Enhanced Photocatalytic Performances of CeO2/TiO2 Nanobelt Heterostructures

CeO₂/TiO₂ nanobelt heterostructures are synthesized via a cost‐effective hydrothermal method. The as‐prepared nanocomposites consist of CeO₂ nanoparticles assembled on the rough surface of TiO₂ nanobelts. In comparison with P25 TiO₂ colloids, surface‐coarsened TiO₂ nanobelts, and CeO₂ nanoparticles, the CeO₂/TiO₂ nanobelt heterostructures exhibit a markedly enhanced photocatalytic activity in the degradation of organic pollutants such as methyl orange (MO) under either UV or visible light irradiation. The enhanced photocatalytic performance is attributed to a novel capture–photodegradation–release mechanism. During the photocatalytic process, MO molecules are captured by CeO₂ nanoparticles, degraded by photogenerated free radicals, and then released to the solution. With its high degradation efficiency, broad active light wavelength, and good stability, the CeO₂/TiO₂ nanobelt heterostructures represent a new effective photocatalyst that is low‐cost, recyclable, and will have wide application in photodegradation of various organic pollutants. The new capture–photodegradation–release mechanism for improved photocatalysis properties is of importance in the rational design and synthesis of new photocatalysts.     

p-n异质结NiO/TiO2纳米复合材料的构建及应用研究进展

TiO_2和NiO分别作为n型和p型半导体材料,通过复合构建p-n异质结NiO/TiO_2纳米复合材料可以促进光生电子-空穴对的分离,从而提高光电性能。综述了不同形貌的p-n异质结NiO/TiO_2纳米复合材料的构建,如纳米球、纳米棒和纳米带等,以及其在光催化、锂离子电池、染料敏化太阳能电池和传感器等领域中的最新研究进展。     

Structure,Synthesis, and Applications of TiO2 Nanobelts

TiO₂ semiconductor nanobelts have unique structural and functional properties, which lead to great potential in many fields, including photovoltaics, photocatalysis, energy storage, gas sensors, biosensors, and even biomaterials. A review of synthetic methods, properties, surface modification, and applications of TiO₂ nanobelts is presented here. The structural features and basic properties of TiO₂ nanobelts are systematically discussed, with the many applications of TiO₂ nanobelts in the fields of photocatalysis, solar cells, gas sensors, biosensors, and lithium‐ion batteries then introduced. Research efforts that aim to overcome the intrinsic drawbacks of TiO₂ nanobelts are also highlighted. These efforts are focused on the rational design and modification of TiO₂ nanobelts by doping with heteroatoms and/or forming surface heterostructures, to improve their desirable properties. Subsequently, the various types of surface heterostructures obtained by coupling TiO₂ nanobelts with metal and metal oxide nanoparticles, chalcogenides, and conducting polymers are described. Further, the charge separation and electron transfer at the interfaces of these heterostructures are also discussed. These properties are related to improved sensitivity and selectivity for specific gases and biomolecules, as well as enhanced UV and visible light photocatalytic properties. The progress in developments of near‐infrared‐active photocatalysts based on TiO₂ nanobelts is also highlighted. Finally, an outline of important directions of future research into the synthesis, modification, and applications of this unique material is given.     

Enhanced Photocatalytic Property of Reduced Graphene Oxide/TiO2 Nanobelt Surface Heterostructures Constructed by an In Situ Photochemical Reduction Method

A facile method is proposed to assemble graphene oxide (GO) on the surface of a TiO₂ nanobelt followed by an in situ photocatalytic reduction to form reduced graphene oxide (rGO)/TiO₂ nanobelt surface heterostructures. The special colloidal properties of GO and TiO₂ nanobelt are exploited as well as the photocatalytic properties of TiO₂. Using water–ethanol solvent mixtures, GO nanosheets are tightly wrapped around the surface of the TiO₂ nanobelts through an aggregation process and are then reduced in situ under UV‐light irradiation to form rGO/TiO₂ nanobelt surface heterostructures. The heterostructures enhance the separation of the photoinduced carriers, which results in a higher photocurrent due to the special electronic characteristics of rGO. Compared to TiO₂ nanobelts, the rGO/TiO₂ nanobelt surface heterostructures possess higher photocatalytic activity for the degradation of methyl orange and for the production of hydrogen from water, as well as excellent recyclability, with no loss of activity over five cycles.     

