Composites of In/C hexagonal nanorods and graphene nanosheets for high-performance electromagnetic wave absorption

In recent years,electromagnetic wave(EMW)absorption has been extensively investigated for solving EMW radiation and pollution.The metal-organic frameworks(MOFs)have attracted attention due to their low density and unique structure,which can meet the requirements of strong reflection loss(RL)and wide absorption bandwidth of EMW absorption materials.In this manuscript,indium nanoparticles/porous carbon(In/C)nanorods composites were prepared via the pyrolysis of nanorods-like In-MOFs at a low temperature of450°C.Indium nanoparticles are evenly attached and embedded on porous carbon.Low electrical conductivity of In/C nanorods is unfavorable to EMW absorption performance,which is due to the low temperature carbonization.Thus,graphene(Gr)nanosheets with high electrical conductivity are introduced to adjust electromagnetic parameters of In/C nanorods for enhancing EMW absorption.The minimum RL of the In/C-Gr-4 composite is up to-43.7 dB with a thin thickness of 1.30 mm.In addition,when the thickness is further reduced to 1.14 mm,the minimum RL of-39.3 dB at 16.1 GHz and effective absorption bandwidth of 3.7 GHz(from 14.3 to 18.0 GHz)can be achieved.This work indicates that In/C-Gr composites show excellent EMW absorption performance.

Investigation of photoelectrocatalytic degradation mechanism of methylene blue by a-Fe_(2)O_(3) nanorods array

Efficiently and thoroughly degrading organic dyes in wastewater is of great importance and challenge.Herein,vertically oriented mesoporous a-Fe_(2)O_(3)nanorods array(a-Fe_(2)O_(3)-NA)is directly grown on fluorine-doped tin oxide(FTO)glass and employed as the photoanode for photoelectrocatalytic degradation of methylene blue simulated dye wastewater.The Ovsites on the a-Fe_(2)O_(3)-NA surface are the active sites for methylene blue(MB)adsorption.Electrons transfer from the adsorbed MB to Fe-O is detected.Compared with electrocatalytic and photocatalytic degradation processes,the photoelectrocatalytic(PEC)process exhibited the best degrading performance and the largest kinetic constant.Hydroxyl,superoxide free radicals,and photo-generated holes play a jointly leading role in the PEC degradation.A possible degrading pathway is suggested by liquid chromatography-mass spectroscopy analysis.This work demonstrates that photoelectrocatalysis by a-Fe_(2)O_(3)-NA has a remarkable superiority over photocatalysis and electrocatalysis in MB degradation.The in-depth investigation of photoelectrocatalytic degradation mechanism in this study is meaningful for organic wastewater treatment.

From kesterite 2D nanosheets to wurtzite 1D nanorods:controllable synthesis of Cu-Zn-Sn-S and their application in electrocatalytic hydrogen evolution

As typical quarternary copper-based chalcogenides,Cu–Zn–Sn–S nanocrystals(CZTS NCs)have emerged as a newfashioned electrocatalyst in hydrogen evolution reactions(HERs).Oleylamine(OM),a reducing surfactant and solvent,plays a significant role in the assisting synthesis of CZTS NCs due to the ligand effect.Herein,we adopted a facile one-pot colloidal method for achieving the structure evolution of CZTS NCs from 2D nanosheets to 1D nanorods assisted through the continuous addition of OM.During the process,the mechanism of OM-induced morphology evolution was further discussed.When merely adding pure 1-dodecanethiol(DDT)as the solvent,the CZTS nanosheets were obtained.As OM was gradually added to the reaction,the CZTS NCs began to grow along the sides of the nanosheets and gradually shrink at the top,followed by the formation of stable nanorods.In acidic electrolytic conditions,the CZTS NCs with 1.0 OM addition display the optimal HER activity with a low overpotential of 561 m V at 10 m A/cm^(2) and a small Tafel slope of 157.6 m V/dec compared with other CZTS samples.The enhancement of HER activity could be attributed to the contribution of the synergistic effect of the diverse crystal facets to the reaction.

