Band Diagram Insights into the Kinetic and Thermodynamic Engineering of Tandem Photocatalytic Cells.

In this work, we theoretically investigate the impact of kinetic and thermodynamic properties on the performance of photocatalytic cells operating in an unassisted tandem configuration, including electron affinity and ionization energies, recombination rates, and reaction rates. To this end, we present general rules and metrics for identifying and isolating the origin of an observed shift in the onset potential at either the photoanode or the photocathode of these devices. The correlation between kinetic and thermodynamic shifts in the onset potential is demonstrated through the use of band diagrams and key comparable features within readily accessible characterization tools: current-voltage plots are taken both under illumination and in the dark and further coupled with Mott-Schottky plots.

On the application of Marcus-Hush theory to small polaron chemical dynamics in oxides: its relationship to the Holstein model and the importance of lattice-orbital symmetries.

The chemical dynamics of small polaron hopping within oxides is often interpreted through two-site variations on Marcus-Hush theory, while from a physics perspective small polaron hopping is more often approached from Holstein's solid-state formalism. Here we seek to provide a chemically oriented viewpoint, focusing on small polaron hopping in oxides, concerning these two phenomenological frameworks by employing both tight-binding modelling and first-principles calculations. First, within a semiclassical approach the Marcus-Hush relations are overviewed as a two-site reduction of Holstein's model.

First-principles redox energy estimates under the condition of satisfying the general form of Koopmans' theorem: An atomistic study of aqueous iron.

In this work, we explore the relative accuracy to which a hybrid functional, in the context of density functional theory, may predict redox properties under the constraint of satisfying the general form of Koopmans' theorem. Taking aqueous iron as our model system within the framework of first-principles molecular dynamics, direct comparison between computed single-particle energies and experimental ionization data is assessed by both (1) tuning the degree of hybrid exchange, to satisfy the general form of Koopmans' theorem, and (2) ensuring the application of finite-size corrections. These finite-size corrections are benchmarked through classical molecular dynamics calculations, extended to large atomic ensembles, for which good convergence is obtained in the large supercell limit.

Evolution of Surface Oxidation on TaN as Probed by a Photoelectrochemical Method.

In this work, we present an in situ method to probe the evolution of photoelectrochemically driven surface oxidation on photoanodes during active operation in aqueous solutions. A standard solution of KFe(CN)-KPi was utilized to benchmark the photocurrent and assess progressive surface oxidation on TaN in various oxidizing solutions. In this manner, a proportional increase in the surface oxygen concentration was detected with respect to oxidation time and further correlated with a continuous decline in the photocurrent.

Ergodic and Nonergodic Dynamics of Oxygen Vacancy Migration at the Nanoscale in Inorganic Perovskites.

Perovskites are widely utilized either as a primary component or as a substrate in which the dynamics of charged oxygen vacancy defects play an important role. Current knowledge regarding the dynamics of vacancy mobility in perovskites is solely based upon volume- and/or time-averaged measurements. This impedes our understanding of the basic physical principles governing defect migration in inorganic materials.

Interpreting interfacial semiconductor-liquid capacitive characteristics impacted by surface states: a theoretical and experimental study of CuGaS.

Semiconductor-liquid interfaces are essential to the operation of many energy devices. Crucially, the operational characteristics of such devices are dependent upon both the flat band potential and doping concentration present in their solid-state semiconducting region. Traditionally, capacitive "linear" Mott-Schottky plots have often been utilized to extract these two parameters.

Fully Quantized Electron Transfer Observed in a Single Redox Molecule at a Metal Interface.

Long-range electron transfer is a ubiquitous process that plays an important role in electrochemistry, biochemistry, organic electronics, and single molecule electronics. Fundamentally, quantum mechanical processes, at their core, manifest through both electron tunneling and the associated transition between quantized nuclear vibronic states (intramolecular vibrational relaxation) mediated by electron-nuclear coupling. Here, we report on measurements of long-range electron transfer at the interface between a single ferrocene molecule and a gold substrate separated by a hexadecanethiol quantum tunneling barrier.

