Ultrafast Two-Electron Transfer in a CdS Quantum Dot-Extended-Viologen Cyclophane Complex.

Time-resolved optical spectroscopies reveal multielectron transfer from the biexcitonic state of a CdS quantum dot to an adsorbed tetracationic compound cyclobis(4,4'-(1,4-phenylene) bipyridin-1-ium-1,4-phenylene-bis(methylene)) (ExBox(4+)) to form both the ExBox(3+•) and the doubly reduced ExBox(2(+•)) states from a single laser pulse. Electron transfer in the single-exciton regime occurs in 1 ps. At higher excitation powers the second electron transfer takes ∼5 ps, which leads to a mixture of redox states of the acceptor ligand. The doubly reduced ExBox(2(+•)) state has a lifetime of ∼10 ns, while CdS(+•):ExBox(3+•) recombines with multiple time constants, the longest of which is ∼300 µs. The long-lived charge separation and ability to accumulate multiple charges on ExBox(4+) demonstrate the potential of the CdS:ExBox(4+) complex to serve as a platform for two-electron photocatalysis.

Photocatalytic Conversion of Nitrobenzene to Aniline through Sequential Proton-Coupled One-Electron Transfers from a Cadmium Sulfide Quantum Dot.

This paper describes the use of cadmium sulfide quantum dots (CdS QDs) as visible-light photocatalysts for the reduction of nitrobenzene to aniline through six sequential photoinduced, proton-coupled electron transfers. At pH 3.6-4.3, the internal quantum yield of photons-to-reducing electrons is 37.1% over 54 h of illumination, with no apparent decrease in catalyst activity. Monitoring of the QD exciton by transient absorption reveals that, for each step in the catalytic cycle, the sacrificial reductant, 3-mercaptopropionic acid, scavenges the excitonic hole in ∼5 ps to form QD(•-); electron transfer to nitrobenzene or the intermediates nitrosobenzene and phenylhydroxylamine then occurs on the nanosecond time scale. The rate constants for the single-electron transfer reactions are correlated with the driving forces for the corresponding proton-coupled electron transfers. This result suggests, but does not prove, that electron transfer, not proton transfer, is rate-limiting for these reactions. Nuclear magnetic resonance analysis of the QD-molecule systems shows that the photoproduct aniline, left unprotonated, serves as a poison for the QD catalyst by adsorbing to its surface. Performing the reaction at an acidic pH not only encourages aniline to desorb but also increases the probability of protonated intermediates; the latter effect probably ensures that recruitment of protons is not rate-limiting.

Mechanisms for adsorption of methyl viologen on CdS quantum dots.

This paper describes the surface composition-dependent binding of the dichloride salt of methyl viologen (MV2+) to CdS quantum dots (QDs) enriched, to various degrees, with either Cd or S at the surface. The degree of enrichment is controlled synthetically and by postsynthetic dilution of the QDs in their solvent, THF. NMR shows the Cd-enriched QDs to contain a relatively dense (2.8 ligands/nm2) surface layer of oleic acid, in the form of Cd-oleate, and S-enriched QDs to contain relatively sparse (1.0 ligands/nm2) surface density of native ligands containing both oleic acid and octadecene. Electron transfer-mediated photoluminescence quenching of the QDs by MV2+ serves as a probe for the binding affinity of MV2+ for the surfaces of the QDs. Diluting Cd-enriched QDs removes Cd-oleate from the surface, exposing the stoichiometric CdS surface beneath and increasing the quenching efficiency of MV2+, whereas diluting S-enriched QD does not change their surface chemistry or the efficiency with which they are quenched by MV2+. The photoluminescence quenching data for all of the surface chemistries we studied fit well to a Langmuir model that accounts for binding of MV2+ through two reaction mechanisms: (i) direct adsorption of MV2+ to exposed stoichiometric CdS surfaces (with an equilibrium adsorption constant of 1.5×10(5) M(-1)), and (ii) adsorption of MV2+ to stoichiometric CdS surfaces upon displacement of weakly bound Cd-oleate complexes (with an equilibrium displacement constant of 3.5×10(3) M(-1)). Ab initio calculations of the binding energy for adsorption of the dichloride salt of MV2+ on Cd- and S-terminated surfaces reveal a substantial preference of MV2+ for S-terminated lattices due to alignment of the positively charged nitrogens on MV2+ with the negatively charged sulfur. These findings suggest a strategy to maximize the adsorption of redox-active molecules in electron transfer-active geometries through synthetic and postsynthetic manipulation of the inorganic surface.

Norrish Type I surface photochemistry for butyrophenone on TiO2(110).

