A tridentate NNN Ni(II) complex, shown to be an electrocatalyst for aqueous H2 production at low overpotentials, is studied by using temperature-dependent paramagnetic (1)H NMR. The NMR T1 relaxation rates, temperature dependence of the chemical shifts, and dc SQUID magnetic susceptibility are correlated to DFT chemical shifts and compared with the properties of a diamagnetic Zn analogue comple...

Amorphous molybdenum sulfide (MoSx) is covalently anchored to reduced graphene oxide (r-GO) via a simple one-pot reaction, thereby inducing the reduction of GO and simultaneous doping of heteroatoms on the GO. The oxygen atoms form a bridged between MoSx and GO and play a crucial role in the fine dispersion of the MoSx particles, control of planar MoSx growth, and increase of exposed active sul...

Fuel cells are appealing for a variety of energy needs, but the high materials and manufacturing costs have hampered their commercialization. The limited availability and the high cost of the currently used platinum catalysts, for example, pose a serious problem in their practical application. We report here non-platinum electrocatalyst systems, such as Pd-Co-Au and Pd-Ti, that are proposed fro...

Efficient and low-cost electrocatalysts for the hydrogen evolution reaction are highly desired for future renewable energy systems. Described herein is the reduction of water to hydrogen using a metal-free carbon nitride electrocatalyst which operates in neutral and alkaline environments. An efficient, easy, and general method for growing ordered carbon nitride on different electrodes was devel...

We report the preparation of a dicobalt compound with two singly proton-bridged cobaloxime units linked by a central [BO4] bridge. Reaction of a doubly proton-bridged cobaloxime complex with trimethyl borate afforded the compound in good yield. Single-crystal X-ray diffraction studies confirmed the bridging nature of the [BO4] moiety. Using electrochemical methods, the dicobalt complex was foun...

A glucose-O2 biofuel cell, consisting only of two electrocatalyst coated 7-mum diameter, 2-cm long carbon fibers is reported. The cell operated continuously at 0.52 V at 37 degrees C in a physiological buffer solution for a week, producing 1.9 muW during the first and 1.0 muW during the last day, generating in the period 0.9 J of electrical energy while passing a charge of 1.7 C. If a similar d...

We have characterized the covalent binding of the CO(2) reduction electrocatalyst ReC0A (Re(CO)(3)Cl(dcbpy) (dcbpy =4,4'-dicarboxy-2,2'-bipyridine)) to the TiO(2) rutile (001) surface. The analysis based on sum frequency generation (SFG) spectroscopy and density functional theory (DFT) calculations indicates that ReC0A binds to TiO(2) through the carboxylate groups in bidentate or tridentate li...

The hydrogen evolution reaction (HER) via water splitting requires the development of advanced and inexpensive electrocatalysts to replace expensive platinum (Pt)-based catalysts. The scalable hydrothermal synthesis of SnS on N-reduced graphene (N-rGr) sheets is presented for the first time, which is used as a highly-active electrocatalyst with long-term stability in acidic, neutral, and alkali...

The tris(2-pyridyl)phosphine oxide (Py3PO) complex [Ru(Py3PO)(bpy)(OH2)] 2+ (bpy is 2,20-bipyridine) is a pH-dependent water oxidation electrocatalyst that accelerates dramatically with increasing pH—up to 780 s 1 at pH 10 ( 1 V overpotential). Despite retaining the pentakis(pyridine) ligand arrangement common to previously reported catalysts, the tripodal Py3PO ligand framework supports much f...

The complex [Ru(tpy)(bpy)(S)](2+) (tpy = 2,2':6',2''-terpyridine, bpy = 2,2'-bipyridine, S = solvent) is an electrocatalyst for water or proton reduction to hydrogen and for reduction of acetone to iso-propanol in CH3CN. Electrocatalysis is initiated by sequential 1e(-) reductions at the tpy and bpy ligands followed by addition of water to give a ruthenium hydride intermediate. Significant rate...