Composition Of Cs Research Articles

Hollow tubular sea-urchin structure with high catalytic activity of NiCo2Se4@CS2 cathodes for high-performance Al/S batteries

The shuttle effect of aluminum polysulfides (AlPSs) have been a source of concern for studying Al/S batteries. Due to the weak adsorption of CS composites, research on cathode materials for Al/S batteries has been delayed. As it is generally known that Al2S3 decomposition demands a large Gibbs free energy, this work has tried to reduce the Al2S3 decomposition potential energy. Herein, the Ni/Co bimetallic selenide reduces the energy barrier conversion and mitigates the polarization effects, while morphology control enables the storage and anchoring of S, alleviating the shuttle effect. Additionally, the intermediate products serve as single-atom catalysts, increasing the active sites, synergistically enhancing the ion diffusion kinetics. DFT calculations verify that NiCo2Se4 has a moderate Gibbs free energy change during the rate-limiting step of S reduction and the most robust adsorption energy to Al2S3. NiCo2Se4@CS2/Al has a remaining capacity of 135 mAh/g after 450 cycles (at 200 mA g−1), pioneering novel ideas for the development of Al/S batteries.

Facile synthesis of phase-adjustable CsPbBr<sub>3</sub>-Cs<sub>4</sub>PbBr<sub>6</sub> composite nanocrystals and <i>in-situ</i> study of phase transformation process

All-inorganic cesium lead halide perovskites have shown great potential applications in optoelectronic field due to their fascinating optical properties. Although perovskite materials have achieved great success in various fields, their inherent ionic properties and high dynamic surface properties have led to their poor stability, hindering their applications. The preparation of CsPbBr<sub>3</sub>-Cs<sub>4</sub>PbBr<sub>6</sub> nanocrystals has proven to be an effective strategy to enhance their photoluminescence properties and stability. Herein, we report an easy synthesis of CsPbBr<sub>3</sub>-Cs<sub>4</sub>PbBr<sub>6</sub> nanocrystals with a diphase structure at room temperature by using Cs-OA, Pb-OA and TOABr as precursors in toluene. It is found that the phase transformation and the relative composition between CsPbBr<sub>3</sub> and Cs<sub>4</sub>PbBr<sub>6</sub> are dependent on the concentration of TOABr and the ratio of Cs/Pb. The <i>in-situ</i> PL experiments reveal that the formation of ~12 nm CsPbBr<sub>3</sub> nanocubes experiences the fast nucleation, the focusing growth of size-distribution in early growth stage and Ostwald ripening growth in the later stage at a TOABr concentration of 0.16 mmol. With the increase of concentration of TOABr or molar ratio of Cs/Pb > 1 (Cs/Pb < 1), [PbBr<sub>4</sub>]<sup>2–</sup> complex and [PbBr<sub>3</sub>]<sup>–</sup> complex can coexist and compete with each other in toluene, and the CsPbBr<sub>3</sub> nucleations dominate in the early stage, then CsPbBr<sub>3-</sub>Cs<sub>4</sub>PbBr<sub>6</sub> nanocomposites are gradually formed on CsPbBr<sub>3</sub> nucleations as photoluminescence centers due to the continuous generation of [PbBr<sub>4</sub>]<sup>2–</sup> complex between TOABr and Pb<sup>2+</sup>. The relative composition of Cs<sub>4</sub>PbBr<sub>6</sub> in CsPbBr<sub>3-</sub>Cs<sub>4</sub>PbBr<sub>6</sub> nanocomposites can be improved from 4% to 85% with the concentration of TOABr increasing or Cs/Pb < 1. The optimized CsPbBr<sub>3</sub>-Cs<sub>4</sub>PbBr<sub>6</sub> composite nanocrystals possess high PLQY and stability. Our work provides an understanding of the mechanism of phase transformation in cesium lead halide perovskite materials.

Predicting ruminal degradability and chemical composition of corn silage using near-infrared spectroscopy and multivariate regression.

