Highly sensitive detection of estradiol by a SERS sensor based on TiO₂ covered with gold nanoparticles

• Andrea Brognara,
• Ili F. Mohamad Ali Nasri,
• Beatrice R. Bricchi,
• Andrea Li Bassi,
• Caroline Gauchotte-Lindsay,
• Matteo Ghidelli and
• Nathalie Lidgi-Guigui

Beilstein J. Nanotechnol. 2020, 11, 1026–1035, doi:10.3762/bjnano.11.87

• different size distributions and densities. Figure 2 shows the two boundary cases of 3 and 15 nm of evaporated Au on a TiO2 film deposited at 12 Pa. The observations were similar for the 8 Pa films. The effects of heat treatment are clearly visible. In the case of 15 nm of Au (Figure 2c,d), a continuous

Structural optical and electrical properties of a transparent conductive ITO/Al–Ag/ITO multilayer contact

• Aliyu Kabiru Isiyaku,
• Ahmad Hadi Ali and
• Nafarizal Nayan

Beilstein J. Nanotechnol. 2020, 11, 695–702, doi:10.3762/bjnano.11.57

• of an ITO sandwich electrode with Ag alloy against heat treatment at 450 °C was carried out by Roh et al. [30]. An appreciable durability and stability of the Ag films was observed. In the present work, the structural, optical and electrical properties of an Al–Ag bilayer between ITO layers (ITO/Al

• heat treatment lowers the trade-off between transparency and conductivity by reducing structural defects in the films. The sheet resistance of the multilayer structure of the IAAI film can be expressed as [29]: where is the total sheet resistance of the IAAI film, RAl and RAg are the sheet resistance

• overcome by adding a thin layer of Al, Au, Pd, or Cr to the Ag film to improve the adhesion [4][25][26]. Optical and electrical properties of ITO films are enhanced by post-deposition annealing especially at high temperatures [7]. Gulen et al. [27] exposed pure ITO films deposited by sputtering to heat

Preparation, characterization and photocatalytic performance of heterostructured CuO–ZnO-loaded composite nanofiber membranes

• Wei Fang,
• Liang Yu and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 631–650, doi:10.3762/bjnano.11.50

• environmental monitoring, industry, aviation, and transportation. In this paper, heterostructured CuO–ZnO-loaded CNF membranes (CNFMs) were prepared successfully by a combination of electrospinning, heat treatment, and hydrothermal synthesis. The influence of the synthesis parameters on morphology, structure

• work [37], bubble-electrospinning was used to prepare Cu(Ac)2/Zn(Ac)2/PVDF/PAN on a large scale. Subsequently, PVDF/PAN CNFMs loaded with CuO and ZnO nanocrystals were prepared using heat treatment and hydrothermal synthesis. However, the diameter distribution of CNFMs obtained by bubble

• the CNFMs were not investigated, which is very important to obtain high-quality CNFMs. Therefore, in the present study, heterostructured CuO–ZnO-loaded CNFMs were prepared using a combination of electrospinning, heat treatment, and hydrothermal synthesis. The effects of electrospinning, heat treatment

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 310–322, doi:10.3762/bjnano.11.23

• can markedly affect the nanoscale porosity [13][14][15][16][17][18][19][20][21]. Hence, a combined in-depth elucidation of meso/microporosity and the graphene-based structure upon heat treatment is pursued in this study to obtain a profound understanding of the relationship between the changes in the

• disorder in the material. That is, with increasing disorder of a material a higher micropore volume is expected. Because with higher carbonization temperature the graphene sheets as well as their stacking become more ordered, the meso/microporosity is expected to depend on the heat treatment temperature

• porosity on the precursor materials is expected as some materials are better graphitizable than others. For instance, resin-based carbon materials are not graphitizable, while pitch-based carbon materials develop a comparably high structural order upon heat treatment and can be converted into graphite. The

High-performance asymmetric supercapacitor made of NiMoO₄ nanorods@Co₃O₄ on a cellulose-based carbon aerogel

