贵金属纳米颗粒的表面等离子共振研究

通过修正的Mie理论分别对单金属Ag、单金属Cu和Cu核Ag壳纳米颗粒/玻璃复合材料的吸收光谱进行了理论计算.计算结果表明,对单金属Ag纳米颗粒/玻璃复合材料,Ag的吸收峰位于425nm左右,不随颗粒尺寸变化而发生偏移;对单金属Cu纳米颗粒/玻璃复合材料,Cu的吸收峰也不随尺寸变化发生偏移但强度较弱;对Cu核Ag壳纳米...     

Visualizing Plasmon Coupling in Closely Spaced Chains of Ag Nanoparticles by Electron Energy‐Loss Spectroscopy

Anisotropic plasmon coupling in closely spaced chains of Ag nanoparticles is visualized using electron energy‐loss spectroscopy in a scanning transmission electron microscope. For dimers as the simplest chain, mapping the plasmon excitations with nanometer spatial resolution and an energy resolution of 0.27 eV intuitively identifies two coupling plasmons. The in‐phase mode redshifts from the ultraviolet region as the interparticle spacing is reduced, reaching the visible range at 2.7 eV. Calculations based on the discrete‐dipole approximation confirm its optical activeness, where the longitudinal direction is constructed as the path for light transportation. Two coupling paths are then observed in an inflexed four‐particle chain.     

Enhancing Photodynamic Therapy through Resonance Energy Transfer Constructed Near‐Infrared Photosensitized Nanoparticles

Photodynamic therapy (PDT) is an important cancer treatment modality due to its minimally invasive nature. However, the efficiency of existing PDT drug molecules in the deep‐tissue‐penetrable near‐infrared (NIR) region has been the major hurdle that has hindered further development and clinical usage of PDT. Thus, herein a strategy is presented to utilize a resonance energy transfer (RET) mechanism to construct a novel dyad photosensitizer which is able to dramatically boost NIR photon utility and enhance singlet oxygen generation. In this work, the energy donor moiety (distyryl‐BODIPY) is connected to a photosensitizer (i.e., diiodo‐distyryl‐BODIPY) to form a dyad molecule ( RET‐BDP ). The resulting RET‐BDP shows significantly enhanced absorption and singlet oxygen efficiency relative to that of the acceptor moiety of the photosensitizer alone in the NIR range. After being encapsulated with biodegradable copolymer pluronic F‐127‐folic acid (F‐127‐FA), RET‐BDP molecules can form uniform and small organic nanoparticles that are water soluble and tumor targetable. Used in conjunction with an exceptionally low‐power NIR LED light irradiation (10 mW cm^?2), these nanoparticles show superior tumor‐targeted therapeutic PDT effects against cancer cells both in vitro and in vivo relative to unmodified photosensitizers. This study offers a new method to expand the options for designing NIR‐absorbing photosensitizers for future clinical cancer treatments.     

High Spatial Resolution Mapping of Localized Surface Plasmon Resonances in Single Gallium Nanoparticles

Plasmonics has emerged as an attractive field driving the development of optical systems in order to control and exploit light–matter interactions. The increasing interest around plasmonic systems is pushing the research of alternative plasmonic materials, spreading the operability range from IR to UV. Within this context, gallium appears as an ideal candidate, potentially active within a broad spectral range (UV–VIS–IR), whose optical properties are scarcely reported. Importantly, the smart design of active plasmonic materials requires their characterization at high spatial and spectral resolution to access the optical fingerprint of individual nanostructures, attainable by transmission electron microscopy techniques (i.e., by means of electron energy‐loss spectroscopy, EELS). Therefore, the optical response of individual Ga nanoparticles (NPs) by means of EELS measurements is analyzed, in order to spread the understanding of the plasmonic response of Ga NPs. The results show that single Ga NPs may support several plasmon modes, whose nature is extensively discussed.     

Dominance of Plasmonic Resonant Energy Transfer over Direct Electron Transfer in Substantially Enhanced Water Oxidation Activity of BiVO4 by Shape‐Controlled Au Nanoparticles

The performance of plasmonic Au nanostructure/metal oxide heterointerface shows great promise in enhancing photoactivity, due to its ability to confine light to the small volume inside the semiconductor and modify the interfacial electronic band structure. While the shape control of Au nanoparticles (NPs) is crucial for moderate bandgap semiconductors, because plasmonic resonance by interband excitations overlaps above the absorption edge of semiconductors, its critical role in water splitting is still not fully understood. Here, first, the plasmonic effects of shape‐controlled Au NPs on bismuth vanadate (BiVO₄) are studied, and a largely enhanced photoactivity of BiVO₄ is reported by introducing the octahedral Au NPs. The octahedral Au NP/BiVO₄ achieves 2.4 mA cm^?2 at the 1.23 V versus reversible hydrogen electrode, which is the threefold enhancement compared to BiVO₄. It is the highest value among the previously reported plasmonic Au NPs/BiVO₄. Improved photoactivity is attributed to the localized surface plasmon resonance; direct electron transfer (DET), plasmonic resonant energy transfer (PRET). The PRET can be stressed over DET when considering the moderate bandgap semiconductor. Enhanced water oxidation induced by the shape‐controlled Au NPs is applicable to moderate semiconductors, and shows a systematic study to explore new efficient plasmonic solar water splitting cells.     

