Water oxidation kinetics of nanoporous BiVO4 photoanodes functionalised with nickel/iron oxyhydroxide electrocatalysts

In this work, spectroelectrochemical techniques are employed to analyse the catalytic water oxidation performance of a series of three nickel/iron oxyhydroxide electrocatalysts deposited on FTO and BiVO₄, at neutral pH. Similar electrochemical water oxidation performance is observed for each of the FeOOH, Ni(Fe)OOH and FeOOHNiOOH electrocatalysts studied, which is found to result from a balance between degree of charge accumulation and rate of water oxidation. Once added onto BiVO₄ photoanodes, a large enhancement in the water oxidation photoelectrochemical performance is observed in comparison to the un-modified BiVO₄. To understand the origin of this enhancement, the films were evaluated through time-resolved optical spectroscopic techniques, allowing comparisons between electrochemical and photoelectrochemical water oxidation. For all three catalysts, fast hole transfer from BiVO₄ to the catalyst is observed in the transient absorption data. Using operando photoinduced absorption measurements, we find that water oxidation is driven by oxidised states within the catalyst layer, following hole transfer from BiVO₄. This charge transfer is correlated with a suppression of recombination losses which result in remarkably enhanced water oxidation performance relative to un-modified BiVO₄. Moreover, despite similar electrocatalytic behaviour of all three electrocatalysts, we show that variations in water oxidation performance observed among the BiVO₄/MOOH photoanodes stem from differences in photoelectrochemical and electrochemical charge accumulation in the catalyst layers. Under illumination, the amount of accumulated charge in the catalyst is driven by the injection of photogenerated holes from BiVO₄, which is further affected by the recombination loss at the BiVO₄/MOOH interface, and thus leads to deviations from their behaviour as standalone electrocatalysts.

Elucidating the role of charge accumulation and reaction kinetics in governing the performance of Ni/Fe oxyhydroxides as electrocatalysts and as co-catalysts on BiVO₄ photoanodes water oxidation.     

Electrochemical oxidation of molecular nitrogen to nitric acid – towards a molecular level understanding of the challenges

Nitric acid is manufactured by oxidizing ammonia where the ammonia comes from an energy demanding and non-eco-friendly, Haber–Bosch process. Electrochemical oxidation of N₂ to nitric acid using renewable electricity could be a promising alternative to bypass the ammonia route. In this work, we discuss the plausible reaction mechanisms of electrochemical N₂ oxidation (N₂OR) at the molecular level and its competition with the parasitic oxygen evolution reaction (OER). We suggest the design strategies for N₂ oxidation electro-catalysts by first comparing the performance of two catalysts – TiO₂(110) (poor OER catalyst) and IrO₂(110) (good OER catalyst), towards dinitrogen oxidation and then establish trends/scaling relations to correlate OER and N₂OR activities. The challenges associated with electrochemical N₂OR are highlighted.

Electrochemical oxidation of N₂ to HNO₃ (N₂OR) is explored in conjunction with parasitic oxygen evolution reaction (OER) on a poor and a good OER catalyst, TiO₂ and IrO₂. We develop scaling relations to correlate OER and N₂OR activities on oxides.     

Effects of ruthenium hydride species on primary amine synthesis by direct amination of alcohols over a heterogeneous Ru catalyst

Heterogeneously catalysed synthesis of primary amines by direct amination of alcohols with ammonia has long been an elusive goal. In contrast to reported Ru-based catalytic systems, we report that Ru–MgO/TiO₂ acts as an effective heterogeneous catalyst for the direct amination of a variety of alcohols to primary amines at low temperatures of ca. 100 °C without the introduction of H₂ gas. The present system could be applied to a variety of alcohols and provides an efficient synthetic route for 2,5-bis(aminomethyl)furan (BAMF), an attention-getting biomonomer. The high catalytic performance can be rationalized by the reactivity tuning of Ru–H species using MgO. Spectroscopic measurements suggest that MgO enhances the reactivity of hydride species by electron donation from MgO to Ru.

