共查询到20条相似文献,搜索用时 15 毫秒
1.
2.
Organic–inorganic perovskites have demonstrated an impressive potential for the design of the next generation of solar cells. Perovskite solar cells (PSCs) are currently considered for scaling up and commercialization. Many of the lab‐scale preparation methods are however difficult to scale up or are environmentally unfriendly. The highest efficient PSCs are currently prepared using the antisolvent method, which utilizes a significant amount of an organic solvent to induce perovskite crystallization in a thin film. An antisolvent‐free method is developed in this work using flash infrared annealing (FIRA) to prepare methylammonium lead iodide (MAPbI3) PSCs with a record stabilized power conversion efficiency of 18.3%. With an irradiation time of fewer than 2 s, FIRA enables the coating of glass and plastic substrates with pinhole‐free perovskite films that exhibit micrometer‐size crystalline domains. This work discusses the FIRA‐induced crystallization mechanism and unveils the main parameters controlling the film morphology. The replacement of the antisolvent method and the larger crystalline domains resulting from flash annealing make FIRA a highly promising method for the scale‐up of PSC manufacture. 相似文献
3.
Jacobus J. van Franeker Koen H. Hendriks Bardo J. Bruijnaers Martinus W. G. M. Verhoeven Martijn M. Wienk René A. J. Janssen 《Liver Transplantation》2017,7(7)
Layer deposition of organometal halide perovskites for solar cells usually involves tedious experimentation to establish the optimum processing conditions. Important parameters are the time and temperature of thermal annealing. Here, it is demonstrated that in situ photoluminescence allows to determine the optimal annealing procedure without fabricating complete solar cells. A deposition method is used in which dense layers of perovskite crystals are formed within seconds in ambient air by hot casting a mixture of lead acetate, lead chloride, and methylammonium iodide. The as‐cast perovskite layers are highly luminescent because charge carriers are unable to reach the charge extraction layers that quench the photoluminescence. Thermal annealing enhances charge transport and quenches the photoluminescence, but deteriorates the photovoltaic performance via decomposition of the perovskite if applied for a too long time. It is demonstrated that the optimal annealing time coincides with the time required for the in situ measured photoluminescence intensity to reach its baseline value for annealing temperatures in the range of 80–100 °C. This results in efficient (>14%) perovskite solar cells and shows that in situ photoluminescence is a simple but powerful tool for in‐line quality monitoring of perovskite films. 相似文献
4.
Keqing Huang Yongyi Peng Yaxin Gao Jiao Shi Hengyue Li Xindi Mo Han Huang Yongli Gao Liming Ding Junliang Yang 《Liver Transplantation》2019,9(44)
Flexible perovskite solar cells (f‐PSCs) have attracted great attention due to their promising commercial prospects. However, the performance of f‐PSCs is generally worse than that of their rigid counterparts. Herein, it is found that the unsatisfactory performance of planar heterojunction (PHJ) f‐PSCs can be attributed to the undesirable morphology of electron transport layer (ETL), which results from the rough surface of the flexible substrate. Precise control over the thickness and morphology of ETL tin dioxide (SnO2) not only reduces the reflectance of the indium tin oxide (ITO) on polyethylene 2,6‐naphthalate (PEN) substrate and enhances photon collection, but also decreases the trap‐state densities of perovskite films and the charge transfer resistance, leading to a great enhancement of device performance. Consequently, the f‐PSCs, with a structure of PEN/ITO/SnO2/perovskite/Spiro‐OMeTAD/Ag, exhibit a power conversion efficiency (PCE) up to 19.51% and a steady output of 19.01%. Furthermore, the f‐PSCs show a robust bending resistance and maintain about 95% of initial PCE after 6000 bending cycles at a bending radius of 8 mm, and they present an outstanding long‐term stability and retain about 90% of the initial performance after >1000 h storage in air (10% relative humidity) without encapsulation. 相似文献
5.
Ziran Zhao Feidan Gu Haixia Rao Senyun Ye Zhiwei Liu Zuqiang Bian Chunhui Huang 《Liver Transplantation》2019,9(3)
Metal halide perovskite solar cells (PSCs) have emerged as promising candidates for photovoltaic technology with their power conversion efficiencies over 23%. For prototypical organic–inorganic metal halide perovskites, their intrinsic instability poses significant challenges to the commercialization of PSCs. Recently, the scientific community has done tremendous work in composition engineering to develop more robust light‐absorbing layers, including mixed‐ion hybrid perovskites, low‐dimensional hybrid perovskites, and all‐inorganic perovskites. This review provides an overview of the impact of these perovskites on the efficiency and long‐term stability of PSCs. 相似文献
6.
