Structure-Tailored Surface Oxide on Cu-Ga Intermetallics Enhances CO2 Reduction Selectivity to Methanol at Ultralow Potential.

Electrochemical CO2 reduction reaction (eCO2 RR) is performed on two intermetallic compounds formed by copper and gallium metals (CuGa2 and Cu9 Ga4 ). Among them, CuGa2 selectively converts CO2 to methanol with remarkable Faradaic efficiency of 77.26% at an extremely low potential of -0.3 V vs RHE. The high performance of CuGa2 compared to Cu9 Ga4 is driven by its unique 2D structure, which retains surface and subsurface oxide species (Ga2 O3 ) even in the reduction atmosphere. The Ga2 O3 species is mapped by X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS) techniques and electrochemical measurements. The eCO2 RR selectivity to methanol are decreased at higher potential due to the lattice expansion caused by the reduction of the Ga2 O3 , which is probed by in situ XAFS, quasi in situ powder X-ray diffraction, and ex situ XPS measurements. The mechanism of the formation of methanol is visualized by in situ infrared (IR) spectroscopy and the source of the carbon of methanol at the molecular level is confirmed from the isotope-labeling experiments in presence of 13 CO2 . Finally, to minimize the mass transport limitations and improve the overall eCO2 RR performance, a poly(tetrafluoroethylene)-based gas diffusion electrode is used in the flow cell configuration.

Unraveling the Role of Site Isolation and Support for Semihydrogenation of Phenylacetylene.

Intermetallic compounds (IMCs) composed of transition metals and post-transition metals function as superior heterogeneous catalysts in comparison to their monometallic and bimetallic alloy counterparts. Rendering IMCs in their nanomaterial iterations further enhances their efficiency. Herein, we demonstrate the role of PdIn as well-dispersed intermetallic nanoparticles (IMNPs) for the semihydrogenation of phenylacetylene selectively to styrene at ambient conditions. Higher selectivity of PdIn was explained with the help DOS calculations. We have explored the role of a few well-known silica-based supports such as SBA-15 and MCM-41, providing insight into how they affect catalysis. As an additional support we have explored previously reported JNC-1, a mesoporous carbon material obtained via a templated strategy using SBA-15. PdIn supported on SBA-15 and JNC-1 displayed the best dispersion, while also exhibiting the most catalytic activity due to the unique nature of the porous structure.