Synthesis of Few‐Layer MoS2 Nanosheet‐Coated TiO2 Nanobelt Heterostructures for Enhanced Photocatalytic Activities

MoS₂ nanosheet‐coated TiO₂ nanobelt heterostructures—referred to as TiO₂@MoS₂—with a 3D hierarchical configuration are prepared via a hydrothermal reaction. The TiO₂ nanobelts used as a synthetic template inhibit the growth of MoS₂ crystals along the c‐axis, resulting in a few‐layer MoS₂ nanosheet coating on the TiO₂ nanobelts. The as‐prepared TiO₂@MoS₂ heterostructure shows a high photocatalytic hydrogen production even without the Pt co‐catalyst. Importantly, the TiO₂@MoS₂ heterostructure with 50 wt% of MoS₂ exhibits the highest hydrogen production rate of 1.6 mmol h^?1g^?1. Moreover, such a heterostructure possesses a strong adsorption ability towards organic dyes and shows high performance in photocatalytic degradation of the dye molecules.     

Controlled-fabrication,morphology formation mechanism of TiO2-B nanobelts with NiO-doping

The NiO/TiO₂-B hybrid nanomaterials were synthesized by a hydrothermal process and subsequently a uniform precipitation-method. The phase and morphology of the NiO/TiO₂-B hybrid nanomaterials can be controlled to be either nanoparticles or nanosheets by varying the experimental conditions, e.g., the reaction time, the concentration of Ni(NO₃)₂·6H₂O, and the precipitants. We systematically studied the mechanism of morphology evolution which is mainly affected by the reaction conditions. It is found that the NiO nanosheets are intensively and perpendicularly aggregated on the TiO₂-B nanobelts. The mechanisms of the nanosheets growth and the formation of NiO/TiO₂-B hybrid nanomaterials were discussed based on their morphology evolution processes. The NiO/TiO₂-B hybrid nanomaterials deliver a high discharge capacity of 395 mAh g^− 1 and 96.2% capacity retentions over 50 cycles, implying excellent cycling stability with reversible capacity which is 7.8% higher than that of isolated TiO₂-B nanobelts. This excellent electrochemical performance of the morphology-controlled NiO/TiO₂-B hybrid nanomaterials has a significant potential for lithium-ion battery application.     

Fabrication, structure, and enhanced photocatalytic properties of hierarchical CeO2 nanostructures/TiO2 nanofibers heterostructures

Combining the versatility of electrospinning technique and hydrothermal growth of nanostructures enabled the fabrication of hierarchical CeO₂/TiO₂ nanofibrous mat. The as-prepared hierarchical heterostructure consisted of CeO₂ nanostructures growing on the primary TiO₂ nanofibers. Interestingly, not only were secondary CeO₂ nanostructures successfully grown on TiO₂ nanofibers substrates, but also the CeO₂ nanostructures were uniformly distributed without aggregation on TiO₂ nanofibers. By selecting different alkaline source, CeO₂/TiO₂ heterostructures with CeO₂ nanowalls or nanoparticles were facilely fabricated. The photocatalytic studies suggested that the CeO₂/TiO₂ heterostructures showed enhanced photocatalytic efficiency of photodegradation of dye pollutants compared with bare TiO₂ nanofibers under UV light irradiation.     

Facile fabrication of hierarchical BiVO<Subscript>4</Subscript>/TiO<Subscript>2</Subscript> heterostructures for enhanced photocatalytic activities under visible-light irradiation

BiVO₄/TiO₂ nanocomposites were fabricated by a facile wet-chemical process, followed by the synthesis of TiO₂ hierarchical spheres via hydrothermal method. The BiVO₄/TiO₂ nanocomposites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV–Vis diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy. The results showed that prepared TiO₂ presented hierarchical spherical morphology self-assembled by nanoparticles and an anatase–brookite mixed crystal phase. The introduction of monoclinic BiVO₄ components retained the hierarchical structures and expanded the light response to around 510 nm. Type II BiVO₄/TiO₂ heterostructured nanocomposites exhibited improved photocatalytic degradation towards methylene blue under visible-light irradiation, especially for the composite photocatalysts with atomic Ti/Bi?=?10, which showed double degradation rate than that of pure BiVO₄. The enhanced photocatalytic mechanism of the heterostructured BiVO₄/TiO₂ nanocomposites was discussed as well.     

