Curvature dependent onset of quantum tunneling in subnanometer gaps.

The quantum tunneling in subnanometer gap sizes in gold dimers is studied in order to account for the dependency of the onset of quantum tunneling on the dimer's radius and accordingly the gap wall's curvature, realized in experiments. Several nanodimers both nanowires and nanospheres with various radii and gap sizes are modelled and simulated based on the quantum corrected model, determining the onset of the quantum tunneling. Results show that the onset of quantum tunneling is both dependent on the gap size as well as on the dimer's radius. As larger dimers result in larger effective conductivity volumes, the influence of the quantum tunneling begins in larger gap sizes in larger dimers.

In Situ Monitoring of Palladium-Catalyzed Chemical Reactions by Nanogap-Enhanced Raman Scattering using Single Pd Cube Dimers.

The central dilemma in label-free in situ surface-enhanced Raman scattering (SERS) for monitoring of heterogeneously catalyzed reactions is the need of plasmonically active nanostructures for signal enhancement. Here, we show that the assembly of catalytically active transition-metal nanoparticles into dimers boosts their intrinsically insufficient plasmonic activity at the monomer level by several orders of magnitude, thereby enabling the in situ SERS monitoring of various important heterogeneously catalyzed reactions at the single-dimer level. Specifically, we demonstrate that Pd nanocubes (NCs), which alone are not sufficiently plasmonically active as monomers, can act as a monometallic yet bifunctional platform with both catalytic and satisfactory plasmonic activity via controlled assembly into single dimers with an ∼1 nm gap. Computer simulations reveal that the highest enhancement factors (EFs) occur at the corners of the gap, which has important implications for the SERS-based detection of catalytic conversions: it is sufficient for molecules to come in contact with the "hot spot corners", and it is not required that they diffuse deeply into the gap. For the widely employed Pd-catalyzed Suzuki-Miyaura cross-coupling reaction, we demonstrate that such Pd NC dimers can be employed for in situ kinetic SERS monitoring, using a whole series of aryl halides as educts. Our generic approach based on the controlled assembly into dimers can easily be extended to other transition-metal nanostructures.

A fresh look at the structure of aromatic thiols on Au surfaces from theory and experiment.

A detailed study of the adsorption structure of self-assembled monolayers of 4-nitrothiophenol on the Au(111) surface was performed from a theoretical perspective via first-principles density functional theory calculations and experimentally by Raman and vibrational sum frequency spectroscopy (vSFS) with an emphasis on the molecular orientation. Simulations-including an explicit van der Waals (vdW) description-for different adsorbate structures, namely, for (3×3), (2 × 2), and (3 × 3) surface unit cells, reveal a significant tilting of the molecules toward the surface with decreasing coverage from 75° down to 32° tilt angle. vSFS suggests a tilt angle of 50°, which agrees well with the one calculated for a structure with a coverage of 0.25. Furthermore, calculated vibrational eigenvectors and spectra allowed us to identify characteristic in-plane (NO2 scissoring) and out-of-plane (C-H wagging) modes and to predict their strength in the spectrum in dependence of the adsorption geometry. We additionally performed calculations for biphenylthiol and terphenylthiol to assess the impact of multiple aromatic rings and found that vdW interactions are significantly increasing with this number, as evidenced by the absorption energy and the molecule adopting a more upright-standing geometry.

Particle Size-Dependent Onset of the Tunneling Regime in Ideal Dimers of Gold Nanospheres.

We report on the nanoparticle-size-dependent onset of quantum tunneling of electrons across the subnanometer gaps in three different sizes (30, 50, and 80 nm) of highly uniform gold nanosphere (AuNS) dimers. For precision plasmonics, the gap distance is systematically controlled at the level of single C-C bonds via a series of alkanedithiol linkers (C2-C16). Parallax-corrected high-resolution transmission electron microscope (HRTEM) imaging and subsequent tomographic reconstruction are employed to resolve the nm to subnm interparticle gap distances in AuNS dimers. Single-particle scattering experiments on three different sizes of AuNS dimers reveal that for the larger dimers the onset of quantum tunneling regime occurs at larger gap distances: 0.96 ± 0.04 nm (C6) for 80 nm, 0.83 ± 0.03 nm (C5) for 50 nm, and 0.72 ± 0.02 nm (C4) for 30 nm dimers. 2D nonlocal and quantum-corrected model (QCM) calculations qualitatively explain the physical origin for this experimental observation: the lower curvature of the larger particles leads to a higher tunneling current due to a larger effective conductivity volume in the gap. Our results have possible implications in scenarios where precise geometrical control over plasmonic properties is crucial such as in hybrid (molecule-metal) and/or quantum plasmonic devices. More importantly, this study constitutes the closest experimental results to the theory for a 3D sphere dimer system and offers a reference data set for comparison with theory/simulations.

A switchable DNA origami/plasmonic hybrid device with a precisely tuneable DNA-free interparticle gap.

We here show a reconfigurable DNA/plasmonic nanodevice with a precisely tunable and DNA-free interparticle gap. The nanodevice comprises two DNA boxes for the size-selective incorporation of nanoparticles in a face-to-face orientation and an underlying switchable DNA platform for the controlled and reversible adjustment of the interparticle distance.