• Meixia Wang,
• Jing Zhang,
• Xibin Yi,
• Benxue Liu,
• Xinfu Zhao and
• Xiaochan Liu

Beilstein J. Nanotechnol. 2020, 11, 240–251, doi:10.3762/bjnano.11.18

• aerogel precursor, which was produced from microcrystalline cellulose (MC). Second, the produced CA was used as the backbone for the growth of NiMoO4 nanorods employing a hydrothermal method followed by heat treatment. By this approach, NiMoO4/CA composites were obtained, in which the NiMoO4 nanorods

The effect of heat treatment on the morphology and mobility of Au nanoparticles

• Sven Oras,
• Sergei Vlassov,
• Simon Vigonski,
• Boris Polyakov,
• Mikk Antsov,
• Vahur Zadin,
• Rünno Lõhmus and
• Karine Mougin

Beilstein J. Nanotechnol. 2020, 11, 61–67, doi:10.3762/bjnano.11.6

• , Latvia 10.3762/bjnano.11.6 Abstract In the present paper, we investigate the effect of heat treatment on the geometry and mobility of Au nanoparticles (NPs) on a Si substrate. Chemically synthesized Au NPs of diameter ranging from 5 to 27 nm were annealed at 200, 400, 600 and 800 °C for 1 h. A change in

• from the ellipsometry measurements presented in Figure 7. How exactly the rapid growth of the SiO2 layer may be related to the drastic increase in friction remains unclear and can be the subject for future studies. Overall, we demonstrated that heat treatment, which is widely used as a surfactant

• of the SiO2 layer. Both processes are highly temperature-dependent, exhibiting drastic enhancement above 700 °C. Overall, we demonstrated that heat treatment, which is widely used for surfactant removal prior to nanomanipulation experiments, can have an extensive effect on the mobility of Au NPs

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• synthesized by hydrothermal treatment of a glucose solution yielding carbon spheres with sizes of 330 ± 50 nm, followed by nitrogen doping via heat treatment in ammonia atmosphere. The influence of a) varying the nitrogen doping temperature (550–1000 °C) and b) of a catalytic graphitization prior to nitrogen

• -synthetic heat treatment in ammonia atmosphere (see the review by Daems and co-workers [7]). The direct comparison of the N content of NCS-850 and NCS-1000 with the g-NCS-850 and g-NCS-1000 spheres reveals that substitutional N-doping of the amorphous carbon matrix is easier than that of the graphitic one

• of oxygen, hydrogen and carbon atoms due to gasification and the arrangement to turbostratic-type carbon after heat treatment, as described in more detail in our former publication [36]. The g-NCS samples of lower reaction temperatures (g-NCS-550 and g-NCS-700) are very similar to their NCS

Synthesis and acetone sensing properties of ZnFe₂O₄/rGO gas sensors

• Kaidi Wu,
• Yifan Luo,
• Ying Li and
• Chao Zhang

Beilstein J. Nanotechnol. 2019, 10, 2516–2526, doi:10.3762/bjnano.10.242

• acetone at low temperature, even at room temperature [32]. Hence, with the aim to fabricate a high-performance acetone gas sensor, we prepared hollow spheres of ZnFe2O4 and ZnFe2O4/rGO composites using a one-pot solvothermal method followed by a high-temperature heat treatment process in an inert

• -temperature heat treatment process in an inert atmosphere. Firstly, the aqueous dispersion solution of GO (0.5 mg/mL) was further treated with ultrasound for 2 h. Then, different amounts of the GO solution (0, 0.242, 0.602, 1.205 and 2.410 mL) were added to the homogeneous solution of isopropanol (30 mL) and

A novel all-fiber-based LiFePO₄/Li₄Ti₅O₁₂ battery with self-standing nanofiber membrane electrodes

• Li-li Chen,
• Hua Yang,
• Mao-xiang Jing,
• Chong Han,
• Fei Chen,
• Xin-yu Hu,
• Wei-yong Yuan,
• Shan-shan Yao and
• Xiang-qian Shen

