Core-shell nanostructured Cu-based bi-metallic electrocatalysts for co-production of ethylene and acetate.

Direct electrocatalytic CCU routes to produce a myriad of valuable chemicals (e.g., methanol, acetic acid, ethylene, propanol, among others) will allow the chemical industry to shift away from the conventional fossil-based production. Electrofuels need to go beyond the current electroreduction of CO2 to CO, and we will here demonstrate the continuous flow electroreduction of syngas (i.e., CO and H2), which are the products from CO2-to-CO, with enhanced product selectivity (∼90% towards ethylene). To overcome current drawbacks, including bicarbonate formation that resulted in low CO2 utilisation and low C2+ product selectivity, the development of nanostructured core-shell bi-metallic electrocatalysts for direct electrochemical reduction of syngas to C2+ is proposed. Electrosynthesis of ethylene is performed in a state-of-the-art continuous flow three-compartment cell to produce ethylene (cathodic gas phase product) and acetate (cathodic liquid phase product), simultaneously.

Highly selective CO2 photoreduction to CO on MOF-derived TiO2.

Metal-Organic Framework (MOF)-derived TiO2, synthesised through the calcination of MIL-125-NH2, is investigated for its potential as a CO2 photoreduction catalyst. The effect of the reaction parameters: irradiance, temperature and partial pressure of water was investigated. Using a two-level design of experiments, we were able to evaluate the influence of each parameter and their potential interactions on the reaction products, specifically the production of CO and CH4. It was found that, for the explored range, the only statistically significant parameter is temperature, with an increase in temperature being correlated to enhanced production of both CO and CH4. Over the range of experimental settings explored, the MOF-derived TiO2 displays high selectivity towards CO (98%), with only a small amount of CH4 (2%) being produced. This is notable when compared to other state-of-the-art TiO2 based CO2 photoreduction catalysts, which often showcase lower selectivity. The MOF-derived TiO2 was found to have a peak production rate of 8.9 × 10-4 µmol cm-2 h-1 (2.6 µmol g-1 h-1) and 2.6 × 10-5 µmol cm-2 h-1 (0.10 µmol g-1 h-1) for CO and CH4, respectively. A comparison is made to commercial TiO2, P25 (Degussa), which was shown to have a similar activity towards CO production, 3.4 × 10-3 µmol cm-2 h-1 (5.9 µmol g-1 h-1), but a lower selectivity preference for CO (3 : 1 CH4 : CO) than the MOF-derived TiO2 material developed here. This paper showcases the potential for MIL-125-NH2 derived TiO2 to be further developed as a highly selective CO2 photoreduction catalyst for CO production.

Investigation of CO2 Photoreduction in an Annular Fluidized Bed Photoreactor by MP-PIC Simulation.

Carbon dioxide (CO2) photoreduction is a promising process for both mitigating CO2 emissions and providing chemicals and fuels. A gas-solid two-phase annular fluidized bed photoreactor (FBPR) would be preferred for this process due to its high mass-transfer rate and easy operation. However, CO2 photoreduction using the FBPR has not been widely researched to date. The Lagrangian multiphase particle-in-cell (MP-PIC) simulation with computational fluid dynamic models is a new and robust approach to explore the multiphase reaction system in the gas-solid fluidized bed. Therefore, the purpose of this paper is to investigate CO2 photoreduction in the FBPR by MP-PIC modeling to understand the intrinsic mechanism of solid flow, species mass transfer, and CO2 photoreaction. The MP-PIC models for solid flow in the FBPR were validated by the bed expansion height and bubble size. The results showed the particle stress of the Lun model, the drag of the Ergun-WenYu (Gidaspow) model, and the coefficient of restitution e = 0.95 with the wall parameters e w = 0.9 and µw = 0.6 are the best fit to the experimental empirical correlations. The MP-PIC models developed in this work proved to be better than the Eulerian two-fluid modeling in the prediction of the bed expansion height and bubble size. It was also found from the simulation results that the maximum radiation intensity is in the half reactor height area, and the photocatalytic reaction mainly occurred around the inner wall. It showed that the gas velocity and catalyst loading were two crucial operating parameters to control the process. The results reported here can provide guidance for the operation and reactor design of the CO2 photoreduction process.

Core-shell TiO2-x-CuyO microspheres for photogeneration of cyclic carbonates under simulated sunlight.

Propylene carbonates are important organic solvents and feedstocks for different applications, including synthesis of polymers and Li-batteries. The generation of propylene carbonate utilising anthropogenic CO2 and renewable solar energy offers an alternative sustainable process with a closed loop carbon cycle. The development of microstructured photocatalysts with desired properties, including high degree of product selectivity, wide range of optical properties, and maximised conversion yield, plays an important role for effective production of propylene carbonate from CO2. A hierachical hollow core with a double shell of TiO2-x-Cu2O-CuO was fabricated using the versatile solvothermal-microwave synthesis method. The fabricated sample revealed effective cascading of photogenerated electrons and holes that promoted the conversion of propylene carbonate (i.e., 1.6 wt%) under 1 Sun irradiation.

