Potential Dependent Reorientation Controlling Activity of a Molecular Electrocatalyst.

The activity of molecular electrocatalysts depends on the interplay of electrolyte composition near the electrode surface, the composition and morphology of the electrode surface, and the electric field at the electrode-electrolyte interface. This interplay is challenging to study and often overlooked when assessing molecular catalyst activity. Here, we use surface specific vibrational sum frequency generation (VSFG) spectroscopy to study the solvent and potential dependent activation of Mo(bpy)(CO)4, a CO2 reduction catalyst, at a polycrystalline Au electrode. We find that the parent complex undergoes potential dependent reorientation at the electrode surface when a small amount of N-methyl-2-pyrrolidone (NMP) is present. This preactivates the complex, resulting in greater yields at less negative potentials, of the active electrocatalyst for CO2 reduction.

Pulsed Electrolysis with a Nickel Molecular Catalyst Improves Selectivity for Carbon Dioxide Reduction.

Pulsed electrolysis can significantly improve carbon dioxide reduction on metal electrodes, but the effect of short (millisecond to seconds) voltage steps on molecular electrocatalysts is largely unstudied. In this work, we investigate the effect pulse electrolysis has on the selectivity and stability of the homogeneous electrocatalyst [Ni(cyclam)]2+ at a carbon electrode. By tuning the potential and pulse duration, we achieve a significant improvement in CO Faradaic efficiencies (85%) after 3 h, double that of the system under potentiostatic conditions. The improved activity is due to in situ catalyst regeneration from an intermediate that occurs as part of the catalyst's degradation pathway. This study demonstrates the wider opportunity to apply pulsed electrolysis to molecular electrocatalysts to control activity and improve selectivity.

Manganese Carbonyl Complexes as Selective Electrocatalysts for CO2 Reduction in Water and Organic Solvents.

The electrochemical reduction of CO2 provides a way to sustainably generate carbon-based fuels and feedstocks. Molecular CO2 reduction electrocatalysts provide tunable reaction centers offering an approach to control the selectivity of catalysis. Manganese carbonyl complexes, based on [Mn(bpy)(CO)3Br] and its derivatives (bpy = 2,2'-bipyridine), are particularly interesting due to their ease of synthesis and the use of a first-row earth-abundant transition metal. [Mn(bpy)(CO)3Br] was first shown to be an active and selective catalyst for reducing CO2 to CO in organic solvents in 2011. Since then, manganese carbonyl catalysts have been widely studied with numerous reports of their use as electrocatalysts and photocatalysts and studies of their mechanism.This class of Mn catalysts only shows CO2 reduction activity with the addition of weak Brønsted acids. Perhaps surprisingly, early reports showed increased turnover frequencies as the acid strength is increased without a loss in selectivity toward CO evolution. It may have been expected that the competing hydrogen evolution reaction could have led to lower selectivity. Inspired by these works we began to explore if the catalyst would work in protic solvents, namely, water, and to explore the pH range over which it can operate. Here we describe the early studies from our laboratory that first demonstrated the use of manganese carbonyl complexes in water and then go on to discuss wider developments on the use of these catalysts in water, highlighting their potential as catalysts for use in aqueous CO2 electrolyzers.Key to the excellent selectivity of these catalysts in the presence of Brønsted acids is a proton-assisted CO2 binding mechanism, where for the acids widely studied, lower pKa values actually favor CO2 binding over Mn-H formation, a precursor to H2 evolution. Here we discuss the wider literature before focusing on our own contributions in validating this previously proposed mechanism through the use of vibrational sum frequency generation (VSFG) spectroelectrochemistry. This allowed us to study [Mn(bpy)(CO)3Br] while it is at, or near, the electrode surface, which provided a way to identify new catalytic intermediates and also confirm that proton-assisted CO2 binding operates in both the "dimer" and primary (via [Mn(bpy)(CO)3]-) pathways. Understanding the mechanism of how these highly selective catalysts operate is important as we propose that the Mn complexes will be valuable models to guide the development of new proton/acid tolerant CO2 reduction catalysts.