Mozhgan Yavari Mohammad Mazloum‐Ardakani Somayeh Gholipour Nevena Marinova Juan Luis Delgado Silver‐Hamill Turren‐Cruz Konrad Domanski Nima Taghavinia Michael Saliba Michael Grätzel Anders Hagfeldt Wolfgang Tress 《Liver Transplantation》2018,8(12)
In the past few years, organic–inorganic metal halide ABX3 perovskites (A = Rb, Cs, methylammonium, formamidinium (FA); B = Pb, Sn; X = Cl, Br, I) have rapidly emerged as promising materials for photovoltaic applications. Tuning the film morphology by various deposition techniques and additives is crucial to achieve solar cells with high performance and long‐term stability. In this work, carbon nanoparticles (CNPs) containing functional groups are added to the perovskite precursor solution for fabrication of fluorine‐doped tin oxide/TiO2/perovskite/spiro‐OMeTAD/gold devices. With the addition of CNPs, the perovskite films are thermally more stable, contain larger grains, and become more hydrophobic. NMR experiments provide strong evidence that the functional groups of the CNPs interact with FA cations already in the precursor solution. The fabricated solar cells show a power‐conversion efficiency of 18% and negligible hysteresis. 相似文献
7.
8.
Perovskite Solar Cells: Understanding the Doping Effect on NiO: Toward High‐Performance Inverted Perovskite Solar Cells (Adv. Energy Mater. 19/2018)
下载免费PDF全文
![点击此处可从《Liver Transplantation》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Wei Chen Yinghui Wu Jing Fan Aleksandra B. Djurišić Fangzhou Liu Ho Won Tam Annie Ng Charles Surya Wai Kin Chan Dong Wang Zhu‐Bing He 《Liver Transplantation》2018,8(19)
9.
Understanding the Doping Effect on NiO: Toward High‐Performance Inverted Perovskite Solar Cells
下载免费PDF全文
![点击此处可从《Liver Transplantation》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Wei Chen Yinghui Wu Jing Fan Aleksandra B. Djurišić Fangzhou Liu Ho Won Tam Annie Ng Charles Surya Wai Kin Chan Dong Wang Zhu‐Bing He 《Liver Transplantation》2018,8(19)
High‐quality hole transport layers are prepared by spin‐coating copper doped nickel oxide (Cu:NiO) nanoparticle inks at room temperature without further processing. In agreement with theoretical calculations predicting that Cu doping results in acceptor energy levels closer to the valence band maximum compared to gap states of nickel vacancies in undoped NiO, an increase in the conductivity in Cu:NiO films compared to NiO is observed. Cu in Cu:NiO can be found in both Cu+ and Cu2+ states, and the substitution of Ni2+ with Cu+ contributes to both increased carrier concentration and carrier mobility. In addition, the films exhibit increased work function, which together with the conductivity increase, enables improved charge transfer and extraction. Furthermore, recombination losses due to lower monomolecular Shockley‐Read‐Hall recombination are reduced. These factors result in an improvement of all photovoltaic performance parameters and consequently an increased efficiency of the inverted planar perovskite solar cells. A power conversion efficiency (PCE) exceeding 20% could be achieved for small‐area devices, while PCE values of 17.41 and 18.07% are obtained for flexible devices and large area (1 cm2) devices on rigid substrates, respectively. 相似文献
10.
Recent Progress on Hole‐Transporting Materials for Emerging Organometal Halide Perovskite Solar Cells
下载免费PDF全文
![点击此处可从《Liver Transplantation》网站下载免费的PDF全文](/ch/ext_images/free.gif)
In less than three years, the photovoltaic community has witnessed a rapid emergence of a new class of solid‐state heterojunction solar cells based on solution‐processable organometal halide perovskite absorbers. The energy conversion efficiency of solid‐state perovskite solar cells (PSCs) has been quickly increased to a certified value of 20.1% by the end of 2014 because of their unique characteristics, such as a broad spectral absorption range, large absorption coefficient, high charge carrier mobility and diffusion length. Here, the focus is specifically on recent developments of hole‐transporting materials (HTMs) in PSCs, which are essential components for achieving high solar cell efficiencies. Some fundamentals with regard to PSCs are first presented, including the history of PSCs, device architectures and general operational principles of PSCs as well as various techniques developed for the fabrications of uniform and dense perovskite complexes. A broad range of the state‐of‐the‐art HTMs being used in PSCs are then discussed in detail. Finally, an outlook on the design of more efficient HTMs for highly efficient PSCs is addressed. 相似文献
11.
