1. ACS Appl. Mater. Interfaces | Research Article
Approximately 800-nm-Thick Pinhole-Free Perovskite Films via Facile Solvent Retarding Process for Efficient Planar Solar Cells
Zhongcheng Yuan, Yingguo Yang, Zhongwei Wu, Sai Bai, Weidong Xu, Tao Song, Xingyu Gao, Feng Gao, and Baoquan Sun
Device performance of organometal halide perovskite solar cells significantly depends on the quality and thickness of perovskite absorber films. However, conventional deposition methods often generate pinholes within ∼300 nm-thick perovskite films, which are detrimental to the large area device manufacture. Here we demonstrated a simple solvent retarding process to deposit uniform pinhole free perovskite films with thicknesses up to ∼800 nm. Solvent evaporation during the retarding process facilitated the components separation in the mixed halide perovskite precursors, and hence the final films exhibited pinhole free morphology and large grain sizes. In addition, the increased precursor concentration after solvent-retarding process led to thick perovskite films. Based on the uniform and thick perovskite films prepared by this convenient process, a champion device efficiency up to 16.8% was achieved. We believe that this simple deposition procedure for high quality perovskite films around micrometer thickness has a great potential in the application of large area perovskite solar cells and other optoelectronic devices.
2. Applied Physics Letters | Research Article
Rong Yang, Li Zhang, Yu Cao, Yanfeng Miao, You Ke, Yingqiang Wei, Qiang Guo, Ying Wang, Zhaohua Rong, Nana Wang, Renzhi Li, Jianpu Wang, Wei Huang, and Feng Gao
Appl. Phys. Lett. 111, 073302 (2017); doi: 10.1063/1.4999630
Wei Zou, Renzhi Li, Shuting Zhang, Yunlong Liu, Nana Wang, Yu Cao, Yanfeng Miao, Mengmeng Xu, Qiang Guo, Dawei Di, Li Zhang, Chang Yi, Feng Gao, Richard H. Friend, Jianpu Wang & Wei Huang
Nature Communications, volume 9, Article number: 608 (2018) doi:10.1038/s41467-018-03049-7
Efficiency roll-off is a major issue for most types of light-emitting diodes (LEDs), and its origins remain controversial. Here we present investigations of the efficiency roll-off in perovskite LEDs based on two-dimensional layered perovskites. By simultaneously measuring electroluminescence and photoluminescence on a working device, supported by transient photoluminescence decay measurements, we conclude that the efficiency roll-off in perovskite LEDs is mainly due to luminescence quenching which is likely caused by non-radiative Auger recombination. This detrimental effect can be suppressed by increasing the width of quantum wells, which can be easily realized in the layered perovskites by tuning the ratio of large and small organic cations in the precursor solution. This approach leads to the realization of a perovskite LED with a record external quantum efficiency of 12.7%, and the efficiency remains to be high, at approximately 10%, under a high current density of 500 mA cm−2.
4. Advanced Materials | Communication
Weihua Ning Feng Wang Bo Wu Jun Lu Zhibo Yan Xianjie Liu Youtian Tao Jun‐Ming Liu Wei Huang Mats Fahlman Lars Hultman Tze Chien Sum* Feng Gao*
Advanced Materials, https://doi.org/10.1002/adma.201706246
Developing environmentally friendly perovskites has become important in solving the toxicity issue of lead‐based perovskite solar cells. Here, the first double perovskite (Cs2AgBiBr6) solar cells using the planar structure are demonstrated. The prepared Cs2AgBiBr6 films are composed of high‐crystal‐quality grains with diameters equal to the film thickness, thus minimizing the grain boundary length and the carrier recombination. These high‐quality double perovskite films show long electron–hole diffusion lengths greater than 100 nm, enabling the fabrication of planar structure double perovskite solar cells. The resulting solar cells based on planar TiO2 exhibit an average power conversion efficiency over 1%. This work represents an important step forward toward the realization of environmentally friendly solar cells and also has important implications for the applications of double perovskites in other optoelectronic devices.
