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基于高性能和环保型的钙钛矿太阳能电池的器件建模

Device modeling of high performance and eco-friendly based perovskite solar cell.

作者信息

Alipour Alireza, Alipour Hossein

机构信息

Department of Physics, Illinois Institute of Technology, Chicago, IL, 60616, USA.

Department of Electrical Engineering, Azad University of Lahijan, Lahijan, Gilan, 1616, Iran.

出版信息

Sci Rep. 2024 Jul 4;14(1):15427. doi: 10.1038/s41598-024-66485-0.

Abstract

Developing environmentally friendly and highly efficient inverted perovskite solar cells (PSCs) encounters significant challenges, specifically the potential toxicity and degradation of thin films in hybrid organic-inorganic photovoltaics (PV). We employed theoretical design strategies that produce hysteresis-reduced, efficient, and stable PSCs based on composition and interface engineering. The devices include a mixed-organic-cation perovskite formamidinium methylammonium tin iodide ( ) as an absorber layer and zinc oxide (ZnO) together with a passivation film phenyl-C61-butyric acid methyl ester ( ) as a double-electron transport layer (DETL). Furthermore, a nickel oxide (NiO) layer and a trap-free junction copper iodide (CuI) are used as a double-hole transport layer (DHTL). The optoelectronic characterization measurements were carried out to understand the physical mechanisms that govern the operation of the devices. The high power conversion efficiencies (PCEs) of 24.27% and 23.50% were achieved in 1D and 2D simulations, respectively. This study illustrates that composition and interface engineering enable eco-friendly perovskite solar cells, improving performance and advancing clean energy.

摘要

开发环境友好且高效的倒置钙钛矿太阳能电池(PSC)面临重大挑战,特别是在混合有机-无机光伏(PV)中薄膜的潜在毒性和降解问题。我们采用了基于成分和界面工程的理论设计策略,以生产具有减少滞后现象、高效且稳定的PSC。这些器件包括一种混合有机阳离子钙钛矿甲脒甲基碘化锡铵( )作为吸收层,以及氧化锌(ZnO)与钝化膜苯基-C61-丁酸甲酯( )作为双电子传输层(DETL)。此外,氧化镍(NiO)层和无陷阱结碘化铜(CuI)用作双空穴传输层(DHTL)。进行了光电特性测量,以了解控制器件运行的物理机制。在一维和二维模拟中分别实现了24.27%和23.50%的高功率转换效率(PCE)。这项研究表明,成分和界面工程能够实现环保型钙钛矿太阳能电池,提高性能并推动清洁能源发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7527/11224425/75c17e529d3e/41598_2024_66485_Fig1_HTML.jpg

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