Au@Ag Core-shell Nanorods Self-assembled on Polyelectrolyte Multilayers for Ultra-High Sensitivity SERS Fiber Probes

We demonstrated a chemical process in the fabrication of a SERS fiber probe with an ultrahigh sensitivity.The synthesis was carried out by preparing Au@Ag core-shell nanorods (Au@Ag-NRs) selfassembled on polyelectrolyte (PE) multilayers,for which Au@Ag-NRs were controlled by adjusting the silver layer thickness.The effect of silver layer thickness of Au@Ag-NRs on the SERS performance of the fiber probe was investigated.The SERS fiber probe shows the best performance when the silver layer thickness is controlled at 8.57 nm.Under the condition of optimizing silver layer thickness,the fiber probe exhibits ultra-high sensitivity (i e,10^(-10) M crystalline violet,CV),good reproducibility (i e,RSD of 3.5%) and stability.Besides,electromagnetic field distribution of the SERS fiber probe was also investigated.The strongest enhancement is found within the core of fiber,whereas a weakened electromagnetic field exists in the fiber cladding layer.The SERS fiber probe can be a good candidate in ultra-trace detection for biomedical and environmental areas.

Structural, Optical and Photocatalytic Properties of Cu2+ Doped ZnO Nanorods with Using HMTA Solvent Prepared by Hydrothermal Method

In this experiment, Cu2+ doped ZnO (Cu-ZnO) nanorods materials have been fabricated by hydrothermal method. Cu2+ ions were doped into ZnO with ratios of 2, 5 and 7 mol.% (compared to the mole’s number of Zn2+). The hexamethylenetetramine (HMTA) solvent used for the fabrication of Cu-ZnO nanorods with the mole ratio of Zn2+:HMTA = 1:4. The characteristics of the materials were analyzed by techniques, such as XRD, Raman shift, SEM and UV-vis diffuse reflectance spectra (DRS). The photocatalytic properties of the materials were investigated by the decomposition of the methylene blue (MB) dye solution under ultraviolet light. The results show that the size of Cu-ZnO nanorods was reduced when the Cu2+ doping ratio increased from 2 mol.% to 7 mol.%. The decomposition efficiency of the MB dye solution reached 92% - 97%, corresponding to the Cu2+ doping ratio changed from 2 - 7 mol.% (after 40 minutes of ultraviolet irradiation). The highest efficiency for the decomposition of the MB solution was obtained at a Cu2+ doping ratio of 2 mol.%.

Manifolding active sites and in situ/operando electrochemical-Raman spectroscopic studies of single-metal nanoparticle-decorated CuO nanorods in furfural biomass valorization to H_(2) and 2-furoic acid

Here,CuO nanorods fabricated via pulsed laser ablation in liquids were decorated with Ir,Pd,and Ru NPs(loading~7 wt%) through pulsed laser irradiation in the liquids process.The resulting NPs-decorated CuO nanorods were characterized spectroscopically and employed as multifunctional electrocatalysts in OER,HER,and the furfural oxidation reactions(FOR).Ir-CuO nanorods afford the lowest overpotential of~345 mV(HER) and 414 mV(OER) at 10 mA cm^(-2),provide the highest 2-furoic acid yield(~10.85 mM) with 64.9% selectivity,and the best Faradaic efficiency~72.7% in 2 h of FOR at 1.58 V(vs.RHE).In situ electrochemical-Raman analysis of the Ir-CuO detects the formation of the crucial intermediates,such as Cu(Ⅲ)-oxide,Cu(OH)_(2),and Ir_x(OH)_y,on the electrode-electrolyte surface,which act as a promoter for HER and OER.The Ir-CuO ‖ Ir-CuO in a coupled HER and FOR-electrolyzer operates at~200 mV lower voltage,compared with the conventional electrolyzer and embodies the dual advantage of energy-saving H_(2) and 2-furoic acid production.

Manipulating d-d orbital hybridization induced by Mo-doped Co_(9)S_(8) nanorod arrays for high-efficiency water electrolysis

Precisely refining the electronic structure of electrocatalysts represents a powerful approach to further optimize the electrocatalytic performance.Herein,we demonstrate an ingenious d-d orbital hybridization concept to construct Mo-doped Co_(9)S_(8) nanorod arrays aligned on carbon cloth(CC)substrate(abbreviated as Mo-Co_(9)S_(8)@CC hereafter)as a high-efficiency bifunctional electrocatalyst toward water electrolysis.It has experimentally and theoretically validated that the 4d-3d orbital coupling between Mo dopant and Co site can effectively optimize the H_(2)O activation energy and lower H^(*)adsorption energy barrier,thereby leading to enhanced hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)activities.Thanks to the unique electronic and geometrical advantages,the optimized Mo-Co_(9)S_(8)@CC with appropriate Mo content exhibits outstanding bifunctional performance in alkaline solution,with the overpotentials of 75 and 234 mV for the delivery of a current density of 10 mA cm^(-2),small Tafel slopes of 53.8 and 39.9 mV dec~(-1)and long-term stabilities for at least 32 and 30 h for HER and OER,respectively.More impressively,a water splitting electrolylzer assembled by the self-supported Mo-Co_(9)S_(8)@CC electrode requires a low cell voltage of 1.53 V at 10 mA cm^(-2)and shows excellent stability and splendid reversibility,demonstrating a huge potential for affordable and scalable electrochemical H_(2) production.The innovational orbital hybridization strategy for electronic regulation herein provides an inspirable avenue for developing progressive electrocatalysts toward new energy systems.

