Time-resolved vibrational spectroscopic study of molecular nanoaggregate photocatalysts.

The controlled aggregation of organic chromophores into supramolecular structures offers a way to control and tune photocatalytic activity. However, the underlying mechanisms of charge transfer and accumulation are still unclear. Time-resolved vibrational spectroscopy is a powerful structural probe for studying photogenerated intermediates. Here, we employ time-resolved infrared (TRIR) spectroscopy to study CNP (2,6-bis(4-cyanophenyl)-4-(9-phenyl-9H-carbazol-3-yl)pyridine-3,5-dicarbonitrile) and its supramolecular aggregates. We show that excitation of the charge transfer (CT) band of semi-crystalline nanofibers (CNP-f) gives rise to long-lived delocalised polarons, which form within the instrument response timescale. By contrast the CNP nanospheres (CNP-s) give rise to a shorter lived polaron that appears to have a greater degree of localization. CNP-f and CNP-s are known to show markedly different levels of photocatalytic activity for hydrogen and hydrogen peroxide formation which are rationalised owing to these differences in photodynamics immediately following photon absorption.

Alkali metal cations enhance CO2 reduction by a Co molecular complex in a bipolar membrane electrolyzer.

The electrochemical reduction of CO2 is a promising pathway for converting CO2 into valuable fuels and chemicals. The local environment at the cathode of CO2 electrolyzers plays a key role in determining activity and selectivity, but currently some mechanisms are still under debate. In particular, alkali metal cations have been shown to enhance the selectivity of metal catalysts, but their role remains less explored for molecular catalysts especially in high-current electrolyzers. Here, we investigated the enhancement effects of cations (Na+, K+, Cs+) on Co phthalocyanine (CoPc) in a state-of-the-art reverse-biased bipolar membrane electrolyzer. When added to the anolyte, these cations increased the Faradaic efficiency for CO, except in the case of Na+ in which the effect was transient, but the effects are convoluted with the transport process through the membrane. Alternatively, these cations can also be added directly to the cathode as chloride salts, allowing the use of a pure H2O anolyte feed, leading to sustained improved CO selectivity (61% at 100 mA cm-2 after 24 h). Our results show that cation addition is a simple yet effective strategy for improving the product selectivity of molecular electrocatalysts, opening up new avenues for tuning their local environment for CO2 reduction.This article is part of the discussion meeting issue 'Green carbon for the chemical industry of the future'.

Conjugated Polymer/Recombinant Escherichia coli Biohybrid Systems for Photobiocatalytic Hydrogen Production.

Biohybrid photocatalysts are composite materials that combine the efficient light-absorbing properties of synthetic materials with the highly evolved metabolic pathways and self-repair mechanisms of biological systems. Here, we show the potential of conjugated polymers as photosensitizers in biohybrid systems by combining a series of polymer nanoparticles with engineered Escherichia coli cells. Under simulated solar light irradiation, the biohybrid system consisting of fluorene/dibenzo [b,d]thiophene sulfone copolymer (LP41) and recombinant E. coli (i.e., a LP41/HydA BL21 biohybrid) shows a sacrificial hydrogen evolution rate of 3.442 mmol g-1 h-1 (normalized to polymer amount). It is over 30 times higher than the polymer photocatalyst alone (0.105 mmol g-1 h-1), while no detectable hydrogen was generated from the E. coli cells alone, demonstrating the strong synergy between the polymer nanoparticles and bacterial cells. The differences in the physical interactions between synthetic materials and microorganisms, as well as redox energy level alignment, elucidate the trends in photochemical activity. Our results suggest that organic semiconductors may offer advantages, such as solution processability, low toxicity, and more tunable surface interactions with the biological components over inorganic materials.

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.

Studying the cation dependence of CO2 reduction intermediates at Cu by in situ VSFG spectroscopy.