Ru–MgO/TiO₂ exhibited high catalytic performance for direct amination of alcohols based on the acceleration effects of MgO.     

Direct observation of the evolving metal–support interaction of individual cobalt nanoparticles at the titania and silica interface

Understanding the metal–support interaction (MSI) is crucial to comprehend how the catalyst support affects performance and whether this interaction can be exploited in order to design new catalysts with enhanced properties. Spatially resolved soft X-ray absorption spectroscopy (XAS) in combination with Atomic Force Microscopy (AFM) and Scanning Helium Ion-Milling Microscopy (SHIM) has been applied to visualise and characterise the behaviour of individual cobalt nanoparticles (CoNPs) supported on two-dimensional substrates (SiO_xSi(100) (x < 2) and rutile TiO₂(110)) after undergoing reduction–oxidation–reduction (ROR). The behaviour of the Co species is observed to be strongly dependent on the type of support. For SiO_xSi a weaker MSI between Co and the support allows a complete reduction of CoNPs although they migrate and agglomerate. In contrast, a stronger MSI of CoNPs on TiO₂ leads to only a partial reduction under H₂ at 773 K (as observed from Co L₃-edge XAS data) due to enhanced TiO₂ binding of surface-exposed cobalt. SHIM data revealed that the interaction of the CoNPs is so strong on TiO₂, that they are seen to spread at and below the surface and even to migrate up to ∼40 nm away. These results allow us to better understand deactivation phenomena and additionally demonstrate a new understanding concerning the nature of the MSI for Co/TiO₂ and suggest that there is scope for careful control of the post-synthetic thermal treatment for the tuning of this interaction and ultimately the catalytic performance.

Understanding the metal–support interaction (MSI) is crucial to comprehend how the catalyst support affects performance and whether this interaction can be exploited in order to design new catalysts with enhanced properties.     

The dome of gold nanolized for catalysis

Gold is noble in bulk but turns out to be a superior catalyst at the nanoscale when supported on oxides, in particular titania. The critical thickness for activity, namely two-layer gold particles on titania, observed two decades ago represents one of the most influential mysteries in the recent history of heterogeneous catalysis. By developing a Bayesian optimization controlled global potential energy surface exploration tool with machine learning potential, here we determine the atomic structures of gold particles within ∼2 nm on a TiO₂ surface. We show that the smallest stable Au nanoparticle is Au₂₄ which is pinned on the oxygen-rich TiO₂ and exhibits an unprecedented dome architecture made by a single-layer Au sheet but with an apparent two-atomic-layer height. Importantly, this has the highest activity for CO oxidation at room temperature. The physical origin of the high activity is the outstanding electron storage ability of the nano-dome, which activates the lattice oxygen of the oxide. The determined CO oxidation mechanism, the simulated rate and the fitted apparent energy barrier are consistent with known experimental facts, providing key evidence for the presence of both the high-activity Au dome and the low-activity close-packed Au particles in real catalysts. The future direction for the preparation of active and stable Au-based catalysts is thus outlined.

The smallest stable Au particle Au₂₄O₄ on TiO₂ surface is determined by the machine learning assisted global optimization, exhibiting a dome architecture made by a single-layer sheet and the highest activity for CO oxidation at room temperature.     

