Results
- Showing results for:
- Reset all filters
Search results
-
Journal articleHeiba HF, Bullen JC, Kafizas A, et al., 2024,
Role of the Sn-TiO2/Ti-SnO2 Heterojunction in Enhancing the Photocatalytic Oxidation of Arsenite (AsIII) through the Promotion of Charge Carrier Lifetime.
, ACS Appl Mater Interfaces, Vol: 16, Pages: 69239-69252This study proposes the heterojunction photocatalyst, Sn-doped TiO2/Ti-doped SnO2 (herein named Sn1Ti1O2), as a promising alternative to pure TiO2. Sn1Ti1O2 demonstrates improved light harvesting efficiency over TiO2 by generating longer-lived electron-hole (eCB--hVB+) pairs, while also displaying a smaller band gap compared to pure TiO2. Consequently, we show that it is a promising candidate for the photocatalytic oxidation (PCO) of AsIII to the less toxic and more readily removable form AsV. Transient absorption spectroscopy (TAS) shows increased eCB--hVB+ recombination half-lives from ∼0.5 ms in TiO2 to ∼1 ms in Sn1Ti1O2. The initial transient absorption signal for Sn1Ti1O2 is twice that of pure TiO2, suggesting early time scale (pre-μs) suppression of (eCB--hVB+) recombination. Moreover, TAS showed that Sn1Ti1O2 possesses more reactive charge carriers than TiO2 under reactions with chemical scavengers. For the first time, TAS experiments were conducted using both a colorimetric indicator (molybdate) and AsIII to determine the PCO kinetics from AsIII to AsV. The TAS molybdate─AsIII experiment results indicate that the oxidation process occurs on the sub-microsecond time scale, with a notable increase in absorption at ∼700 nm, providing evidence of the formation of the AsV─molybdate blue complex. PCO experiments showed that •OH radicals played the predominant role during PCO, followed by superoxide radicals (O2•─). •OH scavengers including isopropanol, rebamipide anhydrous, and dimethyl sulfoxide (DMSO) reduce the PCO yield of AsIII to 21, 30, and 23%, respectively. While O2•─ scavengers including superoxide dismutase (SOD) and p-benzoquinone suppressed the PCO yield of AsIII to a lesser degree, with yields of 35 and 49% seen, respectively. The effects of irradiance intensity, salinity, pH, AsIII concentration, and photocatalyst mass on both the quantum efficiency (QE) and PCO kinetics were investigated. The Sn1Ti1O2 catalyst exh
-
Journal articleHeiba HF, Bullen JC, Kafizas A, et al., 2024,
Engineered Sn-TiO2@SnO2 and SnO2@Sn-TiO2 heterophotocatalysts for enhanced As(III) remediation: a comprehensive bulk and surface characterization and precise photocatalytic oxidation rates determination
, Colloids and Surfaces A: Physicochemical and Engineering Aspects, Vol: 702, ISSN: 0927-7757Arsenite, As(III), is a highly toxic form of arsenic that poses a significant risk to human health if present in drinking water. Oxidation of As(III) to the less toxic As(V) using TiO2 as photocatalyst is an attractive solution in water treatment applications but challenged the high bandgap energy. In this study, we investigate the potential of doping TiO2 with Sn to reduce the bandgap and hence to improve the photocatalytic oxidation (PCO). To this end, we studied first the effect of varying Sn:TiO2 molar doping on the structure of the newly synthesized SnO2@TiO2 and Sn-TiO2@SnO2 hetero photocatalysts. We found that at low Sn:TiO2 doping ratios (0.1Sn:1TiO2), SnO2 tends to float on the surface and form a coat around the TiO2 (SnO2@Sn-TiO2), whereas at higher doping ratio (1Sn:1TiO2) a Sn-TiO2 coat forms alongside SnO2 clusters in the core of the catalyst (Sn-TiO2@SnO2). We assessed the PCO and observed significant shifts to lower conduction and valence band edge energies and a reduction of the bandgap at higher doping ratios. The smallest bandgap was 2.87 eV with a doping ratio of 1Sn:1TiO2. Sn-TiO2@SnO2 and as SnO2@Sn-TiO2 improved the PCO of TiO2 by ∼30 and 46 %, respectively. We finally determined the rate constant (k) for the As(III) oxidation using a combination of spectrochemical and surface sensitive techniques and determined for a 1Sn:1TiO2 (i.e. Sn-TiO2@SnO2) catalyst a value of 0.055 ±0.002 min−1, i.e., 78 folds faster than using only TiO2. We conclude that Sn doping of TiO2 is a very promising approach for improving the PCO of As(III) in water treatment.