Heterostructured BiOI@La(OH)_3 nanorods with enhanced visible light photocatalytic NO removal

Heterostructured BiOI@La（OH）3 nanorod photocatalysts were prepared by a facile chemical impregnation method.The enhanced visible light absorption and charge carrier separation can be simultaneously realized after the introduction of BiOI particles into La（OH）3 nanorods.The BiOI@La（OH）3 composites were applied for visible light photocatalytic oxidization of NO in air and exhibited an enhanced activity compared with BiOI and pure La（OH）3 nanorods.The results show that the energy levels between the La（OH）3 and BiOI phases matched well with each other,thus forming a heterojunctioned BiOI@La（OH）3 structure.This band structure matching could promote the separation and transfer of photoinduced electron-hole pairs at the interface,resulting in enhanced photocatalytic performance under visible light irradiation.The photocatalytic performance of BiOI@La（OH）3 is shown to be dependent on the mass ratio of BiOI to La（OH）3.The highest photocatalytic performance can be achieved when the mass ratio of BiOI to La（OH）3 is controlled at 1.5.A further increase of the mass ratio of BiOI weakened the redox abilities of the photogenerated charge carriers.A new photocatalytic mechanism for BiOI@La（OH）3 heterostructures is proposed,which is directly related to the efficient separation of photogenerated charge carriers by the heterojunction.Importantly,the as-prepared BiOI@La（OH）3 heterostructures exhibited a high photochemical stability after multiple reaction runs.Our findings demonstrate that BiOI is an effective component for the formation of a heterostructure with the properties of a wide bandgap semiconductor,which is of great importance for extending the light absorption and photocatalytic activity of wide bandgap semiconductors into visible light region.

Preparation, friction and wear properties of hydrophobic lanthanum borate nanorods in rapeseed oil

Oleic acid (denoted as OA) surface-caped lanthanum borate nanorods, abbreviated as OA/LaBO3·H2O, were prepared via hydrothermal method. The microstructures of the as-prepared OA/LaBO3·H2O nanorods were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The friction and wear properties of OA/LaBO3·H2O nanorods in rapeseed oil were evaluated with a four-ball tribo-tester. The results show that the as-prepared OA/LaBO3·H2O nanorods are hydrophobic and display nanorods morphology with uniform diameter of about 50 nm and length of up to 500 nm. In the meantime, OA/LaBO3·H2O nanorods can obviously improve the anti-wear and friction-reducing capacities of rapeseed oil, and the optimal anti-wear and friction-reducing properties of rapeseed oil were obtained at an OA/LaBO3·H2O content of 1% (mass fraction).

Synthesis and Characterization of GaN Nanorods by Ammoniating Ga_2O_3 /Co Films Deposited on Si(111) Substrates

GaN nanorods are successfully synthesized on Si（111） substrates with magnetron sputtering through ammoniating Ga2O3/Co films at 950℃. X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy,and Fourier-transform infrared spectroscopy are used to characterize the samples. The results demonstrate that the nanorods are single-crystal GaN with a hexagonal wurtzite structure and possess relatively smooth surfaces. The growth mechanism of GaN nanorods is also discussed.

Preparation of MnxNi0.5-xZn0.5Fe2O4 Nanorods by the Co-precipitation Method

MnxNi0.5-xZn0.5Fe2O4 nanorods were successfully synthesized by the thermal treatment of rod-like precursors that were fabricated by the co-precipitation of Mn2＋, Ni2＋, and Fe2＋ in the lye. The phase, morphology, and particle diameter were examined by the X-ray diffraction and transmission electron microscopy. The magnetic properties of the samples were studied using a vibrating sample magnetometer. nanorods with a diameter of 35 nm and an The results indicated that pure Ni0.5-xZn0.5Fe2O4 aspect ratio of 15 were prepared. It was found that the diametei of the MnxNi0.5-xZn0.5Fe2O4（0≤x≤0.5） samples increased, the length and the aspect .ratio decreased, with an increase in x value. When x=0.5, the diameter and the aspect ratio of the sample reached up to 50 nm and 7-8, respectively. The coercivity of the samples first increased and then decreased with the increase in the x value. The coercivity of the samples again increased when the x value was higher than 0.4. When x=0.5, the coercivity of the MnxNi0.5-xZn0.5Fe2O4 sample reached the maximal value （134.3 Oe） at the calcination temperature of 600 ℃. The saturation magnetization of the samples first increased and then. decreased with the increase in the x value. When x=0.2, the saturation magnetizat：ion of the sample reached the maximal value （68.5 emu/g） at the calcination temperature of 800 ℃.

