TiO2 nanoflower photocatalysts: Synthesis, modifications and applications in wastewater treatment for removal of emerging organic pollutants.

Titanium dioxide (TiO2) has been considered as one of the most promising photocatalysts nanomaterials and is being used in a variety of fields of energy and environment under sunlight irradiation via photocatalysis. Highly efficient photocatalytic materials require the design of the proper structure with excellent morphology, interfacial structures, optical and surface properties, etc. Which are the key points to realize effective light-harvesting for photocatalytic applications. Hierarchical TiO2 based nanoflower structures (i.e., 3D nanostructures) possess such characteristics and have attracted much attention in recent years. The uniqueness of TiO2 nanoflowers (NFs) with a coarse texture and arranged structures demonstrates higher photocatalytic activity. This review deals with the hydrothermal synthesis of 3D TiO2 NFs and effect of shape/size as well as various key synthesis parameters to improve their optoelectronic and photocatalytic properties. Furthermore, to improve their photocatalytic properties, various strategies such as doping engineering and heterojunction/nanocomposite formation with other functional nanomaterials have been discussed followed by their potential applications in photocatalytic degradation of various emerging pollutants discharged into the wastewater from various sources. Importance of such 3D nanoarchitecutres and future research in other fields of current interest in environments are discussed.

Two-Dimensional High-Entropy Selenides for Boosting Visible-Light-Driven Photocatalytic Performance.

High-entropy materials (HEMs) have garnered extensive attention owing to their diverse and captivating physicochemical properties. Yet, fine-tuning morphological properties of HEMs remains a formidable challenge, constraining their potential applications. To address this, we present a rapid, low-energy consumption diethylenetriamine (DETA)-assisted microwave hydrothermal method for synthesizing a series of two-dimensional high-entropy selenides (HESes). Subsequently, the obtained HESes are harnessed for photocatalytic water splitting. Noteworthy is the optimized HESes, Cd0.9Zn1.2Mn0.4Cu1.8Cr1.2Se4.5, showcasing an output rate of hydrogen of 16.08 mmol h-1 g-1 and a quantum efficiency of ca. 30% under 420 nm monochromatic LED irradiation. It is revealed that the photocatalytic performance of these HESes stems not only from the enlarged specific surface area and enhanced photogenerated charge carrier utilization efficiency but also from the promoted formation of the Cd-Hads bond, influenced by multiple principal elements on the Cd. These findings provide a guide for the design of HEMs tailored for various applications.

A high-performance C@Na5V12O32 nanowire electrode derived from the reconstruction of carbon quantum dots.

Vanadate electrodes are potential candidates for lithium-ion batteries (LIBs) due to their large theoretical specific capacity. However, their easy dissolution in the electrolyte, large structural changes, low conductivity and capacity decay during cycling hinder their further application. Herein, a lithium-ion battery electrode of Na5V12O32 (NVO) nanowires covered with a carbon film and formed by the reconstruction of carbon quantum dots (CDs) was obtained using an in situ capping strategy. Remarkably, the carbon film could prevent direct contact between the NVO nanowires and the electrolyte, thus slowing down the occurrence of side reactions and avoiding the dissolution of the NVO nanowires. Among the electrodes treated at different temperatures, the C@NVO-400 electrode exhibits high capacity and excellent cycling stability as the electrode of LIBs, with a discharge specific capacity of 779.1 and 315.5 mAh g-1 after 400 and 1000 cycles at a current density of 0.1 and 2 A g-1, respectively. An in situ coating strategy is proposed here to contribute to the further development of coated vanadate electrodes for high-performance LIBs.

Graphene oxide as an emerging sole adsorbent and photocatalyst: Chemistry of synthesis and tailoring properties for removal of emerging contaminants.

Contaminants of emerging concern (CEC) contain a wide range of compounds, such as pharmaceutical waste, pesticides, herbicides, industrial chemicals, organic dyes, etc. Their presence in the surrounding has extensive and multifaceted effects on human health as they have the potential to persist in the environment, accumulate in biota, and disrupt ecosystems. In this regard, various remediation methods involving different kind of functional nanomaterials with unique properties have been developed. The functional nanomaterials can provide several mechanisms for water pollutant removal, such as adsorption, catalysis, and disinfection, in a single platform. Graphene oxide (GO) is a two-dimensional carbon-based material that has an extremely large surface area and a large number of active sites. Recent advances in synthesising GO have shown great progress in tailoring its various physiochemical, optical, surface, structural properties etc., making it better adsorbent and photocatalysts. In this review, sole adsorbent and standalone photocatalytic performances of GO for the removal of CEC have been discussed in light of tailoring its adsorption and photocatalytic properties through novel synthesis routes and optimizing synthesis parameters. This review also examines various models describing the structure of GO and its surface/structural modifications for improved adsorption and photocatalytic properties. The article provides valuable information for the production of efficient and cost-effective GO-based sole adsorbents and photocatalysts as compared to the traditional materials. Furthermore, future prospective and challenges for sole GO nanostructures to compete with traditional adsorbents and photocatalysts have been discussed providing interesting avenues for future research.

Tunable Interfacial Charge Transfer in a 2D-2D Composite for Efficient Visible-Light-Driven CO2 Conversion.