The aim of this study was to develop and validate regression models to predict the chemical composition and ruminal degradation parameters of corn silage by near-infrared spectroscopy (NIR). Ninety-four samples were used to develop and validate the models to predict corn silage composition. A subset of 23 samples was used to develop and validate models to predict ruminal degradation parameters of corn silage. Wet chemistry methods were used to determine the composition values and ruminal degradation parameters of the corn silage samples. The dried and ground samples had their NIR spectra scanned using a poliSPECNIR 900-1700 model NIR sprectrophotometer (ITPhotonics S.r.l, Breganze, IT.). The models were developed using regression by partial least squares (PLS), and the ordered predictor selection (OPS) method was used. In general, the regression models obtained to predict the corn silage composition (P>0.05), except the model for organic matter (OM), adequately estimated the studied properties. It was not possible to develop prediction models for the potentially degradable fraction in the rumen of OM and crude protein and the degradation rate of OM. The regression models that could be obtained to predict the ruminal degradation parameters showed correlation coefficient of calibration between 0.530 and 0.985. The regression models developed to predict CS composition accurately estimated the CS composition, except the model for OM. The NIR has potential to be used by nutritionists as a rapid prediction tool for ruminal degradation parameters in the field.

The migration behavior of cesium during plasma gasification melting process of spent radioactive resins by thermodynamic calculation

Plasma gasification melting is an effective method of spent radioactive resin disposal. However, the equilibrium distribution and migration of Cs during the plasma gasification melting process is still unclear. In this study, the volatilization behavior of Cs during the plasma gasification melting process of spent resins was investigated by thermodynamic model. The composition of the stable phase and the release of Cs from the stable phase in the three systems of Cs-C-O, Cs-S-O and Cs-N-O were calculated by HSC Chemistry. The possible composition of Cs during the plasma gasification melting process of spent resins was determined. At the same time, the thermodynamic simulation of spent resins in the temperature range of 300–1800 °C was carried out, and the morphological distribution of Cs during the plasma gasification melting process of spent resins was calculated and analyzed, which will provide theoretical guidance for subsequent experimental research. The results showed that Cs2CO3, Cs2SO4 and Cs2O were identified as the stable phases of each system at 1200 °C in air atmosphere. The existent forms of Cs in the three stages of plasma pyrolysis, gasification and melting are different. In the plasma pyrolysis and melting stage, Cs mainly enters the gas phase in the form of gaseous Cs and CsOH. In the plasma gasification stage, Cs mainly enters the gas phase in the form of gaseous Cs and Cs2SO4. By comparing with the results of some literature, the accuracy of thermodynamic calculation is proved. The migration and transformation law of Cs during the plasma gasification melting process of spent radioactive resins is revealed.

Silicon/Carbon Nanoparticles Assembled with Multifunction Carbon Nanotubes/Sheets as High-Performance Anode of Lithium-Ion Batteries

Silicon as an electrode material in the lithium-ion battery application scenario has been hindered by its significant volumetric expansion and intricate synthesis processes. In this research, we have successfully synthesized Si@C/carbon nanotubes/carbon sheets (Si@C-CNTs/CS) composites by employing a simple one-pot method along with modified magnesium thermal reaction, which involves melamine to prevent high temperature. The resulting multifunctional Si@C-CNTs/CS composites demonstrate enhanced stability during volume change in silicon, resulting in both higher capacity compared to conventional carbon coating layer and improved conductivity of the materials. The results indicate that the Si@C-CNTs/CS composites exhibit a high discharge-specific capacity of up to 2981.64 mAh g−1 at 0.5 A g−1 current density and retain a discharge-specific capacity of 1487.71 mAh g−1 even after 300 cycles. Therefore, the double-layer carbon network structure of carbon nanotubes/carbon nanosheets can provide an efficient and simple preparation method for high-performance Si-base anode materials in practical applications.

Dynamics of drop formation and characterization of additive manufactured CS/AgNP/PVA composite membranes

AbstractThis study investigated the dynamics of drop formation and the printability of chitosan/silver nanoparticles composite fluid (CS/AgNP) modified with polyvinyl alcohol (PVA) using an inkjet 3D printer. It specifically investigated the relationship between rheological properties and fluid mechanical properties in determining the minimum drop velocity for 3D printing of modified CS ink. Proper matching of modified CS fluid rheological properties to the established physical parameters generated adequate droplets on glass substrates and formed membrane composites. The dynamic viscosity of the CS ink decreased with an increase in the concentration of PVA, which resulted in the disruption of existing molecular forces within the CS/AgNP polymer chains, suggesting that the solvent (PVA) was responsible for reducing the shear stress, surface tension, and viscosity of the composite membranes and subsequently improving the flow rates of the CS matrix at the nozzle orifice. Optimized drop velocity of 1.77 m/s yielded adequate formation of the CS/AgNP/PVA membrane composite with enhanced surface morphology, while an increase in drop velocity to 2.5 m/s brought about the formation of satellite droplets with irregular surface structures in printed CS composites. Therefore, adherence to minimum fluid drop velocity is fundamental to effective inkjet printing of composite membranes.

