Impact of the anodization time on the photocatalytic activity of TiO₂ nanotubes

• Jesús A. Díaz-Real,
• Geyla C. Dubed-Bandomo,
• Juan Galindo-de-la-Rosa,
• Luis G. Arriaga,
• Janet Ledesma-García and
• Nicolas Alonso-Vante

Beilstein J. Nanotechnol. 2018, 9, 2628–2643, doi:10.3762/bjnano.9.244

• length, fluorine content, and capacitance of the space charge region increased, affecting the opto-electronic properties (bandgap, bathochromic shift, band-edge position) and surface hydrophilicity of TiO2 NTs. These properties are at the origin of the photocatalytic activity (PCA), as proved with the

• photooxidation of methylene blue. Keywords: fluorine doping; nanotubes; photocatalytic activity; photoelectrochemistry; titanium(IV) oxide (TiO2); Introduction TiO2 started to attract great interest after Fujishima and Honda reported [1] on its photoelectrochemical (PEC) properties in 1972. Numerous features

• ] observed that a water-based electrolyte containing NH4F induced a co-doping with F and N in the TNTs. Their study suggested that a combination of applied potential and annealing temperature were responsible for the high photocatalytic activity (PCA) of their materials in the oxidation of methyl orange. In

Nanocellulose: Recent advances and its prospects in environmental remediation

• Katrina Pui Yee Shak,
• Yean Ling Pang and
• Shee Keat Mah

Beilstein J. Nanotechnol. 2018, 9, 2479–2498, doi:10.3762/bjnano.9.232

• ]. Although cellulose alone exhibits limited photocatalytic activity under UV or visible light irradiation, many semiconductor materials have been added to enhance the photocatalytic activity. Several research groups have demonstrated photocatalytic wastewater treatment using cellulose-based metal oxide

Hierarchical heterostructures of Bi₂MoO₆ microflowers decorated with Ag₂CO₃ nanoparticles for efficient visible-light-driven photocatalytic removal of toxic pollutants

• Shijie Li,
• Wei Jiang,
• Shiwei Hu,
• Yu Liu,
• Yanping Liu,
• Kaibing Xu and
• Jianshe Liu

Beilstein J. Nanotechnol. 2018, 9, 2297–2305, doi:10.3762/bjnano.9.214

• photocatalytic activity [37]. However, it is unstable under illumination. Previous studies found that the good stability of Ag2CO3 could be achieved through the rational construction of heterojunctions, such as Ag2CO3/Bi2WO6 [37], Ag2O/Ag2CO3 [38], Ag2CO3/Bi2O2CO3 [39], Ag2CO3/C3N4 [40], Ag/Ag2CO3/BiVO4 [41

• ] Ag2CO3/AgBr/ZnO [42], and Ag/Ag2CO3/Bi2MoO6 [32]. The band structure of Ag2CO3 matches well with that of Bi2MoO6 [32]. Moreover, morphology modulation is another significant way to enhance photocatalytic activity. Three-dimensional nanostructures endow materials with unique physicochemical properties

• as a function of the time. Again, ACO/BMO-30 displayed the highest activity, with degradation efficiencies of 94.9% for MO, 100% for MB, and 78.9% for TC. The photocatalytic activity in the degradation of TC of ACO/BMO-30 was further compared with that of Ag/Ag2CO3/Bi2MoO6 [32], and of Ag2MoO4

A visible-light-controlled platform for prolonged drug release based on Ag-doped TiO₂ nanotubes with a hydrophobic layer

• Caihong Liang,
• Jiang Wen and
• Xiaoming Liao

Beilstein J. Nanotechnol. 2018, 9, 1793–1801, doi:10.3762/bjnano.9.170

• -layer titania nanotubes (TNTs) fabricated using by an in situ voltage up-anodization process. The visible-light photocatalytic activity is improved by loading Ag onto the TNTs by NaBH4 reduction. Then, the TNTs containing Ag nanoparticles were modified with dodecanethiol (NDM) to create a hydrophobic

Controllable one-pot synthesis of uniform colloidal TiO₂ particles in a mixed solvent solution for photocatalysis