Electron Transfer in Dye‐Sensitised Semiconductors Modified with Molecular Cobalt Catalysts: Photoreduction of Aqueous Protons

A visible‐light driven H₂ evolution system comprising of a Ru^II dye ( RuP ) and Co^III proton reduction catalysts ( CoP ) immobilised on TiO₂ nanoparticles and mesoporous films is presented. The heterogeneous system evolves H₂ efficiently during visible‐light irradiation in a pH‐neutral aqueous solution at 25 °C in the presence of a hole scavenger. Photodegradation of the self‐assembled system occurs at the ligand framework of CoP , which can be readily repaired by addition of fresh ligand, resulting in turnover numbers above 300 mol H₂ (mol CoP )^?1 and above 200,000 mol H₂ (mol TiO₂ nanoparticles)^?1 in water. Our studies support that a molecular Co species, rather than metallic Co or a Co‐oxide precipitate, is responsible for H₂ formation on TiO₂. Electron transfer in this system was studied by transient absorption spectroscopy and time‐correlated single photon counting techniques. Essentially quantitative electron injection takes place from RuP into TiO₂ in approximately 180 ps. Thereby, upon dye regeneration by the sacrificial electron donor, a long‐lived TiO₂ conduction band electron is formed with a half‐lifetime of approximately 0.8 s. Electron transfer from the TiO₂ conduction band to the CoP catalysts occurs quantitatively on a 10 μs timescale and is about a hundred times faster than charge‐recombination with the oxidised RuP . This study provides a benchmark for future investigations in photocatalytic fuel generation with molecular catalysts integrated in semiconductors.     

SDS-induced multi-stage unfolding of a small globular protein through different denatured states revealed by single-molecule fluorescence

Ionic surfactants such as sodium dodecyl sulfate (SDS) unfold proteins in a much more diverse yet effective way than chemical denaturants such as guanidium chloride (GdmCl). But how these unfolding processes compare on a molecular level is poorly understood. Here, we address this question by scrutinising the unfolding pathway of the globular protein S6 in SDS and GdmCl with single-molecule Förster resonance energy transfer (smFRET) spectroscopy. We show that the unfolding mechanism in SDS is strikingly different and convoluted in comparison to denaturation in GdmCl. In contrast to the reversible two-state unfolding behaviour in GdmCl characterised by kinetics on the timescale of seconds, SDS demonstrated not one, but four distinct regimes of interactions with S6, dependent on the surfactant concentration. At ≤1 mM SDS, S6 and surfactant molecules form quasi-micelles on a minute timescale; at millimolar [SDS], the protein denatures through an unfolded/denatured ensemble of highly heterogeneous states on a multi-second timescale; at tens of millimolar of SDS, the protein unfolds into a micelle-packed conformation on the second timescale; and >50 mM SDS, the protein unfolds with millisecond timescale dynamics. We propose a detailed model for multi-stage unfolding of S6 in SDS, which involves at least three different types of denatured states with different level of compactness and dynamics and a continually changing landscape of interactions between protein and surfactant. Our results highlight the great potential of single-molecule fluorescence as a direct probe of nanoscale protein structure and dynamics in chemically complex surfactant environments.

Multi-stage unfolding of S6 in SDS involving various types of denatured states with different levels of compactness and dynamics.     

Photocatalyst-independent photoredox ring-opening polymerization of O-carboxyanhydrides: stereocontrol and mechanism

Photoredox ring-opening polymerization of O-carboxyanhydrides allows for the synthesis of polyesters with precisely controlled molecular weights, molecular weight distributions, and tacticities. While powerful, obviating the use of precious metal-based photocatalysts would be attractive from the perspective of simplifying the protocol. Herein, we report the Co and Zn catalysts that are activated by external light to mediate efficient ring-opening polymerization of O-carboxyanhydrides, without the use of exogenous precious metal-based photocatalysts. Our methods allow for the synthesis of isotactic polyesters with high molecular weights (>200 kDa) and narrow molecular weight distributions (M_w/M_n < 1.1). Mechanistic studies indicate that light activates the oxidative status of a Co^III intermediate that is generated from the regioselective ring-opening of the O-carboxyanhydride. We also demonstrate that the use of Zn or Hf complexes together with Co can allow for stereoselective photoredox ring-opening polymerizations of multiple racemic O-carboxyanhydrides to synthesize syndiotactic and stereoblock copolymers, which vary widely in their glass transition temperatures.

