Reducing energy loss via adjusting the anode work function and perovskite layer morphology for the efficient and stable hole transporting layer-free perovskite solar cells

2021 ◽  
pp. 133948
Author(s):  
Jiankai Zhang ◽  
Yapeng Sun ◽  
Huangzhong Yu
Materials ◽  
2019 ◽  
Vol 12 (13) ◽  
pp. 2037 ◽  
Author(s):  
Siva Uthayaraj ◽  
D. Karunarathne ◽  
G. Kumara ◽  
Thanihaichelvan Murugathas ◽  
Shivatharsiny Rasalingam ◽  
...  

This study focuses on employing cuprous iodide (CuI) as a hole-transporting material (HTM) in fabricating highly efficient perovskite solar cells (PSCs). The PSCs were made in air with either CuI or 2,2′,7,7′-Tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9′-spirobifluorene (spiro-OMeTAD) as HTMs. A simple and novel pressing method was employed for incorporating CuI powder layer between perovskite layer and Pt top-contact to fabricate devices with CuI, while spiro-OMeTAD was spin-coated between perovskite layer and thermally evaporated Au top-contact to fabricate devices with spiro-OMeTAD. Under illuminations of 100 mW/cm2 with an air mass (AM) 1.5 filter in air, the average short-circuit current density (JSC) of the CuI devices was over 24 mA/cm2, which is marginally higher than that of spiro-OMeTAD devices. Higher JSC of the CuI devices can be attributed to high hole-mobility of CuI that minimizes the electron-hole recombination. However, the average power conversion efficiency (PCE) of the CuI devices were lower than that of spiro-OMeTAD devices due to slightly lower open-circuit voltage (VOC) and fill factor (FF). This is probably due to surface roughness of CuI powder. However, optimized devices with solvent-free powder pressed CuI as HTM show a promising efficiency of over 8.0 % under illuminations of 1 sun (100 mW/cm2) with an air mass 1.5 filter in air, which is the highest among the reported efficiency values for PSCs fabricated in an open environment with CuI as HTM.


Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 872 ◽  
Author(s):  
Zahra Rezay Marand ◽  
Ahmad Kermanpur ◽  
Fathallah Karimzadeh ◽  
Eva M. Barea ◽  
Ehsan Hassanabadi ◽  
...  

Inorganic hole-transporting materials (HTMs) for stable and cheap inverted perovskite-based solar cells are highly desired. In this context, NiOx, with low synthesis temperature, has been employed. However, the low conductivity and the large number of defects limit the boost of the efficiency. An approach to improve the conductivity is metal doping. In this work, we have synthesized cobalt-doped NiOx nanoparticles containing 0.75, 1, 1.25, 2.5, and 5 mol% cobalt (Co) ions to be used for the inverted planar perovskite solar cells. The best efficiency of the devices utilizing the low temperature-deposited Co-doped NiOx HTM obtained a champion photoconversion efficiency of 16.42%, with 0.75 mol% of doping. Interestingly, we demonstrated that the improvement is not from an increase of the conductivity of the NiOx film, but due to the improvement of the perovskite layer morphology. We observe that the Co-doping raises the interfacial recombination of the device but more importantly improves the perovskite morphology, enlarging grain size and reducing the density of bulk defects and the bulk recombination. In the case of 0.75 mol% of doping, the beneficial effects do not just compensate for the deleterious one but increase performance further. Therefore, 0.75 mol% Co doping results in a significant improvement in the performance of NiOx-based inverted planar perovskite solar cells, and represents a good compromise to synthesize, and deposit, the inorganic material at low temperature, without losing the performance, due to the strong impact on the structural properties of the perovskite. This work highlights the importance of the interface from two different points of view, electrical and structural, recognizing the role of a low doping Co concentration, as a key to improve the inverted perovskite-based solar cells’ performance.


2021 ◽  
Author(s):  
Yang Cheng ◽  
Quanping Wu ◽  
Ming Luo ◽  
Haolin Wang ◽  
Song Xue ◽  
...  

As the sandwiched hole transporting materials (HTMs) layers are in direct contact with up-coated perovskite layer and bottom electrode in p-i-n structured perovskite (i-PSCs), the film quality of HTMs determines...


2017 ◽  
Vol 5 (9) ◽  
pp. 4527-4534 ◽  
Author(s):  
Riski Titian Ginting ◽  
Mi-Kyoung Jeon ◽  
Kwang-Jae Lee ◽  
Won-Yong Jin ◽  
Tae-Wook Kim ◽  
...  

The penetration of moisture/O2 into the perovskite solar cells (PSCs) causes shifts of iodine distribution within the perovskite layer and facilitates diffusion of iodine towards the hole transporting layer. Interestingly, these negative effects can be prevented by a simple encapsulation process and further prolong the stability of PSCs.


Nanoscale ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 4241-4248
Author(s):  
Mengyao Hao ◽  
Weijie Chi ◽  
Zesheng Li

Newly developed organoboron HTMs show strong interface binding ability and fast charge transfer from the perovskite layer to the HTM layer.


2016 ◽  
Vol 4 (26) ◽  
pp. 10130-10134 ◽  
Author(s):  
Yong Li ◽  
Kunyuan Lu ◽  
Xufeng Ling ◽  
Jianyu Yuan ◽  
Guozhen Shi ◽  
...  

Schematic illustration of the dual function of C60–N on the perovskite layer: first, to reduce the work function of the Al electrode and second, to passivate the perovskite surface.


2018 ◽  
Vol 2 (12) ◽  
pp. 2778-2787 ◽  
Author(s):  
Ajay K. Baranwal ◽  
Hiroyuki Kanda ◽  
Naoyuki Shibayama ◽  
Seigo Ito

CuSCN and carbon pastes were printed on perovskite layer.


Nano Research ◽  
2016 ◽  
Vol 9 (6) ◽  
pp. 1600-1608 ◽  
Author(s):  
Weibo Yan ◽  
Yu Li ◽  
Senyun Ye ◽  
Yunlong Li ◽  
Haixia Rao ◽  
...  

2019 ◽  
Vol 5 (6) ◽  
pp. eaaw2543 ◽  
Author(s):  
Yuhang Liu ◽  
Seckin Akin ◽  
Linfeng Pan ◽  
Ryusuke Uchida ◽  
Neha Arora ◽  
...  

Preventing the degradation of metal perovskite solar cells (PSCs) by humid air poses a substantial challenge for their future deployment. We introduce here a two-dimensional (2D) A2PbI4 perovskite layer using pentafluorophenylethylammonium (FEA) as a fluoroarene cation inserted between the 3D light-harvesting perovskite film and the hole-transporting material (HTM). The perfluorinated benzene moiety confers an ultrahydrophobic character to the spacer layer, protecting the perovskite light-harvesting material from ambient moisture while mitigating ionic diffusion in the device. Unsealed 3D/2D PSCs retain 90% of their efficiency during photovoltaic operation for 1000 hours in humid air under simulated sunlight. Remarkably, the 2D layer also enhances interfacial hole extraction, suppressing nonradiative carrier recombination and enabling a power conversion efficiency (PCE) >22%, the highest reported for 3D/2D architectures. Our new approach provides water- and heat-resistant operationally stable PSCs with a record-level PCE.


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