Beilstein J. Nanotechnol. 2019, 10, 2229–2237, doi:10.3762/bjnano.10.215

• grains in the fibers. SEM images of LiFePO4 and Li5Ti4O12 nanofiber membranes are shown in Figure 3. It can be seen that the fiber membranes after heat treatment exhibit a 3D network structure, which is the reason for the high flexibility of the electrode. The high-magnification SEM images show uniform

• . Conclusion LiFePO4 and Li4Ti5O12 nanofiber membrane materials were successfully obtained by electrospinning and subsequent heat treatment. The nanofiber membranes were directly used as free-standing electrodes in LIBs and showed superior electrochemical performance. The battery consisting of these two

Processing nanoporous organic polymers in liquid amines

• Jeehye Byun,
• Damien Thirion and
• Cafer T. Yavuz

Beilstein J. Nanotechnol. 2019, 10, 1844–1850, doi:10.3762/bjnano.10.179

• responsible for the dissolution of polymers. The obtained polymer film exhibited high CO2-philicity by having nitrogen-rich surfaces. The film could be also turned into a fine carbon film by heat treatment in inert atmosphere. Results and Discussion Processing COP-100 in liquid amines COP-100 is a network

• cracked film surface (Figure 2f). The boundary layers between the granules were not demarcated as the heat treatment went on for 3 min (Figure 2g). After 5 min, as all the pieces were combined and covered with excess EDA, the surface became very clean, leading to a flawless film (Figure 2h). Since the

• nanoporous covalent organic polymer (COP-100) was dissolved in liquid amines via simple heat treatment, and the polymer solution could be processed into either nanoparticles or films. FTIR revealed that the carbonyl groups in the polymers were reactive sites that helped to solubilize the structures in liquid

Layered double hydroxide/sepiolite hybrid nanoarchitectures for the controlled release of herbicides

• Ediana Paula Rebitski,
• Margarita Darder and
• Pilar Aranda

Beilstein J. Nanotechnol. 2019, 10, 1679–1690, doi:10.3762/bjnano.10.163

• hybrid nanoarchitectures with 2:1, 1:1, 0.5:1 and 0.3:1 theoretical LDH/Sep weight ratio. After the addition of the salts, the system was kept under magnetic stirring and N2 flux for 24 h. The solid was washed and recovered by centrifugation and then subjected to a controlled heat treatment at 60 or 150

Upcycling of polyurethane waste by mechanochemistry: synthesis of N-doped porous carbon materials for supercapacitor applications

• Christina Schneidermann,
• Pascal Otto,
• Desirée Leistenschneider,
• Sven Grätz,
• Claudia Eßbach and
• Lars Borchardt

Beilstein J. Nanotechnol. 2019, 10, 1618–1627, doi:10.3762/bjnano.10.157

• ) as binder to the N-doped carbon material, which was ground under heat treatment in a mortar. The resulting dough-like material was rolled out to a thickness of 100–200 µm and then cut out to a round electrode with a diameter of 10 mm. The electrodes were dried in a vacuum oven at 120 °C for 24 h. For

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

• vortex flow. Appropriate flow rates yielded two-dimensional films of the carbon nanoring molecule with uniform thickness of a few nanometres. The monolayer films were transferred from the water surface to a solid substrate by hand. Further heat treatment under inert gas atmosphere led to the formation of

• C60 molecules by liquid–liquid interfacial precipitation using a carbon disulfide solution of C60 and isopropyl alcohol. Under optimized conditions, these mesoporous C60 microbelts extended to lengths of the order of centimetres. Heat treatment of the obtained C60 microbelts converts them into two

High-temperature resistive gas sensors based on ZnO/SiC nanocomposites

• Vadim B. Platonov,
• Marina N. Rumyantseva,
• Alexander S. Frolov,
• Alexey D. Yapryntsev and
• Alexander M. Gaskov

Beilstein J. Nanotechnol. 2019, 10, 1537–1547, doi:10.3762/bjnano.10.151

• dispersed silicon carbide (SiC). In this work, ZnO and SiC nanofibers were synthesized by electrospinning of polymer solutions followed by heat treatment, which is necessary for polymer removal and crystallization of semiconductor materials. ZnO/SiC nanocomposites (15–45 mol % SiC) were obtained by mixing