-
Journal articleDutta A, Porat H, Goldreich A, et al., 2024,
Laser exfoliated 2D MXene for supercapacitor applications
, Chemical Engineering Journal, Vol: 500, ISSN: 1385-8947MXenes-based compounds, particularly Ti3C2Tx, have been studied intensively as electrodes for supercapacitors due to their layered structure and high conductivity, enabling facile ion diffusion and charge transfer. However, tight restacking of the 2D layers in these materials limits their practical, accessible surface area, thereby impeding their capacity and rate capability performance. To mitigate this phenomenon, we present a new approach using a processing method based on laser beam irradiation to modify Ti3C2Tx films. We found that the laser treatment induces chemical and morphological changes, ultimately optimizing the stacking arrangement of the MXene electrodes and consequently enhancing their capacity in both neutral and acidic electrolytes. Furthermore, the laser-modified MXene electrodes demonstrate excellent rate capabilities, showing 84 % retention at extreme rates of 0.5 V compared to only 33 % of the original Ti3C2Tx electrodes. Finally, we discuss the chemical and physical changes induced by the laser treatments and their influence on the electrochemical behavior of the lasered MXene. The principles of laser exfoliation discovered in this study can be implemented in broader 2D materials for various applications.
-
Journal articleAlimard P, Gong C, Itskou I, et al., 2024,
Achieving high photocatalytic NOx removal activity using a Bi/BiOBr/TiO2 composite photocatalyst.
, Chemosphere, Vol: 368Fossil fuel combustion generates nitrogen oxides (NO + NO2 = NOx), which pose threats to the environment and human health. Although commercial products containing titanium dioxide (TiO2) can remedy NOx pollution by photocatalysis, they only function in the ultraviolet (UV). On the other hand, bismuth oxybromide (BiOBr) is active in the visible. BiOBr is stable, affordable, and non-toxic, making it an appealing alternative. In addition, nanoparticulate Bi metal can further enhance visible light absorption through its surface plasmon properties and charge carrier lifetime by spatially separating charge. In this study, to enhance the visible-light activity of TiO2-based photocatalysts for NOx pollution, a composite of Bi-decorated BiOBr/TiO2 was synthesised using a solvothermal method across varying the Ti/Bi atomic ratio (0.2, 2.2, 4.4, and 6.6), and synthesis duration (6h, 12h, and 18h). The photocatalytic performance of the synthesised composites for NO gas removal was investigated using an adapted ISO method (22197-1:2016). Analysis showed that the preferential growth of the (010) crystal facet in BiOBr and the presence of Bi metal both play an important role in the superior photocatalytic activity seen in our Bi-decorated BiOBr/TiO2 composite. The composites were characterised using X-ray diffraction (XRD), attenuated total reflectance - Fourier transform infrared spectroscopy (ATR-FTIR), high-resolution scanning electron microscopy (HR-SEM), UV-Vis diffuse reflectance (DRS) spectroscopy, transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Brunauer-Emmett-Teller (BET) analysis, thermogravimetric analysis (TGA), and diffuse reflectance transient absorption spectroscopy (DR-TAS). Our research shows that the Bi/BiOBr-TiO2 composite synthesised through a 12h solvothermal method with
-
Journal articleZhao S, Jia C, Shen X, et al., 2024,
The aerosol-assisted chemical vapour deposition of Mo-doped BiVO4 photoanodes for solar water splitting: an experimental and computational study