Zero-Gap Bipolar Membrane Electrolyzer for Carbon Dioxide Reduction Using Acid-Tolerant Molecular Electrocatalysts.

The scaling-up of electrochemical CO2 reduction requires circumventing the CO2 loss as carbonates under alkaline conditions. Zero-gap cell configurations with a reverse-bias bipolar membrane (BPM) represent a possible solution, but the catalyst layer in direct contact with the acidic environment of a BPM usually leads to H2 evolution dominating. Here we show that using acid-tolerant Ni molecular electrocatalysts selective (>60%) CO2 reduction can be achieved in a zero-gap BPM device using a pure water and CO2 feed. At a higher current density (100 mA cm-2), CO selectivity decreases, but was still >30%, due to reversible product inhibition. This study demonstrates the importance of developing acid-tolerant catalysts for use in large-scale CO2 reduction devices.

Dynamics of Solid-Electrolyte Interphase Formation on Silicon Electrodes Revealed by Combinatorial Electrochemical Screening.

Revealing how formation protocols influence the properties of the solid-electrolyte interphase (SEI) on Si electrodes is key to developing the next generation of Li-ion batteries. SEI understanding is, however, limited by the low-throughput nature of conventional characterisation techniques. Herein, correlative scanning electrochemical cell microscopy (SECCM) and shell-isolated nanoparticles for enhanced Raman spectroscopy (SHINERS) are used for combinatorial screening of the SEI formation under a broad experimental space (20 sets of different conditions with several repeats). This novel approach reveals the heterogeneous nature and dynamics of the SEI electrochemical properties and chemical composition on Si electrodes, which evolve in a characteristic manner as a function of cycle number. Correlative SECCM/SHINERS has the potential to screen thousands of candidate experiments on a variety of battery materials to accelerate the optimization of SEI formation methods, a key bottleneck in battery manufacturing.

Photocatalytic Overall Water Splitting Under Visible Light Enabled by a Particulate Conjugated Polymer Loaded with Palladium and Iridium.

Polymer photocatalysts have received growing attention in recent years for photocatalytic hydrogen production from water. Most studies report hydrogen production with sacrificial electron donors, which is unsuitable for large-scale hydrogen energy production. Here we show that the palladium/iridium oxide-loaded homopolymer of dibenzo[b,d]thiophene sulfone (P10) facilitates overall water splitting to produce stoichiometric amounts of H2 and O2 for an extended period (>60 hours) after the system stabilized. These results demonstrate that conjugated polymers can act as single component photocatalytic systems for overall water splitting when loaded with suitable co-catalysts, albeit currently with low activities. Transient spectroscopy shows that the IrO2 co-catalyst plays an important role in the generation of the charge separated state required for water splitting, with evidence for fast hole transfer to the co-catalyst.

Electrochemical carbon dioxide reduction in ionic liquids at high pressure.

Imidazolium ionic liquids are potentially useful solvents for both carbon dioxide reduction conversion and capture. In particular electrocatalytic CO2 reduction has been shown to occur at low overpotentials using a 1-ethyl-3-methylimidazolium trifluoromethanesulfonate ([EMIM][OTf]) and water mixed solvent. A limitation of such solvent systems is their viscosity, making it hard to maintain reasonable catalytic current densities without energy intensive stirring/agitation of the electrolyte. Here we explore the electrochemical reduction of CO2 at high pressures (0.1 to 5.1 MPa) and demonstrate a correlation between the volume of expansion of the ionic liquid and the achieved catalytic current density. The improved electrocatalytic behaviour is proposed to be due to both the increased bulk CO2 concentration and the improved mass transport properties of the gas-expanded ionic liquid. These initial studies at pressure represent a step towards realising an integrated CO2 capture and utilisation system based around a common ionic liquid.