Decoration of Cu nanowires with chemically modified TiO2 nanoparticles for their improved photocatalytic performance

In this work, TiO₂ nanoparticles/Cu nanowires (TiO₂NPs@CuNWs) binary composites with tunable coverage of TiO₂ nanoparticles were prepared by a facile method of mixing oleic acid-modified TiO₂ nanoparticles with as-prepared Cu nanowires. Characterization studies including X-ray diffraction spectroscopy, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and high-resolution transmission electron microscopy were applied to investigate the structure and morphology of the as-synthesized TiO₂NPs@CuNWs binary composites. The photocatalytic activity of TiO₂NPs@CuNWs binary composites was examined by photodegradation of methyl orange. The enhanced photocatalytic efficiency of TiO₂NPs@CuNWs nanocomposites was ascribed to the moderate specific surface area, mesoporous structures, and the electron sink effect of the Cu nanowires. In principle, our investigation indicates that the TiO₂@Cu self-assembled nanostructures can be a promising candidate of composite photocatalysts.     

Enhanced photoelectrochemical properties of TiO2 nanorod arrays decorated with CdS nanoparticles

TiO₂ nanorod arrays (TiO₂ NRAs) sensitized with CdS nanoparticles were fabricated via successive ion layer adsorption and reaction (SILAR), and TiO₂ NRAs were obtained by oxidizing Ti NRAs obtained through oblique angle deposition. The TiO₂ NRAs decorated with CdS nanoparticles exhibited excellent photoelectrochemical and photocatalytic properties under visible light, and the one decorated with 20 SILAR cycles CdS nanoparticles shows the best performance. This can be attributed to the enhanced separation of electrons and holes by forming heterojunctions of CdS nanoparticles and TiO₂ NRAs. This provides a promising way to fabricate the material for solar energy conversion and wastewater degradation.     

Investigation on solar photocatalytic activity of TiO2 loaded composite: TiO2/Eggshell, TiO2/Clamshell and TiO2/CaCO3

The TiO₂/Eggshell, TiO₂/Clamshell and TiO₂/CaCO₃ loaded composites were prepared by sol-gel method and characterized by XRD and SEM. Their photocatalytic activities were measured through the degradation of Acid Red B under solar light irradiation. The influences of TiO₂ loaded content, heat-treated temperature and time on the photocatalytic activities were reviewed. The effects of irradiation time and dye initial concentration on the photocatalytic degradation were also investigated. The results showed that the photocatalytic activity can be greatly enhanced by appropriate TiO₂ loaded content.     

Preparation of metal ion (Fe and Ni) doped TiO2 nanoparticles supported on ZSM-5 zeolite and investigation of its photocatalytic activity

Metal ion doped TiO₂ nanoparticles supported on ZSM-5 zeolite (M-TiO₂/ZSM-5 composites, M = Fe or Ni) were synthesized by hydrothermal method. The prepared composites were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV–vis diffuse reflectance spectra (DRS). The photocatalytic activities of composites were evaluated by degradation of yellow GX aqueous solution under ambient condition. Fe-TiO₂/ZSM-5 composite showed to be more efficient catalyst for degradation of dye molecules as compared with Ni-TiO₂/ZSM-5 and TiO₂/ZSM-5. Its higher photocatalytic activity is attributed to the effective separation of charge carriers that will be discussed in this paper in detail.     