Crystal Structure and Photocatalytic Properties of the CsV0.625Te1.375O6 Mixed‐Valence β‐Pyrochlore Compound

AbstractA new β‐pyrochlore compound with complex composition of Cs(V3+0.0625V5+0.5625Te4+0.34375Te6+1.03125)O6 has been synthesized by a solid‐state reaction and characterized by single‐crystal X‐ray diffraction and thermal analysis. The compound possesses the typical cubic symmetry with space group , however some of the oxygen atoms shift from the special position 48 f to the general crystallographic positions 32e, 96 g and 96 h. This shift is caused by complex B‐site composition with mixed‐valence vanadium and tellurium atoms, especially the presence of the large Te4+ ion. The locations of the valence band and conduction band edges were determined experimentally under vacuum conditions by X‐ray photoelectron spectroscopy, UV‐visible and impedance spectroscopy and evaluated theoretically for water solutions. The photocatalytic ability of the compound under visible light irradiation was determined using the methylene blue decomposition process as an example. The nature of the active radical species and possible dye degradation pathway were suggested according to experimental data.

Preparation of zeolite framework adsorbents and evaluation of their acetone adsorption performance

The serious damage caused by volatile organic compounds (VOCs) to the environment and human health has attracted worldwide attention. Adsorption methods are among of the most promising VOC emission reduction technologies, with high cost-effectiveness, simple operation, and low energy consumption. The use of an appropriate adsorbent is very important for the removal of VOCs. Based on the preparation of high-performance materials with ideal pore structure and effective adsorption of acetone, in this paper we prepared the zeolite framework adsorbents SiO2@ZIF-67 and SiO2@ZIF-67/Cs as well as the high-temperature calcined C–SiO2@ZIF-67/Cs composites. The results of acetone adsorption tests showed that C–SiO2@ZIF-67/Cs had 55.7% and 32.4% higher adsorption capacity for acetone than SiO2@ZIF-67 and SiO2@ZIF-67/Cs, respectively. The high-temperature calcination can increase the specific surface area, greatly improving the adsorption capacity of the composite for acetone. The composite maintained good adsorption efficiency after five adsorption–desorption tests.

Traditional Importance, Phytochemistry, Pharmacology, and Toxicological Attributes of the Promising Medicinal Herb Carissa spinarum L.

Carissa spinarum L. (Apocynaceae), commonly known as Garna or Jungli Karonda, has a rich history of use in indigenous traditional medicinal systems owing to its tremendous medicinal and nutritional benefits. The present review aims to discuss the traditional uses, ethnopharmacology, bioactive composition, toxicity analysis, and biotechnological applications of Carissa spinarum L. (CS) to identify the gap between current applications and research conducted on this plant. We collected the literature published before December 2022 on the phytochemical composition, pharmacological properties, and biotechnological applications of CS. Literature in English from scientific databases such as Google Scholar, PubMed, ScienceDirect, Springer, and Wiley, along with books on CS, was analyzed and summarized to prepare this review. The plant taxonomy was verified using the “World Flora Online” database. The in vitro and in vivo pharmacological studies on CS revealed its anthelmintic, anticonvulsant, anti-arthritic, anti-inflammatory, antimicrobial, antioxidant, antidiabetic, hepatoprotective, vasorelaxant, antihypertensive, antitumor, wound-healing, anti-venom, and antipyretic effects. Toxicological studies on CS also indicated the absence of any adverse effects even at high doses after oral administration. Although CS showed remarkable therapeutic activities against several diseases—such as diabetes, cancer, inflammation, and hepatitis B virus—there are several drawbacks in previous reports, including the lack of information on the drug dose, standards, controls, and mechanism of action of the extract or the phytocompounds responsible for its activity. Extensive research with proper in vivo or in vitro model systems is required to validate its reported activities.

