ABSTRACT
Nanostructured catalyst-integrated electrodes with remarkably reduced catalyst loadings, high catalyst utilization and facile fabrication are urgently needed to enable cost-effective, green hydrogen production via proton exchange membrane electrolyzer cells (PEMECs). Herein, benefitting from a thin seeding layer, bottom-up grown ultrathin Pt nanosheets (Pt-NSs) were first deposited on thin Ti substrates for PEMECs via a fast, template- and surfactant-free electrochemical growth process at room temperature, showing highly uniform Pt surface coverage with ultralow loadings and vertically well-aligned nanosheet morphologies. Combined with an anode-only Nafion 117 catalyst-coated membrane (CCM), the Pt-NS electrode with an ultralow loading of 0.015 mgPt cm-2 demonstrates superior cell performance to the commercial CCM (3.0 mgPt cm-2), achieving 99.5% catalyst savings and more than 237-fold higher catalyst utilization. The remarkable performance with high catalyst utilization is mainly due to the vertically well-aligned ultrathin nanosheets with good surface coverage exposing abundant active sites for the electrochemical reaction. Overall, this study not only paves a new way for optimizing the catalyst uniformity and surface coverage with ultralow loadings but also provides new insights into nanostructured electrode design and facile fabrication for highly efficient and low-cost PEMECs and other energy storage/conversion devices.
ABSTRACT
Control of electroosmotic flows in a two-layer microfluidic device with crossed channels is used to counteract Brownian diffusion in aqueous solution for three-dimensional trapping of a single nanoparticle or molecule within the probe volume of a confocal fluorescence microscope. A field programmable gate array sorts and counts photons into four channels synchronous with laser pulses in four beams focused to waists slightly offset from the center of the confocal volume and uses the counts to update voltages between the four fluidic inlets every 13.5 µs. Trapping is demonstrated for 40 nm nanoparticles for up to 240 s, 20 nm nanoparticles for up to 25 s, and single molecules of streptavidin-Alexa 647 for up to 1.2 s.
ABSTRACT
Cost-effective pharmaceutical drug discovery depends on increasing assay throughput while reducing reagent needs. To this end, we are developing an ultrasensitive, fluorescence-based platform that incorporates a nano/micro-fluidic chip with an array of closely spaced channels for parallelized optical readout of single-molecule assays. Here we describe the use of direct femtosecond laser machining to fabricate several hundred closely spaced channels on the surfaces of fused silica substrates. The channels are sealed by bonding to a microscope cover slip spin-coated with a thin film of poly(dimethylsiloxane). Single-molecule detection experiments are conducted using a custom-built, wide-field microscope. The array of channels is epi-illuminated by a line-generating red diode laser, resulting in a line focus just a few microns thick across a 500 micron field of view. A dilute aqueous solution of fluorescently labeled biomolecules is loaded into the device and fluorescence is detected with an electron-multiplying CCD camera, allowing acquisition rates up to 7 kHz for each microchannel. Matched digital filtering based on experimental parameters is used to perform an initial, rapid assessment of detected fluorescence. More detailed analysis is obtained through fluorescence correlation spectroscopy. Simulated fluorescence data is shown to agree well with experimental values.
Subject(s)
Biological Assay/methods , Microfluidic Analytical Techniques/methods , Nanotechnology/methods , Lasers , Spectrometry, FluorescenceABSTRACT
We present a multipolar tensor analysis of second-harmonic radiation from arrays of noncentrosymmetric L-shaped gold nanoparticles. Our approach is based on the fundamental differences in the radiative properties of electric dipoles and higher multipoles, which give rise to differences in the nonlinear response tensors for the reflected and transmitted second-harmonic signals. The results are analyzed by dividing the tensors into symmetric (dipolar) and antisymmetric (higher multipolar) parts between the two directions. The nonlinear response is found to be dominated by a tensor component, not resolved earlier [Phys. Rev. Lett. 98, 167403 (2007)], which is associated with chiral symmetry breaking of the sample and which also contains a strong multipolar contribution. The results are explained by a phenomenological model where asymmetrically-distributed defects on opposite sides of the particles give rise to dipolar and quadrupolar second-harmonic emission.
ABSTRACT
We provide experimental evidence of higher multipole (magnetic dipole and electric quadrupole) radiation in second-harmonic (SH) generation from arrays of metal nanoparticles. Fundamental differences in the radiative properties of electric dipoles and higher multipoles yield opposite interference effects observed in the SH intensities measured in the reflected and transmitted directions. These interference effects clearly depend on the polarization of the fundamental field, directly indicating the importance of multipole effects in the nonlinear response. We estimate that higher multipoles contribute up to 20% of the total emitted SH field amplitude for certain polarization configurations.
ABSTRACT
We demonstrate that second-harmonic generation (SHG) from arrays of non-centrosymmetric T-shaped gold nanodimers with a nanogap arises from asymmetry in the local fundamental field distribution and is not related strictly to nanogap size. Calculations show that the local field contains orthogonal polarization components not present in the exciting field, which yield the dominant SHG response. The strongest SHG responses occur through the local surface susceptibility of the particles for a fundamental field distributed asymmetrically at the particle perimeters. Weak responses result from more symmetric distributions despite high field enhancement in the nanogap. Nearly constant field enhancement persists for relatively large nanogap sizes.
ABSTRACT
We use two-beam second-harmonic generation to perform a quantitative tensor analysis of the effective dipolar surface nonlinearity and the separable multipolar bulk nonlinearity for BK7 glass. The most straightforward, self-consistent interpretation of the results is obtained when the effective surface response is assumed to have approximate Kleinman symmetry and the bulk contribution is dominated by magnetic, rather than quadrupole, effects.
ABSTRACT
The symmetry of metal nanostructures may be broken by their overall features or small-scale defects. To separate the roles of these two mechanisms in chiral symmetry breaking, we prepare gold nanostructures with chirality occurring on different levels. Linear optical measurements reveal small chiral signatures, whereas the chiral responses from second-harmonic generation are enormous. The responses of all structures are remarkably similar, suggesting that uncontrollable defects play an important role in symmetry breaking.
ABSTRACT
We present a method for determining the refractive-index profile of polymer optical fiber preforms through a direct-deflection measurement. The method is simple to use, compact, and has good resolution. The profile is obtained from the deflection data by numerically integrating the differential-ray equation for a radial refractive-index gradient. Corrections for topographical deviations are also discussed. Results for both graded-index and step-index fibers are presented.