, Journal of Materials Chemistry A, Vol: 12, Pages: 26645-26666, ISSN: 2050-7488BiVO4 is one of the most promising light absorbing materials for use in photoelectrochemical (PEC) water splitting devices. Although intrinsic BiVO4 suffers from poor charge carrier mobility, this can be overcome by Mo-doping. However, for Mo-doped BiVO4 to be applied in commercial PEC water splitting devices, scalable routes to high performance materials need to be developed. Herein, we propose a scalable aerosol-assisted chemical vapour deposition (AA-CVD) route to high performance Mo-doped BiVO4. The materials were characterised using X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), atomic force microscopy (AFM), UV-visible absorption spectroscopy, and a range of PEC tests. By studying a range of Mo-precursor doping levels (0 to 12% Mo : V), an optimum precursor doping level was found (6% Mo : V); substituting V5+ sites in the host structure as Mo6+. In PEC water oxidation the highest performing material showed an onset of photocurrent (Jon) at ∼0.6 VRHE and a theoretical solar photocurrent (TSP) of ∼1.79 mA cm−2 at 1.23 VRHE and 1 sun irradiance. Importantly, Mo-doping was found to induce a phase change from monoclinic clinobisvanite (m-BiVO4), found in undoped BiVO4, to tetragonal scheelite (t-BiVO4). The effect of Mo-doping on the phase stability, structural and electronic properties was examined with all-electron hybrid exchange density functional theory (DFT) calculations. Doping into V and Bi sites at 6.25 and 12.5 at% was calculated for t-BiVO4 and m-BiVO4 phases. In accord with our observations, 6.25 at% Mo doping into the V sites in t-BiVO4 is found to be energetically favoured over doping into m-BiVO4 (by 2.33 meV per Mo atom inserted). The computed charge density is consistent with n-doping of the lattice as Mo6+ replaces V5+ generating an occupied mid-gap state ∼0.4 eV below the conduction band minimum (CBM) which is primarily of Mo-4d character. Doubling this do
-
Journal articleItskou I, Kafizas A, Nevjestic I, et al., 2024,
Effects of phosphorus doping on amorphous boron nitride’s chemical, sorptive, optoelectronic, and photocatalytic properties
, The Journal of Physical Chemistry C, Vol: 128, Pages: 13249-13263, ISSN: 1932-7447Amorphous porous boron nitride (BN) represents a versatile material platform with potential applications in adsorptive molecular separations and gas storage, as well as heterogeneous and photo-catalysis. Chemical doping can help tailor BN’s sorptive, optoelectronic, and catalytic properties, eventually boosting its application performance. Phosphorus (P) represents an attractive dopant for amorphous BN as its electronic structure would allow the element to be incorporated into BN’s structure, thereby impacting its adsorptive, optoelectronic, and catalytic activity properties, as a few studies suggest. Yet, a fundamental understanding is missing around the chemical environment(s) of P in P-doped BN, the effect of P-doping on the material features, and how doping varies with the synthesis route. Such a knowledge gap impedes the rational design of P-doped porous BN. Herein, we detail a strategy for the successful doping of P in BN (P-BN) using two different sources: phosphoric acid and an ionic liquid. We characterized the samples using analytical and spectroscopic tools and tested them for CO2 adsorption and photoreduction. Overall, we show that P forms P–N bonds in BN akin to those in phosphazene. P-doping introduces further chemical/structural defects in BN’s structure, and hence more/more populated midgap states. The selection of P source affects the chemical, adsorptive, and optoelectronic properties, with phosphoric acid being the best option as it reacts more easily with the other precursors and does not contain C, hence leading to fewer reactions and C impurities. P-doping increases the ultramicropore volume and therefore CO2 uptake. It significantly shifts the optical absorption of BN into the visible and increases the charge carrier lifetimes. However, to ensure that these charges remain reactive toward CO2 photoreduction, additional materials modification strategies should be explored in future work. These strategies could include the
-
Journal articleJeong SB, Heo KJ, Yoo JH, et al., 2024,
Photobiocidal activity of TiO2/UHMWPE composite activated by reduced graphene oxide under white light