• Jong Tae Moon,
• Seung Ki Lee and
• Ji Bong Joo

Beilstein J. Nanotechnol. 2018, 9, 1715–1727, doi:10.3762/bjnano.9.163

• phase or high crystallinity are essential. Highly crystallized TiO2 is generally considered to not only reduce the recombination of electron–hole pairs, but to also extend the lifetime of photogenerated charges that result in the enhancement of photocatalytic activity [7]. During photocatalysis, it is

• surface and prevent surface reactions, and in turn, hamper the photocatalytic activity [25]. In order to address the above issues, TiO2 photocatalysts are often synthesized in the form of a porous colloidal particle in sub-micrometer dimensions [8][26][27]. They can be calcined at high temperature, which

• , large surface area, uniform photocatalytic activity for each particle, and improved accessibility for the reactant molecules. To fabricate the uniform, colloidal TiO2 spheres, several synthetic methods have been reported including hydrothermal, solvothermal, and sol–gel processes [10][26][28][29

Sulfur-, nitrogen- and platinum-doped titania thin films with high catalytic efficiency under visible-light illumination

• Boštjan Žener,
• Lev Matoh,
• Giorgio Carraro,
• Bojan Miljević and
• Romana Cerc Korošec

Beilstein J. Nanotechnol. 2018, 9, 1629–1640, doi:10.3762/bjnano.9.155

• , band gap measurements). The photocatalytic activity of the prepared thin films was determined by measuring the degradation rate of plasmocorinth B (PB), an organic pigment used in the textile industry, which can pose an environmental risk when expelled into wastewater. A kinetic model for adsorption

• and subsequent degradation was used to fit the experimental data. The results have shown an increase in photocatalytic activity under visible-light illumination of nonmetal and metal doped and co-doped titania thin films compared to an undoped sample. Keywords: doping; photocatalysis; sol–gel

• environmental applications, such as water treatment [9][10][11] and air purification [12]. One of the important factors affecting the photocatalytic activity of TiO2 is its specific surface area. By increasing the specific surface area (porosity) of TiO2, the photocatalytic activity can be increased. One of the

Sheet-on-belt branched TiO₂(B)/rGO powders with enhanced photocatalytic activity

• Huan Xing,
• Wei Wen and
• Jin-Ming Wu

Beilstein J. Nanotechnol. 2018, 9, 1550–1557, doi:10.3762/bjnano.9.146

• TiO2(B) is usually adopted to construct phase junctions with anatase TiO2 for applications in photocatalysis to facilitate charge separation; its intrinsic photocatalytic activity, especially when in the form of one- or three-dimensional nanostructures, has been rarely reported. In this study, a sheet

• assist the photodegradation of phenol in water under UV light illumination. The enhanced photocatalytic activity can be attributed to the significantly increased surface area and enhanced charge separation. Keywords: branched nanostructure; photocatalysis; reduced graphene oxide; TiO2(B); Introduction

• safety and rate capability [11][17][18][19][20]. For photocatalytic applications, TiO2(B) is usually combined with anatase TiO2 to construct a multiphase heterostructure to enhance charge separation and in turn the photocatalytic activity [21][22][23][24][25]. For example, Yang et al. synthesized anatase

Cr(VI) remediation from aqueous environment through modified-TiO₂-mediated photocatalytic reduction

• Rashmi Acharya,
• Brundabana Naik and
• Kulamani Parida

Beilstein J. Nanotechnol. 2018, 9, 1448–1470, doi:10.3762/bjnano.9.137

• TiO2 as a photocatalyst and the importance of its modification for photocatalytic reduction of Cr(VI) has also been addressed. In this review, the photocatalytic activity of TiO2 after modification with carbon-based advanced materials, metal oxides, metal sulfides and noble metals towards reduction of

• Cr(VI) was evaluated and compared with that of bare TiO2. The photoactivity of dye-sensitized TiO2 for reduction of Cr(VI) was also discussed. The mechanism for enhanced photocatalytic activity was highlighted and attributed to the resultant properties, namely, effective separation of photoinduced

