Maximizing Ion Permselectivity in MXene/MOF Nanofluidic Membranes for High-Efficient Blue Energy Generation

Key Words:CARBON-DIOXIDE; NANOCLUSTERS; CATALYSIS; EVOLUTION

Abstract:Atomically precise metal nanoclusters (NCs) have emerged as a new class of ultrasmall nanoparticles with both free valence electrons and precise structures (from the metal core to the organic ligand shell) and provide great opportunities to understand the relationship between their structures and properties, such as electrocatalytic CO<INF>2</INF> reduction reaction (eCO<INF>2</INF>RR) performance, at the atomic level. Herein, we report the synthesis and the overall structure of the phosphine and iodine co-protected Au<INF>4</INF>(PPh<INF>3</INF>)<INF>4</INF>I<INF>2</INF> (Au<INF>4</INF>) NC, which is the smallest multinuclear Au superatom with two free e<SUP>-</SUP> reported so far. Single-crystal X-ray diffraction reveals a tetrahedral Au<INF>4</INF> core stabilized by four phosphines and two iodides. Interestingly, the Au<INF>4</INF> NC exhibits much higher catalytic selectivity for CO (FE<INF>CO</INF>: > 60%) at more positive potentials (from -0.6 to -0.7 V vs. RHE) than Au<INF>11</INF>(PPh<INF>3</INF>)<INF>7</INF>I<INF>3</INF> (FE<INF>CO</INF>: < 60%), a larger 8 e<SUP>-</SUP> superatom, and Au(i)PPh<INF>3</INF>Cl complex; whereas the hydrogen evolution reaction (HER) dominates the electrocatalysis when the potential becomes more negative (FE<INF>H<INF>2</INF></INF> of Au<INF>4</INF> = 85.8% at -1.2 V vs. RHE). Structural and electronic analyses reveal that the Au<INF>4</INF> tetrahedron becomes unstable at more negative reduction potentials, resulting in decomposition and aggregation, and consequently the decay in catalytic performance of Au based catalysts towards the eCO<INF>2</INF>RR.

Volume:5

Issue:12

Translation or Not:no