La(III) loaded Fe(III) cross–linked chitosan composites for efficient removal of phosphate from wastewater: Performance and mechanisms

The cost–effective removal and recovery of phosphate from wastewater is of great importance to controlling eutrophication and alleviating the phosphorus resource exhaustion crisis. Herein, chitosan (Cs) encapsulated bimetallic lanthanum (La) and iron (Fe) metal(hydro) oxides (La/Fe–Cs) composites were fabricated using a co–precipitated method for enhanced phosphate removal and recovery. The La/Fe–Cs composites had rough and raised spongy–like surfaces coated with La/Fe (hydr)oxide particles with a high specific surface area of 109.84 m2 g−1, providing more potential binding sites for phosphate capture. The La/Fe–Cs composites with a 1:2 La–to–Fe molar ratio exhibited a maximum adsorption capacity of 67.52 mg g−1 for phosphate at 308 K, calculated using the Langmuir model, which was 211% higher than that of monometallic Fe–Cs composites. Meanwhile, this composite also showed a high phosphate removal rate (63–95%) in an extensive applicable pH range (3.00–10.00) and rapid adsorption within 10 min (up to 94%). Moreover, the adsorption of phosphate by La/Fe–Cs composites was mildly disturbed against co–existing ions of NO3−, Cl−, and humic acid, while adsorption capacities were reduced by almost 13–45% with the existence of SO42−, HCO3−, and CO32−. The FTIR, XPS, and DFT results suggested that La–doped facilitated phosphate removal and the predominant mechanisms involved electrostatic interaction, surface precipitation, and inner–sphere complexation processes. Additionally, La/Fe–Cs composites also illustrated excellent efficiencies in simultaneous scavenging phosphate and ammonia from eutrophication and poultry wastewater. These results highlight bimetallic La/Fe–Cs composites are promising candidates for efficient elimination and recovery of phosphate from real wastewater, and subsequently could be used as slow–release fertilizers or soil amendments.

A novel cytoskeletal action of xylosides.

Proteoglycan glycosaminoglycan (GAG) chains are attached to a serine residue in the protein through a linkage series of sugars, the first of which is xylose. Xylosides are chemicals which compete with the xylose at the enzyme xylosyl transferase to prevent the attachment of GAG chains to proteins. These compounds have been employed at concentrations in the millimolar range as tools to study the role of GAG chains in proteoglycan function. In the course of our studies with xylosides, we conducted a dose-response curve for xyloside actions on neural cells. To our surprise, we found that concentrations of xylosides in the nanomolar to micromolar range had major effects on cell morphology of hippocampal neurons as well as of Neuro2a cells, affecting both actin and tubulin cytoskeletal dynamics. Such effects/morphological changes were not observed with higher xyloside concentrations. We found a dose-dependent alteration of GAG secretion by Neuro2a cells; however, concentrations of xylosides which were effective in altering neuronal morphology did not cause a large change in the rate of GAG chain secretion. In contrast, both low and high concentrations of xylosides altered HS and CS composition. RNAseq of treated cells demonstrated alterations in gene expression only after treatment with millimolar concentration of xylosides that had no effect on cell morphology. These observations support a novel action of xylosides on neuronal cells.

Fabrication of Novel Chitosan–Hydroxyapatite Nanostructured Thin Films for Biomedical Applications

In this study, we develop chitosan–hydroxyapatite (CS–HAp) composite layers that were deposited on Si substrates in radio frequency (RF) magnetron sputtering discharge in argon gas. The composition and structure of CS–HAp composite layers were investigated by analytical techniques, such as Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), metallographic microscopy (MM), and atomic force microscopy (AFM). On the other hand, in the present study the second order derivative of FT-IR–ATR spectra, for compositional analyses of CS–HAp, were used. The SEM, MM, and AFM data have shown the formation of CS–HAp composite layers. The surface of CS–HAp composite layers showed uniform growth (at an Ar gas working pressure of p = 2 × 10−3 mbar). The surface of the CS–HAp composites coatings became more nanostructured, becoming granular as the gas pressure increased from 5 × 10−3 to 1.2 × 10−2 mbar. However, our studies revealed that the surface morphology of the CS–HAp composite layers varies with the Ar gas working pressure. At the same time, optical properties are slightly influenced by Ar pressure. Their unique physicochemical properties make them suitable for various applications in the biomedical field, if we consider the already proven antimicrobial properties of chitosan. The antifungal properties and the capacity of the CS–HAp composite layers to inhibit the development of fungal biofilms were also demonstrated using the Candida albicans ATCC 10231 (C. albicans) fungal strain.