• with carbon-based advanced materials, noble metals, oxides and sulfides of transition metals for enhanced photocatalytic activity towards degradation of Cr(VI). The photocatalytic reduction of Cr(VI) over dye-sensitized TiO2 is also briefly discussed. The present review article has been divided into

Ag₂WO₄ nanorods decorated with AgI nanoparticles: Novel and efficient visible-light-driven photocatalysts for the degradation of water pollutants

• Shijie Li,
• Shiwei Hu,
• Wei Jiang,
• Yanping Liu,
• Yu Liu,
• Yingtang Zhou,
• Liuye Mo and
• Jianshe Liu

Beilstein J. Nanotechnol. 2018, 9, 1308–1316, doi:10.3762/bjnano.9.123

• photocatalytic performance for dye degradation under light irradiation [30][31][36][37]. Unfortunately, due to its wide bandgap of about 3.1 eV, Ag2WO4 has limited photocatalytic activity under sunlight, which severely limits its application and illustrates the urgency for optimization of Ag2WO4 to overcome

• nanorods as the Ag source. The as-prepared AgI/Ag2WO4 heterojunctions exhibited remarkably higher photocatalytic activity than pure Ag2WO4 toward the degradation of rhodamine B (RhB), methyl orange (MO) and para-chlorophenol (4-CP) under visible light. Based on a systematic characterization and study, a

• -light photocatalytic activity with an RhB degradation rate of 16.2% after 60 min irradiation due to the unsatisfactory visible-light absorption and fast recombination of photoinduced charge carriers [31][38][44][45]. After hybridization of AgI, all AgI/Ag2WO4 heterojunctions (0.1AgI/Ag2WO4, 0.2AgI

Noble metal-modified titania with visible-light activity for the decomposition of microorganisms

• Maya Endo,
• Zhishun Wei,
• Kunlei Wang,
• Baris Karabiyik,
• Kenta Yoshiiri,
• Paulina Rokicka,
• Bunsho Ohtani,
• Agata Markowska-Szczupak and
• Ewa Kowalska

Beilstein J. Nanotechnol. 2018, 9, 829–841, doi:10.3762/bjnano.9.77

• antimicrobial properties of noble metals with the high photocatalytic activity of modified titania should result in a high purification efficiency of noble metal-modified titania [6][46][47][48][49][50][51][52]. Indeed, in our recent study, noble metal-modified faceted anatase titania (octahedral anatase

• particles; OAP) have shown high activity in both the decomposition of organic compounds and of microorganisms (E. coli and C. albicans) [48]. It has been found that both the intrinsic properties of silver and the photocatalytic activity of silver-modified titania are responsible for the high antibacterial

• increase in activity was observed, especially for the fine anatase sample (ST01, 93.1%). Modification with gold caused a slight increase in activity under UV irradiation reaching 96.2%, 94.2% and 77.5%, respectively. An increase in photocatalytic activity after titania modification with NPs of NMs is not

Facile synthesis of a ZnO–BiOI p–n nano-heterojunction with excellent visible-light photocatalytic activity

• Mengyuan Zhang,
• Jiaqian Qin,
• Pengfei Yu,
• Bing Zhang,
• Mingzhen Ma,
• Xinyu Zhang and
• Riping Liu

Beilstein J. Nanotechnol. 2018, 9, 789–800, doi:10.3762/bjnano.9.72

• Zn/Bi, the morphology varies from nanoplates, flowers to nanoparticles. The heterojunction formed between ZnO and BiOI decreases the recombination rate of photogenerated carriers and enhances the photocatalytic activity of ZnO/BiOI composites. The obtained ZnO/BiOI heterostructured nanocomposites

• exhibit a significant improvement in the photodegradation of rhodamine B under visible light (λ ≥ 420 nm) irradiation as compared to single-phase ZnO and BiOI. A sample with a Zn/Bi ratio of 3:1 showed the highest photocatalytic activity (≈99.3% after 100 min irradiation). The photodegradation tests

