3 phase, leading to an improvement of the external quantum efficiency to nearly 3% in CH3 NH3 PbBr3 LED.

Interface Engineering for All‐Inorganic CsPbI2Br Perovskite Solar Cells with Efficiency over 14%

In this work, a SnO2 /ZnO bilayered electron transporting layer (ETL) aimed to achieve low energy loss and large open-circuit voltage (Voc ) for high-efficiency all-inorganic CsPbI2 Br perovskite solar cells (PVSCs) is introduced. The high-quality CsPbI2 Br film with regular crystal grains and full coverage can be realized on the SnO2 /ZnO surface. The higher-lying conduction band minimum of ZnO facilitates desirable cascade energy level alignment between the perovskite and SnO2 /ZnO bilayered ETL with superior electron extraction capability, resulting in a suppressed interfacial trap-assisted recombination with lower charge recombination rate and greater charge extraction efficiency. The as-optimized all-inorganic PVSC delivers a high Voc of 1.23 V and power conversion efficiency (PCE) of 14.6%, which is one of the best efficiencies reported for the Cs-based all-inorganic PVSCs to date. More importantly, decent thermal stability with only 20% PCE loss is demonstrated for the SnO2 /ZnO-based CsPbI2 Br PVSCs after being heated at 85 °C for 300 h. These findings provide important interface design insights that will be crucial to further improve the efficiency of all-inorganic PVSCs in the future.

Efficient device engineering for inverted non-fullerene organic solar cells with low energy loss

In recent years, the use of non-fullerene acceptors in organic solar cells has rapidly advanced with new acceptor materials, which have enabled devices to achieve a power conversion efficiency greater than 13%. In addition to new acceptor materials’ design, device engineering plays an important role in improving the device performance. In this study, we develop effective device engineering strategies, including thermal annealing and interlayer modification, to improve the device performance from 7.39% to 9.39%. With the use of PTB7-Th as the donor and IDT-BT-R as the non-fullerene acceptor, we achieved an efficient non-fullerene organic solar cell based on an inverted device architecture with a power conversion efficiency as high as 9.39%. It is worthy of note that the energy loss of the optimized device is only around 0.5 eV, which can be attributed to weak recombination and the appropriate high energy level of the charge transfer states within the optimized device.

High performance low-bandgap perovskite solar cells based on a high-quality mixed Sn–Pb perovskite film prepared by vacuum-assisted thermal annealing

Tandem perovskite solar cells are an effective concept to overcome the Shockley–Queisser limit of a single-junction perovskite solar cell. For a high-performance tandem cell, besides a wide-bandgap perovskite top cell, a high-quality low-bandgap perovskite bottom cell with an optimum bandgap of ∼1.2 eV is urgently needed. Moreover, a simple process technique needs to be developed for a high-quality perovskite film with good reproducibility, in order to further simplify the whole tandem-cell fabrication. Accordingly, we develop a simple one-step process (vacuum-assisted thermal annealing) for a high-quality low-bandgap CH3NH3Sn0.5Pb0.5IxCl3−x film, where the absorption edge can exceed 1000 nm. After comparing CH3NH3Sn0.5Pb0.5IxCl3−x films annealed in a vacuum and in a nitrogen environment, we find that vacuum-assisted thermal annealing can result in CH3NH3Sn0.5Pb0.5IxCl3−x films with better film coverage and crystallinity. This process can also accelerate the sublimation of methylammonium chloride and reduce the trap density in the CH3NH3Sn0.5Pb0.5IxCl3−x film. With this process, we successfully fabricated an efficient low-bandgap perovskite solar cell with a power conversion efficiency of more than 12% and good device reproducibility as well as long-term stability.

Recombination Dynamics Study on Nanostructured Perovskite Light-Emitting Devices

The field of organic-inorganic hybrid perovskite light-emitting diodes (PeLEDs) has developed rapidly in recent years. Although the performance of PeLEDs continues to improve through film quality control and device optimization, little research has been dedicated to understanding the recombination dynamics in perovskite thin films. Likewise, little has been done to investigate the effects of recombination dynamics on the overall light-emitting behavior of PeLEDs. Therefore, this study investigates the recombination dynamics of CH3 NH3 PbI3 thin films with differing crystal sizes by measurement of fluence-dependent transient absorption dynamics and time-resolved photoluminescence. The aim is to find out the link between recombination dynamics and device behavior in PeLEDs. It is found that bimolecular and Auger recombination become more efficient as the crystal size decreases and monomolecular recombination rate is affected by the trap density of perovskite. By defining the radiative efficiency Φ(n), which relates to the monomolecular, bimolecular, and Auger recombination, the fundamental recombination properties of CH3 NH3 PbI3 films are discerned in quantitative terms. These findings help us to understand the light emission behavior of PeLEDs. This study takes an important step toward establishing the relationship between film structure, recombination dynamics, and device behavior for PeLEDs, thereby providing useful insights toward the design of better perovskite devices.