Strong Impact of Intramolecular Hydrogen Bonding on the Cathodic Path of [Re(3,3'-dihydroxy-2,2'-bipyridine)(CO)3Cl] and Catalytic Reduction of Carbon Dioxide.

Herein, we present the cathodic paths of the Group-7 metal complex [Re(3,3'-DHBPY)(CO)3Cl] (3,3'-DHBPY = 3,3'-dihydroxy-2,2'-bipyridine) producing a moderately active catalyst of electrochemical reduction of CO2 to CO. The combined techniques of cyclic voltammetry and IR/UV-vis spectroelectrochemistry have revealed significant differences in the chemistry of the electrochemically reduced parent complex compared to the previously published Re/4,4'-DHBPY congener. The initial irreversible cathodic step in weakly coordinating THF is shifted toward much less negative electrode potentials, reflecting facile reductive deprotonation of one hydroxyl group and strong intramolecular hydrogen bonding, O-H···O-. The latter process occurs spontaneously in basic dimethylformamide where Re/4,4'-DHBPY remains stable. The subsequent reduction of singly deprotonated [Re(3,3'-DHBPY-H+)(CO)3Cl]- under ambient conditions occurs at a cathodic potential close to that of the Re/4,4'-DHBPY-H+ derivative. However, for the stabilized 3,3'-DHBPY-H+ ligand, the latter process at the second cathodic wave is more complex and involves an overall transfer of three electrons. Rapid potential step electrolysis induces 1e--reductive cleavage of the second O-H bond, triggering dissociation of the Cl- ligand from [Re(3,3'-DHBPY-2H+)(CO)3Cl]2-. The ultimate product of the second cathodic step in THF was identified as 5-coordinate [Re(3,3'-DHBPY-2H+)(CO)3]3-, the equivalent of classical 2e--reduced [Re(BPY)(CO)3]-. Each reductive deprotonation of the DHBPY ligand results in a redshift of the IR ν(CO) absorption of the tricarbonyl complexes by ca. 10 cm-1, facilitating the product assignment based on comparison with the literature data for corresponding Re/BPY complexes. The Cl- dissociation from [Re(3,3'-DHBPY-2H+)(CO)3Cl]2- was proven in strongly coordinating butyronitrile. The latter dianion is stable at 223 K, converting at 258 K to 6-coordinate [Re(3,3'-DHBPY-2H+)(CO)3(PrCN)]3-. Useful reference data were obtained with substituted parent [Re(3,3'-DHBPY)(CO)3(PrCN)]+ that also smoothly deprotonates by the initial reduction to [Re(3,3'-DHBPY-H+)(CO)3(PrCN)]. The latter complex ultimately converts at the second cathodic wave to [Re(3,3'-DHBPY-2H+)(CO)3(PrCN)]3- via a counterintuitive ETC step generating the 1e- radical of the parent complex, viz., [Re(3,3'-DHBPY)(CO)3(PrCN)]. The same alternative reduction path is also followed by [Re(3,3'-DHBPY-H+)(CO)3Cl]- at the onset of the second cathodic wave, where the ETC step results in the intermediate [Re(3,3'-DHBPY)(CO)3Cl]•- further reducible to [Re(3,3'-DHBPY-2H+)(CO)3]3- as the CO2 catalyst.

Potential and pitfalls: On the use of transient absorption spectroscopy for in situ and operando studies of photoelectrodes.

Here, we discuss the application, advantages, and potential pitfalls of using transient UV/Vis (ultraviolet-visible) absorption spectroscopy to study photoelectrodes for water splitting. We revisit one of the most commonly studied water oxidation photoanodes (α-Fe2O3-x) to provide commentary and guidelines on experiment design and data analysis for transient absorption (TA) studies of photoelectrodes within a photoelectrochemical cell. We also assess the applicability of such in situ TA studies to understand photoelectrodes under operating conditions. A major limitation is that most, if not all, past in situ TA studies have been carried out using only pulsed light sources to generate carriers, with the electrode held in the dark at other times, which is shown to be a poor model for operating conditions. However, with a simple modification of existing TA experiments, a simple operando TA measurement is reported.

