Optical Extinction-Based 3D Nano-Imaging of WS on Gold.

Broadband nanoextinction images recorded in tip-enhanced optical spectroscopy geometry track the 3D topography of a single layer of WS on Au substrate. The described nano-optical method is complementary to conventional atomic force microscopy and offers additional information about the buried material-metal interface that is not accessible using conventional topographic imaging. Beyond 3D optical imaging, we observe large variations in the junction plasmon resonance on the nanoscale.

Tunable Localized Charge Transfer Excitons in Nanoplatelet-2D Chalcogenide van der Waals Heterostructures.

Observation of interlayer, charge transfer (CT) excitons in van der Waals heterostructures (vdWHs) based on 2D-2D systems has been well investigated. While conceptually interesting, these charge transfer excitons are highly delocalized and spatially localizing them requires twisting layers at very specific angles. This issue of localizing the CT excitons can be overcome via making nanoplate-2D material heterostructures (N2DHs) where one of the components is a spatially quantum confined medium.

Core/Shell-Like Localized Emission at Atomically Thin Semiconductor-Au Interface.

Localized emission in atomically thin semiconductors has sparked significant interest as single-photon sources. Despite comprehensive studies into the correlation between localized strain and exciton emission, the impacts of charge transfer on nanobubble emission remains elusive. Here, we report the observation of core/shell-like localized emission from monolayer WSe nanobubbles at room temperature through near-field studies.

Classical vs. quantum plasmon-induced molecular transformations at metallic nanojunctions.

Chemical transformations near plasmonic metals have attracted increasing attention in the past few years. Specifically, reactions occurring within plasmonic nanojunctions that can be detected via surface and tip-enhanced Raman (SER and TER) scattering were the focus of numerous reports. In this context, even though the transition between localized and nonlocal (quantum) plasmons at nanojunctions is documented, its implications on plasmonic chemistry remain poorly understood.

Controlling the Fluctuating Tip-Enhanced Raman Spectra of Chloramben on Silver Nanocubes.

Tip-enhanced Raman (TER) scattering from molecules residing at plasmonic junctions can be used to detect, identify, and image single molecules. This is most evident for flat molecules interrogated under conditions of extreme temperatures and pressure. It is also the case for (bio)molecular systems that feature preferred orientations/conformations under ambient laboratory conditions.

Chemical characterization of microplastic particles formed in airborne waste discharged from sewer pipe repairs.

Microplastic particles are of increasing environmental concern due to the widespread uncontrolled degradation of various commercial products made of plastic and their associated waste disposal. Recently, common technology used to repair sewer pipes was reported as one of the emission sources of airborne microplastics in urban areas. This research presents results of the multi-modal comprehensive chemical characterization of the microplastic particles related to waste discharged in the pipe repair process and compares particle composition with the components of uncured resin and cured plastic composite used in the process.

Subnanometer Visualization of Spatially Varying Local Field Resonances that Drive Tip-Enhanced Optical Spectroscopy.

Our knowledge of the electromagnetic fields that power modern nanoscale optical measurements, including (non)linear tip-enhanced Raman and photoluminescence, chiefly stems from numerical simulations. Aside from idealized in silico vs heterogeneous (nano)structures in the laboratory, challenges in quantitative descriptions of nanoscale light-matter interactions more generally stem from the very nature of the problem, which lies at the interface of classical and quantum theories. This is particularly the case in ultrahigh spatial resolution measurements that are sensitive to local optical field variations that take place on subnanometer length scales.

Probing Local Optical Fields via Ultralow Frequency Raman Scattering from a Corrugated Probe.

We revisit nanoscale local optical field imaging via tip-enhanced Raman scattering (TERS). Rather than taking advantage of molecular reporters to probe different aspects of the local fields, we show how ultralow frequency Raman (ULF) scattering from the (nanocorrugated) metallic probe itself can be used for the same purpose. The bright ULF-TERS response we record allows non-invasive (tapping mode feedback) local field imaging, enables visualization of the local fields of small (≥20 nm) isolated plasmonic particles, and can also be exploited to distinguish between Si and SiO domains with 5 nm spatial resolution.

Tip-Enhanced Raman Chemical and Chemical Reaction Imaging in HO with Sub-3-nm Spatial Resolution.

Reproducible chemical and chemical reaction nanoimaging at solid-liquid interfaces remains challenging, particularly when resolutions on the order of a few nanometers are sought. In this work, we demonstrate the latter through liquid-tip-enhanced Raman (TER) measurements that target gold nanoplates functionalized with 4-mercaptobenzonitrile (MBN). In addition to chemical imaging and local optical field nanovisualization with high spatial resolution, we observe the signatures of 4-mercaptobenzoic acid, which forms as a result of plasmon-induced hydrolysis of MBN.

Influence of surface and intermolecular interactions on the properties of supported polyoxometalates.

Polyoxometalates (POMs) with localized radical or open-shell metal sites have the potential to be used as transformative electronic spin based molecular qubits (MQs) for quantum computing (QC). For practical applications, MQs have to be immobilized in electronically or optically addressable arrays which introduces interactions with supports as well as neighboring POMs. Herein, we synthesized Keggin POMs with both tungsten (W) and vanadium (V) addenda atoms.

High spatial resolution ambient tip-enhanced (multipolar) Raman scattering.

