Inactivation of SARS-CoV-2 and Other Human Coronaviruses Aided by Photocatalytic One-Dimensional Titania Nanotube Films as a Self-Disinfecting Surface.

SARS-CoV-2 and its variants that continue to emerge have necessitated the implementation of effective disinfection strategies. Developing self-disinfecting surfaces can be a potential route for reducing fomite transmissions of infectious viruses. We show the effectiveness of TiO2 nanotubes (T_NTs) on photocatalytic inactivation of human coronavirus, HCoV-OC43, as well as SARS-CoV-2. T_NTs were synthesized by the anodization process, and their impact on photocatalytic inactivation was evaluated by the detection of residual viral genome copies (quantitative real-time quantitative reverse transcription polymerase chain reaction) and infectious viruses (infectivity assays). T_NTs with different structural morphologies, wall thicknesses, diameters, and lengths were prepared by varying the time and applied potential during anodization. The virucidal efficacy was tested under different UV-C exposure times to understand the photocatalytic reaction's kinetics. We showed that the T_NT presence boosts the inactivation process and demonstrated complete inactivation of SARS-CoV-2 as well as HCoV-OC43 within 30 s of UV-C illumination. The remarkable cyclic stability of these T_NTs was revealed through a reusability experiment. The spectroscopic and electrochemical analyses have been reported to correlate and quantify the effects of the physical features of T_NT with photoactivity. We anticipate that the proposed one-dimensional T_NT will be applicable for studying the surface inactivation of other coronaviruses including SARS-CoV-2 variants due to similarities in their genomic structure.

Boosting Photocatalytic Activity Using Reduced Graphene Oxide (RGO)/Semiconductor Nanocomposites: Issues and Future Scope.

Semiconductor nanoparticles are promising materials for light-driven processes such as solar-fuel generation, photocatalytic pollutant remediation, and solar-to-electricity conversion. Effective application of these materials alongside light can assist in reducing the dependence on fossil-fuel driven processes and aid in resolving critical environmental issues. However, severe recombination of the photogenerated charge-carriers is a persistent bottleneck in several semiconductors, particularly those that contain multiple cations. This issue typically manifests in the form of reduced lifetime of the photoexcited electrons-holes leading to a decrease in the quantum efficiency of various light-driven applications. On the other hand, semiconducting oxides or sulfides, coupled with reduced graphene oxide (RGO), have drawn a considerable interest recently, partly because of the RGO enhancing charge separation and transportation through its honeycomb sp2 network structure. High electron mobility, conductivity, surface area, and cost-effectiveness are the hallmark of the RGO. This Mini-Review focuses on (1) examining the approach to the integration of RGO with semiconductors to produce binary nanocomposites; (2) insights into the microstructure interface, which plays a critical role in leveraging charge transport; (3) key examples of RGO composites with oxide and sulfide semiconductors with photocatalysis as application; and (4) strategies that have to be pursued to fully leverage the benefit of RGO in RGO/semiconductors to attain high photocatalytic activity for a sustainable future. This Mini-Review focuses on areas requiring additional exploration to fully understand the interfacial science of RGO and semiconductor, for clarity regarding the interfacial stability between RGO and the semiconductor, electronic coupling at the heterojunction, and morphological properties of the nanocomposites. We believe that this Mini-Review will assist with streamlining new directions toward the fabrication of RGO/semiconductor nanocomposites with higher photocatalytic activity for solar-driven multifunctional applications.

Inactivation of Human Coronavirus by Titania Nanoparticle Coatings and UVC Radiation: Throwing Light on SARS-CoV-2.

The newly identified pathogenic human coronavirus, SARS-CoV-2, led to an atypical pneumonia-like severe acute respiratory syndrome (SARS) outbreak called coronavirus disease 2019 (abbreviated as COVID-19). Currently, nearly 77 million cases have been confirmed worldwide with the highest numbers of COVID-19 cases in the United States. Individuals are getting vaccinated with recently approved vaccines, which are highly protective in suppressing COVID-19 symptoms but there will be a long way before the majority of individuals get vaccinated. In the meantime, safety precautions and effective disease control strategies appear to be vital for preventing the virus spread in public places. Due to the longevity of the virus on smooth surfaces, photocatalytic properties of "self-disinfecting/cleaning" surfaces appear to be a promising tool to help guide disinfection policies for controlling SARS-CoV-2 spread in high-traffic areas such as hospitals, grocery stores, airports, schools, and stadiums. Here, we explored the photocatalytic properties of nanosized TiO2 (TNPs) as induced by the UV radiation, towards virus deactivation. Our preliminary results using a close genetic relative of SAR-CoV-2, HCoV-NL63, showed the virucidal efficacy of photoactive TNPs deposited on glass coverslips, as examined by quantitative RT-qPCR and virus infectivity assays. Efforts to extrapolate the underlying concepts described in this study to SARS-CoV-2 are currently underway.