• indicated that the ZnO/BiOI heterostructured nanocomposites not only exhibit remarkably enhanced and sustainable photocatalytic activity, but also show good recyclability. The excellent photocatalytic activity could be attributed to the high separation efficiency of the photoinduced electron–hole pairs as

Surface-plasmon-enhanced ultraviolet emission of Au-decorated ZnO structures for gas sensing and photocatalytic devices

• T. Anh Thu Do,
• Truong Giang Ho,
• Thu Hoai Bui,
• Quang Ngan Pham,
• Hong Thai Giang,
• Thi Thu Do,
• Duc Van Nguyen and
• Dai Lam Tran

Beilstein J. Nanotechnol. 2018, 9, 771–779, doi:10.3762/bjnano.9.70

• investigated for photocatalytic activity as reported previously [8][20]. The photocatalytic activity of the Pt/ZnO hybrid nanocomposite under photodegradation of rhodamine B (RhB) was higher compared to commercial TiO2 [21]. Here, it is quite reasonable to note that the plasmonic metal NP/metal-oxide

• semiconductor structures are also promising and interesting materials for photocatalytic utilization, in particular relating to the solar light spectrum. It is also worth mentioning that, in fact, there are numerous works that have investigated the photocatalytic activity of these structures based on

• quenching measurements shows that the Au-decorated ZnO structures exhibited an enhancement in electron−hole pair separation, which allows for superior photocatalytic activity. Results and Discussion X-ray diffraction (XRD) patterns of all samples are shown in Figure 1a. For both pure and Au-decorated ZnO, a

Perovskite-structured CaTiO₃ coupled with g-C₃N₄ as a heterojunction photocatalyst for organic pollutant degradation

• Ashish Kumar,
• Christian Schuerings,
• Suneel Kumar,
• Ajay Kumar and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2018, 9, 671–685, doi:10.3762/bjnano.9.62

• )–CaTiO3 (CTCN) organic–inorganic heterojunction photocatalyst was synthesized by a facile mixing method, resulting in the deposition of CaTiO3 (CT) nanoflakes onto the surface of g-C3N4 nanosheets. The photocatalytic activity of the as-synthesized heterojunction (along with the controls) was evaluated by

• studying the degradation of an aqueous solution of rhodamine B (RhB) under UV, visible and natural sunlight irradiation. The CTCN heterojunction with 1:1 ratio of g-C3N4/CT showed the highest photocatalytic activity under sunlight irradiation and was also demonstrated to be effective for the degradation of

• overall photocatalytic activity. Furthermore, the active species trapping experiments validate the major role played by superoxide radicals (O2−•) in the degradation of pollutants. Based on scavenger studies and theoretically calculated band positions, a plausible mechanism for the photocatalytic

Mechanistic insights into plasmonic photocatalysts in utilizing visible light

• Kah Hon Leong,
• Azrina Abd Aziz,
• Lan Ching Sim,
• Pichiah Saravanan,
• Min Jang and
• Detlef Bahnemann

Beilstein J. Nanotechnol. 2018, 9, 628–648, doi:10.3762/bjnano.9.59

• improve photocatalytic efficiency [101]. The LSPR of Ag in a Ag/AgCl composite was found to enhance the local inner electromagnetic field and prolong the lifetime of the charge carriers. Wang et al. observed that Ag@AgBr exhibited enhanced photocatalytic activity as compared to Ag/AgCl by a factor of 1.5

Fabrication and photoactivity of ionic liquid–TiO₂ structures for efficient visible-light-induced photocatalytic decomposition of organic pollutants in aqueous phase

• Anna Gołąbiewska,
• Marta Paszkiewicz-Gawron,
• Aleksandra Sadzińska,
• Wojciech Lisowski,
• Ewelina Grabowska,
• Adriana Zaleska-Medynska and
• Justyna Łuczak

Beilstein J. Nanotechnol. 2018, 9, 580–590, doi:10.3762/bjnano.9.54

• photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS), scanning transmission microscopy (STEM) and the Brunauer–Emmett–Teller (BET) surface area method, whereas the photocatalytic activity was evaluated by the degradation of phenol in aqueous solution under visible light irradiation (λ > 420

