Enhanced Electrical Properties of Bi_(2−x)Sb_(x)Te_(3)Nanoflake Thin Films Through Interface Engineering

The structure–property relationship at interfaces is difficult to probe for thermoelectric materials with a complex interfacial microstructure.Designing thermoelectric materials with a simple,structurally-uniform interface provides a facile way to understand how these interfaces influence the transport properties.Here,we synthesized Bi_(2−x)Sb_(x)Te_(3)(x=0,0.1,0.2,0.4)nanoflakes using a hydrothermal method,and prepared Bi_(2−x)Sb_(x)Te_(3)thin films with predominantly(0001)interfaces by stacking the nanoflakes through spin coating.The influence of the annealing temperature and Sb content on the(0001)interface structure was systematically investigated at atomic scale using aberration-corrected scanning transmission electron microscopy.Annealing and Sb doping facilitate atom diffusion and migration between adjacent nanoflakes along the(0001)interface.As such it enhances interfacial connectivity and improves the electrical transport properties.Interfac reactions create new interfaces that increase the scattering and the Seebeck coefficient.Due to the simultaneous optimization of electrical conductivity and Seebeck coefficient,the maximum power factor of the Bi_(1.8)Sb_(0.2)Te_(3)nanoflake films reaches 1.72 mW m^(−1)K^(−2),which is 43%higher than that of a pure Bi_(2)Te_(3)thin film.

Facile Synthesis of N-Doped Graphene-Like Carbon Nanoflakes as Efficient and Stable Electrocatalysts for the Oxygen Reduction Reaction

A series of N-doped carbon materials(NCs)were synthesized by using biomass citric acid and dicyandiamide as renewable raw materials via a facile onestep pyrolysis method. The characterization of microstructural features shows that the NCs samples are composed of few-layered graphene-like nanoflakes with controlled in situ N doping, which is attributed to the confined pyrolysis of citric acid within the interlayers of the dicyandiamide-derived g-C_3N_4 with high nitrogen contents. Evidently, the pore volumes of the NCs increased with the increasing content of dicyandiamide in the precursor. Among these samples, the NCs nanoflakes prepared with the citric acid/dicyandiamide mass ratio of 1:6, NC-6,show the highest N content of ~6.2 at%, in which pyridinic and graphitic N groups are predominant. Compared to the commercial Pt/C catalyst, the as-prepared NC-6 exhibits a small negative shift of ~66 mV at the half-wave potential, demonstrating excellent electrocatalytic activity in the oxygen reduction reaction. Moreover, NC-6 also shows better long-term stability and resistance to methanol crossover compared to Pt/C. The efficient and stable performance are attributed to the graphene-like microstructure and high content of pyridinic and graphitic doped nitrogen in the sample, which creates more active sites as well as facilitating charge transfer due to the close four-electron reaction pathway. The superior electrocatalytic activity coupled with the facile synthetic method presents a new pathway to cost-effective electrocatalysts for practical fuel cells or metal–air batteries.

Graphene-immobilized flower-like Ni3S2 nanoflakes as a stable binder-free anode material for sodium-ion batteries

A binder-free Ni3S2 electrode was prepared directly on a graphene-coated Ni foam （G/Ni） substrate through surface sulfiding of substrate using thiourea as the sulfur source in this work. The Ni3S2 showed a flower-like morphology and was uniformly distributed on the G/Ni surface. The flower-like Ni3S2 was composed of cross-arrayed nanoflakes with a diameter and a thickness of 1-2 μm and -50 nm, re- spectively. The free space in the flowers and the thin feature of Ni3S2 buffered the volume changes and relieved mechanical strain during re- peated cycling. The intimate contact with the Ni substrate and the fixing effect of graphene maintained the structural stability of the Ni3S2 electrode during cycling. The G/Ni-supported Ni3S2 maintained a reversible capacity of 250 mAh·g^-1 after 100 cycles at 50 mA·g^-1, demon- strating the good cycling stability as a result of the unique microstructure of this electrode material.

BiIO4 Nanoflakes for the Degradation of Phenol under Simulated Solar Light Irradiation

BiIO4 nanoflakes were successfully prepared through a facile hydrothermal method. The as-prepared BiIO4 was characterized by scanning electron microscope(SEM), high-resolution transmission electron microscopy(HRTEM), X-ray diffraction(XRD), energy-dispersive spectroscopy(EDS) and ultraviolet visible diffuse reflectance spectroscopy. BiIO4 nanoflakes showed excellent photocatalytic activity for the degradation of phenol solution under simulated solar irradiation. The influence of synthesis temperature on the morphology, size and photocatalytic performance of BiIO4 was investigated. BiIO4 prepared under 140 ℃ exhibited the highest removal rate of phenol under simulated solar light irradiation. In addition, the parametric studies such as the effect of catalyst loading and phenol solution pH were carried out to optimize the reaction conditions. The active species trapping experiment demonstrated that h+ and ·OH are the major active species during the photocatalytic process.