The nature of the electrolyte cation is known to have a significant impact on electrochemical reduction of CO2 at catalyst|electrolyte interfaces. An understanding of the underlying mechanism responsible for catalytic enhancement as the alkali metal cation group is descended is key to guide catalyst development. Here, we use in situ vibrational sum frequency generation (VSFG) spectroscopy to monitor changes in the binding modes of the CO intermediate at the electrochemical interface of a polycrystalline Cu electrode during CO2 reduction as the electrolyte cation is varied. A CObridge mode is observed only when using Cs+, a cation that is known to facilitate CO2 reduction on Cu, supporting the proposed involvement of CObridge sites in CO coupling mechanisms during CO2 reduction. Ex situ measurements show that the cation dependent CObridge modes correlate with morphological changes of the Cu surface.

Unravelling the Roles of Integral Polypeptides in Excitation Energy Transfer of Photosynthetic RC-LH1 Supercomplexes.

Elucidating the photosynthetic processes that occur within the reaction center-light-harvesting 1 (RC-LH1) supercomplexes from purple bacteria is crucial for uncovering the assembly and functional mechanisms of natural photosynthetic systems and underpinning the development of artificial photosynthesis. Here, we examined excitation energy transfer of various RC-LH1 supercomplexes of Rhodobacter sphaeroides using transient absorption spectroscopy, coupled with lifetime density analysis, and studied the roles of the integral transmembrane polypeptides, PufX and PufY, in energy transfer within the RC-LH1 core complex. Our results show that the absence of PufX increases both the LH1 → RC excitation energy transfer lifetime and distribution due to the role of PufX in defining the interaction and orientation of the RC within the LH1 ring. While the absence of PufY leads to the conformational shift of several LH1 subunits toward the RC, it does not result in a marked change in the excitation energy transfer lifetime.

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.

Monitoring interfacial electric fields at a hematite electrode during water oxidation.

To understand the mechanisms of water oxidation on materials such as hematite it is important that accurate measurements and models of the interfacial fields at the semiconductor liquid junction are developed. Here we demonstrate how electric field induced second harmonic generation (EFISHG) spectroscopy can be used to monitor the electric field across the space-charge and Helmholtz layers in a hematite electrode during water oxidation. We are able to identify the occurrence of Fermi level pinning at specific applied potentials which lead to a change in the Helmholtz potential. Through combined electrochemical and optical measurements we correlate these to the presence of surface trap states and the accumulation of holes (h+) during electrocatalysis. Despite the change in Helmholtz potential as h+ accumulate we find that a population model can be used to fit the electrocatalytic water oxidation kinetics with a transition between a first and third order regime with respect to hole concentration. Within these two regimes there are no changes in the rate constants for water oxidation, indicating that the rate determining step under these conditions does not involve electron/ion transfer, in-line with it being O-O bond formation.

Hybrid photocathode based on a Ni molecular catalyst and Sb2Se3 for solar H2 production.

We report a H2 evolving hybrid photocathode based on Sb2Se3 and a precious metal free molecular catalyst. Through the use of a high surface area TiO2 scaffold, we successfully increased the Ni molecular catalyst loading from 7.08 ± 0.43 to 45.76 ± 0.81 nmol cm-2, achieving photocurrents of 1.3 mA cm-2 at 0 V vs. RHE, which is 81-fold higher than the device without the TiO2 mesoporous layer.

Packing-induced selectivity switching in molecular nanoparticle photocatalysts for hydrogen and hydrogen peroxide production.

Molecular packing controls optoelectronic properties in organic molecular nanomaterials. Here we report a donor-acceptor organic molecule (2,6-bis(4-cyanophenyl)-4-(9-phenyl-9H-carbazol-3-yl)pyridine-3,5-dicarbonitrile) that exhibits two aggregate states in aqueous dispersions: amorphous nanospheres and ordered nanofibres with π-π molecular stacking. The nanofibres promote sacrificial photocatalytic H2 production (31.85 mmol g-1 h-1) while the nanospheres produce hydrogen peroxide (H2O2) (3.20 mmol g-1 h-1 in the presence of O2). This is the first example of an organic photocatalyst that can be directed to produce these two different solar fuels simply by changing the molecular packing. These different packings affect energy band levels, the extent of excited state delocalization, the excited state dynamics, charge transfer to O2 and the light absorption profile. We use a combination of structural and photophysical measurements to understand how this influences photocatalytic selectivity. This illustrates the potential to achieve multiple photocatalytic functionalities with a single organic molecule by engineering nanomorphology and solid-state packing.

