Tip-enhanced
Raman scattering (TERS) is a promising optical and
analytical technique for chemical imaging and sensing at single molecule
resolution. In particular, TERS signals generated by a gap-mode configuration
where a silver tip is coupled with a gold substrate can resolve a
single-stranded DNA (ssDNA) molecule with a spatial resolution below
1 nm. To demonstrate the proof of subnanometer resolution, we show
direct nucleic acid sequencing using TERS of a phage ssDNA (M13mp18).
M13mp18 provides a known sequence and, through our deposition strategy,
can be stretched (uncoiled) and attached to the substrate by its phosphate
groups, while exposing its nucleobases to the tip. After deposition,
we scan the silver tip along the ssDNA and collect TERS signals with
a step of 0.5 nm, comparable to the bond length between two adjacent
DNA bases. By demonstrating the real-time profiling of a ssDNA configuration
and furthermore, with unique TERS signals of monomeric units of other
biopolymers, we anticipate that this technique can be extended to
the high-resolution imaging of various nanostructures as well as the
direct sequencing of other important biopolymers including RNA, polysaccharides,
and polypeptides.
Monitoring and controlling the neutral and charged excitons (trions) in two-dimensional (2D) materials are essential for the development of high-performance devices. However, nanoscale control is challenging because of diffraction-limited spatial resolution of conventional far-field techniques. Here, we extend the classical tip-enhanced photoluminescence based on tip-substrate nanocavity to quantum regime and demonstrate controlled nano-optical imaging, namely, tip-enhanced quantum plasmonics. In addition to improving the spatial resolution, we use the scanning probe to control the optoelectronic response of monolayer WS2 by varying the neutral/charged exciton ratio via charge tunneling in Au-Ag picocavity. We observe trion “hot spots” generated by varying the picometer-scale probe-sample distance and show the effects of weak and strong coupling, which depend on the spatial location. Our experimental results are in agreement with simulations and open an unprecedented view of a new range of quantum plasmonic phenomena with 2D materials that will help to design new quantum optoelectronic devices.
The timing of formation of the low‐gradient, internally drained landscape of the Tibetan Plateau is fundamental to understanding the evolution of the plateau as a whole. Well‐dated sedimentary records of internal drainage of rivers into lakes are used to reveal the timing of this evolution. Here we redate the youngest continental sedimentary successions of central Tibet in the Lunpola Basin and propose a new age range of ca. 35 to 9 Ma, significantly younger than previously thought. We demonstrate long‐standing internal drainage in central Tibet since the late Eocene and stable sedimentary environments, source regions, and low topographic relief since at least the early Miocene. We suggest that sediment aggradation of internal drainage and reduction of hillslope gradients by erosion dominate the formation of low‐relief landscapes and that the late Cenozoic drainage basins in central Tibet developed in response to flow in the lower crust and/or mantle lithosphere.
Lateral flow assay (LFA) has long been used as a biomarker detection technique. It has advantages such as low cost, rapid readout, portability, and ease of use. However, its qualitative readout process and lack of sensitivity are limiting factors. We report a photon-counting approach to accurately quantify LFAs while enhancing sensitivity. In particular, we demonstrate that the density of SARS-CoV-2 antibodies can be quantified and measured with an enhanced sensitivity using this simple laser optical analysis.
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