• example spectra for IL–TiO2 obtained at IL:TBOT molar ratio of 1:10 and 1:3). Therefore, this enhanced absorbance of the light in the visible spectrum is expected to enhance the photocatalytic activity in the visible region for the target reaction. This observation is well verified by the photocatalytic

• or during synthesis and preparation. Photocatalytic activity The photocatalytic activity of the IL–TiO2 samples was evaluated by phenol degradation induced by visible-light irradiation (using an optical filter with λ > 420 nm). All photocatalysts exhibited better photocatalytic properties than the

Influence of the preparation method on the photocatalytic activity of Nd-modified TiO₂

• Patrycja Parnicka,
• Paweł Mazierski,
• Tomasz Grzyb,
• Wojciech Lisowski,
• Ewa Kowalska,
• Bunsho Ohtani,
• Adriana Zaleska-Medynska and
• Joanna Nadolna

Beilstein J. Nanotechnol. 2018, 9, 447–459, doi:10.3762/bjnano.9.43

• (SHT) methods. The as-prepared samples were characterized by X-ray diffraction (XRD), BET surface area measurements, scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), luminescence spectroscopy and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the

• photocatalytic efficiency of phenol and toluene degradation under vis irradiation in the presence of 0.25% Nd-TiO2(HT) reached 0.62 and 3.36 μmol·dm−1·min−1, respectively. Photocatalytic activity tests in the presence of Nd-TiO2 and scavenger confirm that superoxide radicals were responsible for the visible

• TiO2, which leads to enhanced surface adsorption properties of TiO2 and indirectly increases the photocatalytic activity of the photocatalysts [13][14]. Moreover, it has been reported that the presence of RE ions slowed down the rate of the charge-carrier recombination processes [15]. Besides, RE ions

Facile synthesis of ZnFe₂O₄ photocatalysts for decolourization of organic dyes under solar irradiation

• Arjun Behera,
• Debasmita Kandi,
• Sanjit Manohar Majhi,
• Satyabadi Martha and
• Kulamani Parida

Beilstein J. Nanotechnol. 2018, 9, 436–446, doi:10.3762/bjnano.9.42

• , FESEM, UV–vis DRS, PL, FTIR and photocurrent measurements. The photocatalytic activity of the prepared material is studied with regard to the degradation of rhodamine B (Rh B) and Congo red under solar irradiation. The kinetic study showed that the material exhibits zeroth and first order reaction

• the organic dyes (i.e., Congo red, Rh B, malachite green methylene blue) to CO2, H2O and the corresponding mineral acids [19][24]. Movahedi et al. have prepared ZnFe2O4 through precipitation tested the photocatalytic activity of ZnFe2O4 in the degradation of 5 ppm Congo red obtaining 64% degradation

• in 120 min [19]. The photocatalytic activity of ZnFe2O4 has also been tested in the degradation of Rh B [24]. Zhao et al. have synthesized ZnFe2O4 through chemical etching followed by calcination and reported a degradation rate of 31% in 3 h [24]. Doong and co-workers have prepared ZnFe2O4 through a

Photocatalytic and adsorption properties of TiO₂-pillared montmorillonite obtained by hydrothermally activated intercalation of titanium polyhydroxo complexes

• Mikhail F. Butman,
• Nikolay L. Ovchinnikov,
• Nikita S. Karasev,
• Nataliya E. Kochkina,
• Alexander V. Agafonov and
• Alexandr V. Vinogradov

Beilstein J. Nanotechnol. 2018, 9, 364–378, doi:10.3762/bjnano.9.36

• crystallinity (nanocrystals) representing a mixture of anatase and rutile phases. The structures exhibit improved adsorption and photocatalytic activity as a result of hydrothermally activated intercalation of titanium polyhydroxo complexes (i.e., TiCl4 hydrolysis products) in a solution with a concentration