One-step synthesis of fluorescence-enhanced carbon dots for Fe (III) on−off−on sensing, bioimaging and light-emitting devices

Carbon quantum dots (CDs), as one of the most potential fluorescent sensing materials, have attracted lots of attention in recent years. However, the low quantum yields, complicated separation and purification procedures have limited its application and large-scale production. In this paper, a facile and universal method was successfully developed to synthesize CDs-silica (SiO2) spheres composites (CS composites), which not only demonstrates 10-fold fluorescence enhancement compared with single CDs but also enables the purification with a simple centrifugation step. Meanwhile, fabricated composites also presented superior photoluminescence (PL) stability and high PL intensity, even in some tough environments such as acid/alkali aqueous solution, high/low temperature, and high ion concentration aqueous solution. This simple, fast, low-cost, and efficient synthesis method would potentially expand the application of CDs for clinical analysis, optical sensing (ferric ion (Fe3+) and pyrophosphate), bioimaging and light-emitting diodes (LEDs).

Green Synthesis of A Novel MXene–CS Composite Applied in Treatment of Cr(VI) Contaminated Aqueous Solution

The considerable amount of Cr(VI) pollutants in the aqueous environment is a significant environmental concern that cannot be ignored. A series of novel Mxene–CS inorganic–organic composite nanomaterials synthesized by using the solution reaction method was applied to treat the Cr(VI) contaminated water. The Mxene–CS composites were characterized through SEM (scanning electron microscope), XRD (X–ray diffraction), XPS (X–ray photoelectron spectroscopy), and FTIR (Fourier transform infrared). The XRD patterns (observed at 2θ of 18.1°, 35.8°, 41.5°, and 60.1°) and the FT–IR spectra (-NH2 group for 1635 and 1517 cm−1, and -OH group for 3482 cm−1) illustrated that CS was successfully loaded on the Mxene. The effects of solution pH, the dosage of Mxene–CS, and duration time on the adsorption of Cr(VI) by synthesized Mxene–CS were investigated. The removal efficiency of Cr(VI) was increased from 12.9% to 40.5% with Mxene–CS dosage ranging from 0.02 to 0.12 g/L. The adsorption process could be well fitted by the pseudo–second–order kinetics model, indicating chemisorption occurred. The Langmuir isotherm model could be better to describe the process with a maximum adsorption capacity of 43.1 mg/g. The prepared novel Mxene–CS composite was considered as an alternative for adsorption of heavy metals from wastewater.

Effect of Initial CoII Salts on the Composition and Structure of Cs–CoII Dimethylmalonates

Effect of Initial CoII Salts on the Composition and Structure of Cs–CoII Dimethylmalonates

Composition-tuned MAPbBr3 nanoparticles with addition of Cs+ cations for improved photoluminescence.

Hybrid organic–inorganic lead halide perovskite nanoparticles are promising candidates for optoelectronic applications. This investigation describes the structural and optical properties of MAxCs1−xPbBr3 mixed cation colloidal nanoparticles spanning the complete compositional range of Cs substitution. A monotonic progression in the cubic lattice parameter (a) with changes in the Cs+ content confirmed the formation of mixed cation materials. More importantly, time-resolved photoluminescence (TRPL) revealed the optimized 13 mol% Cs nanoparticle composition exhibits the longest charge carrier lifetime and enhancement in radiative pathways. This sample also showed the highest photoluminescence quantum yield (PLQY) of ∼88% and displays ∼100% improvement in the PLQY of pure MAPbBr3 and CsPbBr3. Prototype LEDs fabricated from MA0.87Cs0.13PbBr3 were demonstrated.

Chemical composition and study on liquefaction optimization of chestnut shells

Abstract Chestnut shell (CS) is a by-product of some food sector companies. The aim of this study was to test the suitability of this material to be liquefied with polyalcohols, optimizing the main liquefaction parameters in order to use the liquefied material for the production of high added value products. As the chemical composition of the fruit shell depends on the variation in the soil, climate, and species, the chemical composition of CS was determined. Liquefaction was performed with 50:50 ethyleneglycol:glycerol catalyzed by sulfuric acid. Different tests were carried out and several parameters were tested: particle size, temperature 130–190°C, and time 15–120 min. Chemical composition of CSs was determined. The main component found was lignin with 47.0%, which is higher than α-cellulose with around 20.5%, hemicelluloses 15.2%, and extractives in ethanol 8.8%. For the tested parameters, the best liquefaction yield was obtained at 190°C, 30 min, and a 40–60 particle size.