Effects of Carbon Allotrope Interface on the Photoactivity of Rutile One-Dimensional (1D) TiO2 Coated with Anatase TiO2 and Sensitized with CdS Nanocrystals.

The assembly of a large-bandgap one-dimensional (1D) oxide-conductive carbon-chalcogenide nanocomposite and its surface, optical, and photoelectrochemical properties are presented. Microscopy, surface analysis, and optical spectroscopy results are reported to provide insights into the assembly of the nanostructure. We have investigated (i) how the various carbon allotropes (C60), reduced graphene oxide (RGO), carbon nanotubes (CNTs), and graphene quantum dots (GQDs) can be integrated at the interface of the 1D TiO2 and zero-dimensional (0D) CdS nanocrystals; (ii) the carbon allotrope and CdS loading effects; (iii) the impact of the carbon allotrope presence on 0D CdS nanocrystals; and (iv) how they promote light absorbance. Subsequently, the functioning of the integrated nanostructured assembly in a photoelectrochemical cell has been systematically investigated. These studies include (i) chronoamperometry, (ii) impedance measurements or EIS, and (iii) linear sweep voltammetry. The results indicate that the presence of a GQD interface shows the most enhancement in the photoelectrochemical properties. The optimized photocurrent values were respectively noted to be 2.8, 2.2, 1.9, and 1.6 mA/cm(2), indicating JGQD > JRGO > JCNT > Jfullerene. Furthermore, the annealing conditions have indicated that ammonia treatment leads to an increase in the photoelectrochemical responses when using any form of the carbon allotropes.

Free energy dependence of pure phase iron doped bismuth titanate from first principles calculations.

A density functional theory study of Fe substitutions in Bi2Ti2O7 photocatalyst (Fe-BTO) is presented. It models an experiment where H2 production of Fe-BTO peaked for samples loaded with 1% Fe concentration then decreased for samples with heavier loadings. The total energy calculations were used to determine defect formation energies and the chemical potential landscape that suggests the observed formation of Fe2O3 (in samples at 2% Fe concentration) was detrimental to H2 production. Doping configurations as a function of oxygen chemical potential are discussed, and the chemical potential ranges that avoid formation of the Fe2O3 phase in Fe-BTO are predicted.

Encapsulating Bi2Ti2O7 (BTO) with reduced graphene oxide (RGO): an effective strategy to enhance photocatalytic and photoelectrocatalytic activity of BTO.

Multimetal oxides (AxByOz) offer a higher degree of freedom compared to single metal oxides (AOx) in that these oxides facilitate (i) designing nanomaterials with greater stability, (ii) tuning of the optical bandgap, and (iii) promoting visible light absorption. However, all AxByOz materials such as pyrochlores (A2B2O7)--referred to here as band-gap engineered composite oxide nanomaterials or BECONs--are traditionally prone to severe charge recombination at their surface. To alleviate the charge recombination, an effective strategy is to employ reduced graphene oxide (RGO) as a charge separator. The BECON and the RGO with oppositely charged functional groups attached to them can be integrated at the interface by employing a simple electrostatic self-assembly approach. As a case study, the approach is demonstrated using the Pt-free pyrochlore bismuth titanate (BTO) with RGO, and the application of the composite is investigated for the first time. When tested as a photocatalyst toward hydrogen production, an increase of ∼ 250% using BTO in the presence of RGO was observed. Further, photoelectrochemical measurements indicate an enhancement of ∼ 130% in the photocurrent with RGO inclusion. These two results firmly establish the viability of the electrostatic approach and the inclusion of RGO. The merits of the RGO addition is identified as (i) the RGO-assisted improvement in the separation of the photogenerated charges of BTO, (ii) the enhanced utilization of the charges in a photocatalytic process, and (iii) the maintenance of the BTO/RGO structural integrity after repeated use (established through reusability analysis). The success of the self-assembly strategy presented here lays the foundation for developing other forms of BECONs, belonging to perovskites (ABO3), sillenite (A12BO20), or delafossite (ABO2) groups, hitherto written off due to limited or no photoelectrochemicalactivity.