Facile synthesis of nano-TiO2/stellerite composite with efficient photocatalytic degradation of phenol

In this paper, we report a kind of nano-TiO₂/stellerite composite with enhanced photoactivity, which was synthesized by a typical homogeneous precipitation method followed by a calcination crystallization process using natural stellerite as support. The as-prepared composites were characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen adsorption-desorption, high resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). The results showed that TiO₂ loading amounts and calcination temperatures had significant influence on the adsorption and photocatalytic degradation properties of phenol. Moreover, it was indicated that the TiO₂ nanoparticles (NPs) with smaller grain size (around 12.0?nm) and narrower size distributions were uniformly deposited on the surface of stellerite as a layer of film. Compared with commercial P25, the received composite exhibited more superior photocatalytic degradation performance towards phenol. The enhanced photocatalytic degradation performance should result from the better dispersibility of TiO₂ NPs and higher separation efficiency of photogenerated electron-hole pairs. This work may set foundation for the practical application of this new composite photocatalyst in the field of wastewater treatment.     

Synthesis and visible-light photocatalytic activity of Bi-doped TiO2 nanobelts

Bi-doped anatase TiO₂ nanobelts were synthesized from layer-structural titanate nanobelts using two-step hydrothermal treatment approach. X-ray diffraction (XRD) patterns and transmission electron microscopic (TEM) images show that the doping of Bi³⁺ cations does not change the crystal structure and morphology of TiO₂ nanobelts. The energy-dispersive X-ray (EDX) and inductively coupled plasma-mass spectrometry (ICP-MS) analytic results suggest that the doping cations mainly exist near the surface of the TiO₂ nanobelts. The ultraviolet-visible (UV-vis) absorption spectra show that the absorption edge for the samples with Bi³⁺ has red shift as compared with that of undoped TiO₂ nanobelts, and correspondingly, the photocatalytic degradation of methylene blue under visible-light illumination is enhanced with the increase of Bi-doping content.     

碳纳米管修饰LaFeO3/TiO2复合材料的光催化性能与机理

采用超声辅助溶胶凝胶法制备了LaFeO₃颗粒,进一步以碳纳米管(CNTs)为基底和钛酸丁酯为前体,通过一步水热法煅烧合成CNTs/TiO₂/LaFeO₃(CTF)三元异质结光催化复合材料。通过扫描电子显微镜(SEM)、X射线衍射分析(XRD)、氮气吸附-解吸等温线(BET)、紫外-可见分光光度计(UV-Vis)、光致发光光谱(PL)等表征手段对材料的形貌与特征结构、比表面积和孔径结构以及光学特征进行了分析,并在紫外光下通过降解活性黑五(RB5)测试样品的光催化性能。结果表明,以CNTs作为载体,能够有效提升LaFeO₃/TiO₂复合材料的光催化性能。当CNTs在复合材料中的质量占比为5%时,150 W汞灯照射下RB5的50 min去除率可达99.5%。CNTs一方面通过增加复合材料的比较面积为催化反应的进行提供了更多的活性位点,更为重要的是,CNTs作为光生载流子传输的通道加快了电荷分离效率,提升了复合材料的降解能力和催化反应动力学进程。     

Unique and hierarchically structured novel Co<Subscript>3</Subscript>O<Subscript>4</Subscript>/NiO nanosponges with superior photocatalytic activity against organic contaminants

In the present study, novel Co₃O₄/NiO nanosponges designed for the photocatalytic degradation of organic contaminants were synthesized by a simple precipitation technique. The formation of sponge-like nanostructures was clearly evident through the TEM analysis. The photocatalytic efficiency was tested against rhodamine B (RhB) and congo red (CR) dye solutions. Co₃O₄/NiO nanosponges showed excellent and enhanced photocatalytic efficacy compared to those of Co₃O₄, NiO nanoparticles, and standards like TiO₂ and ZnO. The influence of paramount important operational parameters was explored and the conditions for the best photocatalytic efficiency were optimized. The trapping experiment revealed that the reactive oxygen species (ROS) identified was $OH radical. These findings certainly open up a new way for synthesizing a morphology dependent photocatalyst.     

