Highly Selective Electroreduction of Carbon Dioxide Using Defect-Driven Catalysis.

The production of methanol from the electrochemical reduction of CO is a promising method of mitigating climate change while simultaneously producing a useful liquid fuel. In this study, we design self-assembled monolayers (SAMs) of thiols on metal and metal oxide electrodes that operate via cooperative catalysis between the thiolated surface sites and exposed electrode defect sites. This defect-driven mechanism enables the fabrication of SAM-modified ZnO electrodes that yield methanol with an extraordinarily high Faradaic efficiency of up to 92%.

Hybrid bilayer membranes as platforms for biomimicry and catalysis.

Hybrid bilayer membrane (HBM) platforms represent an emerging nanoscale bio-inspired interface that has broad implications in energy catalysis and smart molecular devices. An HBM contains multiple modular components that include an underlying inorganic surface with a biological layer appended on top. The inorganic interface serves as a support with robust mechanical properties that can also be decorated with functional moieties, sensing units and catalytic active sites.

Investigating Formate, Sulfate, and Halide Anions in Reversible Zinc Electrodeposition Dynamic Windows.

Reversible metal electrodeposition (RME) is an emerging and promising method for designing dynamic windows with electrically controllable transmission, excellent color neutrality, and wide dynamic range. Zn is a viable option for metal-based dynamic windows due to its fast switching kinetics and reversibility despite its very negative deposition voltage. In this manuscript, we study the effect of the supporting electrolyte anions for Zn electrodeposition on transparent tin-doped indium oxide.

Nanostructured Ni-Cu Electrocatalysts for the Oxygen Evolution Reaction.

Ni-based materials are promising electrocatalysts for the oxygen evolution reaction (OER) for water splitting in alkaline media. We report the synthesis and OER electrocatalysis of both Ni-Cu nanoparticles (20-50 nm in diameter) and Ni-Cu nanoclusters (<20 metal atoms). Analysis of mass spectral data from matrix-assisted laser desorption/ionization and electrospray ionization techniques demonstrates that discrete heterobimetallic Ni-Cu nanoclusters capped with glutathione ligands were successfully synthesized.

Hybrid Dynamic Windows with Color Neutrality and Fast Switching Using Reversible Metal Electrodeposition and Cobalt Hexacyanoferrate Electrochromism.

Dynamic windows, which electronically switch between clear and dark states on demand, save energy in buildings and automobiles by minimizing the lighting, heating, and cooling costs. In this study, we design dynamic windows by combining reversible metal electrodeposition (RME) and electrochromism, two promising approaches for optoelectronics. These hybrid dynamic windows tint on both electrodes.

Dual Tinting Dynamic Windows Using Reversible Metal Electrodeposition and Prussian Blue.

Electronically tintable windows based on reversible metal electrodeposition are a promising alternative to electrochromic materials due to the high optical contrast imparted by the opacity of thin metal films. While traditional metal-based dynamic windows utilize a metal counter electrode frame, metal electrodeposition on the working electrode must be paired with a plane-parallel counter electrode that facilitates transverse ion migration to enable uniform metal electrodeposition on a large scale. In this manuscript, we develop dynamic windows that combine reversible Bi electrodeposition on the working electrode with a Prussian blue counter electrode that acts as both a charge storage layer that intercalates K ions and an anodically coloring material.

Membrane-Modified Metal Triazole Complexes for the Electrocatalytic Reduction of Oxygen and Carbon Dioxide.

In this manuscript, an electrochemical architecture is designed that controls the kinetics of proton transfer to metal triazole complexes for electrocatalytic O and CO reduction. Self-assembled monolayers of these catalysts are attached to a glassy carbon electrode and covered with a lipid monolayer containing proton carriers, which acts as a proton-permeable membrane. The O reduction voltammograms on carbon are similar to those obtained on membrane-modified Au electrodes, which through the control of proton transfer rates, can be used to improve the selectivity of O reduction.

Controlling Proton and Electron Transfer Rates to Enhance the Activity of an Oxygen Reduction Electrocatalyst.

An electrochemical approach is developed that allows for the control of both proton and electron transfer rates in the O reduction reaction (ORR). A dinuclear Cu ORR catalyst was prepared that can be covalently attached to thiol-based self-assembled monolayers (SAMs) on Au electrodes using azide-alkyne click chemistry. Using this architecture, the electron transfer rate to the catalyst is modulated by changing the length of the SAM, and the proton transfer rate to the catalyst is controlled with an appended lipid membrane modified with proton carriers.

Effect of Concentration on the Electrochemistry and Speciation of the Magnesium Aluminum Chloride Complex Electrolyte Solution.

Magnesium batteries offer an opportunity to use naturally abundant Mg and achieve large volumetric capacities reaching over four times that of conventional Li-based intercalation anodes. High volumetric capacity is enabled by the use of a Mg metal anode in which charge is stored via electrodeposition and stripping processes, however, electrolytes that support efficient Mg electrodeposition and stripping are few and are often prepared from highly reactive compounds. One interesting electrolyte solution that supports Mg deposition and stripping without the use of highly reactive reagents is the magnesium aluminum chloride complex (MACC) electrolyte.

Proton transfer dynamics dictate quinone speciation at lipid-modified electrodes.

