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Free-standing membrane incorporating single-atom catalysts for ultrafast electroreduction of low-concentration nitrate

The release of wastewaters containing relatively low levels of nitrate (NO 3 ⁻) results in sufficient contamination to induce harmful algal blooms and to elevate drinking water NO 3 ⁻ concentrations to potentially hazardous levels. In particular, the facile triggering of algal blooms by ultra-low concentrations of NO 3 ⁻ necessitates the development of efficient methods for NO 3 ⁻ destruction. However, promising electrochemical methods suffer from weak mass transport under low reactant concentrations, resulting in long treatment times (on the order of hours) for complete NO 3 ⁻ destruction. In this study, we present flow-through electrofiltration via an electrified membrane incorporating nonprecious metal single-atom catalysts for NO 3 ⁻ reduction activity enhancement and selectivity modification, achieving near-complete removal of ultra-low concentration NO 3 ⁻ (10 mg-N L -1 ) with a residence time of only a few seconds (10 s). By anchoring Cu single atoms supported on N-doped carbon in a carbon nanotube interwoven framework, we fabricate a free-standing carbonaceous membrane featuring high conductivity, permeability, and flexibility. The membrane achieves over 97% NO 3 ⁻ removal with high N 2 selectivity of 86% in a single-pass electrofiltration, which is a significant improvement over flow-by operation (30% NO 3 ⁻ removal with 7% N 2 selectivity). This high NO 3 ⁻ reduction performance is attributed to the greater adsorption and transport of nitric oxide under high molecular collision frequency coupled with a balanced supply of atomic hydrogen through H 2 dissociation during electrofiltration. Overall, our findings provide a paradigm of applying a flow-through electrified membrane incorporating single-atom catalysts to improve the rate and selectivity of NO 3 ⁻ reduction for efficient water purification.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Materials Data on Mg3N2 by Materials Project

Mg3N2 is Corundum-like structured and crystallizes in the cubic Ia-3 space group. The structure is three-dimensional. Mg2+ is bonded to four N3- atoms to form a mixture of corner and edge-sharing MgN4 tetrahedra. There are a spread of Mg–N bond distances ranging from 2.10–2.20 Å. There are two inequivalent N3- sites. In the first N3- site, N3- is bonded to six equivalent Mg2+ atoms to form a mixture of corner and edge-sharing NMg6 octahedra. The corner-sharing octahedral tilt angles are 55°. In the second N3- site, N3- is bonded to six equivalent Mg2+ atoms to form a mixture of distorted corner and edge-sharing NMg6 octahedra. The corner-sharing octahedra tilt angles range from 55–56°.

36 MATERIALS SCIENCE↗

Materials Data on Mg3N by Materials Project

Mg3N is beta Cu3Ti-like structured and crystallizes in the hexagonal P6_3/mmc space group. The structure is three-dimensional. Mg is bonded in a 12-coordinate geometry to eight equivalent Mg and four equivalent N atoms. There are two shorter (2.73 Å) and six longer (2.89 Å) Mg–Mg bond lengths. There are two shorter (2.81 Å) and two longer (2.84 Å) Mg–N bond lengths. N is bonded to twelve equivalent Mg atoms to form a mixture of face and corner-sharing NMg12 cuboctahedra.

36 MATERIALS SCIENCE↗

Materials Data on MgN8 by Materials Project

MgN8 crystallizes in the tetragonal I4/m space group. The structure is two-dimensional and consists of two MgN8 sheets oriented in the (0, 0, 1) direction. Mg2+ is bonded in an octahedral geometry to six N+0.25- atoms. There are four shorter (2.09 Å) and two longer (2.36 Å) Mg–N bond lengths. There are three inequivalent N+0.25- sites. In the first N+0.25- site, N+0.25- is bonded in a single-bond geometry to one Mg2+ atom. In the second N+0.25- site, N+0.25- is bonded in a linear geometry to two equivalent N+0.25- atoms. Both N–N bond lengths are 1.18 Å. In the third N+0.25- site, N+0.25- is bonded in a distorted bent 150 degrees geometry to one Mg2+ and one N+0.25- atom.

36 MATERIALS SCIENCE↗