Hierarchical hyper-branched titania nanorods with tuneable selectivity for CO2 photoreduction.

Utilising captured CO2 and converting it into solar fuels can be extremely beneficial in reducing the constantly rising CO2 concentration in the atmosphere while simultaneously addressing energy crisis issues. Hence, many researchers have focused their work on the CO2 photoreduction reaction for the last 4 decades. Herein, the titania hyper-branched nanorod (HBN) thin films, with a novel hierarchical dendritic morphology, revealed enhanced CO2 photoreduction performance. The HBNs exhibited enhanced photogenerated charge production (66%), in comparison with P25 (39%), due to the unique hyper-branched morphology. Furthermore, the proposed HBN thin films exhibited a high degree of control over the product selectivity, by undergoing a facile phase-altering treatment. The selectivity was shifted from 91% towards CO, to 67% towards CH4. Additionally, the HBN samples showed the potential to surpass the conversion rates of the benchmark P25 TiO2 in both CO and CH4 production. To further enhance the selectivity and overall performance of the HBNs, RuO2 was incorporated into the synthesis, which enhanced the CH4 selectivity from 67% to 74%; whereas the incorporation of CuO revealed a selectivity profile comparative to P25.

Synthesis of TiO2-x/W18O49 hollow double-shell and core-shell microspheres for CO2 photoreduction under visible light.

TiO2-x/W18O49 with core-shell or double-shelled hollow microspheres were synthesized through a facile multi-step solvothermal method. The formation of the hollow microspheres with a double-shell was a result of the Kirkendall effect during the solvothermal treatment with concentrated NaOH. The advanced architecture significantly enhanced the electronic properties of TiO2-x/W18O49, improving by more than 30 times the CO2 photoreduction efficiency compared to the pristine W18O49. Operando DRIFTS measurements revealed that the yellow TiO2-x was a preferable CO2 adsorption and conversion site.

Alkali modified P25 with enhanced CO2 adsorption for CO2 photoreduction.

To improve the CO2 adsorption on the photocatalyst, which is an essential step for CO2 photoreduction, solid solutions were fabricated using a facile calcination treatment at 900 °C. Using various alkalis, namely NaOH, Na2CO3, KOH, K2CO3, the resulted samples presented a much higher CO2 adsorption capacity, which was measured with the pulse injection of CO2 on the temperature programmed desorption workstation, compared to the pristine Evonik P25. As a result, all of the fabricated solid solutions produced higer yield of CO under UV light irradiation due to the increased basicity of the solid solutions even though they possessed only the rutile polymorph of TiO2. The highest CO2 adsorption capacity under UV irradiation was observed in the sample treated with NaOH, which contained the highest amount of isolated hydroxyls, as shown in the FTIR studies.

Raspberry-Like Microspheres of Core-Shell Cr2 O3 @TiO2 Nanoparticles for CO2 Photoreduction.

To promote the interaction of p-n semiconductors, raspberry-like microspheres of core-shell Cr2 O3 @TiO2 nanoparticles have been fabricated through a five-step process. Raman spectroscopy of products calcined at various temperatures reveal that the titania shell causes crystal distortion of the Cr2 O3 core, without changing the microstructures of the fabricated core-shell microspheres. In situ and time-resolved synchrotron-based powder XRD reveals the formation of monoclinic TiO2 in the fourth step, but these monoclinic TiO2 nanocrystals undergo a phase transition when the applied calcination temperature is above 550 °C. As a result, TiO2 (B), a magnéli phase of Ti4 O7 and Cr2 Ti6 O15 compounds, resulting from inner doping between Cr2 O3 and TiO2 , is formed. The close interaction of Cr2 O3 and TiO2 forms a p-n junction that decreases the recombination of photogenerated electron-hole pairs, leading to enhanced production of CH4 by photocatalytic reduction of CO2 .

Photo-generation of cyclic carbonates using hyper-branched Ru-TiO2.

Anthropogenic CO2 is the main contributor to the increased concentration of greenhouse gases in the atmosphere, and thus utilising waste CO2 for the production of valuable chemicals is a very appealing strategy for reducing CO2 emissions. The catalytic fixation of CO2 with epoxides for the production of cyclic carbonates has gained increasing attention from the research community in search of an alternative to the homogeneous catalytic routes, which are currently being used in industry. A novel photocatalytic heterogeneous approach to generate cyclic carbonates is demonstrated in this work. Hyper-branched microstructured Ru modified TiO2 nanorods decorated with RuO2 nanoparticles, supported on fluorine-doped tin oxide (FTO) glass were fabricated for the first time and were used to catalyse the photo-generation of propylene carbonates from propylene oxides. Propylene carbonate was used as a reference for cyclic carbonates. The photo-generation of cyclic carbonates from epoxides and CO2 was carried out at a maximum temperature of 55 °C at 200 kPa in a stainless steel photoreactor with a quartz window, under solar irradiation for 6 h. The best performing photocatalyst exhibited an estimated selectivity of 83% towards propylene carbonates under the irradiation of a solar simulator.