Relating Franck-Condon blockade to redox chemistry in the single-particle picture.

In this work, we explore Franck-Condon blockade in the "redox limit," where nuclear relaxation processes occur much faster than the rate of electron transfer. To this end, the quantized rate expressions for electron transfer are recast in terms of a quantized redox density of states (DOS) within a single phonon mode model. In the high temperature regime, this single-particle picture formulation of electron transfer is shown to agree well with the semi-classical rate and DOS expressions developed by Gerischer and Hopfield.

Electrical Stressing Induced Monolayer Vacancy Island Growth on TiSe.

To ensure practical applications of atomically thin transition metal dichalcogenides, it is essential to characterize their structural stability under external stimuli such as electric fields and currents. Using vacancy monolayer islands on TiSe surfaces as a model system, we have observed nonlinear area evolution and growth from triangular to hexagonal driven by scanning tunneling microscopy (STM) subjected electrical stressing. The observed growth dynamics represent a 2D departure from the linear area growth law expected for bulk vacancy clustering.

Measuring Spatially Resolved Collective Ionic Transport on Lithium Battery Cathodes Using Atomic Force Microscopy.

One of the main challenges in improving fast charging lithium-ion batteries is the development of suitable active materials for cathodes and anodes. Many materials suffer from unacceptable structural changes under high currents and/or low intrinsic conductivities. Experimental measurements are required to optimize these properties, but few techniques are able to spatially resolve ionic transport properties at small length scales.

Electron transfer from the perspective of electron transmission: Biased non-adiabatic intermolecular reactions in the single-particle picture.

In this work, we revisit Hopfield's formulation of non-adiabatic electron transfer between uncorrelated redox species within the single-particle picture description of electron transmission commonly applied in solid-state systems. The formulation is applied to a model system, similar to that often found in solid-state electron tunneling studies, consisting of redox species separated by an insulating tunneling barrier. Redox tunneling across such an insulator is predicted to demonstrate a marked asymmetry, ranging from one to three orders of magnitude between forward and reverse bias electron transfer rates, when reactants possess dissimilar reorganization energies.

The role of relative rate constants in determining surface state phenomena at semiconductor-liquid interfaces.

In this work, we present a theoretical study of surface state occupation statistics at semiconductor-liquid interfaces, as it pertains to the evolution of H and O through water splitting. Our approach combines semiclassical charge transport and electrostatics at the semiconductor-liquid junction, with a master rate equation describing surface state mediated electron/hole transfer. As a model system we have studied the TiO-water junction in the absence of illumination, where it is shown that surface states might not always equilibrate with the semiconductor.

Phase-Field-Crystal Model for Electromigration in Metal Interconnects.

We propose an atomistic model of electromigration (EM) in metals based on a recently developed phase-field-crystal (PFC) technique. By coupling the PFC model's atomic density field with an applied electric field through the EM effective charge parameter, EM is successfully captured on diffusive time scales. Our framework reproduces the well-established EM phenomena known as Black's equation and the Blech effect, and also naturally captures commonly observed phenomena such as void nucleation and migration in bulk crystals.

Interfacial Screening in Ultrafast Voltammetry: A Theoretical Study of Redox-Active Monolayers.

The impact of interfacial screening on electron transfer (ET) at ultrashort time scales is theoretically investigated on redox active monolayers by linear sweep voltammetry (LSV). The charging current associated with the nanosecond screening process is an important experimental determinant in finding both the reorganization energy (λ) and electronic coupling (|M|) through ultrafast methods. On the one hand, time dependent decay of the charging current mitigates its impact on the current contribution from faradaic processes, while on the other hand, allowing substantial decay translates into a reduced upper-bound of applicable scan rates, which are crucial for ultrafast characterization.