, Nano Letters: a journal dedicated to nanoscience and nanotechnology, Vol: 24, Pages: 9155-9162, ISSN: 1530-6984Herein, we introduce a photobiocidal surface activated by white light. The photobiocidal surface was produced through thermocompressing a mixture of titanium dioxide (TiO2), ultra-high-molecular-weight polyethylene (UHMWPE), and reduced graphene oxide (rGO) powders. A photobiocidal activity was not observed on UHMWPE-TiO2. However, UHMWPE-TiO2@rGO exhibited potent photobiocidal activity (>3-log reduction) against Staphylococcus epidermidis and Escherichia coli bacteria after a 12 h exposure to white light. The activity was even more potent against the phage phi 6 virus, a SARS-CoV-2 surrogate, with a >5-log reduction after 6 h exposure to white light. Our mechanistic studies showed that the UHMWPE-TiO2@rGO was activated only by UV light, which accounts for 0.31% of the light emitted by the white LED lamp, producing reactive oxygen species that are lethal to microbes. This indicates that adding rGO to UHMWPE-TiO2 triggered intense photobiocidal activity even at shallow UV flux levels.
-
Journal articleReddick C, Sotelo-Vazquez C, Tam B, et al., 2024,
Photoelectrochemical disinfection efficiency of WO3-based photoanodes: development of multifunctional photoelectrocatalytic materials
, Catalysis Today, Vol: 437, ISSN: 0920-5861Access to safe water is a growing global concern, with millions lacking acceptable water sources. Photocatalysis offers eco-friendly water remediation, yet its combination with electrocatalysis for both water treatment and hydrogen production remain underexplored. This study investigates UVA LED photoelectrocatalysis using WO3-based photoanodes, alone or in heterojunction with BiVO4, to purify wastewater and co-produce hydrogen. Tests on polluted water streams containing 105 PFU mL−1 of MS2 bacteriophage virus and 106 CFU mL−1 of E. coli reveal that nanostructured WO3 achieves rapid MS2 disinfection within 5 min. (k= 0.80 min−1), with enhanced efficiency over flat counterparts. However, nanostructuring does not improve E. coli inactivation due to bacterium size constraints. These findings advance the design of tandem photoreactors for dual wastewater purification and energy generation.
-
Journal articleLin Z-P, Li Y, Haque SA, et al., 2024,
Insights from experiment and machine learning for enhanced TiO₂ coated glazing for photocatalytic NOₓ remediation
, Journal of Materials Chemistry A, Vol: 12, Pages: 13281-13298, ISSN: 2050-7488In this study, 58 distinct TiO2-coated glass samples were synthesized via Atmospheric Pressure Chemical Vapour Deposition (APCVD) under controlled synthesis conditions. The crystal properties, optical properties, surface properties and photogenerated charge carrier behaviour of all synthesized samples were characterized by X-ray diffraction (XRD), UV-visible spectroscopy, atomic force microscopy (AFM), and transient absorption spectroscopy (TAS), respectively. The photocatalytic activity of all coatings was systematically assessed against NO gas under near-ISO (22 197-1:2016) test conditions. The most active TiO2 coating showed ∼22.3% and ∼6.6% photocatalytic NO and NOx conversion efficiency, respectively, with this being ∼60 times higher than that of a commercial self-cleaning glass. In addition, we compared the accuracy of different machine learning strategies in predicting photocatalytic oxidation performance based on experimental data. The errors of the best strategy for predicting NO and NOx removal efficiency on the entire data set were ±2.20% and ±0.92%, respectively. The optimal ML strategy revealed that the most influential factors affecting NO photocatalytic efficiency are the sample surface area and photogenerated charge carrier lifetime. We then successfully validated our ML predictions by synthesising a new, high-performance TiO2-coated glass sample in accordance with our ML simulated data. This sample performed better than commercially available self-cleaning glass under a new metric, which comprehensively considered the visible light transmittance (VLT), NO degradation rate and NO2 selectivity of the material. Not only did this research provide a panoramic view of the links between synthesis parameters, physical properties, and NOx removal performance for TiO2-coated glass, but also showed how ML strategies can guide the future design and production of more effective photocatalytic coatings.
