Stabilizing the Ag Electrode and Reducing J–V Hysteresis through Suppression of Iodide Migration in Perovskite Solar Cells

2017 ◽  
Vol 9 (41) ◽  
pp. 36338-36349 ◽  
Author(s):  
Jiangzhao Chen ◽  
Donghwa Lee ◽  
Nam-Gyu Park
Solar RRL ◽  
2018 ◽  
Vol 2 (9) ◽  
pp. 1800118 ◽  
Author(s):  
Jie Wang ◽  
Xiaolian Chen ◽  
Fangyuan Jiang ◽  
Qun Luo ◽  
Lianping Zhang ◽  
...  

Solar RRL ◽  
2018 ◽  
Vol 2 (9) ◽  
pp. 1870207 ◽  
Author(s):  
Jie Wang ◽  
Xiaolian Chen ◽  
Fangyuan Jiang ◽  
Qun Luo ◽  
Lianping Zhang ◽  
...  

2019 ◽  
Vol 198 ◽  
pp. 11-18 ◽  
Author(s):  
Liangxin Zhu ◽  
Chong Chen ◽  
Yujuan Weng ◽  
Fumin Li ◽  
Qiang Lou

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3463
Author(s):  
Mohammad Aminul Islam ◽  
Hamidreza Mohafez ◽  
Khan Sobayel ◽  
Sharifah Fatmadiana Wan Muhamad Hatta ◽  
Abul Kalam Mahmud Hasan ◽  
...  

Perovskite solar cells (PSCs) have already achieved efficiencies of over 25%; however, their instability and degradation in the operational environment have prevented them from becoming commercially viable. Understanding the degradation mechanism, as well as improving the fabrication technique for achieving high-quality perovskite films, is crucial to overcoming these shortcomings. In this study, we investigated details in the changes of physical properties associated with the degradation and/or decomposition of perovskite films and solar cells using XRD, FESEM, EDX, UV-Vis, Hall-effect, and current-voltage (I-V) measurement techniques. The dissociation, as well as the intensity of perovskite peaks, have been observed as an impact of film degradation by humidity. The decomposition rate of perovskite film has been estimated from the structural and optical changes. The performance degradation of novel planner structure PSCs has been investigated in detail. The PSCs were fabricated in-room ambient using candle soot carbon and screen-printed Ag electrode. It was found that until the perovskite film decomposed by 30%, the film properties and cell efficiency remained stable.


2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Dazheng Chen ◽  
Shangzheng Pang ◽  
Weidong Zhu ◽  
Hongxiao Zhang ◽  
Long Zhou ◽  
...  

Four-terminal tandem solar cells employing a perovskite top cell and crystalline silicon (Si) bottom cell offer a simpler pathway to surpass the efficiency limit of market-leading single-junction silicon solar cells. To obtain cost-effective top cells, it is crucial to develop transparent conductive electrodes with low parasitic absorption and manufacturing cost. The commonly used indium tin oxide (ITO) shows some drawbacks, like the increasing prices and high-energy magnetron sputtering process. Transparent metal electrodes are promising candidates owing to the simple evaporation process, facile process conditions, and high conductivity, and the cheaper silver (Ag) electrode with lower parasitic absorption than gold may be the better choice. In this work, efficient semitransparent perovskite solar cells (PSCs) were firstly developed by adopting the composite cathode of an ultrathin Ag electrode at its percolation threshold thickness (11 nm), a molybdenum oxide optical coupling layer, and a bathocuproine interfacial layer. The resulting power conversion efficiency (PCE) is 13.38% when the PSC is illuminated from the ITO side and the PCE is 8.34% from the Ag side, and no obvious current hysteresis can be observed. Furthermore, by stacking an industrial Si bottom cell (PCE = 14.2%) to build a four-terminal architecture, the overall PCEs of 17.03% (ITO side) and 11.60% (Ag side) can be obtained, which are 27% and 39% higher, respectively, than those of the perovskite top cell. Also, the PCE of the tandem cell has exceeded that of the reference Si solar cell by about 20%. This work provides an outlook to fabricate high-performance solar cells via the cost-effective pathway.


2021 ◽  
Vol 58 (1) ◽  
pp. 53-69
Author(s):  
I. Kaulachs ◽  
A. Ivanova ◽  
A. Holsts ◽  
M. Roze ◽  
A. Flerov ◽  
...  

AbstractThe main drawback of the methylammonium lead halide perovskite solar cells is their degradation in ambient atmosphere. To investigate ambient-air-induced cell degradation, spectral dependencies of open-circuit voltage (VOC), fill factor (FF) and the power conversion efficiency (PCE) have been acquired (for the first time reported in literature).Our custom-made measurement system allowed us to perform measurements of the abovementioned entities in situ directly in vacuum during and after thermal deposition of the electrode. We also studied how these parameters in vacuum changed after cell exposure to ambient air for 85 min (50 nm top electrode) and for 180 min (100 nm top Ag electrode). For fresh CH3NH3PbI3–xClx cell (never been in open air) with very high shunt resistance of 3·107 Ω·cm2 (with practically no shorts and therefore FF could be determined mainly by charge carrier recombination processes) we found that FF in vacuum increased along with an increase of the incident photon energy from 0.55 at 760 nm up to 0.82 at 400 nm. Hypothesis considering hot polaron participation in charge carrier photogeneration and recombination processes as well as another competing hypothesis were offered as possible explanations for the observed FF increase.The kinetics of short-circuit photocurrent EQE with a change in pressure was also investigated. It was also shown that perovskite solar cell degradation could be noticeably reduced by increasing the top Ag electrode thickness to at least 100 nm, which could possibly facilitate the usual encapsulation process.


Nanoscale ◽  
2019 ◽  
Vol 11 (45) ◽  
pp. 21824-21833 ◽  
Author(s):  
Jyoti V. Patil ◽  
Sawanta S. Mali ◽  
Chang Kook Hong

Controlling the grain size of the organic–inorganic perovskite thin films using thiourea additives now crossing 2 μm size with >20% power conversion efficiency.


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