Facile deposition of FeNi/Ni hybrid nanoflower electrocatalysts for effective and sustained water oxidation.

Bimetallic iron-nickel (FeNi) compounds are widely studied materials for the oxygen evolution reaction (OER) owing to their high electrocatalytic performance and low cost. In this work, we produced thin films of the FeNi alloy on nickel foam (NF) by using an aerosol-assisted chemical deposition (AACVD) method and examined their OER catalytic activity. The hybrid FeNi/Ni catalysts obtained after 1 and 2 h of AACVD deposition show improved charge transfer and kinetics for the OER due to the strong interface between the FeNi alloy and Ni support. The FeNi/Ni-2h catalyst has higher catalytic activity than the FeNi/Ni-1h catalyst because of its nanoflower morphology that provides a large surface area and numerous active sites for the OER. Therefore, the FeNi/Ni-2h catalyst exhibits low overpotentials of 300 and 340 mV at 50 and 500 mA cm-2 respectively, and excellent stability over 100 h, and ∼0% loss after 5000 cycles in 1 M KOH electrolyte. Furthermore, this catalyst has a small Tafel slope, low charge transfer resistance and high current exchange density and thus surpasses the benchmark IrO2 catalyst. The easy, simple, and scalable AACVD method is an effective way to develop thin film electrocatalysts with high activity and stability.

Low Overpotential Electrochemical Reduction of CO2 to Ethanol Enabled by Cu/CuxO Nanoparticles Embedded in Nitrogen-Doped Carbon Cuboids.

The electrochemical conversion of CO2 into value-added chemicals is a promising approach for addressing environmental and energy supply problems. In this study, electrochemical CO2 catalysis to ethanol is achieved using incorporated Cu/CuxO nanoparticles into nitrogenous porous carbon cuboids. Pyrolysis of the coordinated Cu cations with nitrogen heterocycles allowed Cu nanoparticles to detach from the coordination complex but remain dispersed throughout the porous carbon cuboids. The heterogeneous composite Cu/CuxO-PCC-0h electrocatalyst reduced CO2 to ethanol at low overpotential in 0.5 M KHCO3, exhibiting maximum ethanol faradaic efficiency of 50% at -0.5 V vs. reversible hydrogen electrode. Such electrochemical performance can be ascribed to the synergy between pyridinic nitrogen species, Cu/CuxO nanoparticles, and porous carbon morphology, together providing efficient CO2 diffusion, activation, and intermediates stabilization. This was supported by the notably high electrochemically active surface area, rich porosity, and efficient charge transfer properties.

Electrochemical Reduction of CO2 to C1 and C2 Liquid Products on Copper-Decorated Nitrogen-Doped Carbon Nanosheets.

Due to the significant rise in atmospheric carbon dioxide (CO2) concentration and its detrimental environmental effects, the electrochemical CO2 conversion to valuable liquid products has received great interest. In this work, the copper-melamine complex was used to synthesize copper-based electrocatalysts comprising copper nanoparticles decorating thin layers of nitrogen-doped carbon nanosheets (Cu/NC). The as-prepared electrocatalysts were characterized by XRD, SEM, EDX, and TEM and investigated in the electrochemical CO2 reduction reaction (ECO2RR) to useful liquid products. The electrochemical CO2 reduction reaction was carried out in two compartments of an electrochemical H-Cell, using 0.5 M potassium bicarbonate (KHCO3) as an electrolyte; nuclear magnetic resonance (1H NMR) was used to analyze and quantify the liquid products. The electrode prepared at 700 °C (Cu/NC-700) exhibited the best dispersion for the copper nanoparticles on the carbon nanosheets (compared to Cu/NC-600 & Cu/NC-800), highest current density, highest electrochemical surface area, highest electrical conductivity, and excellent stability and faradic efficiency (FE) towards overall liquid products of 56.9% for formate and acetate at the potential of -0.8V vs. Reversible Hydrogen Electrode (RHE).

Electrochemical Reduction of CO2: A Review of Cobalt Based Catalysts for Carbon Dioxide Conversion to Fuels.

Electrochemical CO2 reduction reaction (CO2RR) provides a promising approach to curbing harmful emissions contributing to global warming. However, several challenges hinder the commercialization of this technology, including high overpotentials, electrode instability, and low Faradic efficiencies of desirable products. Several materials have been developed to overcome these challenges. This mini-review discusses the recent performance of various cobalt (Co) electrocatalysts, including Co-single atom, Co-multi metals, Co-complexes, Co-based metal-organic frameworks (MOFs), Co-based covalent organic frameworks (COFs), Co-nitrides, and Co-oxides. These materials are reviewed with respect to their stability of facilitating CO2 conversion to valuable products, and a summary of the current literature is highlighted, along with future perspectives for the development of efficient CO2RR.

Interconnected Hollow Cobalt Phosphide Grown on Carbon Nanotubes for Hydrogen Evolution Reaction.

Transition-metal phosphides are deemed as potential alternative to platinum for large-scale and sustainable electrocatalytic hydrogen production from water. In this study, facile preparation of interconnected hollow cobalt monophosphide (CoP) supported on carbon nanotubes is demonstrated and evaluated as a low-cost electrocatalyst for hydrogen evolution reaction. Hexamethylenetetramine is used as a structure-directing agent to guide the formation of interconnected cobalt oxide, which further grows into interconnected hollow CoP. Interconnected and hollow microstructural artifacts impart benign attributes, such as enhanced specific and electrochemically active surface area, low intrinsic charge transfer resistance, high interfacial charge transfer kinetics, and improved mass transport, to the electrocatalyst. As a result, the as-prepared electrode exhibits remarkable electrocatalytic performance, low onset (18 mV) and overpotential (η10 = 73 mV); small Tafel slope (54.6 mV dec-1); and high turnover frequency (0.58 s-1 at η = 73 mV). In addition, the electrode shows excellent electrochemical stability.