-
Journal articleTam B, Babacan O, Kafizas A, et al., 2024,
Comparing the net-energy balance of standalone photovoltaic-coupled electrolysis and photoelectrochemical hydrogen production
, Energy and Environmental Science, Vol: 17, Pages: 1677-1694, ISSN: 1754-5692Photovoltaic-coupled electrolysis (PV-E) and photoelectrochemical (PEC) water splitting are two options for storing solar energy as hydrogen. Understanding the requirements for achieving a positive energy balance over the lifetime of facilities using these technologies is important for ensuring sustainability. While neither technology has yet reached full commercialisation, they are also at very different technology readiness levels and scales of development. Here, we model the energy balance of standalone large-scale facilities to evaluate their energy return on energy invested (ERoEI) over time and energy payback time (EPBT). We find that for average input parameters based on present commercialised modules, a PV-E facility shows an EPBT of 6.2 years and ERoEI after 20 years of 2.1, which rises to approximately 3.7 with an EPBT of 2.7 years for favourable parameters using the best metrics amongst large-scale modules. The energy balance of PV-E facilities is influenced most strongly by the upfront embodied energy costs of the photovoltaic component. In contrast, the simulated ERoEI for a PEC facility made with earth abundant materials only peaks at 0.42 after 11 years and about 0.71 after 20 years for facilities with higher-performance active materials. Doubling the conversion efficiency to 10% and halving the degradation rate to 2% for a 10-year device lifetime can allow PEC facilities to achieve an ERoEI after 20 years of 2.1 for optimistic future parameters. We also estimate that recycling the materials used in hydrogen production technologies improves the energy balance by 28% and 14% for favourable-case PV-E and PEC water splitting facilities, respectively.
-
Journal articleYang G, Zhou Y, Wang M, et al., 2023,
Elucidating the effect of nitrogen occupancy on the hydrogen evolution reaction for a series of titanium oxynitride electrocatalysts
, ChemCatChem, Vol: 15, ISSN: 1867-3880Titanium nitride (TiN) shows desirable properties for use as an electrocatalyst and catalyst support, as it possesses high electrical conductivity and excellent corrosion resistance. Any oxygen and humidity present or incomplete nitridation during the synthesis process of nitrides can lead to an increasing oxygen content. However, the role of oxygen contents or nitrogen occupancies in the bulk of the nitrides during the electrocatalytic reactions is not well understood. In this work, we have synthesised a series of titanium oxynitrides with varied bulk nitrogen occupancies by ammonolysis at different temperatures. Higher ammonolysis temperatures will give a higher nitrogen occupancy but result in a lower surface area. The geometric activities towards the hydrogen evolution reaction (HER) have been normalised by the electrochemically active surface areas (ECSA) and the BET surface areas to get the specific activities. Their specific activity towards the HER is found to be strongly correlated with the bulk nitrogen occupancy and a higher bulk nitrogen occupancy is beneficial to the specific HER activities.