• , and liquefied nitrogen adsorption/desorption. The photocatalytic activity of the TiO2-pillared materials was studied using the degradation of anionic (methyl orange, MO) and cationic (rhodamine B, RhB) dyes in water under UV irradiation. The combined effect of adsorption and photocatalysis resulted in

• removal of 100% MO and 97.5% RhB (with an initial concentration of 40 mg/L and a photocatalyst-sorbent concentration of 1 g/L) in about 100 minutes. The produced TiO2-pillared montmorillonite showed increased photocatalytic activity as compared to the commercially available photocatalyst Degussa P25

Sugarcane juice derived carbon dot–graphitic carbon nitride composites for bisphenol A degradation under sunlight irradiation

• Lan Ching Sim,
• Jing Lin Wong,
• Chen Hong Hak,
• Jun Yan Tai,
• Kah Hon Leong and
• Pichiah Saravanan

Beilstein J. Nanotechnol. 2018, 9, 353–363, doi:10.3762/bjnano.9.35

• of g-C3N4. Hence, the charge separation efficiency should not be one of the main factors responsible for the enhancement of the photocatalytic activity of CD/g-C3N4. Instead, the light absorption capability was the dominant factor since the photoreactivity correlated well with the ultraviolet–visible

• extended absorption spectrum from the visible to the near-infrared (NIR) region. This extended spectral absorption allows for the generation of more electrons for the enhancement of BPA degradation. It was determined that the reactive radical species responsible for the photocatalytic activity were the

• superior photocatalytic activity was demonstrated [8]. Guo and co-workers used the electrochemical method to produce CDs from graphite rods. The deposition of CDs onto g-C3N4/ZnO heterojunctions enhanced the degradation of tetracycline by absorbing a wider spectrum of visible light and suppressing the

Bombyx mori silk/titania/gold hybrid materials for photocatalytic water splitting: combining renewable raw materials with clean fuels

• Stefanie Krüger,
• Michael Schwarze,
• Otto Baumann,
• Christina Günter,
• Michael Bruns,
• Christian Kübel,
• Dorothée Vinga Szabó,
• Rafael Meinusch,
• Verónica de Zea Bermudez and
• Andreas Taubert

Beilstein J. Nanotechnol. 2018, 9, 187–204, doi:10.3762/bjnano.9.21

• particle size and preparation procedure on the photocatalytic activity of Au/TiO2 catalysts. Lower Au loadings of 0.25% Au on P25 TiO2 produced more efficient water splitting catalysts than materials with Au loadings of 1.5% or 2.2%. Moreover, the authors showed that 532 nm laser light is more efficient

• diameters of ca. 440 nm and AuNPs with diameters of ca. 60 nm could split water in the visible range, even at low Au fractions of only 1.8% [27]. Finally, Seh et al. showed that TiO2/Au Janus nanoparticles have a higher photocatalytic activity than the corresponding core–shell particles [28]. All materials

• resulting material was thus a macroscopic and mechanically robust object that could simply be retrieved and washed before reuse [32]. Another viable approach for the synthesis of larger and mechanically stable objects with photocatalytic activity is the immobilization of TiO2/Au nanostructures on a scaffold

Facile synthesis of silver/silver thiocyanate (Ag@AgSCN) plasmonic nanostructures with enhanced photocatalytic performance

• Xinfu Zhao,
• Dairong Chen,
• Abdul Qayum,
• Bo Chen and
• Xiuling Jiao

Beilstein J. Nanotechnol. 2017, 8, 2781–2789, doi:10.3762/bjnano.8.277

• the product was investigated based on the time-dependent experiments. Further experiments indicated that the prepared Ag@AgSCN nanostructures with an atomic ratio of Ag/AgSCN = 0.0463 exhibited high photocatalytic activity and long-term stability for the degradation of oxytetracycline (84%) under

• visible-light irradiation. In addition to the microstructure and high specific surface area, the enhanced photocatalytic activity was mainly caused by the surface plasmon resonance of Ag nanoparticles, and the high stability of AgSCN resulted in the long-term stability of the photocatalyst product

