A novel approach for the synthesis of colloidal silver nanoprisms (AgNPrs) with controllable localized surface plasmon resonance (LSPR) via a chemical shape transformation of silver nanospheres (AgNSs) is presented. The shape conversion is carried out by feeding hydrogen peroxide (H 2 O 2 ) solution into a starchstabilized AgNS colloid under ambient conditions. Oxidative dissolution and the mild reducing action of H 2 O 2 under alkaline conditions serve as the principal reactions for the shape transformation process. After addition of H 2 O 2 , the instantaneous shape transformation events can be visualized by the naked eye through the color change of the colloid. Initial concentration of AgNSs, molar ratio of H 2 O 2 : AgNSs, H 2 O 2 injection rate, and mixing efficiency are the key parameters for controlling the LSPR wavelengths of AgNPrs as the in-plane dipole plasmon resonance can be selectively tuned across visible and near infrared regions (i.e., 460-850 nm). The obtained AgNPrs exhibited mixed geometries e.g. hexagonal, truncated triangular, rounded-tip triangular prisms, and circular disks with average bisector lengths of 30 to 120 nm and the thickness of 10 to 20 nm. A colloid of highly concentrated AgNPrs having a final concentration up to 11 mM can be produced within 10 min.
In this study, we demonstrate improved photovoltaic properties in inverted organic thin-film solar cells by simultaneous excitation of grating-coupled surface plasmons and grating-coupled waveguide modes on gold grating surfaces. The cell consists of a glass-ITO substrate/titanium dioxide/poly(3-hexylthiophene-2,5-diyl):phenyl-C61-butyric acid methyl ester/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)/gold structure. The grating structures were fabricated on P3HT:PCBM layers using a nanoimprinting technique with a PDMS stamp. The grating-structured PDMS stamps were fabricated using a DVD-R grating template with a grating pitch, Λ, of 740 nm. Reflectivity measurements made using p-polarized light clearly indicate 2 types of excitation modes, i.e., surface plasmons and waveguide modes, while s-polarized light produces only waveguide modes. Incident photon-to-current efficiency measurements exhibited increased photocurrent wavelengths corresponding to the wavelengths of surface plasmon excitations and waveguide mode excitations. Through the simultaneous excitation of surface plasmons and waveguide modes, short-circuit photocurrents in the grating-structured cells exhibited an improvement of up to 11% in the solar cells, leading to an efficiency increase of 16%.
This review provides an overview of smartphone-based SPR platforms in both reflection and transmission configurations, typical setups, and examples of their use in the analysis of chemical and biological samples.
The study on the shape evolution of metal nanoparticles (MNPs) is crucial to gain an understanding on controlling the shape and size of metal nanostructures. In this work, a detailed study on shape evolution of silver (Ag) nanospheres to nanoplates induced by hydrogen peroxide (H2O2) was performed. According to the growth mechanism of Ag nanoplates, the spectrophotometric method combined with chemometric analysis has potential to reveal the structural evolution process as observed by surface plasmon resonance phenomena. The extinction spectra of the evolving nanostructures were analyzed by factor analysis and error indicator functions. Five major components attributed to the different particle shapes and sizes were theoretically predicted. Furthermore, the concentration profiles and pure spectra of these components were resolved using multivariate curve resolution-alternative least squares (MCR-ALS) analysis. The evolution profiles show that the spherical Ag particles systematically evolved into plate structures of different sizes. Larger nanoplates were obtained when higher concentrations of H2O2 were employed. An evidence of nanoplate disintegration was observed when a large amount of H2O2 was employed. The predicted structural morphologies of each component given by chemometric calculation were in excellent agreement with those observed by transmission electron microscope (TEM) images.
Gold quantum dots (AuQDs) are employed as photosensitizers in organic thin‐film solar cells (OSCs) to improve their photoelectric conversion properties. Three types of AuQDs with different fluorescence emission wavelengths are used: blue (B‐AuQDs), green (G‐AuQDs), and red (R‐AuQDs). AuQDs are loaded into the poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) thin‐film layer of OSCs. UV–vis spectra, atomic force microscope images, current density–voltage characteristics, and impedance spectra of the fabricated devices are measured for the three aforementioned types of AuQDs. All types of AuQDs improve the photoelectric conversion properties, and the G‐AuQD‐loaded OSCs exhibit the best improvement, exhibiting an efficiency increase of 10% compared with OSCs without the AuQDs. The fluorescence/photosensitization of the AuQDs plays an important role in the enhancement of the OSCs. Finite‐difference time‐domain simulations indicate increased electric field intensity due to a small degree of AuQDs aggregation.
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