Synthesis and characterisation of W–Bi–S-tridoped TiO2 nanoparticles with enhanced photocatalytic activity

In the present work, W–Bi–S-tridoped TiO₂ nanoparticles were synthesised by a simple sol–gel method. The structure and morphology of as-prepared W–Bi–S-tridoped TiO₂ were characterised by using X-ray powder diffraction, transmission electron microscopy, scanning electron microscopy and UV–Vis diffuse reflectance spectrum. It was found that the W–Bi–S-tridoped TiO₂ nanoparticles were well crystallised with a small size distribution. The absorption edge of TiO₂ was extended into visible-light region obviously after being doped with W, Bi and S. The photocatalytic degradation of methylene blue was used as a probe reaction to evaluate the efficiency of W, Bi and S doping. The W–Bi–S-tridoped TiO₂ exhibited the best photocatalytic activity, compared with TiO₂, S-TiO₂, W–S–TiO₂ and Bi–S–TiO₂. The mechanism that enhanced photocatalytic activity might be attributed to the synergistic effect of W, Bi and S.     

Self-assembled 3D ACF–rGO–TiO2 composite as efficient and recyclable spongy adsorbent for organic dye removal

Reduced graphene oxide (rGO) nanosheets (NSs) decorated with TiO₂ nanoparticles (NPs) were bound to activated carbon fibers (ACF) forming three-dimensional (3D) macroscopic composites with nanoscale building blocks by a one-pot hydrothermal self-assembly method. The integration of adsorption capacity enhanced by rGO NSs and photocatalytic activity introduced by TiO₂ NPs in the resultant ACF–rGO–TiO₂ composite was demonstrated via the proof-of-concept application of disposing organic dyes, i.e. Rhodamine B (RhB). Moreover, the photocatalytic degradation of laden RhB dye can effectively make ACF–rGO–TiO₂ composites regenerate the adsorption capacity, promoting two practical values: (1) eliminating rather than removing dye pollutants and (2) recycling rather than consuming adsorbents. The synergistic functionalization highlights the potential of 3D ACF–rGO–TiO₂ composite as a promising massive adsorbent with photocatalytic activities for environment purifications.     

Fabrication of magnetic Fe3O4/C/TiO2 composites with nanotube structure and enhanced photocatalytic activity

Magnetic hybrid photocatalysts containing TiO₂ nanotube as outer catalytic layer and Fe₃O₄ as the core, with an amorphous carbon intermediate layer, were synthesised, characterised and applied to degradation of phenol under Xenon lamp irradiation. For the composite, Fe₃O₄/C microspheres were surrounded by anatase TiO₂ nanotubes with a diameter of ～8–10?nm. Photocatalytic performance of the Fe₃O₄/C/TiO₂ nanotube (FCT-NT) composites was also evaluated and showed enhanced activity superior to commercial P25 and homemade TiO₂ particles. The outstanding photocatalytic performance of FCT-NT sample could be attributed to its improved surface area and enhanced capability of optical absorption. Notably, the novel photocatalyst showed excellent magnetic behaviour and could be efficiently separated and collected from the wastewater.     

Structural,morphological and photocatalytic characterisations of Ag-coated anatase TiO2 fabricated by the sol–gel dip-coating method

This study reports on the synthesis, characterisation and environmental applications of immobilised Titanium dioxide (TiO₂) as photocatalyst. Nanostructured thin films have been prepared on glass substrates using a layer-by-layer dip-coating method. The crystalline phase and surface morphology of the thin films were investigated by X-ray diffraction (XRD) pattern and scanning electron microscopy (SEM), respectively. The XRD results show that the TiO₂ thin films crystallise in anatase phase and we have found that the thin films consist of titanium dioxide nanocrystals. SEM shows that the nanoparticles are sintered together to form a compact structure and TiO₂ particles coated with silver nanoclusters were observed. Ag-coated TiO₂ films demonstrated photocatalysis performance when irradiated, and the Ag carrier further showed an electron-scavenging ability to mitigate electron–hole pair recombination, which can improve the photocatalytic efficiency. With the oxidisation and electron-scavenging ability of Ag and the photocatalysis ability of TiO₂, Ag-coated TiO₂ can decolour methyl orange (MO) more than bare TiO₂. It is a new approach to form Ag-coated TiO₂ nanoparticles with a simple system and non-toxic materials. The high photocatalytic effect of Ag-coated TiO₂ nanoparticles on pollutant (MO) suggests that it may have a promising future for water and wastewater treatments.