Highly active catalysts for the oxygen evolution reaction (OER) are required for the development of photoelectrochemical devices that generate hydrogen efficiently from water using solar energy. Here, we identify the origin of a 500-fold OER activity enhancement that can be achieved with mixed (Ni,Fe)oxyhydroxides (Ni(1-x)Fe(x)OOH) over their pure Ni and Fe parent compounds, resulting in one of the most active currently known OER catalysts in alkaline electrolyte. Operando X-ray absorption spectroscopy (XAS) using high energy resolution fluorescence detection (HERFD) reveals that Fe(3+) in Ni(1-x)Fe(x)OOH occupies octahedral sites with unusually short Fe-O bond distances, induced by edge-sharing with surrounding [NiO6] octahedra. Using computational methods, we establish that this structural motif results in near optimal adsorption energies of OER intermediates and low overpotentials at Fe sites. By contrast, Ni sites in Ni(1-x)Fe(x)OOH are not active sites for the oxidation of water.
Electrocatalytic reduction of CO 2 to energy-rich hydrocarbons such as alkanes, alkenes, and alcohols is a very challenging task. So far, only copper has proven to be capable of such a conversion. We report density functional theory (DFT) calculations combined with the Poisson−Boltzmann implicit solvation model to show that single-atom alloys (SAAs) are promising electrocatalysts for CO 2 reduction to C 1 hydrocarbons in aqueous solution. The majority component of the SAAs studied is either gold or silver, in combination with isolated single atoms, M (M = Cu, Ni, Pd, Pt, Co, Rh, and Ir), replacing surface atoms. We envision that the SAA behaves as a one-pot tandem catalyst: first gold (or silver) reduces CO 2 to CO, and the newly formed CO is then captured by M and is further reduced to C 1 hydrocarbons such as methane or methanol. We studied 28 SAAs, and found about half of them selectively favor the CO 2 reduction reaction over the competing hydrogen evolution reaction. Most of those promising SAAs contain M = Co, Rh, or Ir. The reaction mechanism of two SAAs, Rh@Au(100) and Rh@Ag(100), is explored in detail. Both of them reduce CO 2 to methane but via different pathways. For Rh@Au(100), reduction occurs through the pathway *CO → *CHO → *CHOH → *CH + H 2 O (l) → *CH 2 + H 2 O (l) → *CH 3 + H 2 O (l) → * + H 2 O (l) + CH 4(g) ; whereas, for Rh@Ag(100), the pathway is *CO → *CHO → *CH 2 O→ *OCH 3 → *O + CH 4(g) → *OH + CH 4(g) → * + H 2 O (l) + CH 4(g). The minimum applied voltages to drive the two electrocatalytic systems are −1.01 and −1.12 V RHE for Rh@Au(100) and Rh@Ag(100), respectively, at which the Faradaic efficiencies for CO 2 reduction to CO are 60% for gold and 90% for silver. This suggests that SAA can efficiently reduce CO 2 to methane with as small as 40% loss to the hydrogen evolution reaction for Rh@Au(100) and as small as 10% for Rh@Ag(100). We hope these computational results can stimulate experimental efforts to explore the use of SAA to catalyze CO 2 electrochemical reduction to hydrocarbons.
Harnessing renewable electricity to drive the electrochemical reduction of CO 2 is being intensely studied for sustainable fuel production and as a means for energy storage. Copper is the only monometallic electrocatalyst capable of converting CO 2 to value-added products, e.g., hydrocarbons and oxygenates, but suffers from poor selectivity and mediocre activity. Multiple oxidative treatments have shown improvements in the performance of copper catalysts. However, the fundamental underpinning for such enhancement remains controversial. Here, we combine reactivity, in-situ surface-enhanced Raman spectroscopy, and computational investigations to demonstrate that the presence of surface hydroxyl species by co-electrolysis of CO 2 with low concentrations of O 2 can dramatically enhance the activity of copper catalyzed CO 2 electroreduction. Our results indicate that co-electrolysis of CO 2 with an oxidant is a promising strategy to introduce catalytically active species in electrocatalysis.