A unique architecture based on 1 D semiconductor, reduced graphene oxide, and chalcogenide with multifunctional properties.

A unique heterostructured optoelectronic material (HOM), consisting of a reduced graphene oxide (RGO) layer with spatially distributed CdS, suspended by zinc oxide (ZnO) nanorods, is presented. The key features of this HOM are the assembly of the components in a manner so as to realize an effective integration between the constituents and the ability to modify the electronic properties of the RGO. For the first time, the location of RGO (as a suspended layer) along with the tuning of its charge-transport properties (n-/p-type) and its influence on the photo(electro)chemical processes has been examined systematically by using this ZnO/RGO/CdS HOM as a case study. The n-type RGO interlayer facilitates >100 % increase in the photocurrent density and 25 % increase in the photodegradation of a dye, compared to ZnO/CdS, thus demonstrating its multifunctionality. At 3.2 mA cm(-2) , this HOM architecture helps to achieve the highest photocurrent density utilizing ZnO, RGO, and CdS as building blocks in any form. The work is significant for the following reasons: i) other one dimensional (1D) oxides/chalcogenides or 1D oxides/dyes may be designed with similar architectures; ii) HOMs with tunable optical absorbance and charge-transport properties could be realized; iii) related application areas (e.g., sensing or solar fuel generation) should be greatly benefited.

Role of reduced graphene oxide in the critical components of a CdS-sensitized TiO2 -based photoelectrochemical cell.

Nitrogen (N)-doped reduced graphene oxide (nRGO) is systematically incorporated into a TiO(2) -CdS photoelectrochemical (PEC) cell and its role is examined in the three main components of the cell: 1) the CdS-sensitized TiO(2) photoanode, 2) the cathode, and 3) the S(2-)/S(.-) aqueous redox electrolyte. The nRGO layer is sandwiched between TiO(2) nanorods (deposited by using a solvothermal method) and CdS (deposited by using the successive ionic-layer-adsorption and -reaction method). Scanning electron microscopy with energy dispersive X-ray analysis (EDS) reveals the spatial distribution of CdS and nRGO, whereas nRGO formation is evident from Mott Schottky analysis. Chronoamperometry and PEC analysis indicate that upon incorporation of nRGO, a photocurrent density that is at least 27 times higher than that of pristine TiO(2) is achieved; this increase is attributable to the ability of the nRGO to efficiently separate and transport charges. Stability analysis performed by continuous photoillumination over ∼3 h indicates a 26% and 42 % reduction in the photocurrent in the presence and absence of the nRGO respectively. Formation of SO(4)(2-) is identified as the cause for this photocurrent reduction by using X-ray photoelectron spectroscopy. It is also shown that nRGO-coated glass is as effective as a Pt counter electrode in the PEC cell. Unlike the benefits offered by nRGO at the anode and cathode, introducing it in the redox electrolyte is detrimental. Systematic and complementary electrolyte and film-based studies on this aspect reveal evidence of the capacitive behavior of nRGO. Competition between the nRGO and the oxidized electrolyte is identified, based on linear-sweep voltammetry analysis, as the limiting step to efficient charge transport in the electrolyte.

Mn-modified Bi2Ti2O7 photocatalysts: bandgap engineered multifunctional photocatalysts for hydrogen generation.

In this study, a hydrogen generation photocatalyst based on bismuth titanate (Bi2Ti2O7 - BTO) modified with manganese (Mn) has been developed. Mn of varying weight percent was added to construct a modified BTO catalyst (Mn_BTO), in order to enhance the opto-electronic and photocatalytic hydrogen generation capabilities of the pristine BTO. The structural, morphological, and optical properties of the photocatalysts were evaluated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-visible spectrophotometry. The XRD, SEM, and TEM analyses indicate the formation of the pyrochlore BTO phase with particles of dimensions 30 ± 10 nm. The UV-visible study revealed a reduction in the bandgap of Mn_BTO and enhanced absorption in the visible range, compared to the pristine BTO. The catalyst was optimized for maximum hydrogen generation from a water-methanol (sacrificial electron donor) system in a slurry reactor. The photocatalytic hydrogen evolution studies indicate that the Mn_BTO with up to 1 wt% Mn facilitates an optimal 140% increase in the hydrogen yield. The role of formic acid and formaldehyde as additives in photocatalytic hydrogen evolution has also been examined. The effect of Mn content, mechanistic overview, and reusability of the catalyst are discussed.