Sensitivity Tuning through Additive Heterogeneous Plasmon Coupling between 3D Assembled Plasmonic Nanoparticle and Nanocup Arrays

Plasmonic substrates have fixed sensitivity once the geometry of the structure is defined. In order to improve the sensitivity, significant research effort has been focused on designing new plasmonic structures, which involves high fabrication costs; however, a method is reported for improving sensitivity not by redesigning the structure but by simply assembling plasmonic nanoparticles (NPs) near the evanescent field of the underlying 3D plasmonic nanostructure. Here, a nanoscale Lycurgus cup array (nanoLCA) is employed as a base colorimetric plasmonic substrate and an assembly template. Compared to the nanoLCA, the NP assembled nanoLCA (NP‐nanoLCA) exhibits much higher sensitivity for both bulk refractive index sensing and biotin–streptavidin binding detection. The limit of detection of the NP‐nanoLCA is at least ten times smaller when detecting biotin–streptavidin conjugation. The numerical calculations confirm the importance of the additive plasmon coupling between the NPs and the nanoLCA for a denser and stronger electric field in the same 3D volumetric space. Tunable sensitivity is accomplished by controlling the number of NPs in each nanocup, or the number density of the hot spots. This simple yet scalable and cost‐effective method of using additive heterogeneous plasmon coupling effects will benefit various chemical, medical, and environmental plasmon‐based sensors.     

真空镀膜法制备纳米铝颗粒膜及其表面等离激元共振特性研究

采用直流磁控溅射镀膜技术制备了纳米铝颗粒膜,并尝试通过两种方式获得纳米铝的表面等离激元共振吸收峰,一种是先在室温石英基底上沉积纳米铝,再进行真空退火;另一种是在热石英基底上沉积纳米铝。用透射电镜和扫描电子显微镜、X-射线光电子谱、紫外-可见吸收光谱表征了样品的形貌和晶态结构、成份和吸收特性。采用比对的方式,研究了基底温度、沉积时间对两种方法制备的纳米铝表面等离激元共振的影响。结果表明,先沉积纳米铝,再进行真空退火,不能获得表面等离激元共振吸收峰,而在热基底上沉积纳米铝,可以获得明显的表面等离激元共振吸收峰。通过调控沉积时间和沉积温度实现了纳米铝表面等离激元共振峰从紫外光区到可见光区的可控移动。而且,研究发现对于平均厚度大于3 nm的纳米铝薄膜,由于纳米铝氧化具有自限性,其表面等离激元共振特性在空气中稳定且主要取决于纳米铝颗粒的团聚度。本研究对理解纳米铝表面等离激元共振特性及其应用具有指导意义。     

Modulating the Charge Transfer Plasmon in Bridged Au Core-Satellite Homometallic Nanostructures

The localized surface plasmon resonance (LSPR) is one of the important properties for noble metal nanoparticles. Tuning the LSPR on demand thus has attracted tremendous interest. Beyond the size and shape control, manipulating intraparticle coupling is an effective way to tailor their LSPR. The charge transfer plasmon (CTP) is the most important mode of conductive coupling between subunits linked by conductive bridges that are well studied for structures prepared on substrates by lithography method. However, the colloidal synthesis of CTP structure remains a great challenge. This work reports the colloidal synthesis of extraordinary bridged Au core-satellite structures by exploiting the buffer effect of polydopamine shell on Au core for Au atom diffusion, in which the Au bridge is well controlled in terms of width and length. Benefiting from the tunable Au bridges, the resonance energy of the CTP can be readily controlled. As a result, the LSPR absorptions of the core-satellite structures are continuously tuned within the NIR spectral range (from 900 to >1300 nm), demonstrating their great potentials for ultrafast nano-optics and biomedical applications.     