• materials by mixing and heat treatment of electrospun ZnO nanofibers and nanocrystalline silicon carbide of 3C-SiC polytype. The effect of silicon carbide on the structure and electrical properties of composite materials was studied using different techniques. The work is aimed at creating the resistive

• oxide, ZnO, were prepared separately by electrospinning of polymer solutions followed by heat treatment in order to remove the polymer and crystallize the semiconductor material. The annealing conditions for polymer decomposition were determined by thermal analysis. Fabrication of nanocrystalline SiC

Rapid thermal annealing for high-quality ITO thin films deposited by radio-frequency magnetron sputtering

• Petronela Prepelita,
• Ionel Stavarache,
• Doina Craciun,
• Florin Garoi,
• Catalin Negrila,
• Beatrice Gabriela Sbarcea and
• Valentin Craciun

Beilstein J. Nanotechnol. 2019, 10, 1511–1522, doi:10.3762/bjnano.10.149

• treatment on the ITO chemical composition. Using a Tauc plot, values of the optical band gap ranging from 3.17 to 3.67 eV were estimated. These values depend on the heat treatment and the thickness of the sample. Highly conductive indium tin oxide thin films (ρ = 7.4 × 10−5 Ω cm) were obtained after RTA

• optical transmission by 52.8% (from 34.2% to 87% at 550 nm) due to heat treatment at 850 °C in nitrogen atmosphere was reported [24]. Thermal treatments become important when the application of ITO films on a large scale can be demonstrated with excellent performance for various applications [7][8][9][10

Synthesis of P- and N-doped carbon catalysts for the oxygen reduction reaction via controlled phosphoric acid treatment of folic acid

• Rieko Kobayashi,
• Takafumi Ishii,
• Yasuo Imashiro and
• Jun-ichi Ozaki

Beilstein J. Nanotechnol. 2019, 10, 1497–1510, doi:10.3762/bjnano.10.148

• this point, it is worth noting that our previous investigations of the relationship between the ORR activity and oxygen adsorption properties of warped graphitic layers (obtained by oxidative heat treatment of fullerene extraction residues) demonstrated that these two parameters are well correlated [41

Selective gas detection using Mn₃O₄/WO₃ composites as a sensing layer

• Yongjiao Sun,
• Zhichao Yu,
• Wenda Wang,
• Pengwei Li,
• Gang Li,
• Wendong Zhang,
• Lin Chen,
• Serge Zhuivkov and
• Jie Hu

Beilstein J. Nanotechnol. 2019, 10, 1423–1433, doi:10.3762/bjnano.10.140

• ), and absolute ethanol were of analytical grade and purchased from Aladdin Chemical Reagents Company (Shanghai, China). Deionized water (>18.0 MΩ·cm) was used throughout the synthesis process. Synthesis Pure WO3 and Mn3O4/WO3 composites were prepared by the hydrothermal method and a subsequent heat

• treatment. An ethanol solution was prepared by dissolving 0.3 g of WCl6 and various amounts of Mn(CH3COO)2·4H2O in absolute ethanol (60 mL) (Supporting Information File 1, Table S1). Then, the solution was stirred for 45 min to obtain a primrose colored homogeneous solution. Afterwards, the prepared

Warped graphitic layers generated by oxidation of fullerene extraction residue and its oxygen reduction catalytic activity

• Machiko Takigami,
• Rieko Kobayashi,
• Takafumi Ishii,
• Yasuo Imashiro and
• Jun-ichi Ozaki

Beilstein J. Nanotechnol. 2019, 10, 1391–1400, doi:10.3762/bjnano.10.137

• ORR activity of the WGLs was examined using onion-like carbon (OLC) produced by the heat treatment of a nanodiamond [39]. The results showed the highest ORR activity for OLC heat-treated at 1400 °C among the prepared samples (HTT = 1000 °C to 1800 °C). The material formed OLCs composed of WGLs, but

