Matricardi Cristiano, Hanske Christoph, Garcia-Pomar Juan Luis, Langer Judith, Mihi Agustín, Liz-Marzán Luis M
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC) , Campus de la UAB, 08193 Bellaterra , Catalonia , Spain.
CIC biomaGUNE and Ciber-BBN , Paseo de Miramón 182 , 20014 Donostia - San Sebastián , Spain.
ACS Nano. 2018 Aug 28;12(8):8531-8539. doi: 10.1021/acsnano.8b04073. Epub 2018 Aug 17.
Metal colloids are of great interest in the field of nanophotonics, mainly due to their morphology-dependent optical properties, but also because they are high-quality building blocks for complex plasmonic architectures. Close-packed colloidal supercrystals not only serve for investigating the rich plasmonic resonances arising in strongly coupled arrangements but also enable tailoring the optical response, on both the nano- and the macroscale. Bridging these vastly different length scales at reasonable fabrication costs has remained fundamentally challenging, but is essential for applications in sensing, photovoltaics or optoelectronics, among other fields. We present here a scalable approach to engineer plasmonic supercrystal arrays, based on the template-assisted assembly of gold nanospheres with topographically patterned polydimethylsiloxane molds. Regular square arrays of hexagonally packed supercrystals were achieved, reaching periodicities down to 400 nm and feature sizes around 200 nm, over areas up to 0.5 cm. These two-dimensional supercrystals exhibit well-defined collective plasmon modes that can be tuned from the visible through the near-infrared by simple variation of the lattice parameter. We present electromagnetic modeling of the physical origin of the underlying hybrid modes and demonstrate the application of superlattice arrays as surface-enhanced Raman scattering (SERS) spectroscopy substrates which can be tailored for a specific probe laser. We therefore investigated the influence of the lattice parameter, local degree of order, and cluster architecture to identify the optimal configuration for highly efficient SERS of a nonresonant Raman probe with 785 nm excitation.
金属胶体在纳米光子学领域备受关注,主要是由于其依赖形态的光学特性,还因为它们是构建复杂等离子体结构的优质材料。紧密堆积的胶体超晶体不仅可用于研究强耦合排列中产生的丰富等离子体共振,还能在纳米和宏观尺度上定制光学响应。以合理的制造成本跨越这些差异巨大的长度尺度,从根本上来说仍然具有挑战性,但对于传感、光伏或光电子等领域的应用至关重要。我们在此展示一种可扩展的方法来设计等离子体超晶体阵列,该方法基于用具有拓扑图案的聚二甲基硅氧烷模具对金纳米球进行模板辅助组装。实现了六方堆积超晶体的规则正方形阵列,在面积达0.5平方厘米的区域内,周期低至400纳米,特征尺寸约为200纳米。这些二维超晶体展现出定义明确的集体等离子体模式,通过简单改变晶格参数,可将其从可见光调节到近红外光。我们对潜在混合模式的物理起源进行了电磁建模,并展示了超晶格阵列作为表面增强拉曼散射(SERS)光谱学基板的应用,该基板可针对特定探测激光进行定制。因此,我们研究了晶格参数、局部有序度和簇结构的影响,以确定用于785纳米激发的非共振拉曼探针高效SERS的最佳配置。