Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive technique with molecular specificity, making it an ideal analytical tool in various fields. However, the breadth of practical applications of SERS has been severely limited because it is still a great challenge to achieve simultaneously a high sensitivity and a high reproducibility. Herein, we report a highly controllable method to fabricate periodic bowtie SERS substrates with a narrow nanogap, high SERS enhancement, and good uniformity over a large area. The periodic bowtie template is first fabricated over a gold film by holographic lithography (HL), followed by Au deposition to obtain a conductive plasmonic bowtie array. The gap size is then narrowed down by pulsed electrodeposition of Ag simultaneously monitored in situ by electrochemical dark field spectroscopy. Thus, we are able to observe the most sensitive change in the scattering spectra when the gap is just about to merge and obtain uniform SERS substrates with a gap size down to around 5 nm. The average enhancement factor of 5 × 10 7 to 1 × 10 8 is obtained, which is 50 times larger than that from Au nanoparticle-assembled substrates and 140 times larger than that from commercial Klarite chips. This substrate offers a promising opportunity for SERS practical applications.

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Terahertz (THz) sensing of molecular fingerprint enables wide applications in biomedicine and security detection. Conventional detection approaches face big barriers in trace analysis of analyte due to the difficulties of enhancing the broadband molecular absorption. In order to achieve strong broadband wave–matter interaction for the analyte, we propose a method based on THz wave angular scanning on a dielectric metagrating. In virtue of the guided-mode resonance, one can strengthen the local electric field in various trace-amount analytes by tuning the polarization and incident angle, which leads to significant enhancement on the broadband signal of molecular fingerprint. The study paves the way for more applications of THz trace-amount detection.

Time-resolved emission and scattering imaging of plume dynamics and nanoparticle ejection in femtosecond laser ablation of silver thin films

The pixel size of a charge-coupled device (CCD) camera plays a major role in the image resolution, and the square pixels are attributed to the physical anisotropy of the sampling frequency. We synthesize the high sampling frequency directions from multiple frames acquired with different angles to enhance the resolution by 1.4× over conventional CCD orthogonal sampling. To directly demonstrate the improvement of frequency-domain diagonal extension (FDDE) microscopy, lens-free microscopy is used, as its resolution is dominantly determined by the pixel size. We demonstrate the resolution enhancement with a mouse skin histological specimen and a clinical blood smear sample. Further, FDDE is extended to lens-based photography with an ISO 12233 resolution target. This method paves a new way for enhancing the image resolution for a variety of imaging techniques in which the resolution is primarily limited by the sampling pixel size, for example, microscopy, photography, and spectroscopy.

In this paper, we present a modified SOFI algorithm with enhanced temporal resolution: the required number of raw images for SOFI is reduced from hundreds to tens. The modification is intended to eliminate the low-frequency fluctuation and readout noise from the raw image stack, and is achieved by separately utilizing two wavelet-based filters in the temporal and spatial domains of the raw image stack. The high-frequency stochastic fluctuating signal could be extracted effectively, and the efficiency of SOFI could be enhanced. The modified SOFI image could be generated with 25 frames of raw images, and the corresponding acquisition time was 1.25 s.

The study reveals the field-circuit relationship for the light–matter interaction of nanostructure stacks and provides a powerful method for the quick design of functional plasmonic metamaterials.

Open-3DSIM is an open-source reconstruction platform for three-dimensional structured illumination microscopy. We demonstrate its superior performance for artifact suppression and high-fidelity reconstruction relative to other algorithms on various specimens and over a range of signal-to-noise levels. Open-3DSIM also offers the capacity to extract dipole orientation, paving a new avenue for interpreting subcellular structures in six dimensions (xyzθλt). The platform is available as MATLAB code, a Fiji plugin and an Exe application to maximize user-friendliness.