• , as shown in Figure 1d. A TEM image of NNB showed similarities to that of NB-ORG, meaning that the heat treatment of NB-ORG in an inert atmosphere did not cause any structural changes under TEM observation. Figure 2a shows the dependence of the yield on treatment time; there is a rapid decrease in the

• yield with oxidation time up to 2 h, but no significant decrease for the heat treatment in an inert atmosphere (Figure 2e). Figure 2b shows the XRD profiles of the prepared samples. NB-ORG appeared to have two diffraction peaks in the carbon 002 region: one at 2θ = 17° another at 2θ = 23°. The former

Highly ordered mesoporous silica film nanocomposites containing gold nanoparticles for the catalytic reduction of 4-nitrophenol

• Mohamad Azani Jalani,
• Leny Yuliati,
• Siew Ling Lee and
• Hendrik O. Lintang

Beilstein J. Nanotechnol. 2019, 10, 1368–1379, doi:10.3762/bjnano.10.135

• treatment at 210 °C. In contrast, when the material was subjected to calcination as a heat treatment from 190 to 450 °C, the thin film nanocomposites showed an intense d100 X-ray diffraction peak. Moreover, gold nanoparticles inside the thin film nanocomposites were confirmed by the presence of the d111

• very interesting to utilize this nanocomposite for the growth of AuNPs in the silicate nanochannels. Recently, mesoporous silica nanomaterials were not only used as a support to control the size of the AuNPs [28], but also to enhance the thermal stability after heat treatment at high temperature [29

• measurements confirmed the formation of a hexagonal structure in the silicate nanochannels of [Au3Pz3]C10TEG/silicahex. Structural analysis of the nanocomposites after heat treatment The quality of the hexagonal mesostructured silica can be generally evaluated from its ordered or disordered structures by

Alloyed Pt₃M (M = Co, Ni) nanoparticles supported on S- and N-doped carbon nanotubes for the oxygen reduction reaction

• Stéphane Louisia,
• Yohann R. J. Thomas,
• Pierre Lecante,
• Marie Heitzmann,
• M. Rosa Axet,
• Pierre-André Jacques and
• Philippe Serp

Beilstein J. Nanotechnol. 2019, 10, 1251–1269, doi:10.3762/bjnano.10.125

• doping. Elemental and X-ray photoelectron spectroscopy (XPS) analysis results are shown in Table 1. The elemental analysis confirmed the efficiency of the doping, and showed that S-CNT contains a significant amount of residual catalyst (iron, encapsulated in the structure of the tubes). An effect of heat

• treatment on the N-CNTs (besides the reduction of disorder) is to decrease the amount of nitrogen, which decreases from 2.9 to 1.6%. XPS analysis confirmed the bulk analyses and showed that the S-CNT sample also contains a significant amount of surface oxygen groups. The introduction of oxygen may

Concurrent nanoscale surface etching and SnO₂ loading of carbon fibers for vanadium ion redox enhancement

• Jun Maruyama,
• Shohei Maruyama,
• Tomoko Fukuhara,
• Toru Nagaoka and
• Kei Hanafusa

Beilstein J. Nanotechnol. 2019, 10, 985–992, doi:10.3762/bjnano.10.99

• single heat-treatment step. The subsequent thermal oxidation concurrently achieved nanoscale surface etching and loading with SnO2 nanoparticles. The nanoscale-etched and SnO2-loaded surface was characterized by field-emission scanning electron microscopy (FESEM), Raman spectroscopy, and X-ray

• carbonaceous thin film was formed by sublimation, deposition, and pyrolysis of CoPc on the carbon fiber surface during a single heat-treatment step using a conventional crucible. The treatment substantially enriched edge planes and produced an enhanced activity for the positive and negative electrode reactions

• . Results and Discussion Concurrent surface etching and SnO2 loading Graphitic carbon paper (TGP-H-090, Toray, abbreviated as TGP) was used as the substrate. The SnPc-derived carbonaceous thin film (CSnPc; obtained thorugh sublimation, deposition, and pyrolysis of SnPc in a single-step heat treatment in an