Synthesis, Characterization and Luminescent Properties of La2Zr2OT：Eu3＋ Nanorods

The Eu3＋-doped La2Zr207 phosphor with rod-like morphology was successfully synthesized by conventional solid state reaction and hydrothermal method. X-ray diffraction patterns, transmission electron microscopy, and photoluminescence spectra were employed to charac- terize its structure and morphology as well as luminescent properties. The results indicated that the red-emitting phosphor La2Zr207：Eu3＋ had well crystallized and belonged to the cubic structure with space group of Fd3m. The as-obtained product mainly appeared as straight nanorods with an average diameter of 47 nm and length of 50-700 nm. The pos- sible growth mechanism was also discussed. It was found that under blue excitation with a wavelength of 466 nm, the La2Zr2OT：Eu3＋ phosphor exhibited a characteristic red emission at 616 nm that was attributed to the hypersensitive 5D0--＊TF2 electric dipole transition of Eu3＋ ions. Meanwhile, it was more interesting to note that the emission of 5D1--＊TFj （J=0, 1, 2） transitions and the splitting patterns of 5D0---＋TFJ （J--l, 2, 4） transitions of Eu3＋ ions can be observed in the luminescent spectra of La2Zr207：Eu3＋. It was demonstrated that Eu3＋ preferred to occupy a low symmetry site.

Hydrothermal Synthesis and Field Enhancement Behavior of ZnO Nanorods Pattern

We provide a new way to prepare ZnO nanorods pattern from the solution composed of hexamethylenetetramine （HMT） and Zn（NO3）2. The substrate is ITO substrate covered by well ordered Au islands. Since Au and the underneath ITO substrate have two different nucleation rates in the initial stage of heterogeneous nucleation process, the subsequent ZnO growth on the quick nucleating area takes place under diffusion control and is able to confine the synthesis of ZnO nanorods to specific locations. The concentrations of zinc nitrate and HMT are well adjusted to show the possibility of the new route for the patterning of the ZnO nanorods. Furthermore, the nanorods pattern was characterized by X-ray diffraction and photoluminescence and the performance of field emission property from ZnO nanorod patterns was investigated. The ZnO nanorods pattern with a good alignment also shows a good field enhancement behavior with a high value of the field enhancement factor.

Synthesis of GaN Nanorods with Herringbone Morphology

Hexagonal GaN nanorods are synthesized on quartz substrates through ammoniating Ga 2O 3 thin films deposited by radio frequency magnetron sputtering.X ray diffraction (XRD),scanning electron microscopy (SEM),high resolution transmission electron microscopy (HRTEM),and photoluminescence (PL) are used to analyze the synthesized GaN nanorods.Among the products,one dimensional GaN nanostructures owning protuberances on the surface are detected,which show interesting herringbone morphology.The analysis reveals that the herringbone GaN nanorods are polycrystalline composed of overlapping parallelepiped GaN nanocrystals arranged along the major axis.The large blue shift of yellow PL luminescence of the nanorods is observed at room temperature.

Mg(OH)_2 Nanorods Synthesized by A Facile Hydrothermal Method in the Presence of CTAB

Magnesium hydroxide(Mg(OH)_2) nanorods were synthesized by a simple and facile hydrothermal method in the presence of cetyltetramethylammonium bromide(CTAB) as a surfactant. Nanorods of magnesium oxide Mg O were also induced by thermal decomposition of Mg(OH)_2 nanorods at 700. By using disk diffusion technique, the Mg(OH)_2 nanorods were found to exhibit higher antibacterial efficiency against several tested bacterial strains.