Accepted in Advanced Materials, 30 March 2018
5. Chem. Commun. | Communication
Zhongcheng Yuan, Sai Bai,* Zhibo Yan, Jun-Ming Liu and Feng Gao*
We investigate the effect of commonly used solution-processed TiOx, SnO2and ZnO interlayers on the perovskite film crystallization process. We find that the ZnO/perovskite interface can efficiently catalyze the perovskite crystallization even without thermal annealing.
6. ACS Appl. Mater. Interfaces | Research Article
Jianming Yang†, Zhongcheng Yuan‡, Xianjie Liu, Slawomir Braun, Yanqing Li, Jianxin Tang, Feng Gao, Chungang Duan, Mats Fahlman, and Qinye Bao
Organometal halide perovskites are under rapid development, and significant focus has been placed on their stability that currently presents a major obstacle for practical application. Energetics plays a vital role in charge injection/extraction and transport properties in devices. Here, we in situ investigate oxygen- and water-induced energetics degradation in organometal halide perovskite films. Oxygen gas induces an upward shift of the vacuum level of the perovskite films because of the formation of an oxygen-induced surface dipole, water vapor causes a significant vacuum-level downshift, and the valence band binding energy referenced to the Fermi level simultaneously increases so as to keep the ionization potential of the perovskite films unchanged. Moreover, the chemical compositions, crystalline structures, surface morphologies, and dynamical properties also are monitored and analyzed in detail. These results are indispensable to understand the degradation mechanisms and to perform the optimizations of stable materials and devices in the future.
7. J. Phys. Chem. Lett.| Perspective
Xiao-Ke Liu and Feng Gao*
Recently, lead halide perovskite materials have attracted extensive interest, in particular, in the research field of solar cells. These materials are fascinating “soft” materials with semiconducting properties comparable to the best inorganic semiconductors like silicon and gallium arsenide. As one of the most promising perovskite family members, organic–inorganic hybrid Ruddlesden–Popper perovskites (HRPPs) offer rich chemical and structural flexibility for exploring excellent properties for optoelectronic devices, such as solar cells and light-emitting diodes (LEDs). In this Perspective, we present an overview of HRPPs on their structural characteristics, synthesis of pure HRPP compounds and thin films, control of their preferential orientations, and investigations of heterogeneous HRPP thin films. Based on these recent advances, future directions and prospects have been proposed. HRPPs are promising to open up a new paradigm for high-performance LEDs.
28th May, 2018
87. Nature.| Letter
Yu Cao, Nana Wang, He Tian, Jingshu Guo, Yingqiang Wei, Hong Chen, Yanfeng Miao, Wei Zou, Kang Pan, Yarong He, Hui Cao, You Ke, Mengmeng Xu, Ying Wang, Ming Yang, Kai Du, Zewu Fu, Decheng Kong, Daoxin Dai, Yizheng Jin, Gongqiang Li, Hai Li, Qiming Peng, Jianpu Wang & Wei Huang
Light-emitting diodes (LEDs), which convert electricity to light, are widely used in modern society—for example, in lighting, flat-panel displays, medical devices and many other situations. Generally, the efficiency of LEDs is limited by nonradiative recombination (whereby charge carriers recombine without releasing photons) and light trapping. In planar LEDs, such as organic LEDs, around 70 to 80 per cent of the light generated from the emitters is trapped in the device, leaving considerable opportunity for improvements in efficiency. Many methods, including the use of diffraction gratings, low-index grids and buckling patterns, have been used to extract the light trapped in LEDs. However, these methods usually involve complicated fabrication processes and can distort the light-output spectrum and directionality. Here we demonstrate efficient and high-brightness electroluminescence from solution-processed perovskites that spontaneously form submicrometre-scale structures, which can efficiently extract light from the device and retain wavelength- and viewing-angle-independent electroluminescence. These perovskites are formed simply by introducing amino-acid additives into the perovskite precursor solutions. Moreover, the additives can effectively passivate perovskite surface defects and reduce nonradiative recombination. Perovskite LEDs with a peak external quantum efficiency of 20.7 per cent (at a current density of 18 milliamperes per square centimetre) and an energy-conversion efficiency of 12 per cent (at a high current density of 100 milliamperes per square centimetre) can be achieved—values that approach those of the best-performing organic LEDs.