Rapid, ultraviolet-induced, reversibly switchable wettability of superhydrophobic/superhydrophilic surfaces

• Yunlu Pan,
• Wenting Kong,
• Bharat Bhushan and
• Xuezeng Zhao

Beilstein J. Nanotechnol. 2019, 10, 866–873, doi:10.3762/bjnano.10.87

• superhydrophobic (WCA ≈ 165°) to a superhydrophilic (WCA ≈ 0°) state within 10 min upon UV illumination and subsequent recovery to superhydrophobicity occurred after heat treatment. It was found that the changes in the trimethoxy(alkyl)silane upon UV illumination can explain the rapid decrease of the WCA from more

• heat treatment has been previously reported and was explained by the formation of Ti–O–H bonds under UV light, while heating of the surface results in the decrease in the concentration of Ti–O–H bonds [33][34]. As reported, due to the low band gap energy of TiO2, the photo-induced electron–hole pairs

An efficient electrode material for high performance solid-state hybrid supercapacitors based on a Cu/CuO/porous carbon nanofiber/TiO₂ hybrid composite

• Mamta Sham Lal,
• Thirugnanam Lavanya and
• Sundara Ramaprabhu

Beilstein J. Nanotechnol. 2019, 10, 781–793, doi:10.3762/bjnano.10.78

• decompose and offer the porous nature to the fiber during heat treatment [15]. CuO is one of the promising candidates for supercapacitors owning to its natural abundance, ecologically friendly and inexpensive characteristics. Moreover, Cu/CuO-based carbonaceous nanocomposites have emerged as an attractive

• magnified image of PCNF which reveals the presence of pores in PCNF due to removal of PVDF during heat treatment. Figure 5e shows the FE-SEM image of Cu/PCNF and Figure 5f shows the magnified image of Cu/PCNF. Cu nanoparticles embedded due to the electrospinning process are visible on the surface of the Cu

Raman study of flash-lamp annealed aqueous Cu₂ZnSnS₄ nanocrystals

• Yevhenii Havryliuk,
• Oleksandr Selyshchev,
• Mykhailo Valakh,
• Alexandra Raevskaya,
• Oleksandr Stroyuk,
• Constance Schmidt,
• Volodymyr Dzhagan and
• Dietrich R. T. Zahn

Beilstein J. Nanotechnol. 2019, 10, 222–227, doi:10.3762/bjnano.10.20

• larger content of the ligand (according to XPS, 27% O and 40% C in ink0 vs 22% O and 37% C in ink1) or/and probably some structural and compositional changes of the organic matrix initiated through the heat treatment of ink1. The elemental composition of the CZTS NC phase was proved by a survey XPS

• were prepared in aqueous solutions by the reaction of a mixture of mercaptoacetate (MA) complexes of Cu(II), Sn(II), and Zn(II) with sodium sulfide and a subsequent optional heat treatment at about 95 °C. An XPS study reported in [21] showed all the elements of CZTS to be present in the expected

• nitrogen atmosphere. Two types of samples were investigated: an as-synthesized sample “ink0” (the sample purified without heat treatment at 95 °C) [21], and “ink1”, i.e., the same ink heated at 96–98 °C in the dark immediately after synthesis (vials were immersed for 10 min into a boiling water bath). For

Wet chemistry route for the decoration of carbon nanotubes with iron oxide nanoparticles for gas sensing

• Hussam M. Elnabawy,
• Juan Casanova-Chafer,
• Badawi Anis,
• Mostafa Fedawy,
• Mattia Scardamaglia,
• Carla Bittencourt,
• Ahmed S. G. Khalil,
• Eduard Llobet and
• Xavier Vilanova

Beilstein J. Nanotechnol. 2019, 10, 105–118, doi:10.3762/bjnano.10.10

• results for carbon nanotubes decorated with iron oxide nanoparticles of larger size. This is consistent with the literature, in which heat treatment on sensors doped with an optimum doping ratio can cause both an increase in the size of decorating nanoparticles and an enhancement in the response of the