Water Oxidation with Cobalt-Loaded Linear Conjugated Polymer Photocatalysts.

The first examples of linear conjugated organic polymer photocatalysts that produce oxygen from water after loading with cobalt and in the presence of an electron scavenger are reported. The oxygen evolution rates, which are higher than for related organic materials, can be rationalized by a combination of the thermodynamic driving force for water oxidation, the light absorption of the polymer, and the aqueous dispersibility of the relatively hydrophilic polymer particles. We also used transient absorption spectroscopy to study the best performing system and we found that fast oxidative quenching of the exciton occurs (picoseconds) in the presence of an electron scavenger, minimizing recombination.

Photocatalytically active ladder polymers.

Conjugated ladder polymers (cLaPs) are introduced as organic semiconductors for photocatalytic hydrogen evolution from water under sacrificial conditions. Starting from a linear conjugated polymer (cLiP1), two ladder polymers are synthesized via post-polymerization annulation and oxidation techniques to generate rigidified, planarized materials bearing dibenzo[b,d]thiophene (cLaP1) and dibenzo[b,d]thiophene sulfone subunits (cLaP2). The high photocatalytic activity of cLaP1 (1307 µmol h-1 g-1) in comparison to that of cLaP2 (18 µmol h-1 g-1) under broadband illumination (λ > 295 nm) in the presence of a hole-scavenger is attributed to a higher yield of long-lived charges (µs to ms timescale), as evidenced by transient absorption spectroscopy. Additionally, cLaP1 has a larger overpotential for proton reduction and thus an increased driving force for the evolution of hydrogen under sacrificial conditions.

In situ study of the low overpotential "dimer pathway" for electrocatalytic carbon dioxide reduction by manganese carbonyl complexes.

The electrocatalytic reduction of CO2 using [fac-Mn(bpy)(CO)3Br] (bpy = 2,2'-bipyridine) and its derivatives has been the subject of numerous recent studies. However the mechanisms of catalysis are still debated. Here we carry out in situ vibrational sum-frequency generation (VSFG) spectroelectrochemistry to examine how this catalyst behaves at an electrode surface. In particular, a low overpotential pathway involving a dimeric manganese has been reported in several studies using substituted bipyridine ligands. Here, we find that the "dimer pathway" can also occur with the unsubstuituted bipyridine complexes. Specifically we can observe spectroscopic evidence of the interaction between [Mn2(bpy)2(CO)6] with CO2 in the presence of a suitable acid. Detailed VSFG studies of [Mn2(bpy)2(CO)6], including of the potential dependence of the surface ν(CO) mode, allow us to construct a model of how it accumulates and behaves at the electrode surface under potentiostatic control.

Vibrational sum-frequency generation spectroscopy of electrode surfaces: studying the mechanisms of sustainable fuel generation and utilisation.

The electrocatalytic oxidation of water coupled to the reduction of carbon dioxide, to make carbon based products, or the reduction of protons to provide hydrogen, offers a sustainable route to generating useful fuels. However new improved electrocatalysts and electrode materials are needed for these reactions. Similarly fuel cells for fuel utilisation rely on precious metal electrodes and new lower-cost materials are needed. Developing efficient catalysts for sustainable fuel generation can be accelerated with an improved understanding of the underlying mechanisms. Herein, we present a perspective on the use of vibrational sum-frequency generation (VSFG) spectroscopy to study such electrocatalytic mechanisms. We briefly outline the basic principles of VSFG spectroscopy pertinent to the study of electrochemical interfaces. We then review the use of VSFG to study water at charged and electrode interfaces, relevant to the mechanisms of water oxidation, the mechanisms of alcohol oxidation and also molecular electrocatalysts for carbon dioxide reduction.