The photofragmentation of butyrophenone yields benzoate and a propyl radical on oxidized TiO2(110). Oxygen dissociates in native oxygen vacancies to produce reactive oxygen adatoms which react with butyrophenone to create photoactive butyrophenone-O complexes that are sensitive to hole oxidation created upon UV illumination. The same O adatoms also trap one of the primary photoproducts, phenyl-CO, to produce benzoate. The reaction proceeds via a Norrish Type I like process involving α-CC cleavage on the surface, in contrast to the gas phase where a Norrish Type II pathway predominates. The mechanism is probed using mass spectrometry and, for the first time, scanning tunneling microscopy (STM). Our STM experiments show that there is a 1-to-1 correspondence between the immobile butyrophenone-O complex and formation of a benzoate on the surface. We also demonstrate that the benzoate species is in close proximity to the original butyrophenone complex, indicating that benzoate is produced on a time scale more rapid than diffusion of the photoproducts. While the photoproducts of butyrophenone decomposition are similar to ketone oxidation reported previously, butyrophenone reacts via a different starting ground state, based on STM and density functional theory studies. Specifically, butyrophenone does not produce a dioxyalkylene species, which has been proposed to be the photoactive state for other ketones. Based on a combination of STM experiments and density functional theory, we propose that a peroxy-like configuration where the oxygen adatom stabilizes the butyrophenone through its carbonyl oxygen is the surface intermediate that photodecomposes. These results demonstrate the importance of the excited state in determining the photochemistry of ketones on surfaces.

Sequential photo-oxidation of methanol to methyl formate on TiO2(110).

Methyl formate is produced from the photo-oxidation of methanol on preoxidized TiO(2)(110). We demonstrate that two consecutive photo-oxidation steps lead to methyl formate using mass spectrometry and scanning tunneling microscopy. The first step in methanol oxidation is formation of methoxy by the thermal dissociation of the O-H bond to yield adsorbed CH(3)O and water. Formaldehyde is produced via hole-mediated oxidation of adsorbed methoxy in the first photochemical step. Next, transient HCO is made photochemically from formaldehyde. The HCO couples with residual methoxy on the surface to yield methyl formate. Exposure of the titania surface to O(2) is required for these photo-oxidation steps in order to heal surface and near-surface defects that can serve as hole traps. Notably, residual O adatoms are not required for photochemical production of methyl formate or formaldehyde. All O adatoms react thermally with methanol to form methoxy and gaseous water at rt, leaving a surface devoid of O adatoms. The mechanism provides insight into the photochemistry of TiO(2) and suggests general synthetic pathways that are the result of the ability to activate both alkoxides and aldehydes using photons.

Butyrophenone on O-TiO2(110): one-dimensional motion in a weakly confined potential well.

We demonstrate the one-dimensional confinement of weakly bound butyrophenone molecules between strongly bound complexes formed via reaction with oxygen on TiO(2)(110). Butyrophenone weakly bound to Ti rows through the carbonyl oxygen diffuses freely in one dimension along the rows even at 55 K, persisting for many minutes before hopping out of the 1-D well. Quantitative analysis yields an estimate of the migration barrier of 0.11 eV and a frequency factor of 6.5 × 10(9) Hz. These studies demonstrate that weakly bound organic molecules can be confined on a surface by creating molecular barriers, potentially altering their assembly.

Molecular imaging of reductive coupling reactions: interstitial-mediated coupling of benzaldehyde on reduced TiO2(110).

We report the first visualization of a reactive intermediate formed from coupling two molecules on a surface-a diolate formed from benzaldehyde coupling on TiO(2)(110). The diolate, imaged using scanning tunneling microscopy (STM), is reduced to gaseous stilbene upon heating to ∼400 K, leaving behind two oxygen atoms that react with reduced Ti interstitials that migrate to the surface, contrary to the popular expectation that strong bonds in oxygenated molecules react only with oxygen vacancies at the surface. Our work further provides both experimental and theoretical evidence that Ti interstitials drive the formation of diolate intermediates. Initially mobile monomers migrate together to form paired features, identified as diolates that bond over two adjacent five-coordiante Ti atoms on the surface. Our work is of broad importance because it demonstrates the possibility of imaging the distribution and bonding configurations of reactant species on a molecular scale, which is a critical part of understanding surface reactions and the development of surface morphology during the course of reaction.

McMurry chemistry on TiO(2)(110): Reductive C=C coupling of benzaldehyde driven by titanium interstitials.

