scholarly journals Solid-State Solar Cells Based on TiO2 Nanowires and CH3NH3PbI3 Perovskite

Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 404
Author(s):  
Abdul Sami ◽  
Arsalan Ansari ◽  
Muhammad Dawood Idrees ◽  
Muhammad Musharraf Alam ◽  
Junaid Imtiaz

Perovskite inorganic-organic solar cells are fabricated as a sandwich structure of mesostructured TiO2 as electron transport layer (ETL), CH3NH3PbI3 as active material layer (AML), and Spiro-OMeTAD as hole transport layer (HTL). The crystallinity, structural morphology, and thickness of TiO2 layer play a crucial role to improve the overall device performance. The randomly distributed one dimensional (1D) TiO2 nanowires (TNWs) provide excellent light trapping with open voids for active filling of visible light absorber compared to bulk TiO2. Solid-state photovoltaic devices based on randomly distributed TNWs and CH3NH3PbI3 are fabricated with high open circuit voltage Voc of 0.91 V, with conversion efficiency (CE) of 7.4%. Mott-Schottky analysis leads to very high built-in potential (Vbi) ranging from 0.89 to 0.96 V which indicate that there is no depletion layer voltage modulation in the perovskite solar cells fabricated with TNWs of different lengths. Moreover, finite-difference time-domain (FDTD) analysis revealed larger fraction of photo-generated charges due to light trapping and distribution due to field convergence via guided modes, and improved light trapping capability at the interface of TNWs/CH3NH3PbI3 compared to bulk TiO2.

2018 ◽  
Vol 6 (29) ◽  
pp. 14255-14261 ◽  
Author(s):  
Huan Li ◽  
Guoqing Tong ◽  
Taotao Chen ◽  
Hanwen Zhu ◽  
Guopeng Li ◽  
...  

A derivative-phase CsPb2Br5 is introduced into inorganic perovskite solar cells, which will effectively eliminate interface defects, lower the energy barrier of electron transport layer and suppress the recombination at the interface of hole transport layer in the devices.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2151
Author(s):  
Syed Shah ◽  
Muhammad Sayyad ◽  
Karim Khan ◽  
Jinghua Sun ◽  
Zhongyi Guo

Application of MXene materials in perovskite solar cells (PSCs) has attracted considerable attention owing to their supreme electrical conductivity, excellent carrier mobility, adjustable surface functional groups, excellent transparency and superior mechanical properties. This article reviews the progress made so far in using Ti3C2Tx MXene materials in the building blocks of perovskite solar cells such as electrodes, hole transport layer (HTL), electron transport layer (ETL) and perovskite photoactive layer. Moreover, we provide an outlook on the exciting opportunities this recently developed field offers, and the challenges faced in effectively incorporating MXene materials in the building blocks of PSCs for better operational stability and enhanced performance.


2021 ◽  
Vol 2083 (2) ◽  
pp. 022011
Author(s):  
Rui Huang ◽  
Jiyu Tang

Abstract Perovskite solar cells have attracted the attention of the researchers in the last couple of years as a potential photovoltaic device. However, the use of expensive hole transport materials (HTM) in these devices often restricts their commercial adaptability. Thus exploring cost-effective, efficient HTL and ETL materials remain an important challenge to the researchers. In this work, simulation studies are carried out considering cupric oxide (CuO), a relatively inexpensive material as hole transport materials for planar heterojunction perovskite solar cells. The photo-voltaic performance of CuO based hole transport layer (HTL) has been estimated in combination with several electron transport materials (ETM) that include TiO2,SnO2,ZnO, CdS, ZnSe,PCBM and Cd1-xZnxS. Studies predict that among these materials, the Cd1-xZnxS electron transport layer (ETL) could be the most promising to result high photo-voltaic efficiency in combination to CuO based HTL. Also, the thickness and optical band gap of perovskite absorber are optimized in order to achieve maximum photo-voltaic efficiency. The cell efficiency of FTO / Cd1-xZnxS/CH3NH3PbI3/CuO/carbon structure is predicted 25.24% under optimized operational conditions with Voc, Jsc and Fill Factor of 1.1eV,26.32mA/cm2 and 87.14% respectively.


Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1269 ◽  
Author(s):  
Wu ◽  
Thakur ◽  
Chiang ◽  
Chandel ◽  
Wang ◽  
...  

