聚合物/AgPt双金属纳米粒子协同作用:通过控制合成和基质集成优化等离子体耐久性。

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Abeer Fahes, Lavinia Balan, Caroline Andreazza-Vignolle, Claudia de Melo, Didier Zanghi, Pascal Andreazza
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引用次数: 0

摘要

研究人员开发了一种结合紫外线诱导聚合和超高真空原子气相沉积的创新方法,在无孔聚二丙二醇二丙烯酸酯(PDGDA)基质中合成并分散了2-3 nm的AgPt双金属纳米颗粒(BNPs),超越了传统的多孔聚合物策略。这种方法提供了前所未有的对BNPs和一般纳米合金结构特性的控制,聚合物基质在调节纳米颗粒形成、空间排列和尺寸均匀性方面起着关键作用。PDGDA基体通过空间稳定和可控扩散增强了纳米颗粒的稳定性,在长时间高温退火过程中有效地保持了小纳米颗粒尺寸(~ 2.4-2.8 nm)和低分散性(σ D/D = 0.16)。通过连续退火至320℃,纳米颗粒(NPs)的约束显著加快,这增加了聚合物链的迁移率,降低了粘度,实现了快速扩散,同时保持了聚合物基体的结构完整性。这一过程大大缩短了包埋时间,从室温下的12天到加热后的几乎瞬间包埋。成功的约束归因于关键的热力学因素,这些因素促进了聚合物网络中的界面相互作用和颗粒迁移。实验结果表明,嵌入的AgPt BNPs具有独特的紫外等离子体特性,具有长期稳定性。由于两种金属之间的协同效应,制备的AgPt纳米粒子比纯铂纳米粒子表现出明显更强的局部表面等离子体共振(LSPRs)。促进这种增强的因素包括银的高导电性和相对较低的光学损耗,电磁耦合和局部电场增强,突出了这些BNPs在先进等离子体动力学方面的潜力。本研究解决了对吸收紫外线的生物物种的表面增强拉曼散射(SERS)检测和开发更高效的广谱太阳能电池的日益增长的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymer/AgPt bimetallic nanoparticle synergy: optimizing plasmonic durability through controlled synthesis and matrix integration.

An innovative approach combining UV-induced polymerization and ultra-high vacuum (UHV) atomic vapor deposition was developed to synthesize and disperse 2-3 nm AgPt bimetallic nanoparticles (BNPs) within a non-porous poly (dipropylene glycol diacrylate) (PDGDA) matrix, surpassing conventional porous polymer strategies. This method offers unprecedented control over the structural properties of BNPs and in general nanoalloys, with the polymer matrix playing a critical role in regulating nanoparticle formation, spatial arrangement, and size uniformity. The PDGDA matrix enhances nanoparticle stability through steric stabilization and controlled diffusion, effectively maintaining small nanoparticle sizes (∼2.4-2.8 nm) and low dispersity (σ D/D = 0.16) during extended high-temperature annealing. Confinement of nanoparticles (NPs) was significantly accelerated by successive thermal annealing to 320 °C, which increased polymer chain mobility and reduced viscosity, enabling rapid diffusion while preserving the structural integrity of the polymer matrix. This process dramatically reduced the embedding time from 12 days at room temperature to near-instantaneous incorporation upon heating. Successful confinement is attributed to key thermodynamic factors that promote interfacial interactions and particle mobility within the polymer network. Experimental results reveal distinctive UV plasmonic properties of the embedded AgPt BNPs with long-term stability. The produced AgPt BNPs exhibit significantly stronger localized surface plasmon resonances (LSPRs) than pure platinum nanoparticles, attributed to synergistic effects between the two metals. Factors contributing to this enhancement include silver's high electrical conductivity and relatively low optical losses, electromagnetic coupling, and localized electric field enhancement, highlighting the potential of these BNPs for advanced plasmonics. This research addresses the growing demand for surface-enhanced Raman scattering (SERS) detection of UV-absorbing biospecies and the development of more efficient broad-spectrum solar cells.

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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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