Photocatalytic CO2 conversion for hydrocarbon fuel production has been known as one of the most promising strategies for achieving carbon neutrality. Yet, its conversion efficiency remains unsatisfactory mainly due to its severe charge-transfer resistance and slow charge kinetics. Herein, a tunable interfacial charge transfer on an oxygen-vacancies-modified bismuth molybdate nanoflower assembled by 2D nanosheets (BMOVs) and 2D bismuthene composite (Bi/BMOVs) is demonstrated for photocatalytic CO2 conversion. Specifically, the meticulous design of the Ohmic contact formed between BMOVs and bismuthene can allow the modulation of the interfacial charge-transfer resistance. According to density functional theory (DFT) simulations, it is ascertained that such exceptional charge kinetics is attributed to the tunable built-in electric field (IEF) of the Ohmic contact. As such, the photocatalytic CO2 reduction performance of the optimized Bi/BMOVs (CO and CH4 productions rate of 169.93 and 4.65 µmol g-1 h-1 , respectively) is ca. 10 times higher than that of the pristine BMO (CO and CH4 production rates of 16.06 and 0.51 µmol g-1 h-1 , respectively). The tunable interfacial resistance of the Ohmic contact reported in this work can shed some important light on the design of highly efficient photocatalysts for both energy and environmental applications.

Formation of Highly Conductive Interfaces in Crystalline Ionic Liquid-Gated Unipolar MoTe2/h-BN Field-Effect Transistor.

2H MoTe2 (molybdenum ditelluride) has generated significant interest because of its superconducting, nonvolatile memory, and semiconducting of new materials, and it has a large range of electrical properties. The combination of transition metal dichalcogenides (TMDCs) and two dimensional (2D) materials like hexagonal boron nitride (h-BN) in lateral heterostructures offers a unique platform for designing and engineering novel electronic devices. We report the fabrication of highly conductive interfaces in crystalline ionic liquid-gated (ILG) field-effect transistors (FETs) consisting of a few layers of MoTe2/h-BN heterojunctions. In our initial exploration of tellurium-based semiconducting TMDs, we directed our attention to MoTe2 crystals with thicknesses exceeding 12 nm. Our primary focus centered on investigating the transport characteristics and quantitatively assessing the surface interface heterostructure. Our transconductance (gm) measurements indicate that the very efficient carrier modulation with an ILG FET is two times larger than standard back gating, and it demonstrates unipolarity of the device. The ILG FET exhibited highly unipolar p-type behavior with a high on/off ratio, and it significantly increased the mobility in MoTe2/h-BN heterochannels, achieving improvement as one of the highest recorded mobility increments. Specifically, we observed hole and electron mobility values ranging from 345 cm2 V-1 s-1 to 285 cm2 V-1 s-1 at 80 K. We predict that our ability to observe the intrinsic, heterointerface conduction in the channels was due to a drastic reduction of the Schottky barriers, and electrostatic gating is suggested as a method for controlling the phase transitions in the few layers of TMDC FETs. Moreover, the simultaneous structural phase transitions throughout the sample, achieved through electrostatic doping control, presents new opportunities for developing phase change devices using atomically thin membranes.

Effect of Alumina Incorporation on the Surface Mineralization and Degradation of a Bioactive Glass (CaO-MgO-SiO2-Na2O-P2O5-CaF2)-Glycerol Paste.

This study investigates the dissolution behavior as well as the surface biomineralization in simulated body fluid (SBF) of a paste composed of glycerol (gly) and a bioactive glass in the system CaO-MgO-SiO2-Na2O-P2O5-CaF2 (BG). The synthesis of the bioactive glass in an alumina crucible has been shown to significantly affect its bioactivity due to the incorporation of aluminum (ca. 1.3-1.4 wt %) into the glass network. Thus, the kinetics of the hydroxyapatite (HA) mineralization on the glass prepared in the alumina crucible was found to be slower than that reported for the same glass composition prepared in a Pt crucible. It is considered that the synthesis conditions lead to the incorporation of small amount of aluminum into the BG network and thus delay the HA mineralization. Interestingly, the BG-gly paste was shown to have significantly higher bioactivity than that of the as-prepared BG. Structural analysis of the paste indicate that glycerol chemically interacts with the glass surface and strongly alter the glass network architecture, thus generating a more depolymerized network, as well as an increased amount of silanol groups at the surface of the glass. In particular, BG-gly paste features early intermediate calcite precipitation during immersion in SBF, followed by hydroxyapatite formation after ca. seven days of SBF exposure; whereas the HA mineralization seems to be suppressed in BG, probably a consequence of the incorporation of aluminum into the glass network. The results obtained within the present study reveal the positive effect of using pastes based on bioactive glasses and organic carriers (here alcohols) which may be of interest not only due to their advantageous visco-elastic properties, but also due to the possibility of enhancing the glass bioactivity upon surface interactions with the organic carrier.

Deterring gun crime materially using forensic coatings.

Surface coatings that can help deter and solve gun crime are described. These nanoengineered coatings have been applied and evaluated on brass cartridge cases, where they increase associative forensic evidence through nanotag donation to the handler and the retention of handler's DNA. In future we expect this approach to be used for other surfaces and conditions.