This article summarizes lessons learnt from ambient tip-enhanced Raman (TER) mapping of molecules interacting with plasmonic nanostructures. It is shown that numerous physical and chemical phenomena contribute to high-resolution TER spectral images. As a result, selectively tracking interfacial chemical transformations TERS is more challenging than currently appreciated.

Ambient Tip-Enhanced Two Photon Photoluminescence from CdSe/ZnS Quantum Dots.

Nonlinear nano-optical measurements that combine ultrafast spectroscopy with tools of scanning probe microscopy are scarce. This is particularly the case when high spatial resolution on the order of a few nanometers is sought after in experiments performed under ambient laboratory conditions. In this work, we demonstrate the latter through measurements that track two-photon photoluminescence from aggregates of CdSe/ZnS quantum dots with sub-5 nm spatial resolution.

Excited-State-Selective Ultrafast Relaxation Dynamics and Photoisomerization of -4,4'-Azopyridine.

Excited-state dynamics of -4,4'-azopyridine in ethanol is studied using femtosecond transient absorption with 30 fs temporal resolution. Exciting the system at three different wavelengths, 460 and 290 (275) nm, to access the S * and S * electronic states, respectively, reveals a 195 cm vibrational coherence, which suggests that the same mode is active in both * and * relaxation channels. Following S-excitation, relaxation proceeds via a nonrotational pathway, where a fraction of the * population is trapped in a planar minimum (lifetime, 2.

Integrated photoelectrochemical energy storage cells prepared by benchtop ion soft landing.

The exceptional photochromic and redox properties of polyoxometalate anions, PWO, have been exploited to develop an integrated photoelectrochemical energy storage cell for conversion and storage of solar energy. Elimination of strongly coordinating cations using benchtop ion soft landing leads to a ∼370% increase in the maximum power output of the device. Additionally, the photocathode displayed a pronounced color change from clear to blue upon irradiation, which warrants the potential application of the IPES cell in advanced smart windows and photochromic lenses.

Nano-optical Visualization of Interlayer Interactions in WSe/WS Heterostructures.

The interplay between excitons and phonons governs the optical and electronic properties of transition metal dichalcogenides (TMDs). Even though a number of linear and nonlinear optical-, electron-, and photoelectron-based approaches have been developed and/or adopted to characterize excitons and phonons in single/few-layer TMDs and their heterostructures, no existing method is capable of directly probing ultralow-frequency and interlayer phonons on the nanoscale. To this end, we developed ultralow-frequency tip-enhanced Raman spectroscopy, which allows spectrally and spatially resolved chemical and structural nanoimaging of WSe/WS heterostructures.

A Closer Look at Tip-Enhanced Raman Chemical Reaction Nanoimages.

Tip-enhanced Raman spectroscopy (TERS) is a powerful technique that enables ultrahigh spatial resolution and ultrasensitive chemical imaging. This technique's ability to track plasmon-induced/enhanced chemical reactions in real space has gained increasing popularity in recent years. In this study, we expose inherent difficulties associated with assigning TERS signatures that accompany chemical transformations.

Tip-Enhanced Raman Scattering on Both Sides of the Schrödinger Equation.

Historically, molecular spectroscopists have focused their attention to the right-hand side of the Schrödinger equation. Our major goal had and still has to do with determining a (bio)molecular system's Hamiltonian operator. From a theoretical spectroscopist's perspective, this entails varying the parameters of a model Hamiltonian until the predicted observables agree with their experimental analogues.

Multimodal Tip-Enhanced Nonlinear Optical Nanoimaging of Plasmonic Silver Nanocubes.

Optical field localization at plasmonic tip-sample nanojunctions has enabled high-spatial-resolution chemical analysis through tip-enhanced linear optical spectroscopies, including Raman scattering and photoluminescence. Here, we illustrate that nonlinear optical processes, including parametric four-wave mixing (4WM), second-harmonic/sum-frequency generation (SHG and SFG), and two-photon photoluminescence (TPPL), can be enhanced at plasmonic junctions and spatiospectrally resolved simultaneously with few-nm spatial resolution under ambient conditions. Through a detailed analysis of our spectral nanoimages, we find that the efficiencies of the local nonlinear signals are determined by sharp tip-sample junction resonances that vary over the few-nanometer length scale.

Imaging Charged Exciton Localization in van der Waals WSe/MoSe Heterobilayers.

Exciton localization in transition-metal dichalcogenide monolayers is behind a variety of interesting phenomena and applications, including broad-spectrum solar cells and single-photon emissions. Strain fields at the periphery of topographically distinct features such as nanoscopic bubbles were recently associated with localized charge-neutral excitons. Here, we use tip-enhanced photoluminescence (PL) to visualize excitons in WSe/MoSe heterobilayers (HBL).

From SERS to TERS and Beyond: Molecules as Probes of Nanoscopic Optical Fields.

A detailed understanding of the interaction between molecules and plasmonic nanostructures is important for several exciting developments in (bio)molecular sensing and imaging, catalysis, as well as energy conversion. While much of the focus has been on the nanostructures that generate enhanced and nano-confined optical fields, we herein highlight recent work from our groups that uses the molecular response in surface and tip enhanced Raman scattering (SERS and TERS, respectively) to investigate different aspects of the local fields. TERS provides access to ultra-confined volumes, and as a result can further explore and explain ensemble-averaged SERS measurements.