Ultrafast dynamics of the dipole moment reversal in a polar organic monolayer.

Pyridine layers on Cu(110) possess a strong electric field due to the large dipole of adsorbed pyridine. This electric field is visible as an enhanced sum frequency response from both the copper surface electrons and the aromatic C-H stretch of pyridine via a third order susceptibility. In response to a visible pump pulse, both surface electron and C-H stretch sum frequency signals are reduced on a subpicosecond time scale. In addition, the relative phase between the two signals changes over a few hundred femtoseconds, which indicates a change in the electronic structure of the adsorbate. We explain the transients as a consequence of the previously observed pyridine dipole field reversal when the pump pulse excites electrons into the pyridine π* orbital. The pyridine anions in the pyridine layer cause a large-scale structural change which alters the pyridine-copper bond, reflected in the altered sum frequency response.

Detection of Metal-Molecule-Metal Junction Formation by Surface Enhanced Raman Spectroscopy.

Vibrational modes play a key role in characterizing metal-molecule-metal junctions, but their detection currently either requires single-molecule sensitivity or the generation of defect-free large-scale junctions. Here we demonstrate that surface-enhanced Raman scattering (SERS) on nonideal surfaces can provide a significant amount of information despite many defects in the layer. We determine the vibrational signature of the molecular electronic junction for palladium ions complexed and reduced on 4-mercaptopyridine adsorbed on rough gold and gold nanoparticles using SERS and density functional theory. We show that these nonideal surfaces can be used to probe kinetics of metal ion complexation and establish the success of electrochemical metallization. SERS on nonideal surfaces is thus revealed as a useful tool to rapidly establish the key process parameters in making molecular electronic junctions before embarking on more detailed studies on single molecules or single crystal surfaces.

Discrimination between hydrogen bonding and protonation in the spectra of a surface-enhanced Raman sensor.

We investigate the surface-enhanced Raman spectra of 4-mercaptopyridine on gold in a variety of acids. 4-Mercaptopyridine is a known pH sensor which exhibits characteristic spectral changes when the pH is changed. Here we show with the help of experiment and density functional calculations that the ring breathing mode is also highly sensitive to hydrogen bonding. Its spectral signature is a broad band with up to three contributions from free, protonated and hydrogen-bonded 4-mercaptopyridine. Unlike pyridine in solution, where protonation leads to a higher ring breathing frequency than hydrogen-bonding, we find that protonated adsorbed 4-mercaptopyridine possesses a frequency which is lower than the corresponding hydrogen-bonded species. The Raman spectra indicate an orientation change of the aromatic ring in acidic solutions, which could be caused by a cation/π interaction between protonated and deprotonated 4-mercaptopyridine. As the frequencies of the three species are well separated, adsorbed 4-mercaptopyridine can probe more complex changes in the solution environment than just pH.

Desorption of CO from individual ruthenium porphyrin molecules on a copper surface via an inelastic tunnelling process.

The coordination of CO to metalloporphyrins changes their electronic and magnetic properties. Here we locally desorb CO molecules from a single ruthenium tetraphenylporphyrin carbonyl (CO-RuTPP) on Cu(110) using STM. The desorption is triggered by the injection of holes into the occupied states of the adsorbate using an unusual two-carrier process.

Stabilization of Insulin by Adsorption on a Hydrophobic Silane Self-Assembled Monolayer.

The interaction between many proteins and hydrophobic functionalized surfaces is known to induce ß-sheet and amyloid fibril formation. In particular, insulin has served as a model peptide to understand such fibrillation, but the early stages of insulin misfolding and the influence of the surface have not been followed in detail under the acidic conditions relevant to the synthesis and purification of insulin. Here we compare the adsorption of human insulin on a hydrophobic (-CH3-terminated) silane self-assembled monolayer to a hydrophilic (-NH3(+)-terminated) layer. We monitor the secondary structure of insulin with Fourier transform infrared attenuated total reflection and side-chain orientation with sum frequency spectroscopy. Adsorbed insulin retains a close-to-native secondary structure on both hydrophobic and hydrophilic surfaces for extended periods at room temperature and converts to a ß-sheet-rich structure only at elevated temperature. We propose that the known acid stabilization of human insulin and the protection of the aggregation-prone hydrophobic domains on the insulin monomer by adsorption on the hydrophobic surface work together to inhibit fibril formation at room temperature.

Coverage dependent non-adiabaticity of CO on a copper surface.