Gelation enabled charge separation following visible light excitation using self-assembled perylene bisimides.

Perylene bisimides (PBIs) can be functionalised to enable controlled aggregation into complex supramolecular structures and are promising materials for photovoltaic and solar fuel applications. Amino acid appended PBIs such as PBI-alanine (PBI-A) have been found to form photoconductive films containing worm-like structures that enable charge transport. However, despite being strong chromophores in the visible region, when PBI-A films are prepared by drying down solutions, activity only occurs under UV illumination. This limits potential applications. The requirement for UV illumination has previously been suggested to be due to the large ion-pair energy in the low dielectric environment of the dried samples. Hydrogel films, rehydrated xerogels and dry xerogels of PBI-A can also be prepared offering an ideal sample set to examine the influence of hydration on charge-separation. Using transient absorption (TA) spectroscopy, we demonstrate a correlation between water content and efficiency of generation of long-lived charge separated states within the PBI-A materials, highlighting their potential, particularly for light-driven water splitting.

Directing the mechanism of CO2 reduction by a Mn catalyst through surface immobilization.

Immobilization of a Mn polypyridyl CO2 reduction electrocatalyst on nanocrystalline TiO2 electrodes yields an active heterogeneous system and also significantly triggers a change in voltammetric and catalytic behaviour, relative to in solution. A combination of spectroelectrochemical techniques are presented here to elucidate the mechanism of the immobilized catalyst in situ.

The Role of Electrode-Catalyst Interactions in Enabling Efficient CO2 Reduction with Mo(bpy)(CO)4 As Revealed by Vibrational Sum-Frequency Generation Spectroscopy.

Group 6 metal carbonyl complexes ([M(bpy)(CO)4], M = Cr, Mo, W) are potentially promising CO2 reduction electrocatalysts. However, catalytic activity onsets at prohibitively negative potentials and is highly dependent on the nature of the working electrode. Here we report in situ vibrational SFG (VSFG) measurements of the electrocatalyst [Mo(bpy)(CO)4] at platinum and gold electrodes. The greatly improved onset potential for electrocatalytic CO2 reduction at gold electrodes is due to the formation of the catalytically active species [Mo(bpy)(CO)3]2- via a second pathway at more positive potentials, likely avoiding the need for the generation of [Mo(bpy)(CO)4]2-. VSFG studies demonstrate that the strength of the interaction between initially generated [Mo(bpy)(CO)4]•- and the electrode is critical in enabling the formation of the active catalyst via the low energy pathway. By careful control of electrode material, solvent and electrolyte salt, it should therefore be possible to attain levels of activity with group 6 complexes equivalent to their much more widely studied group 7 analogues.

Photochemical CO2 reduction using structurally controlled g-C3N4.

Graphitic carbon nitride (g-C3N4) synthesised from a urea precursor is an excellent CO2 reduction photocatalyst using [Co(bpy)n]2+ as a co-catalyst. A five-fold increase in activity for the highly polymerised urea derived g-C3N4 is achieved compared to alternative precursors. Transient absorption, time-resolved and steady-state emission studies indicate that the enhanced activity is related to both an increased driving force for photoelectron transfer and a greater availability of photogenerated charges.

Acid Treatment Enables Suppression of Electron-Hole Recombination in Hematite for Photoelectrochemical Water Splitting.

We report a strategy for efficient suppression of electron-hole recombination in hematite photoanodes. Acid-treated hematite showed a substantially enhanced photocurrent density compared to untreated samples. Electrochemical impedance spectroscopy studies revealed that the enhanced photocurrent is partly due to improved efficiency of charge separation. Transient absorption spectroscopic studies coupled to electrochemical measurements indicate that, in addition to improved bulk electrochemical properties, acid-treated hematite has significantly decreased surface electron-hole recombination losses owing to a greater yield of the trapped photoelectrons being extracted to the external circuit.