Qifei Wang Wenhao Zhang Zhihui Zhang Shuang Liu Jiawen Wu Yanjun Guan Anyi Mei Yaoguang Rong Yue Hu Hongwei Han 《Liver Transplantation》2020,10(5)
Controlling the crystallization of organic–inorganic hybrid perovskite is of vital importance to achieve high performing perovskite solar cells. The growth mechanism of perovskites has been intensively studied in devices with planar structures and traditional structures. However, for the printable mesoscopic perovskite solar cells, it is difficult to study the crystallization mechanism of perovskite owing to the complicated mesoporous structure. Here, a solvent evaporation controlled crystallization method to achieve ideal crystallization in the mesoscopic structure is provided. Combining results of scanning electron microscope and X‐ray diffraction, it is found that adjusting the evaporation rate of solvent can control the crystallization rate of perovskite and a model for the crystallization process during annealing in mesoporous structures is proposed. Finally, a homogeneous pore filling in the mesoscopic structure without any additives is successfully achieved and a stabilized power conversion efficiency of 16.26% using ternary‐cation perovskite absorber is realized. The findings will provide better understanding of perovskite crystallization in printable mesoscopic perovskite solar cells and pave the way for the commercialization of perovskite solar cells. 相似文献
12.
Meng Li Zhao‐Kui Wang Ying‐Guo Yang Yun Hu Shang‐Lei Feng Jin‐Miao Wang Xing‐Yu Gao Liang‐Sheng Liao 《Liver Transplantation》2016,6(21)
The development of effective and stable hole transporting materials (HTMs) is very important for achieving high‐performance planar perovskite solar cells (PSCs). Herein, copper salts (cuprous thiocyanate (CuSCN) or cuprous iodide (CuI)) doped 2,2,7,7‐tetrakis(N,N‐di‐p‐methoxyphenylamine)‐9,9‐spirobifluorene (spiro‐OMeTAD) based on a solution processing as the HTM in PSCs is demonstrated. The incorporation of CuSCN (or CuI) realizes a p‐type doping with efficient charge transfer complex, which results in improved film conductivity and hole mobility in spiro‐OMeTAD:CuSCN (or CuI) composite films. As a result, the PCE is largely improved from 14.82% to 18.02% due to obvious enhancements in the cell parameters of short‐circuit current density and fill factor. Besides the HTM role, the composite film can suppress the film aggregation and crystallization of spiro‐OMeTAD films with reduced pinholes and voids, which slows down the perovskite decomposition by avoiding the moisture infiltration to some extent. The finding in this work provides a simple method to improve the efficiency and stability of planar perovskite solar cells. 相似文献
13.
Efficient Indium‐Doped TiOx Electron Transport Layers for High‐Performance Perovskite Solar Cells and Perovskite‐Silicon Tandems
下载免费PDF全文
![点击此处可从《Liver Transplantation》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Jun Peng The Duong Xianzhong Zhou Heping Shen Yiliang Wu Hemant Kumar Mulmudi Yimao Wan Dingyong Zhong Juntao Li Takuya Tsuzuki Klaus J. Weber Kylie R. Catchpole Thomas P. White 《Liver Transplantation》2017,7(4)
In addition to a good perovskite light absorbing layer, the hole and electron transport layers play a crucial role in achieving high‐efficiency perovskite solar cells. Here, a simple, one‐step, solution‐based method is introduced for fabricating high quality indium‐doped titanium oxide electron transport layers. It is shown that indium‐doping improves both the conductivity of the transport layer and the band alignment at the ETL/perovskite interface compared to pure TiO2, boosting the fill‐factor and voltage of perovskite cells. Using the optimized transport layers, a high steady‐state efficiency of 17.9% for CH3NH3PbI3‐based cells and 19.3% for Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3‐based cells is demonstrated, corresponding to absolute efficiency gains of 4.4% and 1.2% respectively compared to TiO2‐based control cells. In addition, a steady‐state efficiency of 16.6% for a semi‐transparent cell is reported and it is used to achieve a four‐terminal perovskite‐silicon tandem cell with a steady‐state efficiency of 24.5%. 相似文献
14.
15.
Yang Wang Mingzhu Li Huizeng Li Yangjie Lan Xue Zhou Chang Li Xiaotian Hu Yanlin Song 《Liver Transplantation》2019,9(25)
Novel photovoltaic perovskite solar cells (PSCs) with high‐efficient photovoltaic property are largely in thrall to the uncertain perovskite grain size and inevitable defects. Here, inspired by the competitive growth between tree and grass in the forest system, a competitive perovskite grain growth approach via micro‐contact print (MicroCP) method (CD disk as templates) for printing wettability‐patterned substrate is proposed, aiming to achieve large‐grained perovskite and avoid discontinuous perovskite films caused by the low wettability of substrates. A MicroCP process is employed to construct a patterned wettability surface for the perovskite competitive growth mechanism on the electrode surface. This approach modifies the substrates quickly, ensures the uniform coverage of perovskite due to the function of ‐NH2 and Pb2+ bonds, and converts the perovskite films composed of small grains and pinholes into high‐quality perovskite films, free from pinholes and made up of large grains, resulting in efficiencies over 20% for the MicroCP PSCs. 相似文献
16.