Photoredox ring-opening polymerization of O-carboxyanhydrides allows for the synthesis of functionalized polyesters with high molecular weights, narrow molecular weight distributions, and various tacticities.     

Modulation of the superficial electronic structure via metal–support interaction for H2 evolution over Pd catalysts

Electronic interactions can radically enhance the performance of supported metal catalysts and are critical for fundamentally understanding the nature of catalysts. However, at the microscopic level, the details of such interactions tuning the electronic properties of the sites on the metal particle''s surface and metal–support interface remain obscure. Herein, we found polarized electronic metal–support interaction (pEMSI) in oxide-supported Pd nanoparticles (NPs) describing the enhanced accumulation of electrons at the surface of NPs (superficial Pd^δ−) with positive Pd atoms distributed on the interface (interfacial Pd^δ+). More superficial Pd^δ− species mean stronger pEMSI resulting from the synergistic effect of moderate Pd–oxide interaction, high structural fluxionality and electron transport activity of Pd NPs. The surface Pd^δ− species are responsible for improved catalytic performance for H₂ evolution from metal hydrides and formates. These extensive insights into the nature of supported-metal NPs may open new avenues for regulating a metal particle''s electronic structure precisely and exploiting high-performance catalysts.

A new type of electronic effect, polarized metal-support interaction (pEMSI), in oxide-supported Pd nanoparticles describing the enhanced accumulation of electrons at the superficial surface is responsible for improved catalytic H₂ evolution.     

Low-temperature deposition and crystallization of RuO2/TiO2 on cotton fabric for efficient solar photocatalytic degradation of o-toluidine

A green low-temperature deposition and crystallization method was developed to uniformly coat RuO₂/TiO₂ nanocomposite onto cotton fabrics for efficient solar photocatalysis. The sequential growth of anatase TiO₂ and rutile RuO₂ on the surface of the cotton was confirmed by XRD, Raman and XPS characterizations. After the deposition of RuO₂, the optical properties of RuO₂/TiO₂/Cotton revealed better visible light absorption and higher charge mobility, and XPS spectra showed that the peaks of Ti 2p_3/2 and O 1 s shifted towards the lower binding energies due to the interfacial charge transfer at the robust RuO₂/TiO₂ mediated with Ti–O–Ru bonding. The photocatalytic performances of the RuO₂/TiO₂/Cotton were evaluated towards the photodegradation of o-toluidine (o-TD), an aromatic amine widely used in the chemical industry. Compared with TiO₂/Cotton, RuO₂/TiO₂/Cotton exhibited a remarkable improvement in the photocatalytic activity. The presence of RuO₂ on the surface of TiO₂/Cotton narrowed the band gap and improved the absorption of visible light. Moreover, the successful formation of a robust heterogeneous interface between TiO₂ and RuO₂ suppressed the charge carrier (e^–/h⁺) recombination effectively. With the RuO₂/TiO₂ coating chemically bound to the cotton fibers, RuO₂/TiO₂/Cotton delivered long-term stability in photocatalytic activity and high mechanical durability even after 20 washing times. Our facile and scalable synthesis strategy paved a universal route to efficient immobilization of visible-light-responsible TiO₂-based photocatalysts on the low-heat-resistant substrates for various applications.

Graphical abstract

     

In situ K-edge X-ray absorption spectroscopy of the ligand environment of single-site Au/C catalysts during acetylene hydrochlorination

The replacement of HgCl₂/C with Au/C as a catalyst for acetylene hydrochlorination represents a significant reduction in the environmental impact of this industrial process. Under reaction conditions atomically dispersed cationic Au species are the catalytic active site, representing a large-scale application of heterogeneous single-site catalysts. While the metal nuclearity and oxidation state under operating conditions has been investigated in catalysts prepared from aqua regia and thiosulphate, limited studies have focused on the ligand environment surrounding the metal centre. We now report K-edge soft X-ray absorption spectroscopy of the Cl and S ligand species used to stabilise these isolated cationic Au centres in the harsh reaction conditions. We demonstrate the presence of three distinct Cl species in the materials; inorganic Cl⁻, Au–Cl, and C–Cl and how these species evolve during reaction. Direct evidence of Au–S interactions is confirmed in catalysts prepared using thiosulfate precursors which show high stability towards reduction to inactive metal nanoparticles. This stability was clear during gas switching experiments, where exposure to C₂H₂ alone did not dramatically alter the Au electronic structure and consequently did not deactivate the thiosulfate catalyst.