-
Journal articleWilson AA, Shalvey TP, Kafizas A, et al., 2023,
Analysis of charge trapping and long lived hole generation in SrTiO<sub>3</sub> photoanodes
, SUSTAINABLE ENERGY & FUELS, Vol: 7, Pages: 5066-5075, ISSN: 2398-4902Charge carrier dynamics studies of SrTiO3 under applied bias offer the opportunity to gain unique insights into what underpins its state-of-the-art photocatalytic water splitting activity. Herein, time resolved spectroscopic measurements are employed, to investigate the impact of applied bias on the transient and steady state charge carrier dynamics of SrTiO3 across μs–s timescales, and simultaneously measure charge extraction kinetics. A high density of Ti3+ defect states in SrTiO3 photoanodes are identified and associated with prevalent electron trapping into deep states, which is in competition with electron extraction and limits the photocurrent. Despite the high density of trapped electrons, an intrinsically long lifetime for photogenerated holes in SrTiO3 photoanodes is observed using transient absorption spectroscopy, even in the absence of applied bias. This is important for overcoming the slow kinetics and hole accumulation associated with the water oxidation reaction, and for enabling good performance in photocatalytic systems where bias cannot be applied.
-
Journal articleQuan Y, YiO MHN, Li Y, et al., 2023,
Influence of Bi co-catalyst particle size on the photocatalytic activity of BiOI microflowers in Bi/BiOI junctions - a mechanistic study of charge carrier behaviour
, Journal of Photochemistry and Photobiology A: Chemistry, Vol: 443, ISSN: 1010-6030Herein, we investigate the effect of Bi particle size in BiOI/Bi junctions on their photocatalytic function towards NO gas. BiOI microflowers (BiOI) and BiOI microflowers decorated with micron-sized Bi particles (BiOI/Bi MPs) were produced by a solvothermal method. BiOI decorated with nano-sized Bi particles (BiOI/Bi NPs) were produced by a reduction process. All samples were physically characterised by XRD, FT-IR, SEM, HR-TEM coupled with EDX analysis, DR-UV–visible and PL spectroscopy and functionally characterised by photocatalytic testing towards NO gas, TAS and EPR spectroscopy.Their photocatalytic activity towards NO gas was measured following ISO protocol (ISO 22197–1:2016). The best performing BiOI-based sample was BiOI/Bi NPs, showing NO and NOx conversion efficiencies of ∼33 and ∼11% under UVA light, and ∼26 and ∼8.1% under visible light, respectively. The BiOI and BiOI/Bi MPs samples showed significantly lower activities, displaying overall NOx conversion efficiencies of ∼3.5 and ∼0.8% under UVA light, respectively. Importantly, the best performing BiOI/Bi NPs samples showed visible light activity that was at least 6 times higher than that of a commercial TiO2 benchmark (CristalACTiVTM PC-S7). TAS measurements showed that charge carriers were significantly longer lived in the BiOI/Bi NPs sample (t50% from 10 μs of ∼90 μs) than the BiOI and BiOI/Bi MPs samples (t50% from 10 μs of ∼50 μs). This was attributed to the significant degree of interfacial contact formed between Bi and BiOI in the BiOI/Bi NPs sample, which enhanced charge carrier separation. EPR studies showed that this interfacial contact between BiOI and Bi likely promoted the formation of VO, which may have contributed to enhancement seen in photocatalytic activity in the BiOI/Bi junction.
-
Journal articleMeng Z, Pastor E, Selim S, et al., 2023,
Operando IR optical control of localized charge carriers in BiVO4 photoanodes
, Journal of the American Chemical Society, Vol: 145, Pages: 17700-17709, ISSN: 0002-7863In photoelectrochemical cells (PECs) the photon-to-current conversion efficiency is often governed by carrier transport. Most metal oxides used in PECs exhibit thermally activated transport due to charge localization via the formation of polarons or the interaction with defects. This impacts catalysis by restricting the charge accumulation and extraction. To overcome this transport bottleneck nanostructuring, selective doping and photothermal treatments have been employed. Here we demonstrate an alternative approach capable of directly activating localized carriers in bismuth vanadate (BiVO4). We show that IR photons can optically excite localized charges, modulate their kinetics, and enhance the PEC current. Moreover, we track carriers bound to oxygen vacancies and expose their ∼10 ns charge localization, followed by ∼60 μs transport-assisted trapping. Critically, we demonstrate that localization is strongly dependent on the electric field within the device. While optical modulation has still a limited impact on overall PEC performance, we argue it offers a path to control devices on demand and uncover defect-related photophysics.