Sheng Fu Xiaodong Li Li Wan Yulei Wu Wenxiao Zhang Yueming Wang Qinye Bao Junfeng Fang 《Liver Transplantation》2019,9(35)
Stability has become the main obstacle for the commercialization of perovskite solar cells (PSCs) despite the impressive power conversion efficiency (PCE). Poor crystallization and ion migration of perovskite are the major origins of its degradation under working condition. Here, high‐performance PSCs incorporated with pyridine‐2‐carboxylic lead salt (PbPyA2) are fabricated. The pyridine and carboxyl groups on PbPyA2 can not only control crystallization but also passivate grain boundaries (GBs), which result in the high‐quality perovskite film with larger grains and fewer defects. In addition, the strong interaction among the hydrophobic PbPyA2 molecules and perovskite GBs acts as barriers to ion migration and component volatilization when exposed to external stresses. Consequently, superior optoelectronic perovskite films with improved thermal and moisture stability are obtained. The resulting device shows a champion efficiency of 19.96% with negligible hysteresis. Furthermore, thermal (90 °C) and moisture (RH 40–60%) stability are improved threefold, maintaining 80% of initial efficiency after aging for 480 h. More importantly, the doped device exhibits extraordinary improvement of operational stability and remains 93% of initial efficiency under maximum power point (MPP) tracking for 540 h. 相似文献
17.
Perovskite Solar Cells: High‐Efficiency Low‐Temperature ZnO Based Perovskite Solar Cells Based on Highly Polar,Nonwetting Self‐Assembled Molecular Layers (Adv. Energy Mater. 5/2018)
下载免费PDF全文
![点击此处可从《Liver Transplantation》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Randi Azmi Wisnu Tantyo Hadmojo Septy Sinaga Chang‐Lyoul Lee Sung Cheol Yoon In Hwan Jung Sung‐Yeon Jang 《Liver Transplantation》2018,8(5)
18.
Il Jeon Jungjin Yoon Unsoo Kim Changsoo Lee Rong Xiang Ahmed Shawky Jun Xi Junseop Byeon Hyuck Mo Lee Mansoo Choi Shigeo Maruyama Yutaka Matsuo 《Liver Transplantation》2019,9(27)
Double‐walled carbon nanotubes are between single‐walled carbon nanotubes and multiwalled carbon nanotubes. They are comparable to single‐walled carbon nanotubes with respect to the light optical density, but their mechanical stability and solubility are higher. Exploiting such advantages, solution‐processed transparent electrodes are demonstrated using double‐walled carbon nanotubes and their application to perovskite solar cells is also demonstrated. Perovskite solar cells which harvest clean solar power have attracted a lot of attention as a next‐generation renewable energy source. However, their eco‐friendliness, cost, and flexibility are limited by the use of transparent oxide conductors, which are inflexible, difficult to fabricate, and made up of expensive rare metals. Solution‐processed double‐walled carbon nanotubes can replace conventional transparent electrodes to resolve such issues. Perovskite solar cells using the double‐walled carbon nanotube transparent electrodes produce an operating power conversion efficiency of 17.2% without hysteresis. As the first solution‐processed electrode‐based perovskite solar cells, this work will pave the pathway to the large‐size, low‐cost, and eco‐friendly solar devices. 相似文献
19.
20.
Ming‐Hua Li Shun‐Chang Liu Fa‐Zheng Qiu Zhen‐Yun Zhang Ding‐Jiang Xue Jin‐Song Hu 《Liver Transplantation》2020,10(21)
CsPbI2Br is emerging as a promising all‐inorganic material for perovskite solar cells (PSCs) due to its more stable lattice structure and moisture resistance compared to CsPbI3, although its device performance is still much behind this counterpart. Herein, a preannealing process is developed and systematically investigated to achieve high‐quality CsPbI2Br films by regulating the nucleation and crystallization of perovskite. The preannealing temperature and time are specifically optimized for a dopant‐free poly(3‐hexylthiophene) (P3HT)‐based device to target dopant‐induced drastic performance degradation for spiro‐OMeTAD‐based devices. The resulting P3HT‐based device exhibits comparable power conversion efficiency (PCE) to spiro‐OMeTAD‐based devices but much enhanced ambient stability with over 95% PCE after 1300 h. A diphenylamine derivative is introduced as a buffer layer to improve the energy‐level mismatch between CsPbI2Br and P3HT. A record‐high PCE of 15.50% for dopant‐free P3HT‐based CsPbI2Br PSCs is achieved by alleviating the open‐circuit voltage loss with the buffer layer. These results demonstrate that the preannealing processing together with a suitable buffer layer are applicable strategies for developing dopant‐free P3HT PSCs with high efficiency and stability. 相似文献