In situ chlorine and sulphur XAS shows a dynamic ligand environment around cationic Au single-sites during acetylene hydrochlorination.     

Room temperature conductance switching in a molecular iron(iii) spin crossover junction

Herein, we report the first room temperature switchable Fe(iii) molecular spin crossover (SCO) tunnel junction. The junction is constructed from [Fe^III(qsal-I)₂]NTf₂ (qsal-I = 4-iodo-2-[(8-quinolylimino)methyl]phenolate) molecules self-assembled on graphene surfaces with conductance switching of one order of magnitude associated with the high and low spin states of the SCO complex. Normalized conductance analysis of the current–voltage characteristics as a function of temperature reveals that charge transport across the SCO molecule is dominated by coherent tunnelling. Temperature-dependent X-ray absorption spectroscopy and density functional theory confirm the SCO complex retains its SCO functionality on the surface implying that van der Waals molecule—electrode interfaces provide a good trade-off between junction stability while retaining SCO switching capability. These results provide new insights and may aid in the design of other types of molecular devices based on SCO compounds.

Herein, we report the first room temperature switchable Fe(iii) molecular spin crossover (SCO) tunnel junction.     

Identifying key mononuclear Fe species for low-temperature methane oxidation

The direct functionalization of methane into platform chemicals is arguably one of the holy grails in chemistry. The actual active sites for methane activation are intensively debated. By correlating a wide variety of characterization results with catalytic performance data we have been able to identify mononuclear Fe species as the active site in the Fe/ZSM-5 zeolites for the mild oxidation of methane with H₂O₂ at 50 °C. The 0.1% Fe/ZSM-5 catalyst with dominant mononuclear Fe species possess an excellent turnover rate (TOR) of 66 mol_MeOH mol_Fe⁻¹ h⁻¹, approximately 4 times higher compared to the state-of-the-art dimer-containing Fe/ZSM-5 catalysts. Based on a series of advanced in situ spectroscopic studies and ¹H- and ¹³C- nuclear magnetic resonance (NMR), we found that methane activation initially proceeds on the Fe site of mononuclear Fe species. With the aid of adjacent Brønsted acid sites (BAS), methane can be first oxidized to CH₃OOH and CH₃OH, and then subsequently converted into HOCH₂OOH and consecutively into HCOOH. These findings will facilitate the search towards new metal-zeolite combinations for the activation of C–H bonds in various hydrocarbons, for light alkanes and beyond.

The monomeric Fe species in Fe/ZSM-5 have been identified as the intrinsic active sites for the low-temperature methane oxidation.     

Quantification of the mixed-valence and intervalence charge transfer properties of a cofacial metal–organic framework via single crystal electronic absorption spectroscopy