-
Journal articleWang M, Kafizas A, Sathasivam S, et al., 2023,
ZnO/BiOI heterojunction photoanodes with enhanced photoelectrochemical water oxidation activity
, Applied Catalysis B: Environmental, Vol: 331, ISSN: 0926-3373ZnO/BiOI heterojunction photoanode thin films were prepared by aerosol-assisted chemical vapour deposition, and the impact of growth temperature and film thickness on the water oxidation functionality was systematically investigated. A top ZnO layer with a thickness of 120 nm (deposited at 350 °C) and a 390 nm thick BiOI layer (deposited at 300 °C) were found to achieve the best photoelectrochemical performance of the heterojunction. The ZnO/BiOI heterojunction exhibited a significant increase in photoelectrochemical activity, with a photocurrent of 0.27 mA·cm−2 observed at 1.1 VRHE (350 nm, 2.58 mW·cm−2), which is ~ 2.2 times higher than that of single-layer ZnO and far higher than that of BiOI. Photoluminescence spectroscopy and transient absorption spectroscopy measurements showed that there was effective charge transfer across the heterojunction which spatially separated charge carriers and increased their lifetime and ability to drive photoelectrochemical water oxidation.
-
Conference paperCreasey G, McCallum T, O'Neill L, et al., 2023,
Materials and reactor development for photoelectrochemical hydrogen production
, Materials for Sustainable Development Conference (MATSUS), Publisher: Fundació de la comunitat valenciana SCITO -
Journal articleNasser SMT, Rana AA, Doffinger R, et al., 2023,
Elevated free interleukin-18 associated with severity and mortality in prospective cohort study of 206 hospitalised COVID-19 patients
, Intensive Care Medicine Experimental, Vol: 11, ISSN: 2197-425XBackgroundDivergence between deterioration to life-threatening COVID-19 or clinical improvement occurs for most within the first 14 days of symptoms. Life-threatening COVID-19 shares clinical similarities with Macrophage Activation Syndrome, which can be driven by elevated Free Interleukin-18 (IL-18) due to failure of negative-feedback release of IL-18 binding protein (IL-18bp). We, therefore, designed a prospective, longitudinal cohort study to examine IL-18 negative-feedback control in relation to COVID-19 severity and mortality from symptom day 15 onwards.Methods662 blood samples, matched to time from symptom onset, from 206 COVID-19 patients were analysed by enzyme-linked immunosorbent assay for IL-18 and IL-18bp, enabling calculation of free IL-18 (fIL-18) using the updated dissociation constant (Kd) of 0.05 nmol. Adjusted multivariate regression analysis was used to assess the relationship between highest fIL-18 and outcome measures of COVID-19 severity and mortality. Re-calculated fIL-18 values from a previously studied healthy cohort are also presented.ResultsRange of fIL-18 in COVID-19 cohort was 10.05–1157.7 pg/ml. Up to symptom day 14, mean fIL-18 levels increased in all patients. Levels in survivors declined thereafter, but remained elevated in non-survivors. Adjusted regression analysis from symptom day 15 onwards showed a 100 mmHg decrease in PaO2/FiO2 (primary outcome) for each 37.7 pg/ml increase in highest fIL-18 (p < 0.03). Per 50 pg/ml increase in highest fIL-18, adjusted logistic regression gave an odds-ratio (OR) for crude 60-day mortality of 1.41 (1.1–2.0) (p < 0.03), and an OR for death with hypoxaemic respiratory failure of 1.90 [1.3–3.1] (p < 0.01). Highest fIL-18 was associated also with organ failure in patients with hypoxaemic respiratory failure, with an increase of 63.67 pg/ml for every additional organ supported (p < 0.01).ConclusionsElevated free IL-
-
Journal articleAnagnostopoulou M, Zindrou A, Cottineau T, et al., 2023,
MOF-Derived Defective Co3O4 Nanosheets in Carbon Nitride Nanocomposites for CO2 Photoreduction and H2 Production
, ACS APPLIED MATERIALS & INTERFACES, Vol: 15, Pages: 6817-6830, ISSN: 1944-8244 -