Colloidal Gold Nanorings and Their Plasmon Coupling with Gold Nanospheres

Gold nanorings are attractive as plasmonic metal nanocrystals because they have a hollow inner cavity. Their enhanced electric field inside the ring cavity is accessible, which is highly desirable for assembling with other optical components and studying their plasmon‐coupling behaviors. However, the lack of robust methods for synthesizing size‐controllable and uniform Au nanorings severely impedes the study of their attractive plasmonic properties and plasmon‐driven applications. Herein, an improved wet‐chemistry method is reported for the synthesis of monodisperse colloidal Au nanorings. Using circular Au nanodisks with different thicknesses and diameters as templates, Au nanorings are synthesized with thicknesses varied from ≈30 to ≈50 nm and cavity sizes varied from ≈90 to ≈40 nm. The produced Au nanorings are assembled with colloidal Au nanospheres to yield Au nanoring–nanosphere heterodimers in sphere‐in‐ring and sphere‐on‐ring configurations on substrates. The sphere‐in‐ring heterodimers exhibit the interesting feature of plasmonic Fano resonance upon the excitation of the dark quadrupolar plasmon mode of the Au nanorings. The open cavity in a nanoring holds a great promise for studying plasmon‐coupled systems, which will facilitate the construction of advanced metamaterials and high‐performance Fano‐based devices.     

基于表面等离子共振GGBP胺耦合绑定的葡萄糖浓度测量影响因素

人体组织液中的葡萄糖浓度与血糖浓度密切相关,微创血糖检测通过测量组织液中的葡萄糖浓度来预测血糖浓度,而组织液中成分复杂,利用对葡萄糖有特异性吸附作用的D-半乳糖／D-葡萄糖结合蛋白（GGBP）胺耦合绑定修饰表面等离子共振（SPR）传感器可以实现葡萄糖选择性测量．但是由于测量过程复杂,需要对影响测量精度的因素进行评价,确定最佳测量条件,以微型SPR传感器为核心搭建了一套葡萄糖浓度测量系统,系统地分析研究了GGBP胺耦合绑定SPR葡萄糖浓度测量过程中的各种影响因素,在不同实验条件下进行了测量实验,获得了蛋白质纯化、蛋白质活性、基线、流速、传质效应、温度和气泡等对测量结果的影响机制,提出了相应的解决方案,优化了测量流程．为标准化和小型化仪器开发提供重要依据．     

Correct Spectral Conversion between Surface‐Enhanced Raman and Plasmon Resonance Scattering from Nanoparticle Dimers for Single‐Molecule Detection

Simultaneous measurement of surface‐enhanced Raman scattering (SERS) and localized surface plasmon resonance (LSPR) in nanoparticle dimers presents outstanding opportunities in molecular identification and in the elucidation of physical properties, such as the size, distance, and deformation of target species. SERS–LSPR instrumentation exists and has been used under limited conditions, but the extraction of SERS and LSPR readouts from a single measurement is still a challenge. Herein, the extraction of LSPR spectra from SERS signals is reported and a tool for measuring the interparticle distance from Raman enhancement data by the standardization of the SERS signal is proposed. The SERS nanoruler mechanism incorporates two important aspects (the LSPR scattering peak shift and the Raman shift for measuring interparticle distance), and signifies their exact one‐to‐one correspondence after spectral correction. The developed methodology is applied to calculate the interparticle distance between nanoparticle dimers from SERS signals, to detect and quantify DNA at the single‐molecule level in a base‐pair‐specific manner. It is also shown that the SERS nanoruler concept can be used in structural analysis for the specific detection of the interaction of immunoglobulin G (IgG) with its target from bianalyte Raman signals with identical shaping at single‐molecule resolution. The SERS profile shaping approach not only offers a new detection mechanism for single molecules, but also has excellent potential for studying protein interactions and the intracellular detection of mRNA.     

Upconversion Luminescence Resonance Energy Transfer (LRET)‐Based Biosensor for Rapid and Ultrasensitive Detection of Avian Influenza Virus H7 Subtype

Avian influenza viruses (AIV) with good adaptation and various mutations have threatened both human and animals’ health. The H7 subtypes have the potential to cause pandemic threats to human health due to the highly pathogenic characteristics. Therefore, it is quite urgent to develop a novel biosensor for rapid and sensitive detection of H7 subtypes. In this work, a biosensor based on luminescence resonance energy transfer (LRET) from BaGdF₅:Yb/Er upconversion nanoparticles (UCNPs) to gold nanoparticles (AuNPs) has been developed for rapid and sensitive H7 subtypes detection. The amino modified capture oligonucleotide probes are covalently linked to poly(ethylenimine) (PEI) modified BaGdF₅:Yb/Er UCNPs. The thiol modified oligonucleotides with H7 hemagglutinin gene sequence are conjugated to surfaces of AuNPs. The hybridization process between complementary strands of H7 Hemagglutinin gene and its probe brings the energy donor and acceptor into close proximity, leading to the quenching of fluorescence of UCNPs. A linear response is obtained ranging from 10 pm to 10 nm and the limit of detection (LOD) is around 7 pm with detection time around 2 hours. This biosensor is expected to be a valuable diagnostic tool for rapid and sensitive detection of AIV.