Gaining a fundamental understanding of charge transfer mechanisms in three-dimensional Metal–Organic Frameworks (MOFs) is crucial to the development of electroactive and conductive porous materials. These materials have potential in applications in porous conductors, electrocatalysts and energy storage devices; however the structure–property relationships pertaining to charge transfer and its quantification are relatively poorly understood. Here, the cofacial Cd(ii)-based MOF [Cd(BPPTzTz)(tdc)]·2DMF (where BPPTzTz = 2,5-bis(4-(pyridin-4-yl)phenyl)thiazolo[5,4-d]thiazole, tdc²⁻ = 2,5-thiophene dicarboxylate) exhibits Intervalence Charge Transfer (IVCT) within its three-dimensional structure by virtue of the close, cofacial stacking of its redox-active BPPTzTz ligands. The mixed-valence and IVCT properties are characterised using a combined electrochemical, spectroelectrochemical and computational approach. Single crystal electronic absorption spectroscopy was employed to obtain the solid-state extinction coefficient, enabling the application of Marcus–Hush theory. The electronic coupling constant, H_ab, of 145 cm⁻¹ was consistent with the localised mixed-valence properties of both this framework and analogous systems that use alternative methods to obtain the H_ab parameter. This work demonstrates the first report of the successful characterisation of IVCT in a MOF material using single crystal electronic absorption spectroscopy and serves as an attractive alternative to more complex methods due to its simplicity and applicability.

Gaining a fundamental understanding of charge transfer mechanisms in three-dimensional Metal–Organic Frameworks (MOFs) is crucial to the development of electroactive and conductive porous materials.     

X-ray scattering reveals ion clustering of dilute chromium species in molten chloride medium

Enhancing the solar energy storage and power delivery afforded by emerging molten salt-based technologies requires a fundamental understanding of the complex interplay between structure and dynamics of the ions in the high-temperature media. Here we report results from a comprehensive study integrating synchrotron X-ray scattering experiments, ab initio molecular dynamics simulations and rate theory concepts to investigate the behavior of dilute Cr³⁺ metal ions in a molten KCl–MgCl₂ salt. Our analysis of experimental results assisted by a hybrid transition state-Marcus theory model reveals unexpected clustering of chromium species leading to the formation of persistent octahedral Cr–Cr dimers in the high-temperature low Cr³⁺ concentration melt. Furthermore, our integrated approach shows that dynamical processes in the molten salt system are primarily governed by the charge density of the constituent ions, with Cr³⁺ exhibiting the slowest short-time dynamics. These findings challenge several assumptions regarding specific ionic interactions and transport in molten salts, where aggregation of dilute species is not statistically expected, particularly at high temperature.

Ion clustering of dilute chromium species was unexpectedly revealed in a high-temperature molten chloride salt, challenging several long-held assumptions regarding specific ionic interactions and transport in molten ionic media.     

Top-down synthesis of polyoxometalate-like sub-nanometer molybdenum-oxo clusters as high-performance electrocatalysts

The top-down fabrication of catalytically active molecular metal oxide anions, or polyoxometalates, is virtually unexplored, although these materials offer unique possibilities, for catalysis, energy conversion and storage. Here, we report a novel top-down route, which enables the scalable synthesis and deposition of sub-nanometer molybdenum-oxo clusters on electrically conductive mesoporous carbon. The new approach uses a unique redox-cycling process to convert crystalline Mo^IVO₂ particles into sub-nanometer molecular molybdenum-oxo clusters with a nuclearity of ∼1–20. The resulting molybdenum-oxo cluster/carbon composite shows outstanding, stable electrocatalytic performance for the oxygen reduction reaction with catalyst characteristics comparable to those of commercial Pt/C. This new material design could give access to a new class of highly reactive polyoxometalate-like metal oxo clusters as high-performance, earth abundant (electro-)catalysts.

The top-down synthesis and deposition of polyoxometalate-like clusters on porous carbon is reported together with the high electrocatalytic oxygen reduction reactivity of the composite.     

Ortho C–H arylation of arenes at room temperature using visible light ruthenium C–H activation

A ruthenium-catalyzed ortho C–H arylation process is described using visible light. Using the readily available catalyst [RuCl₂(p-cymene)]₂, visible light irradiation was found to enable arylation of 2-aryl-pyridines at room temperature for a range of aryl bromides and iodides.

A ruthenium-catalyzed ortho C–H arylation process is described using visible light.     