Hydrothermal Synthesis and Visible-light Photocatalytic Activities of SnS_2 Nanoflakes

SnS2 nanoflakes were successfully synthesized via a simple hydrothermal process. The as-prepared SnS2 samples were characterized by X-ray diffraction（XRD）, scanning electron microscopy（SEM）, nitrogen adsorption-desorption isotherms, and UV-vis diffuse reflectance spectroscopy（DRS）. The photocatalytic activities of the as-prepared SnS2 nanoflakes under visible light irradiation（λ〉420 nm） were evaluated by the degradation of rhodamine B（Rh B）. The effect of hydrothermal temperatures on the photocatalytic efficiency of as-prepared SnS2 nanoflakes was investigated. The experimental result showed that SnS2 nanoflakes synthesized at the temprature of 160 o had higher photocatalytic efficiency and good photocatalytic stability.

Facile fabrication of heterostructure with p-BiOCl nanoflakes and n-ZnO thin film for UV photodetectors

Herein, high-quality n-ZnO film layer on c-sapphire and well-crystallized tetragonal p-BiOCl nanoflakes on Cu foil are prepared, respectively. According to the absorption spectra, the bandgaps of n-ZnO and p-BiOCl are confirmed as ~3.3 and~3.5 eV, respectively. Subsequently, a p-BiOCl/n-ZnO heterostructural photodetector is constructed after a facile mechanical bonding and post annealing process. At –5 V bias, the photocurrent of the device under 350 nm irradiation is ~800 times higher than that in dark, which indicates its strong UV light response characteristic. However, the on/off ratio of In–ZnO–In photodetector is ~20 and the Cu–BiOCl–Cu photodetector depicts very weak UV light response. The heterostructure device also shows a short decay time of 0.95 s, which is much shorter than those of the devices fabricated from pure ZnO thin film and BiOCl nanoflakes. The p-BiOCl/n-ZnO heterojunction photodetector provides a promising pathway to multifunctional UV photodetectors with fast response, high signal-to-noise ratio, and high selectivity.

Oxygen migration triggering molybdenum exposure in oxygen vacancy-rich ultra-thin Bi_(2)MoO_(6) nanoflakes: Dual binding sites governing selective CO_(2) reduction into liquid hydrocarbons

Oxygen vacancy plays vital roles in regulating the electronic and charge distribution of the oxygen deficient materials.Herein,abundant oxygen vacancies are created during assembling the two-dimensional(2D)ultra-thin Bi_(2)MoO_(6) nanoflakes into three dimensional(3D)Bi_(2)MoO_(6) nanospheres,resulting in significantly improved performance for photocatalytical conversion of CO_(2) into liquid hydrocarbons.The increased performance is contributed by two primary sites,namely the abundant oxygen vacancy and the exposed molybdenum(Mo)atom induced by oxygen-migration,as revealed by the theoretical calculation.The oxygen vacancy(Ov)and uncovered Mo atom serving as dual binding sites for trapping CO_(2) molecules render the synchronous fixation-reduction process,resulting in the decline of activation energy for CO_(2) reduction from 2.15 eV on bulk Bi_(2)MoO_(6) to 1.42 eV on Ov-rich Bi_(2)MoO_(6).Such a striking decrease in the activation energy induces the efficient selective generation of liquid hydrocarbons,especially the methanol(C_(2)H_(5) OH)and ethanol(CH_(3) OH).The yields of CH_(3) OH and C_(2)H_(5) OH over the optimal Ov-Bi_(2)MoO_(6) is high up to 106.5 and 10.3μmol g^(-1) respectively,greatly outperforming that on the Bulk-Bi_(2)MoO_(6).