Synthesis of ZnO nanorods and their optical absorption in visible-light region

Single crystalline ZnO nanorods were prepared by the hydrothermal method with synthesized ZnCl2·4Zn（OH）2 as the precursor. Morphologies of the nanorods were controlled by various reaction conditions with cetyltrimethylammonium bromide （CTAB） as the modifying agent. The nanorods were characterized by XRD, TEM, UV-Vis spectra, and IR spectra. The microstructure of holes in nanosize was observed on the surface of the nanorods. The UV-Vis spectra indicate that the as-prepared ZnO nanorods have absorption of visible-hght as well as ultraviolet-light. Therefore, these nanorods may be good candidates for visible-light photocatalysis materials from the viewpoint of practical applications. The reason for visible-light absorption was discussed in this article.

Fluorescent Silicon Nanorods-Based Nanotheranostic Agents for Multimodal Imaging-Guided Photothermal Therapy

The utilization of diagnosis to guide/aid therapy procedures has shown great prospects in the era of personalized medicine along with the recognition of tumor heterogeneity and complexity.Herein,a kind of multifunctional silicon-based nanostructure,i.e.,gold nanoparticles-decorated fluorescent silicon nanorods(Au@SiNRs),is fabricated and exploited for tumor-targeted multimodal imaging-guided photothermal therapy.In particular,the prepared Au@SiNRs feature high photothermal conversion efficiency(~43.9%)and strong photothermal stability(photothermal performance stays constant after five-cycle NIR laser irradiation),making them high-performance agents for simultaneously photoacoustic and infrared thermal imaging.The Au@SiNRs are readily modified with targeting peptide ligands,enabling an enhanced tumor accumulation with a high value of^8.74%ID g?1.Taking advantages of these unique merits,the Au@SiNRs are superbly suitable for specifically ablating tumors in vivo without appreciable toxicity under the guidance of multimodal imaging.Typically,all the mice treated with the Au@SiNRs remain alive,and no distinct tumor recurrence is observed during 60-day investigation.

Hybrid Field-Effect Transistors and Photodetectors Based on Organic Semiconductor and CsPbI_3 Perovskite Nanorods Bilayer Structure

The outstanding performances of nanostructured allinorganic CsPbX_3(X = I, Br, Cl) perovskites in optoelectronic applications can be attributed to their unique combination of a suitable bandgap, high absorption coefficient, and long carrier lifetime, which are desirable for photodetectors. However, the photosensing performances of the CsPbI_3 nanomaterials are limited by their low charge-transport efficiency. In this study, a phototransistor with a bilayer structure of an organic semiconductor layer of 2,7-dioctyl [1] benzothieno[3,2-b] [1] benzothiophene and CsPbI_3 nanorod layer was fabricated. The high-quality CsPbI_3 nanorod layer obtained using a simple dip-coating method provided decent transistor performance of the hybrid transistor device.The perovskite layer efficiently absorbs light, while the organicsemiconductor layer acts as a transport channel for injected photogenerated carriers and provides gate modulation. The hybrid phototransistor exhibits high performance owing to the synergistic function of the photogating effect and field effect in the transistor,with a photoresponsivity as high as 4300 A W^(-1), ultra-high photosensitivity of 2.2 9 106, and excellent stability over 1 month.This study provides a strategy to combine the advantages of perovskite nanorods and organic semiconductors in fabrication of high-performance photodetectors.

Syntheses, Morphologies and Properties of BiOI Nanolamellas and BiSI Nanorods

Well defined BiOI nanolamellas and BiSI nanorods have been synthesized by a solventless method. The phase identity, morphology, growth orientation, and conversion from lamella to rod have been investigated. Several experimental facts suggest that the growth orientations of BiOI nanolamellas and BiSI nanorods are guided by their corresponding crystal structure motifs. The optical band gaps of BiOI and BiSI are measured to be 1.97 and 1.61 eV, and the visible light photocatalytic activity of BiOI lamellas is primarily measured.

Effect of annealing treatment on morphologies and gas sensing properties of ZnO nanorods

The high-temperature stabilization of ZnO nanorods synthesized by hydrothermal treatment was investigated. The structure and morphologies of ZnO nanorods were characterized by XRD and SEM, respectively. The thermal stability of ZnO nanorods was also detected by thermal gravity analyzing. Thermal annealing treatment results indicate that ZnO nanorods are fundamentally stable when annealing temperature is lower than 600 ℃. When annealing temperature is beyond 600℃, the diameters of ZnO nanorods obviously decrease and the aggravating tendency of nanorods between each other also increase. Annealing treatment can greatly influence the gas sensing properties of ZnO nanorods. Comparing with ZnO nanorods without annealing treatment, the gas sensing property of ZnO nanorods to H2 with concentration of 2.5×10-6 can increase from 2.22 to 3.56. ZnO nanorods annealed at 400 ℃ exhibit optimum gas sesing property to H2 gas.