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.

Tuning the local chemical environment of ZnSe quantum dots with dithiols towards photocatalytic CO2 reduction.

Sunlight-driven CO2 reduction to renewable fuels is a promising strategy towards a closed carbon cycle in a circular economy. For that purpose, colloidal quantum dots (QDs) have emerged as a versatile light absorber platform that offers many possibilities for surface modification strategies. Considerable attention has been focused on tailoring the local chemical environment of the catalytic site for CO2 reduction with chemical functionalities ranging from amino acids to amines, imidazolium, pyridines, and others. Here we show that dithiols, a class of organic compounds previously unexplored in the context of CO2 reduction, can enhance photocatalytic CO2 reduction on ZnSe QDs. A short dithiol (1,2-ethanedithiol) activates the QD surface for CO2 reduction accompanied by a suppression of the competing H2 evolution reaction. In contrast, in the presence of an immobilized Ni(cyclam) co-catalyst, a longer dithiol (1,6-hexanedithiol) accelerates CO2 reduction. 1H-NMR spectroscopy studies of the dithiol-QD surface interactions reveal a strong affinity of the dithiols for the QD surface accompanied by a solvation sphere governed by hydrophobic interactions. Control experiments with a series of dithiol analogues (monothiol, mercaptoalcohol) render the hydrophobic chemical environment unlikely as the sole contribution of the enhancement of CO2 reduction. Density functional theory (DFT) calculations provide a framework to rationalize the observed dithiol length dependent activity through the analysis of the non-covalent interactions between the dangling thiol moiety and the CO2 reduction intermediates at the catalytic site. This work therefore introduces dithiol capping ligands as a straightforward means to enhance CO2 reduction catalysis on both bare and co-catalyst modified QDs by engineering the particle's chemical environment.

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.

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.

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.

Time-Resolved Raman Spectroscopy of Polaron Formation in a Polymer Photocatalyst.

Polymer photocatalysts are a synthetically diverse class of materials that can be used for the production of solar fuels such as H2, but the underlying mechanisms by which they operate are poorly understood. Time-resolved vibrational spectroscopy provides a powerful structure-specific probe of photogenerated species. Here we report the use of time-resolved resonance Raman (TR3) spectroscopy to study the formation of polaron pairs and electron polarons in one of the most active linear polymer photocatalysts for H2 production, poly(dibenzo[b,d]thiophene sulfone), P10. We identify that polaron-pair formation prior to thermalization of the initially generated excited states is an important pathway for the generation of long-lived photoelectrons.

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.

Alkaline Water Oxidation Using a Bimetallic Phospho-Boride Electrocatalyst.

New oxygen evolution reaction (OER) electrocatalysts based on low-cost elements, which set new benchmark levels of activity, are vital if water electrolysis is to be applied on a global scale. Herein, a low-cost bimetallic phospho-boride catalyst was developed that showed outstanding OER activity of approximately 195 mV to achieve 10 mA cm-2 in alkaline water electrolysis, with a minimal catalyst loading of 0.3 mg cm-2 . The contrasting electron transfer property of the metal borides and phosphides when combined in phospho-boride modulated the electron density of the Co atom, yielding highly active CoOOH species at lower potentials. The addition of Mo at low levels further enhanced the activity by increasing the surface area and by formation of nano-crystalline domains. The combined contributions from each of the components resulted in a new benchmark mass activity of 666 A g-1 at 300 mV overpotential. This work presents a new avenue towards fabricating electrode materials with exceptional performances.