We have studied the coverage-dependent energy transfer dynamics between hot electrons and CO on Cu(110) with femtosecond visible pump, sum frequency probe spectroscopy. We find that transients of the C-O stretch frequency display a red shift, which increases from 3 cm(-1) at 0.1 ML to 9 cm(-1) at 0.77 ML. Analysis of the transients reveals that the non-adiabatic coupling between the adsorbate vibrational motion and the electrons becomes stronger with increasing coverage. This trend requires the frustrated rotational mode to be the cause of the non-adiabatic behavior, even for relatively weak laser excitation of the adsorbate. We attribute the coverage dependence to both an increase in the adsorbate electronic density of states and an increasingly anharmonic potential energy surface caused by repulsive interactions between neighboring CO adsorbates. This work thus reveals adsorbate-adsorbate interactions as a new way to control adsorbate non-adiabaticity.

Hot hole-induced dissociation of NO dimers on a copper surface.

We use reflection-absorption infrared spectroscopy (RAIRS) to study the photochemistry of NO on Cu(110) in the UV-visible range. We observe that the only photoactive species of NO on Cu(110) is the NO dimer, which is asymmetrically bound to the surface. RAIRS shows that photoinduced dissociation proceeds via breaking of the weak N-N bond of the dimer, photodesorbing one NO(g) to the gas phase and leaving one NO(ads) adsorbed on the surface in a metastable atop position. We model the measured wavelength-dependent cross sections assuming both electron- and hole-induced processes and find that the photochemistry can be described by either electron attachment to a level 0.3 eV above the Fermi energy E(F) or hole attachment to a level 2.2 eV below E(F). While there is no experimental or theoretical evidence for an electron attachment level so close to E(F), an occupied NO-related molecular orbital is known to exist at E(F) - 2.52 eV on the Cu(111) surface [I. Kinoshita, A. Misu, and T. Munakata, J. Chem. Phys. 102, 2970 (1995)]. We, therefore, propose that photoinduced dissociation of NO dimers on Cu(110) in the visible wavelength region proceeds by the creation of hot holes at the top of the copper d-band.

Real-time infrared detection of cyanide flip on silver-alumina NOx removal catalyst.

Spectroscopic studies of the mechanistic steps that occur on supported precious metal catalysts used in industrial and automotive applications are hampered by a dearth of suitable experimental methods. We used femtosecond laser excitation followed by nanosecond time-resolved in situ Fourier-transform infrared spectroscopy to initiate a catalytic reaction on alumina-supported silver catalysts, which are of interest in minimizing nitrogen oxide emissions from fuel-efficient lean-burn engines. We found that the key intermediate step in the reaction between carbon monoxide and nitric oxide is the flip of a cyanide group from a silver nanoparticle to the alumina support (with a lifetime of 2 microseconds), which indicates the central role played by the interface between the metal particle and the oxide support.

The determination of an inhomogeneous linewidth for a strongly coupled adsorbate system.

We present a set of experiments that provide a complete mapping of coherent and incoherent vibrational relaxation times for a molecule on a metal surface, CO/Ir{111}. Included is the first detection of a midinfrared photon echo from a metallic surface, some 15 years after the analogous measurement on a semiconductor surface, which sets a precedent for the ability to manipulate and rephase polarization on a subpicosecond time scale on surfaces. For the C-O stretch in a strongly dipole-coupled CO layer we obtain a total linewidth of 5.6 cm-1, composed of a homogeneous width of 2.7 cm-1 and an inhomogeneous contribution of 3.0 cm-1. Pure dephasing is negligible at liquid nitrogen temperatures, making CO/Ir{111} an attractive model system for quantum computing.

Real-time observation of nonadiabatic surface dynamics: the first picosecond in the dissociation of NO on iridium.

Ultrafast laser pulses on Ir{111} cause a highly temperature-dependent redshift of the intramolecular stretch frequency of adsorbed NO. The time-resolved spectral changes are driven by charge transfer of hot electrons to the NO 2pi*d antibonding orbital, which leads to bending of NO and internal bond weakening. The nonadiabatic change in the NO adsorption geometry follows the charge transfer within a time scale of 700 femtoseconds. This geometrical change is the same as the mechanism predicted for thermally induced dissociation.

Broadband femtosecond sum-frequency spectroscopy of CO on Ru1010 in the frequency and time domains.

CO on Ru[1010] was investigated by broadband femtosecond sum-frequency spectroscopy at 200 K. Approximately half of the frequency shift of 71 cm(-1) over the coverage range from 0.15 to 1.22 monolayers is shown to originate from dipole-dipole coupling, with the remainder due to a chemical shift. Despite low adlayer-surface registration at the highest coverages, the linewidth of the C-O stretch is comparatively low, and is described by homogeneous broadening according to sum-frequency free-induction decay measurements in the time domain. This can be explained by the dominance of the CO dipole coupling strength over the static disorder present in a coincidence structure. As the coverage decreases below 0.3 monolayer, the linewidth increases considerably, indicative of inhomogeneous broadening. Supported by a concomitant frequency change we suggest that at low coverages CO molecules form chains of irregular length in the [0001] direction, as has been shown for other surfaces with similar symmetry.