Chitosan‐Based, Biocompatible, Solution Processable Films for In Vivo Localization of Neural Interface Devices

AbstractChitosan (CS) is a biocompatible, inexpensive organic polymer that is increasingly used in neural tissue applications. However, its intrinsic fluorescence has not yet been leveraged to facilitate localization of neural interface devices, a key procedure to ensure accurate analysis of neurophysiological signals. A process is developed to enable control of mechanical and chemical properties of CS‐based composites, generating freestanding films that are stable in aqueous environments and exhibit concentration‐dependent fluorescence intensity. The shape and location of CS‐coated probes are reliably visualized in vitro and in vivo using fluorescence microscopy. Furthermore, CS neural probe marking is fully compatible with classical immunohistochemical and histological techniques, enabling localization of high spatiotemporal resolution surface electrocorticography arrays in adult rats and mouse pups. CS composites have the potential to simplify and streamline experimental procedures required to efficiently acquire, localize, and interpret neurophysiological data.

Synthesis and Antibacterial Properties of Novel ZnMn2O4-Chitosan Nanocomposites.

The development of productive antibacterial agents from nontoxic materials via a simple methodology has been an immense research contribution in the medicinal chemistry field. Herein, a sol–gel one-pot reaction was used to synthesize hybrid composites of hausmannite–chitosan (Mn3O4–CS) and its innovative derivative zinc manganese oxide–chitosan (ZnMn2O4–CS). Fixed amounts of CS with different metal matrix w/v ratios of 0.5%, 1.0%, 1.5%, and 2.0% for Mn and Zn precursors were used to synthesize ZnMn2O4–CS hybrid composites. X-ray diffraction analysis indicated the formation of polycrystalline tetragonal-structured ZnMn2O4 with a CS matrix in the hybrids. Fourier-transform infrared spectroscopic analysis confirmed the formation of ZnMn2O4–CS hybrids. Detailed investigations of the surface modifications were conducted using scanning electron microscopy; micrographs at different magnifications revealed that the composites’ surface changed depending on the ratio of the source materials used to synthesize the ZnMn2O4–CS hybrids. The antibacterial activity of the Mn3O4–CS and ZnMn2O4–CS composites was tested against various bacterial species, including Bacillus subtilis, Escherichia coli, Salmonella typhi, and Pseudomonas aeruginosa. The zone of inhibition and minimum inhibitory concentration values were deduced to demonstrate the efficacy of the ZnMn2O4–CS nanocomposites as antibacterial agents.

Utilization of Carbon Nanospheres in Photocatalyst Production: From Composites to Highly Active Hollow Structures.

Titanium dioxide–carbon sphere (TiO2–CS) composites were constructed via using prefabricated carbon spheres as templates. By the removal of template from the TiO2–CS, TiO2 hollow structures (HS) were synthesized. The CS templates were prepared by the hydrothermal treatment of ordinary table sugar (sucrose). TiO2–HSs were obtained by removing CSs with calcination. Our own sensitized TiO2 was used for coating the CSs. The structure of the CSs, TiO2–CS composites, and TiO2–HSs were characterized by scanning electron microscopy (SEM), infrared spectroscopy (IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and diffuse reflectance spectroscopy (DRS). The effect of various synthesis parameters (purification method of CSs, precursor quantity, and applied furnace) on the morphology was investigated. The photocatalytic activity was investigated by phenol model pollutant degradation under visible light irradiation (λ > 400 nm). It was established that the composite samples possess lower crystallinity and photocatalytic activity compared to TiO2 hollow structures. Based on XPS measurements, the carbon content on the surface of the TiO2–HS exerts an adverse effect on the photocatalytic performance. The synthesis parameters were optimized and the TiO2–HS specimen having the best absolute and surface normalized photocatalytic efficiency was identified. The superior properties were explained in terms of its unique morphology and surface properties. The stability of this TiO2–HS was investigated via XRD and SEM measurements after three consecutive phenol degradation tests, and it was found to be highly stable as it entirely retained its crystal phase composition, morphology and photocatalytic activity.