We propose a mechanism of water splitting on cobalt oxide surface with atomistic thermodynamic and kinetic details. The density-functional theory studies suggest that the oxidation process could proceed with several nonelectrochemical (spontaneous) intermediate steps, following the initial electrochemical hydroxyl-to-oxo conversion. More specifically, the single oxo sites CoIVO can hop (via surface proton/electron hopping) to form oxo pair CoIV(O)-O-CoIVO, which will undergo nucleophilic attack by a water molecule and form the hydroperoxide CoIII–OOH. Encounter with another oxo would generate a superoxo CoIII–OO, followed by the O2 release. Finally the addition and deprotonation of a fresh water molecule will restart the catalytic cycle by forming the hydroxyl CoIII–OH at this active site. Our theoretical investigations indicate that all nonelectrochemical reactions are kinetically fast and thermodynamically downhill. This hypothesis is supported by recent in situ spectroscopic observations of surface superoxo that is stabilized by hydrogen bonding to adjacent hydroxyl group as an intermediate on fast-kinetics Co catalytic site.
Density functional theory (DFT) calculations are performed to investigate the energetics of the CO 2 electrochemical reduction on metal (M) porphyrin-like motifs incorporated into graphene layers. The objective is to develop strategies that enhance CO 2 reduction while suppressing the competitive hydrogen evolution reaction (HER). We find that there exists a scaling relation between the binding energy of the catalyst to hydrogen and that to COOH, a key intermediate in the reduction of CO 2 to CO; however, the M−H bond is stronger than the M−COOH bond, driving the reaction toward the HER rather than the reduction of CO 2 to CO. This scaling relation holds even with axial ligation to the metal cation coordinated to the porphyrin ring. When 4f lanthanide or 5f actinide elements are used as the reactive center, the scaling relation still holds but the M−COOH bond is stronger than the M−H bond, and the reaction favors the reduction of CO 2 to CO. By contrast, there is no scaling relation between the binding energy of the catalyst to H and that to OCHO, the key intermediate in CO 2 reduction to formic acid. Interestingly, we find that coordination of a ligand to an unoccupied axial site can make the M− OCHO bond stronger than the M−H bond, resulting in preferential formic acid formation. This means that the axial ligand effectively enhances CO 2 reduction to formic acid and suppresses the HER. Our DFT calculations have also identified several promising electrocatalysts for CO 2 reduction to HCOOH with almost zero overpotentials.
1′,2′-j]picene (DDP, 1), a thermally and chemically stable helical arene, can be prepared from 1,4-bis[2-(arylethynyl)phenyl]benzene in four synthetic steps. Its helical backbone, which incorporates an oquinodimethane moiety, was verified by X-ray crystallography, and this structural feature results in a very high barrier to racemization (exceeding 50 kcal/mol). DDP possesses versatile and promising properties, including a small HOMO−LUMO energy gap (1.31 eV for the dimesitylsubstituted derivative 1ab), an electron spin resonance (ESR)active character, a small triplet−singlet energy gap (4.75 kcal/mol), broad photoabsorption covering the ultraviolet, visible, and near-infrared (NIR) regions, two-photon absorption in the NIR range, and respectable ambipolar charge-transport behavior in a solution-processed organic field-effect transistor.
Addition of Fe to Ni-and Co-based (oxy)hydroxides significantly enhances the activity of these materials for electrochemical oxygen evolution reaction (OER). Here, we show that Fe cations bound to the surface of oxidized Au enhance its OER activity, the OER activity increasing with increasing surface concentration of Fe. Density functional theory analysis of the energetics of the OER revealed that oxygen evolution over Fe cations bound to a hydroxylterminated oxidized Au surface (Fe-Au2O3) occurs at an overpotential 0.43 V lower than that at which the OER occurs on hydroxylated Au2O3 (0.86 V). This finding agrees very well with experimental observation and is a consequence of the more optimal binding energetics for the OER reaction intermediates at Fe cations bound to the surface of Au2O3. These findings suggest that the enhanced OER activity reported recently upon low-potential cycling of Au may be due to surface Fe impurities rather than to "superactive" Au(III) surfaquo species.3
We used density functional theory quantum mechanics with periodic boundary conditions to determine the atomistic mechanism underlying catalytic activation of propane by the M1 phase of Mo-V-Nb-Te-O mixed metal oxides. We find that propane is activated by Te═O through our recently established reduction-coupled oxo activation mechanism. More importantly, we find that the C-H activation activity of Te═O is controlled by the distribution of nearby V atoms, leading to a range of activation barriers from 34 to 23 kcal/mol. On the basis of the new insight into this mechanism, we propose a synthesis strategy that we expect to form a much more selective single-phase Mo-V-Nb-Te-O catalyst.
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