Data-powered augmented volcano plots for homogeneous catalysis

Given the computational resources available today, data-driven approaches can propel the next leap forward in catalyst design. Using a data-driven inspired workflow consisting of data generation, statistical analysis, and dimensionality reduction algorithms we explore trends surrounding the thermodynamics of a model hydroformylation reaction catalyzed by group 9 metals bearing phosphine ligands. Specifically, we introduce “augmented volcano plots” as a means to easily visualize the similarity of each catalyst''s complete catalytic cycle energy profile to that of a hypothetical ideal reference profile without relying upon linear scaling relationships. In addition to quickly identifying catalysts that most closely match the ideal thermodynamic catalytic cycle energy profile, these maps also enable a more refined comparison of closely lying species in standard volcano plots. For the reaction studied here, they inherently uncover the presence of multiple sets of scaling relationships differentiated by metal type, where iridium catalysts follow distinct relationships from cobalt/rhodium catalysts and have profiles that more closely match the ideal thermodynamic profile. Reconstituted molecular volcano plots confirm the findings of the augmented volcanoes by showing that hydroformylation thermodynamics are governed by two distinct volcano shapes, one for iridium catalysts and a second for cobalt/rhodium species.

Augmented volcano plots, a tool for comparing and visualizing the similarity of a number of complete catalytic cycle energy profiles to that of an ideal reference profile without relying on linear scaling relationships, are introduced.     

Recent advances in single atom catalysts for the electrochemical carbon dioxide reduction reaction

The electrochemical carbon dioxide reduction reaction (CO₂RR) offers a promising solution to mitigate carbon emission and at the same time generate valuable carbonaceous chemicals/fuels. Single atom catalysts (SACs) are encouraging to catalyze the electrochemical CO₂RR due to the tunable electronic structure of the central metal atoms, which can regulate the adsorption energy of reactants and reaction intermediates. Moreover, SACs form a bridge between homogeneous and heterogeneous catalysts, providing an ideal platform to explore the reaction mechanism of electrochemical reactions. In this review, we first discuss the strategies for promoting the CO₂RR performance, including suppression of the hydrogen evolution reaction (HER), generation of C₁ products and formation of C₂₊ products. Then, we summarize the recent developments in regulating the structure of SACs toward the CO₂RR based on the above aspects. Finally, several issues regarding the development of SACs for the CO₂RR are raised and possible solutions are provided.

The electrochemical carbon dioxide reduction reaction (CO₂RR) offers a promising solution to mitigate carbon emission and at the same time generate valuable carbonaceous chemicals/fuels.     

Defective TiO2 for photocatalytic CO2 conversion to fuels and chemicals

Photocatalytic conversion of CO₂ into fuels and valuable chemicals using solar energy is a promising technology to combat climate change and meet the growing energy demand. Extensive effort is going on for the development of a photocatalyst with desirable optical, surface and electronic properties. This review article discusses recent development in the field of photocatalytic CO₂ conversion using defective TiO₂. It specifically focuses on the different synthesis methodologies adapted to generate the defects and their impact on the chemical, optical and surface properties of TiO₂ and, thus, photocatalytic CO₂ conversion. It also encompasses theoretical investigations performed to understand the role of defects in adsorption and activation of CO₂ and identify the mechanistic pathway which governs the formation and selectivity of different products. It is divided into three parts: (i) general mechanism and thermodynamic criteria for defective TiO₂ catalyzed CO₂ conversion, (ii) theoretical investigation on the role of defects in the CO₂ adsorption–activation and mechanism responsible for the formation and selectivity of different products, and (iii) the effect of variation of physicochemical properties of defective TiO₂ synthesized using different methods on the photocatalytic conversion of CO₂. The review also discusses the limitations and the challenges of defective TiO₂ photocatalysts that need to be overcome for the production of sustainable fuel utilizing solar energy.

This review discusses photocatalytic CO₂ conversion using defective TiO₂, with emphasis on the mechanism, the role of defects on CO₂ adsorption–activation and product selectivity, as well as challenges of defective TiO₂ to produce solar fuels.