Proton-coupled electron transfer (PCET) reactions are ubiquitous in biochemistry and alternative energy schemes. Natural enzymes utilize quinones in proton transfer chains and energy conversion processes. Here, we utilize a bio-inspired hybrid bilayer membrane system to control the reaction mechanism of a quinone molecule covalently bound to an electrode surface.

The Flip-Flop Diffusion Mechanism across Lipids in a Hybrid Bilayer Membrane.

In this study, we examine the mechanism of flip-flop diffusion of proton carriers across the lipid layer of a hybrid bilayer membrane (HBM). The HBM consists of a lipid monolayer appended on top of a self-assembled monolayer containing a Cu-based O2 reduction catalyst on a Au electrode. The flip-flop diffusion rates of the proton carriers dictate the kinetics of O2 reduction by the electrocatalyst.

Proton transfer dynamics control the mechanism of O2 reduction by a non-precious metal electrocatalyst.

Many chemical and biological processes involve the transfer of both protons and electrons. The complex mechanistic details of these proton-coupled electron transfer (PCET) reactions require independent control of both electron and proton transfer. In this report, we make use of lipid-modified electrodes to modulate proton transport to a Cu-based catalyst that facilitates the O2 reduction reaction (ORR), a PCET process important in fuel cells and O2 reduction enzymes.

The Interplay of Al and Mg Speciation in Advanced Mg Battery Electrolyte Solutions.

Mg batteries are an attractive alternative to Li-based energy storage due to the possibility of higher volumetric capacities with the added advantage of using sustainable materials. A promising emerging electrolyte for Mg batteries is the magnesium aluminum chloride complex (MACC) which shows high Mg electrodeposition and stripping efficiencies and relatively high anodic stabilities. As prepared, MACC is inactive with respect to Mg deposition; however, efficient Mg electrodeposition can be achieved following an electrolytic conditioning process.

Photoresponsive molecular switch for regulating transmembrane proton-transfer kinetics.

To control proton delivery across biological membranes, we synthesized a photoresponsive molecular switch and incorporated it in a lipid layer. This proton gate was reversibly activated with 390 nm light (Z-isomer) and then deactivated by 360 nm irradiation (E-isomer). In a lipid layer this stimuli responsive proton gate allowed the regulation of proton flux with irradiation to a lipid-buried O2 reduction electrocatalyst.

Anion transport through lipids in a hybrid bilayer membrane.

In this report, we use a hybrid bilayer membrane (HBM) as an electrochemical platform to study anion diffusion through a lipid monolayer. We first append lipid on a self-assembled monolayer (SAM) that contains a covalently bound Cu(I)/Cu(II) redox center. We then perform cyclic voltammetry (CV) using different anions in bulk solution and extract thermodynamic and kinetic information about anion transport.

Proton switch for modulating oxygen reduction by a copper electrocatalyst embedded in a hybrid bilayer membrane.

Molecular switches gate many fundamental processes in natural and artificial systems. Here, we report the development of an electrochemical platform in which a proton carrier switches the activity of a catalyst. By incorporating an alkyl phosphate in the lipid layer of a hybrid bilayer membrane, we regulate proton transport to a Cu-based molecular oxygen reduction reaction catalyst.

Inhibiting platelet-stimulated blood coagulation by inhibition of mitochondrial respiration.

Platelets are important mediators of blood coagulation that lack nuclei, but contain mitochondria. Although the presence of mitochondria in platelets has long been recognized, platelet mitochondrial function remains largely unaddressed. On the basis of a small amount of literature that suggests platelet mitochondria are functional, we hypothesized that the inhibition of platelet mitochondria disrupts platelet function and platelet-activated blood coagulation.

Hybrid bilayer membrane: a platform to study the role of proton flux on the efficiency of oxygen reduction by a molecular electrocatalyst.

In this report, we present a novel platform to study proton-coupled electron transfer (PCET) by controlling the proton flux using an electrode-supported hybrid bilayer membrane (HBM). Oxygen reduction by an iron porphyrin was used as a model PCET reaction. The proton flux was controlled by incorporating an aliphatic proton carrier, decanoic acid, into the lipid layer of the HBM.

Ferrocene embedded in an electrode-supported hybrid lipid bilayer membrane: a model system for electrocatalysis in a biomimetic environment.

An electrode-supported system in which ferrocene molecules are embedded in a hybrid bilayer membrane (HBM) has been prepared and characterized. The redox properties of the ferrocene molecules were studied by varying the lipid and alkanethiol building blocks of the HBM. The midpoint potential and electron transfer rate of the embedded ferrocene were found to be dependent on the hydrophobic nature of the electrolyte and the distance at which the ferrocene was positioned in the HBM relative to the electrode and the solution.

Inhibition of electrocatalytic O(2) reduction of functional CcO models by competitive, non-competitive, and mixed inhibitors.

Electrocatalytic reduction of O(2) by functional cytochrome C Oxidase (CcO) models is studied in the presence of several known inhibitors like CO, N(3)(-), CN(-), and NO(2)(-). These models successfully reproduce the inhibitions observed in CcO at similar concentrations reported for these inhibitors. Importantly, the data show very different electrochemical responses depending on the nature of the inhibitor, that is, competitive, non-competitive and mixed.