Highly Efficient Electrochemical Nitrate and Nitrogen Reduction to Ammonia under Ambient Conditions on Electrodeposited Cu‐Nanosphere Electrode

Highly Efficient Electrochemical Nitrate and Nitrogen Reduction to Ammonia under Ambient Conditions on Electrodeposited Cu-Nanosphere Electrode

Cu-nanosphere film with a high surface area and dominant (200) facet was fabricated by a simple electrodeposition method. The Cu-nanosphere achieved excellent nitrate reduction reaction (NO3RR), and nitrogen reduction reaction (NRR) performance. The dominance of the Cu (200) facet of the Cu-nanosphere electrocatalyst suppresses the competing hydrogen evolution reaction (HER) and thus exhibits better electrochemical NO3RR and NRR selectivity.


Abstract

The electrochemical reduction reaction of nitrogenous species such as NO3 (NO3RR) and N2 (NRR) is a promising strategy for producing ammonia under ambient conditions. However, low activity and poor selectivity of both NO3RR and NRR remain the biggest problem of all current electrocatalysts. In this work, we fabricated Cu-nanosphere film with a high surface area and dominant with a Cu(200) facet by simple electrodeposition method. The Cu-nanosphere film exhibits high electrocatalytic activity for NO3RR and NRR to ammonia under ambient conditions. In the nitrate environment, the Cu-nanosphere electrode reduced NO3 to yield NH3 at a rate of 5.2 mg/h cm2, with a Faradaic efficiency of 85 % at −1.3 V. In the N2-saturated environment, the Cu-nanosphere electrode reduced N2 to yield NH3 with the highest yield rate of 16.2 μg/h cm2 at −0.5 V, and the highest NH3 Faradaic efficiency of 41.6 % at −0.4 V. Furthermore, the Cu-nanosphere exhibits excellent stability with the NH3 yield rate, and the Faradaic efficiency remains stable after 10 consecutive cycles. Such high levels of NH3 yield, selectivity, and stability at low applied potential are among the best values currently reported in the literature.

Effect of Copper Oxide Nanoparticles on the Performance of Polyvinyl Chloride Membranes

Effect of Copper Oxide Nanoparticles on the Performance of Polyvinyl Chloride Membranes

The strong trade-off between water flux and rejection is a challenge for polymeric membranes. The effect of CuO nanoparticles on the properties and performance of a polyvinyl chloride membrane for removal of bovine serum albumin (BSA) from contaminated surface water is evaluated. A positive impact in terms of surface porosity, permeation flux, antifouling performance, and BSA rejection could be stated.


Abstract

Polyvinyl chloride (PVC)/copper oxide (CuO) nanocomposite membranes were fabricated at different CuO nanoparticles loading levels using the phase inversion method. The fabricated membranes were tested through two filtration cycles in a submerged membrane system to remove bovine serum albumin (BSA) from water. Results showed that the hydrophilicity and porosity of the nanocomposite membranes were enhanced with an increase of CuO nanoparticles loading. The field emission electron microscopy images from the membrane surface demonstrated that the number and size of pores increased with addition of CuO nanoparticles. The atomic force microscopy test displayed that all nanocomposite membranes showed lower surface roughness in comparison to neat PVC membranes. The obtained results from membrane performance indicated that the irreversible fouling ratio for neat PVC membranes in the first and second cycles of filtration decreased for PVC/CuO-1.5 membranes. Compared with the neat PVC membrane, the membrane containing CuO exhibited better capabilities such as the enhanced permeation flux, higher BSA rejection rate, and better antifouling properties.