The Hydrogen Evolution Activity of BaZrS3, BaTiS3, and BaVS3 Chalcogenide Perovskites.

Chalcogenide perovskites are a class of materials with electronic and optoelectronic properties desirable for solar cells, infrared optics, and computing. The oxide counterparts of these chalcogenides have been studied extensively for their electrocatalytic and photoelectrochemical properties. As chalcogenide perovskites are more covalent, conductive, and stable, we hypothesize that they are more viable as electrocatalysts than oxide perovskites. The goal of this synthetic, experimental, and computational study is to examine the hydrogen evolution reaction (HER) activity of three Barium-based chalcogenides in perovskite and related structures: BaZrS3, BaTiS3, and BaVS3. Potential energy surfaces for hydrogen adsorption on surfaces of these materials are calculated using density functional theory and the computational hydrogen electrode model is used to contrast overpotentials with experiment. Although both experiments and computations agree that BaVS3 is the most active of the three materials, high overpotentials of these materials make them less viable than platinum for HER. Our work establishes a framework for future studies in the chemical and electrochemical properties of chalcogenide perovskites.

Vertex Differentiation Strategy for Tuning the Physical Properties of closo-Dodecaborate Weakly Coordinating Anions.

We report the synthesis and characterization of various compounds containing the 1,7,9-hydroxylated closo-dodecahydrododecaborate (B12H9(OH)32-) cluster motif. Specifically, we show how the parent compound can be synthesized on the multigram scale and further perhalogenated, leading to a new class of vertex-differentiated weakly coordinating anions. We show that a postmodification of the hydroxyl groups by alkylation affords further opportunities for tailoring these anions' stability, steric bulk, and solubility properties. The resulting dodecaborate-based salts were subjected to a full thermal and electrochemical stability evaluation, showing that many of these anions maintain thermal stability up to 500 °C and feature no redox activity below ∼1 V vs Fc/Fc+. Mixed hydroxylated/halogenated clusters show enhanced solubility compared to their purely halogenated analogs and retain weakly coordinating properties in the solid state, as demonstrated by ionic conductivity measurements of their Li+ salts.

Electrochemical Cycling of Redox-Active Boron Cluster-Based Materials in the Solid State.

This work demonstrates the first successful electrochemical cycling of a redox-active boron cluster-based material in the solid state. Specifically, we designed and synthesized an ether-functionalized dodecaborate cluster, B12(OCH3)12, which is the smallest redox-active building block in the B12(OR)12 family. This species can reversibly access four oxidation states in solution, ranging from a dianion to a radical cation. We show that a chemically isolated and characterized neutral [B12(OCH3)12]0 cluster can be utilized as a cathode active material in a PEO-based rechargeable all-solid-state cell with a lithium metal anode. The cell exhibits an impressive active material utilization close to 95% at C/20 rate, a high Coulombic efficiency of 96%, and reversibility, with only 4% capacity fade after 16 days of cycling. This work represents a conceptual departure in the development of redox-active components for electrochemical storage and serves as an entry point to a broader class of borane-based materials.

Cobalt and Nickel Phosphates as Multifunctional Air-Cathodes for Rechargeable Hybrid Sodium-Air Battery Applications.

Noble-metal-free bifunctional electrocatalysts are indispensable to realize low-cost and energy-efficient rechargeable metal-air batteries. In addition, power density, energy density, and cycle life of these metal-air batteries can be improved further by utilizing the fast faradaic reactions of metal ions in the catalyst layer together with the oxygen evolution/reduction reactions (OER/ORR) for charge storage. In this work, we propose mixed metal phosphates of nickel and cobalt, NixCo3-x(PO4)2 (x = 0,1, 1.5, 2, and 3), as multifunctional air-cathodes exhibiting bifunctional electrocatalytic activity and reversible metal redox reaction (M3+/2+, M = Ni and Co). Submicron-sized NixCo3-x(PO4)2 particles were synthesized by a solution combustion synthesis technique with urea acting as the fuel. Electrocatalytic activity toward the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in 0.1 M NaOH was systematically tuned by varying the Ni-to-Co ratio. The synthesized NixCo3-x(PO4)2 with x = 1.5 (NCP11) showed superior bifunctional catalytic activity to other samples. Moreover, the catalyst material delivered a specific capacity of ∼110 mAh g-1 by the redox reactions of its metal sites. The hybrid Na-air battery fabricated using the NCP11 catalyst-loaded air-cathode exhibited low overpotential, stable cycling performance, and round-trip energy efficiency exceeding 78% in a 0.1 M NaOH aqueous electrolyte.

Electrodeposited Nickel-Cobalt-Sulfide Catalyst for the Hydrogen Evolution Reaction.

A novel Ni-Co-S-based material prepared by the potentiodynamic deposition from an aqueous solution containing Ni2+, Co2+, and thiourea is studied as an electrocatalyst for the hydrogen evolution reaction (HER) in a neutral phosphate solution. The composition of the catalyst and the HER activity are tuned by varying the ratio of the concentrations of Ni2+ and Co2+ ions in the electrolytes. Under optimized deposition conditions, the bimetallic Ni-Co-S exhibits higher electrocatalytic activity than its monometallic counterparts. The Ni-Co-S catalyst requires an overpotential of 150 mV for the HER onset, and 10 mA cm-2 current density is obtained at 280 mV overpotential. The catalyst exhibits two different Tafel slopes (93 and 70 mV dec-1) indicating two dissimilar mechanisms. It is proposed that the catalyst comprises two types of catalytic active sites, and they contribute selectively toward HER in different potential regions.

High Catalytic Activity of Amorphous Ir-Pi for Oxygen Evolution Reaction.

Large-scale production of hydrogen gas by water electrolysis is hindered by the sluggish kinetics of oxygen evolution reaction (OER) at the anode. The development of a highly active and stable catalyst for OER is a challenging task. Electrochemically prepared amorphous metal-based catalysts have gained wide attention after the recent discovery of a cobalt-phosphate (Co-Pi) catalyst. Herein, an amorphous iridium-phosphate (Ir-Pi) is investigated as an oxygen evolution catalyst. The catalyst is prepared by the anodic polarization of carbon paper electrodes in neutral phosphate buffer solutions containing IrCl3. The Ir-Pi film deposited on the substrate has significant amounts of phosphate and Ir centers in an oxidation state higher than +4. Phosphate plays a significant role in the deposition of the catalyst and also in its activity toward OER. The onset potential of OER on the Ir-Pi is about 150 mV lower in comparison with the Co-Pi under identical experimental conditions. Thus, Ir-Pi is a promising catalyst for electrochemical oxidation of water.

An oxygen evolution Co-Ac catalyst--the synergistic effect of phosphate ions.

Formation of an amorphous cobalt based oxygen evolution catalyst called Co-Pi has been recently reported from a neutral phosphate buffer solution containing Co(2+). But the concentration of Co(2+) is as low as 0.5 mM due to poor solubility of a cobalt salt in phosphate medium. In the present study, a cobalt acetate based oxygen evolution catalyst (Co-Ac) is prepared from a neutral acetate buffer solution, where the solubility of Co(2+) is very high (>100 times in comparison with phosphate buffer solution). The Co-Ac possesses better catalytic activity than the Co-Pi with an additional advantage of easy bulk scale preparation. The comparative studies on the oxygen evolution reaction (OER) activity of Co-Ac and Co-Pi in phosphate and acetate buffer electrolytes reveal that the Co-Ac exhibits enhanced synergistic catalytic activity in phosphate solution, probably due to partial substitution of acetate in the catalyst layer by phosphate, resulting in the formation of a Co-Ac-Pi catalyst.