Selective reductive coupling of benzaldehyde to stilbene is driven by subsurface Ti interstitials on vacuum-reduced TiO(2)(110). A combination of temperature-programmed reaction spectroscopy and scanning tunneling microscopy (STM) provides chemical and structural information which together reveal the dependence of this surface reaction on bulk titanium interstitials. Benzaldehyde reductively couples to stilbene with 100% selectivity and conversions of up to 28% of the adsorbed monolayer in temperature programmed reaction experiments. The activity for coupling was sustained for at least 20 reaction cycles, which indicates that there is a reservoir of Ti interstitials available for reaction and that surface O vacancies alone do not account for the coupling. Reactivity was unchanged after predosing with water so as to fill surface oxygen vacancies, which are not solely responsible for the coupling reaction. The reaction is nearly quenched if O(2) is adsorbed first-a procedure that both fills defects and reacts with Ti interstitials as they migrate to the surface. New titania islands form after reductive coupling of benzaldehyde, based on scanning tunneling microscope images obtained after exposure of TiO(2)(110) to benzaldehyde followed by annealing, providing direct evidence for migration of subsurface Ti interstitials to create reactive sites. The reliance of the benzaldehyde coupling on subsurface defects, and not surface vacancies, over reduced TiO(2)(110), may be general for other reductive processes induced by reducible oxides. The possible role of subsurface, reduced Ti interstitials has broad significance in modeling oxide-based catalysis with reduced crystals.

Adsorption, interaction, and manipulation of dibutyl sulfide on cu{111}.

This paper describes a low-temperature scanning tunneling microscopy (STM) study of a simple thioether, dibutyl sulfide, on a Cu{111} surface. The literature is full of data about thiol-based monolayers; however, relatively little is known about thioether self-assembly. Thioethers are more resilient to oxidation than thiols and offer the potential for control over nanoscale assembly in two dimensions parallel to the surface. Therefore, robust assembly schemes derived from thioethers may offer a new class of self-assembled systems with novel and useful properties. At a medium surface coverage and a temperature of 78 K, dibutyl sulfide grows in small, highly ordered islands in which the ordering is driven by both the molecule-surface dative bonds and intermolecular van der Waals bonding. Annealing to around 120 K allows diffusion and reordering of the molecules and the formation of large, very well ordered domains with little or no defects. We show high-resolution images of the molecular arrays and propose a model for their packing structure. These data suggest the potential use of thioethers for a variety of self-assembly applications that require control over molecular spacing parallel to the surface. We also show how the STM tip can be used to manipulate individual molecules within the ordered structures and that the arrays can act as a nanoscale abacus. The range of motion of the manipulated molecules inside a regular array reflects the potential imposed upon them by their neighbors.

Dimethyl sulfide on Cu{111}: molecular self-assembly and submolecular resolution imaging.

The literature contains many studies of thiol-based, self-assembled monolayers (RSH); however, thioethers (RSR) have barely begun to be explored, despite having the potential advantages of being more resistant to oxidation and allowing for the control of self-assembly parallel to the surface. This paper describes a low-temperature scanning tunneling microscopy investigation of dimethyl sulfide on Cu{111}. Previous work on the adsorption of dibutyl sulfide on Cu{111} revealed that intermolecular van der Waals interactions directed the parallel ordering of dibutyl sulfide molecules in linear rows. Upon annealing to 120 K, small dibutyl sulfide domains reordered into very large, ordered domains free of defects. The current study reveals the effect of the shorter alkyl chain length of dimethyl sulfide on both the rate of diffusion and the packing structure of the molecule. At a medium surface coverage and at 78 K, it was found that dimethyl sulfide is mobile and forms large, ordered islands without the 120 K annealing that was required for dibutyl sulfide to arrange. Also, the molecular packing structure evolves from quadrupole-quadrupole interactions and results in a perpendicular arrangement of neighboring molecules instead of the parallel arrangement observed for dibutyl sulfide. We show high-resolution images of the dimethyl sulfide islands in which submolecular features are revealed. These high-resolution data allow us to propose a structural model for the adsorption site of each dimethyl sulfide molecule within the ordered structures. These results demonstrate that the length of the alkyl side chain is an important factor in determining how thioethers self-assemble on metal surfaces.

Extraordinary atomic mobility of Au{111} at 80 Kelvin: effect of styrene adsorption.

We describe how the presence of styrene, a weakly adsorbed molecule, dramatically restructures the Au{111} surface at temperatures as low as 80 K. The restructuring manifests itself both in mobility of step-edge atoms, as well as changes in the position of the herringbone reconstruction over time. These effects are explained in terms of the preferential adsorption sites of styrene allowing it to assist in atom detachment from step edges, as well as lowering of the energetic barrier for movement of the herringbone reconstruction. This work has important consequences for studies in which Au is used as a support for or as an electrical contact to molecules.