The power conversion efficiency (PCE) of single-junction solar cells was theoretically predicted to be limited by the Shockley–Queisser limit due to the intrinsic potential loss of the photo-excited electrons in the light absorbing materials. Up to now, the optimized GaAs solar cell has the highest PCE of 29.1%, which is close to the theoretical limit of ~33%. To pursue the perfect photovoltaic performance, it is necessary to extend the lifetimes of the photo-excited carriers (hot electrons and hot holes) and to collect the hot carriers without potential loss. Thanks to the long-lived hot carriers in perovskite crystal materials, it is possible to completely convert the photon energy to electrical power when the hot electrons and hot holes can freely transport in the quantized energy levels of the electron transport layer and hole transport layer, respectively. In order to achieve the ideal PCE, the interactions between photo-excited carriers and phonons in perovskite solar cells has to be completely understood.


The researchers now days are avid of solar cells despite the efficiency issues. As lead-based halide perovskite exhibit toxic nature alternatives for the anti- toxic perovskite solar cells(PSCs) are gaining much research. Bis(sulfanylidene )tungsten is a toxic free feasible emerging option with direct band gap of value 1.8 eV. Tungsten disulfide is other chemical name of Bis(sulfanylidene)tungsten. In this paper, perovskite solar cell (PSC) with Bis(sulfanylidene)tungsten (WS2 ) as electron transport layer and spiro-OMeTAD as hole transport layer is modelled and simulated using SCAPS software to analyze performance parameters. The device simulations results are compared for comprehensive defect study of WS2 as ETL. With integration of WS2 and spiro-OMeTAD in the perovskite design, the outcomes are proficient enough with 25.96% of PCE, 22.06 mA/cm2 Jsc, 1.280V Voc and 91.76% FF. Launching the batch setup for absorber layer thickness further resulted with competent PCE 27.78%. The outcomes signified that the toxic-free WS2 based PSC can be a prominent upcoming perspective in terms of environmentally pristine nature and capitulate comparative high efficiency


Science ◽  
2021 ◽  
Vol 371 (6527) ◽  
pp. 390-395
Author(s):  
Jun Peng ◽  
Daniel Walter ◽  
Yuhao Ren ◽  
Mike Tebyetekerwa ◽  
Yiliang Wu ◽  
...  

Polymer passivation layers can improve the open-circuit voltage of perovskite solar cells when inserted at the perovskite–charge transport layer interfaces. Unfortunately, many such layers are poor conductors, leading to a trade-off between passivation quality (voltage) and series resistance (fill factor, FF). Here, we introduce a nanopatterned electron transport layer that overcomes this trade-off by modifying the spatial distribution of the passivation layer to form nanoscale localized charge transport pathways through an otherwise passivated interface, thereby providing both effective passivation and excellent charge extraction. By combining the nanopatterned electron transport layer with a dopant-free hole transport layer, we achieved a certified power conversion efficiency of 21.6% for a 1-square-centimeter cell with FF of 0.839, and demonstrate an encapsulated cell that retains ~91.7% of its initial efficiency after 1000 hours of damp heat exposure.


Nanomaterials ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1666 ◽  
Author(s):  
Jien Yang ◽  
Qiong Zhang ◽  
Jinjin Xu ◽  
Hairui Liu ◽  
Ruiping Qin ◽  
...  

Despite the successful improvement in the power conversion efficiency (PCE) of perovskite solar cells (PSCs), the issue of instability is still a serious challenge for their commercial application. The issue of the PSCs mainly originates from the decomposition of the organic–inorganic hybrid perovskite materials, which will degrade upon humidity and suffer from the thermal environment. In addition, the charge transport layers also influence the stability of the whole devices. In this study, inorganic transport layers are utilized in an inverted structure of PSCs employing CsPbIBr2 as light absorbent layer, in which nickel oxide (NiOx) and cerium oxide (CeOx) films are applied as the hole transport layer (HTL) and the electron transport layer (ETL), respectively. The inorganic transport layers are expected to protect the CsPbIBr2 film from the contact of moisture and react with the metal electrode, thus preventing degradation. The PSC with all inorganic components, inorganic perovskite and inorganic transport layers demonstrates an initial PCE of 5.60% and retains 5.56% after 600 s in ambient air at maximum power point tracking.


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