Enhanced absorption in organic solar cells using core-shell iron-ZnO nanoparticles: optical and numerical simulations

IF 2.6 4区 材料科学 Q3 CHEMISTRY, MULTIDISCIPLINARY Journal of Nanoparticle Research Pub Date : 2025-04-14 DOI:10.1007/s11051-025-06295-1
Mahdi Aghlmandi Sadigh Bagheri
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Abstract

This study utilizes the finite-difference time-domain (FDTD) method to reveal the superior potential of cuboid iron (Fe) nanoparticles (NPs) with a zinc oxide (ZnO) shell for absorption enhancement (AE) in the active layer of organic solar cells (OSCs). The dimensions and arrangement of core-shell Fe-ZnO cuboid NPs on a ZnO substrate were meticulously optimized to achieve the highest AE. Unlike other noble metals, Fe NPs maintain or improve their enhancement capabilities even as the core thickness decreases and the shell thickness increases. In the 300–700 nm wavelength range, where the P3HT:PCBM composite has an intrinsic absorption spectrum, the absorption of ZnO nanostructures devoid of a metal core is reduced to 0.9 times the intrinsic value. In contrast, the absorption of the Fe-ZnO NPs increased to 1.282 times, which is 1.13 times greater than that of the Au NPs in the same structure. Additionally, the optical \(J_{sc}\) achieved by the Fe NPs is 1.75 times greater than the intrinsic \(J_{sc}\), which is 1.26 times greater than that achieved by the Au NPs. The electric field density and absorption density profiles indicate that Fe NPs significantly enhance organic absorption through localized surface plasmon resonance (LSPR), particularly in the red spectrum (700 nm), where P3HT:PCBM has the lowest intrinsic absorption.

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利用核壳氧化铁-氧化锌纳米粒子增强有机太阳能电池的吸收:光学和数值模拟
本研究利用时域有限差分(FDTD)方法揭示了具有氧化锌(ZnO)外壳的长方体铁(Fe)纳米颗粒(NPs)在有机太阳能电池(OSCs)活性层中的吸收增强(AE)的优越潜力。在ZnO衬底上精心优化了核壳铁氧化锌长方体NPs的尺寸和排列,以获得最高的声发射。与其他贵金属不同,铁NPs在芯厚减小、壳厚增加的情况下仍能保持或提高其增强能力。在300-700 nm波长范围内,P3HT:PCBM复合材料具有本征吸收光谱,无金属芯的ZnO纳米结构的吸收降低到本征值的0.9倍。相比之下,Fe-ZnO NPs的吸收率增加到1.282倍,是相同结构下Au NPs的1.13倍。此外,铁纳米粒子获得的光学\(J_{sc}\)比本征\(J_{sc}\)大1.75倍,比金纳米粒子获得的本征大1.26倍。电场密度和吸收密度谱图表明,Fe NPs通过局部表面等离子体共振(LSPR)显著增强有机吸收,特别是在红色光谱(700 nm),其中P3HT:PCBM具有最低的本征吸收。
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来源期刊
Journal of Nanoparticle Research
Journal of Nanoparticle Research 工程技术-材料科学:综合
CiteScore
4.40
自引率
4.00%
发文量
198
审稿时长
3.9 months
期刊介绍: The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size. Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology. The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.
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