Journal articleJiamprasertboon A, Kafizas A, Hawkins E, et al., 2023,
Photocatalytic NOₓ oxidation of BiOCl nanostructure-based films grown using aerosol-assisted chemical vapor deposition
, ACS Applied Nano Material, Vol: 6, Pages: 738-749, ISSN: 2574-0970Coating of photocatalytic nanomaterials on various surfaces enables interesting applications. This work demonstrates the ability of the aerosol-assisted chemical vapor deposition (AACVD) approach to prepare high-quality BiOCl nanostructure-based films and also to tune the nanostructure and photocatalytic properties of the films by varying the solvent and carrier gas. Solvents have a dramatic impact on the surface morphologies and crystallite size. X-ray diffraction (XRD) and grazing incidence X-ray diffraction (GIXRD) analyses indicate that BiOCl crystals displayed preferential growth in the (101) plane in most samples, while both the (101) and (102) planes were favored in films deposited using ethyl acetate and methanol. Surface energy and adsorption energy calculation reveal that the preferred growth depends on the interaction between the Bi atom and solvent molecules. X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDS) characterizations showed that all films did not contain any impurity elements but did contain some oxygen vacancies. The obtained nanostructured BiOCl films show good photocatalytic properties. The highest photocatalytic NOx removal efficiency is achieved in the film prepared using ethyl acetate and air, which we attribute to the large crystallite size and therefore high mobility of the carriers. Herein, we show that different crystal morphologies and sizes of BiOCl have strong impacts on the photocatalytic activity toward NO oxidation, and both factors can be effectively tuned in the AACVD process. Such knowledge may be useful for future research on coating materials for resolving environmental problems.
-
Journal articleWong Y, Li Y, Lin Z, et al., 2022,
Studying the effects of processing parameters in the aerosol-assisted chemical vapour deposition of TiO2 coatings on glass for applications in photocatalytic NOx remediation
, Applied Catalysis A: General, Vol: 648, Pages: 1-12, ISSN: 0926-860XHerein, we employ an aerosol-assisted method (AA-CVD) to produce TiO2 on window glass and study how the process parameters affect their photocatalytic activity towards NOx (NO + NO2) remediation. A range of process parameters are explored to produce 50 unique TiO2 coatings with wide ranging physicochemical properties. The physicochemical properties were examined using X-ray diffraction (XRD), atomic force microscopy (AFM), UV–visible transmission spectroscopy and transient absorption spectroscopy (TAS), and the photocatalytic activity towards NO gas was measured using protocol akin to the ISO (22197-1:2016). The most active sample showed an NO removal of ∼14.4 ± 1.7 % and NOx removal of ∼5.4 ± 0.77 %, which was ∼40 and ∼25 times higher than that of a commercially available self-cleaning window. The links between the process parameters, physicochemical properties and photocatalytic activity were studied in depth, where it was seen that the three most influential physicochemical properties on the observed activity were surface roughness, charge carrier population and charge carrier lifetime. Therefore, we recommend that these properties be targeted in the rational design of more active coatings for applications in photocatalytic NOx remediation.
This data is extracted from the Web of Science and reproduced under a licence from Thomson Reuters. You may not copy or re-distribute this data in whole or in part without the written consent of the Science business of Thomson Reuters.
Contact us
Dr. Andreas Kafizas
Leader - Solar Coatings Group
e-mail: a.kafizas@imperial.ac.uk
tel: +44(0)20 7594 6752
twitter: @CoatingsSolar