Photoassisted enhancement of the electrocatalytic oxidation of formic acid on platinized TiO2 nanotubes.

A solvothermal method is used to deposit Pt nanoparticles on anodized TiO2 nanotubes (T_NT). Surface characterization using SEM, EDX, and XRD indicates the formation of polycrystalline TiO2 nanotubes of 110 ± 10 nm diameter with Pt nanoparticle islands. The application of the T_NT/Pt photoanode has been examined toward simultaneous electrooxidation and photo(electro)oxidation of formic acid (HCOOH). Upon UV-vis photoillumination, the T_NT/Pt photoelectrode generates a current density of 72 mA/cm(2), which is significantly higher (∼39-fold) than that of the T_NT electrode (1.85 mA/cm(2)). This boosting in the overall current is attributable to the enhanced oxidation of formic acid at the T_NT/Pt-electrolyte interface. Further, a series of cyclic voltammetric (CV) responses, of which each anodic scan is switched to photoillumination at a certain applied bias (i.e., 0.2 V, 0.4 V, etc.), is used to identify the role of T_NT/Pt as a promoter for the photoelectrooxidation of formic acid and understand a carbon monoxide (CO)-free pathway. Chronoamperometric (j/t) measurements demonstrate the evidence of an external bias dependent variation in the time lag during the current stabilization. An analysis of the CV plots and j/t profiles suggests the existence of both the charge-transfer controlled process and the diffusion-controlled process during formic acid photoelectrooxidation.

TiO2 nanotube (T_NT) surface treatment revisited: Implications of ZnO, TiCl4, and H2O2 treatment on the photoelectrochemical properties of T_NT and T_NT-CdSe.

The surface treatment of an anodized TiO(2) nanotube (T_NT) is very desirable for enhancing its photoelectrochemical properties and often is a prerequisite to deposition of any overlying layer for photoactivity efficiency improvement. This study provides a comparative analysis of the effects of such surface treatments and the mechanistic insights behind the observed improvements in the performance of the treated T_NTs. T_NT surface treatment using three approaches, viz., TiCl(4), Zn(NH(3))(4)(2+), and H(2)O(2) is examined. TiCl(4) and Zn(NH(3))(4)(2+) treatment results in the formation of discontinuous islands of the respective oxides with 5-10 nm and 15-20 nm diameter particles. TiCl(4) treatment demonstrates an increase of 7.4% in photovoltage and is the most effective of the three approaches. Zn(NH(3))(4)(2+) treatment also results in an ~2% increase in photovoltage. However, a surface treatment of T_NT using H(2)O(2) results only in a favourable shift in flatband potential (80 mV). The T_NTs are rendered ineffective as H(2)O(2) treatment causes the destabilization of the T_NT at the base. Finally, the activity of an overlying chalcogenide layer is improved with the TiCl(4) and Zn(NH(3))(4)(2+) treatment (and not with H(2)O(2)) as evident from the photoelectrochemical responses: (J(T_NT-TiO(2)-CdSe) > J(T_NT-ZnO-CdSe) > J(T_NT-CdSe) > J(T_NT-H(2)O(2)-CdSe)).

1D CdS/PbS heterostructured nanowire synthesis using cation exchange.

Heterostructured CdS nanowires with PbS deposits forming p-n junctions have been synthesized by successive cation exchange. The method developed herein opens up the possibility of preparing a spatially distributed heterojunction-based multifunctional electrode. The (photo)electrochemical activity of the material may be chemically tuned by changing the size and density of the p type PbS nanoparticles.

Robust synthesis of bismuth titanate pyrochlore nanorods and their photocatalytic applications.

A facile and template-free reverse micelle-based method can be employed to synthesize highly crystalline and pure stoichiometric bismuth titanate (Bi(2)Ti(2)O(7)) pyrochlore nanorods 400-500 nm long and 40-50 nm in diameter which demonstrate promising photoactivity.