• and environmental friendlessness. For example, as a typical semiconductor, TiO2 exhibits high photocatalytic degradation performance against a large number of organic pollutants [5][6][7]. However, it is difficult to obtain a high photocatalytic activity under visible-light irradiation with TiO2 as a

CdSe nanorod/TiO₂ nanoparticle heterojunctions with enhanced solar- and visible-light photocatalytic activity

• Fakher Laatar,
• Hatem Moussa,
• Halima Alem,
• Lavinia Balan,
• Emilien Girot,
• Ghouti Medjahdi,
• Hatem Ezzaouia and
• Raphaël Schneider

Beilstein J. Nanotechnol. 2017, 8, 2741–2752, doi:10.3762/bjnano.8.273

• the narrow bandgap of CdSe NRs serves to increase the photoresponse of CdSe/TiO2 composites until ≈725 nm. The CdSe (2 wt %)/TiO2 composite exhibits the highest photocatalytic activity for the degradation of rhodamine B in aqueous solution under simulated sunlight or visible light irradiation. The

• enhancement in photocatalytic activity likely originates from CdSe sensitization of TiO2 and the heterojunction between these materials which facilitates electron transfer from CdSe to TiO2. Due to its high stability (up to ten reuses without any significant loss in activity), the CdSe/TiO2 heterostructured

• separation. The interfacial electron transfer between two semiconductors has gained significant interest because the heterojunction improves both the optical absorption in the visible range and the charge separation yield and thus the charge carrier lifetime [3][4][5][6][7][8]. The photocatalytic activity is

Hydrothermal synthesis of ZnO quantum dot/KNb₃O₈ nanosheet photocatalysts for reducing carbon dioxide to methanol

• Xiao Shao,
• Weiyue Xin and
• Xiaohong Yin

Beilstein J. Nanotechnol. 2017, 8, 2264–2270, doi:10.3762/bjnano.8.226

• . The as-prepared photocatalysts were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis absorption spectroscopy (UV–vis). The photocatalytic activity of the

• excellent nonlinear optical, piezoelectric, ferroelectric, ionic conductivity, selective-ion exchange and photocatalytic properties [6][7][8][9]. Zhang et al. prepared K4Nb6O17 with a sheet-like nanostructure by hydrothermal synthesis and found its photocatalytic activity for degrading acidic red G to be

• much higher than that of the commercial Degussa P25 [10]. Zhou et al. synthesized porous K4Nb6O17 microspheres with large surface area via a homogeneous precipitation method, which showed not only two times higher photocatalytic activity than that of the commercial Degussa P25 (the titanium dioxide

Synthesis and characterization of noble metal–titania core–shell nanostructures with tunable shell thickness

• Bartosz Bartosewicz,
• Marta Michalska-Domańska,
• Malwina Liszewska,
• Dariusz Zasada and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2017, 8, 2083–2093, doi:10.3762/bjnano.8.208

• ][5][6][7][8][9][10][11]. For many applications, however, the use of titanium dioxide in CSNs would be of much greater interest. Useful physicochemical properties of titanium dioxide in its crystalline forms, rutile and anatase, such as high refractive index and photocatalytic activity have led to its

Two-dimensional carbon-based nanocomposites for photocatalytic energy generation and environmental remediation applications

• Suneel Kumar,
• Ashish Kumar,
• Ashish Bahuguna,
• Vipul Sharma and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2017, 8, 1571–1600, doi:10.3762/bjnano.8.159

• charge transfer and better catalytic dispersion to enhance the photocatalytic activity. The 2D carbon-based nanomaterials combine several of the above-mentioned advantages of both 2D and carbon-based materials, and have shown great prospects as catalysts for various applications. As this is currently an

• precursor, exhibited different microstructure and isoelectric points [91]. The g-C3N4 prepared by the thermal condensation method generally exhibit low surface area, which can limit its practical applications, as high specific surface area of catalyst is highly desirable for enhanced photocatalytic activity

• separation and migration of charge carriers to the surface. Higher crystallinity and smaller size of particles play a significant role in enhancing the photocatalytic activity by decreasing the recombination probability of photogenerated charge carriers [4]. It is well known that higher crystallinity leads