Epitaxial Self-Assembly of Interfaces of 2D Metal-Organic Frameworks for Electroanalytical Detection of Neurotransmitters.

This paper identifies the electrochemical properties of individual facets of anisotropic layered conductive metal-organic frameworks (MOFs) based on M3(2,3,6,7,10,11-hexahydroxytriphenylene)2 (M3(HHTP)2) (M = Co, Ni). The electroanalytical advantages of each facet are then applied toward the electrochemical detection of neurochemicals. By employing epitaxially controlled deposition of M3(HHTP)2 MOFs on electrodes, the contribution of the basal plane ({001} facets) and edge sites ({100} facets) of these MOFs can be individually determined using electrochemical characterization techniques. Despite having a lower observed heterogeneous electron transfer rate constant, the {001} facets of the M3(HHTP)2 systems prove more selective and sensitive for the detection of dopamine than the {100} facets of the same MOF, with the limit of detection (LOD) of 9.9 ± 2 nM in phosphate-buffered saline and 214 ± 48 nM in a simulated cerebrospinal fluid. Langmuir isotherm studies accompanied by all-atom MD simulations suggested that the observed improvement in performance and selectivity is related to the adsorption characteristics of analytes on the basal plane versus edge sites of the MOF interfaces. This work establishes that the distinct crystallographic facets of 2D MOFs can be used to control the fundamental interactions between analyte and electrode, leading to tunable electrochemical properties by controlling their preferential orientation through self-assembly.

Rapid and Energetic Solid-State Metathesis Reactions for Iron, Cobalt, and Nickel Boride Formation and Their Investigation as Bifunctional Water Splitting Electrocatalysts.

Metal borides have long-standing uses due to their desirable chemical and physical properties such as high melting points, hardness, electrical conductivity, and chemical stability. Typical metal boride preparations utilize high-energy and/or slow thermal heating processes. This report details a facile, solvent-free single-step synthesis of several crystalline metal monoborides containing earth-abundant transition metals. Rapid and exothermic self-propagating solid-state metathesis (SSM) reactions between metal halides and MgB2 form crystalline FeB, CoB, and NiB in seconds without sustained external heating and with high isolated product yields (∼80%). The metal borides are formed using a well-studied MgB2 precursor and compared to reactions using separate Mg and B reactants, which also produce self-propagating reactions and form crystalline metal borides. These SSM reactions are sufficiently exothermic to theoretically raise reaction temperatures to the boiling point of the MgCl2 byproduct (1412 °C). The chemically robust monoborides were examined for their ability to perform electrocatalytic water oxidation and reduction. Crystalline CoB and NiB embedded on carbon wax electrodes exhibit moderate and stable bifunctional electrocatalytic water splitting activity, while FeB only shows appreciable hydrogen evolution activity. Analysis of catalyst particles after extended electrocatalytic experiments shows that the bulk crystalline metal borides remain intact during electrochemical water-splitting reactions though surface oxygen species may impact electrocatalytic activity.

General Synthetic Strategy to Ordered Mesoporous Carbon Catalysts with Single-Atom Metal Sites for Electrochemical CO2 Reduction.

The electrochemical carbon dioxide reduction reaction (CO2 RR) is a transformative technology to reduce the carbon footprint of modern society. Single-site catalysts have been demonstrated as promising catalysts for CO2 RR, but general synthetic methods for catalysts with high surface area and tunable single-site metal composition still need to be developed to unambiguously investigate the structure-activity relationship crossing various metal sites. Here, a generalized coordination-condensation strategy is reported to prepare single-atom metal sites on ordered mesoporous carbon (OMC) with high surface areas (average 800 m2  g-1 ). This method is applicable to a broad range of metal sites (Fe, Co, Ni, Cu, Pt, Pd, Ru, and Rh) with loadings up to 4 wt.%. In particular, the CO2 RR to carbon monoxide (CO) Faradaic efficiency (FE) with Ni single-site OMC catalyst reaches 95%. This high FE is maintained even under large current density (>140 mA cm-2 ) and in a long-term study (14 h), which suits the urgently needed large-scale applications. Theoretical calculations suggest that the enhanced activity on single-atom Ni sites results from balanced binding energies between key intermediates, COOH and CO, for CO2 RR, as mediated by the coordination sphere.