Emergence of Metallic Properties at LiFePO4 Surfaces and LiFePO4/Li2S Interfaces: An Ab Initio Study.

The atomic and electronic structures of the LiFePO4 (LFP) surface, both bare and reconstructed upon possible oxygenation, are theoretically studied by ab initio methods. On the basis of total energy calculations, the atomic structure of the oxygenated surface is proposed, and the effect of surface reconstruction on the electronic properties of the surface is clarified. While bare LFP(010) surface is insulating, adsorption of oxygen leads to the emergence of semimetallic behavior by inducing the conducting states in the band gap of the system.

A first principles scanning tunneling potentiometry study of an opaque graphene grain boundary in the ballistic transport regime.

We report on a theoretical interpretation of scanning tunneling potentiometry (STP), formulated within the Keldysh non-equilibrium Green's function description of quantum transport. By treating the probe tip as an electron point source/sink, it is shown that this approach provides an intuitive bridge between existing theoretical interpretations of scanning tunneling microscopy and STP. We illustrate this through ballistic transport simulations of the potential drop across an opaque graphene grain boundary, where atomistic features are predicted that might be imaged through high resolution STP measurements.

Chemically homogeneous and thermally reversible oxidation of epitaxial graphene.

With its exceptional charge mobility, graphene holds great promise for applications in next-generation electronics. In an effort to tailor its properties and interfacial characteristics, the chemical functionalization of graphene is being actively pursued. The oxidation of graphene via the Hummers method is most widely used in current studies, although the chemical inhomogeneity and irreversibility of the resulting graphene oxide compromises its use in high-performance devices.

Terminating surface electromigration at the source.

Based on an extensive search across the periodic table utilizing first-principles density functional theory, we discover phosphorus to be an optimal surface electromigration inhibitor on the technologically important Cu(111) surface--the dominant diffusion pathway in modern nanoelectronics interconnects. Unrecognized thus far, such an inhibitor is characterized by energetically favoring (and binding strongly at) the kink sites of step edges. These properties are determined to generally reside in elements that form strong covalent bonds with substrate metal atoms.

Wafer-level photocatalytic water splitting on GaN nanowire arrays grown by molecular beam epitaxy.

We report on the achievement of wafer-level photocatalytic overall water splitting on GaN nanowires grown by molecular beam epitaxy with the incorporation of Rh/Cr(2)O(3) core-shell nanostructures acting as cocatalysts, through which H(2) evolution is promoted by the noble metal core (Rh) while the water forming back reaction over Rh is effectively prevented by the Cr(2)O(3) shell O(2) diffusion barrier. The decomposition of pure water into H(2) and O(2) by GaN nanowires is confirmed to be a highly stable photocatalytic process, with the turnover number per unit time well exceeding the value of any previously reported GaN powder samples.

Formation of graphene p-n superlattices on Pb quantum wedged islands.

On the basis of first-principles calculations within density functional theory, we report on a novel scheme to create graphene p-n superlattices on Pb wedged islands with quantum stability. Pb(111) wedged islands grown on vicinal Si(111) extend over several Si steps, forming a wedged structure with atomically flat tops. The monolayer thickness variation due to the underlying substrate steps is a sizable fraction of the total thickness of the wedged islands and gives rise to a bilayer oscillation in the work function of Pb(111) due to quantum size effects.

Phenylacetylene one-dimensional nanostructures on the Si(100)-2 x 1:H surface.

Using ultrahigh vacuum (UHV) scanning tunneling microscopy (STM), many olefins have been shown to self-assemble on the hydrogen-passivated Si(100)-2 x 1 surface into one-dimensional nanostructures. This paper demonstrates that similar one-dimensional nanostructures can also be realized using alkynes. In particular, UHV STM, sum frequency generation (SFG), and density functional theory (DFT) are employed to study the growth mechanism and binding configuration of phenylacetylene (PA) one-dimensional nanostructures on the Si(100)-2 x 1:H surface.