A microfluidic photoelectrochemical cell for solar-driven CO2 conversion into liquid fuels with CuO-based photocathodes.

Utilising photoelectrochemical (PEC) devices to produce sustainable fuels from water and CO2 is a very attractive strategy, in which sunlight is used to convert the greenhouse gas (CO2) into a usable form of stored chemical energy. While significant progress has been made in the development of efficient photoactive catalysts for PEC reactions, limited efforts have been focused on the reactor design where continuous flow microfluidic PEC reactors are particular promising. In this work, a range of CuO-based thin films were used as photocathodes in a continuous flow microfluidic PEC reactor using CO2-saturated aqueous NaHCO3 solution under simulated AM 1.5 solar irradiation for up to 12 h. The highest photocurrent density obtained was for the α-Fe2O3/CuO photoelectrode yielding -1.0 mA cm-2 at 0.3 V vs. RHE and initial results indicated a solar-to-fuel (STF) efficiency of 0.48%. While the CuO, Cu2O and CuO-Cu2O photoelectrodes virtually only formed formate, the bilayer α-Fe2O3/CuO photocathode produced methanol in addition to formate indicating that combined copper and iron oxides in continuous flow microfluidic PEC cells have great potential of direct solar conversion into useful chemicals.

High-Performance Coral Reef-like Carbon Nitrides: Synthesis and Application in Photocatalysis and Heavy Metal Ion Adsorption.

Synthesis of carbon nitrides (CNx) by refluxing under nitrogen exhibited mixed growth mechanisms of oriented attachment and Ostwald ripening, leading to the formation of coral reef-like microstructures from spherical agglomerates. Some phase transformation from ß-phase to α-phase CNx occurred upon refluxing for 1.5 h, producing a biphasic CNx. The N content relative to C was determined from CHN elemental analysis, and the presence of C═N and terminal groups (i.e., COOH and NH2) was consistent with the Fourier transform infrared, nuclear magnetic resonance, and X-ray photoelectron spectroscopic results. The sample refluxed for 2.0 h (CNx/2.0 h) had the highest surface area of 24.5 m2·g-1 and displayed enhanced adsorption capacities for methylene blue (MB) molecules and heavy metal ions Pb2+ (720 mg·g-1), Cd2+ (480 mg·g-1), and As(V) (220 mg·g-1), which was attributed to the presence of COOH functional groups. CNx samples had a negative surface charge that electrostatically attracted the cationic heavy metal ions as well as MB molecules for subsequent photodecomposition under visible-light illumination. The photocatalytic activity of CNx/2.0 h toward phenol, a common pollutant in aqueous waste, was also demonstrated and a possible photocatalytic route was proposed.

Probing the Effects of Templating on the UV and Visible Light Photocatalytic Activity of Porous Nitrogen-Modified Titania Monoliths for Dye Removal.

Porous nitrogen-modified titania (N-titania) monoliths with tailored morphologies were prepared using phase separation and agarose gel templating techniques. The doping and templating process were simultaneously carried out in a one-pot step using alcohol amine-assisted sol-gel chemistry. The amount of polymer used in the monoliths that were prepared using phase separation was shown to affect both the physical and optical properties: higher poly(ethylene glycol) content increased the specific surface area, porosity, and visible light absorption of the final materials. For the agarose-templated monoliths, the infiltration conditions affected the monolith morphology. A porous monolith with high surface area and the least shrinkage was obtained when the N containing alkoxide precursor was infiltrated into the agarose scaffolds at 60 °C. The effect of the diverse porous morphologies on the photocatalytic activity of N-titania was studied for the decomposition of methylene blue (MB) under visible and UV light irradiation. The highest visible light activity was achieved by the agarose-templated N-titania monolith, in part due to higher N incorporation. This sample also showed better UV activity, partly because of the higher specific surface area (up to 112 m(2) g(-1)) compared to the phase separation-induced monoliths (up to 103 m(2) g(-1)). Overall, agarose-templated, porous N-titania monoliths provided better features for effectively removing the MB contaminant.

Flowerlike WSe2 and WS2 microspheres: one-pot synthesis, formation mechanism and application in heavy metal ion sequestration.

Flowerlike WSe2 and WS2 microspheres were synthesized by a facile and scalable one-pot solvothermal method. Their formation mechanism followed the reaction between dissolved W(CO)6 and dissolved S or melted Se without complete decomposition of W(CO)6 into tungsten. As novel efficient sorbents, WSe2 and WS2 demonstrated outstanding uptake capacities for Pb(2+) and Hg(2+).