Microstructure and properties of high-fraction graphite nanoflakes/6061Al matrix composites fabricated via spark plasma sintering

30-50 wt.%graphite nanoflakes(GNFs)/6061Al matrix composites were fabricated via spark plasma sintering(SPS)at 610℃.The effects of the sintering pressure and GNF content on the microstructure and properties of the composites were investigated.The results indicated that interfacial reactions were inhibited during SPS because no Al4C3 was detected.Moreover,the agglomeration of the GNFs increased,and the distribution orientation of the GNFs decreased with increasing the GNF content.The relative density,bending strength,and coefficient of thermal expansion(CTE)of the composites decreased,while the thermal conductivity(TC)in the X−Y direction increased.As the sintering pressure increased,the GNFs deagglomerated and were distributed preferentially in the X−Y direction,which increased the relative density,bending strength and TC,and decreased the CTE of the composites.The 50wt.%GNFs/6061Al matrix composite sintered at 610℃ under 55 MPa demonstrated the best performance,i.e.,bending strength of 72 MPa,TC and CTE(RT−100℃)of 254 W/(m·K)and 8.5×10^(−6)K^(−1)in the X−Y direction,and 55 W/(m·K)and 9.7×10^(−6)K^(−1)in the Z direction,respectively.

Assembling Co_9S_8 nanoflakes on Co_3O_4 nanowires as advanced core/shell electrocatalysts for oxygen evolution reaction

Rational design of advanced cost-effective electrocatalysts is vital for the development of water electrolysis. Herein, we report a novel binder-free efficient CoS@CoOcore/shell electrocatalysts for oxygen evolution reaction（OER） via a combined hydrothermal-sulfurization method. The sulfurized net-like CoSnanoflakes are strongly anchored on the CoOnanowire core forming self-supported binder-free core/shell electrocatalysts. Positive advantages including larger active surface area of CoSnanoflakes,and reinforced structural stability are achieved in the CoS@CoOcore/shell arrays. The OER performances of the CoS@CoOcore/shell arrays are thoroughly tested and enhanced electrocatalytic performance with lower over-potential(260 m V at 20 m A cm) and smaller Tafel slopes（56 mV dec-1） as well as long-term durability are demonstrated in alkaline medium. Our proposed core/shell smart design may provide a new way to construct other advanced binder-free electrocatalysts for applications in electrochemical catalysis.

Synergistic Effect and Electrochromic Mechanism of Nanoflake Li-doped NiO in LiOH Electrolyte

Inorganic metal oxide electrochromic materials have good application prospects for energy-saving windows in buildings and smart display applications.Therefore,the development of electrochromic films with good cycling stabilities,fast color-change response times,and high coloring efficiencies has attracted considerable attention.In this study,nanoflake Li-doped NiO electrochromic films were prepared using a hydrothermal method,and the films exhibited superior electrochromic performances in the LiOH electrolyte.Li^(+)ions doping increased the ion transmission rates of the NiO films,and effectively promoted the transportation of ions from the electrolyte into NiO films.Meanwhile,the nanoflake microstructure caused the NiO films to have larger specific surface areas,providing more active sites for electrochemical reactions.It was determined that the NiO-Li20%film exhibited an ultra-fast response in the LiOH electrolyte(coloring and bleaching times reached 3 and 1.5 s,respectively).Additionally,the coloration efficiency was 62.1 cm^(2)C^(−1),and good cycling stability was maintained beyond 1500 cycles.Finally,the simulation calculation results showed that Li doping weakened the adsorption strengths of the NiO films to OH^(−),which reduced the generation and decomposition of NiOOH and helped to improve the cycling stabilities of the films.Therefore,the research presented in this article provides a strategy for designing electrochromic materials in the future.

Strain-modulated ultrafast magneto-optic dynamics of graphene nanoflakes decorated with transition-metal atoms

We perform first-principles calculations and coherent laser-matter interaction analyses to investigate the laser-induced ultrafast spin flip on graphene nanoflakes(GNFs)with transition metal elements attached on the boundary[TM&GNFs(TM=Fe,Co,Ni)].It is shown that the spin-flip process on TM&GNFs is highly influenced by the involved element species and the position attached to the nanoflakes.Furthermore,taking Ni&GNF as an example,the first-principles tensile test predicts that the variation of the C-Ni bond length plays an important role in the spin density distribution,especially for the low-lying magnetic states,and can therefore dominate the spin-flip processes.The fastest spin-flip scenario is achieved within 80 fs in a Ni&GNF structure under 10%tensile strain along the C-Ni bond.The local deformation modulation of spin flip provides the precursory guidance for further study of ultrafast magnetization control in GNFs,which could lead to potential applications in future integrated straintronic devices.

Constructing oxygen vacancy‐regulated cobalt molybdate nanoflakes for efficient oxygen evolution reaction catalysis

Oxygen evolution reaction(OER)is the dominant step for plenty of energy conversion and storage technologies.However,the OER suffers from sluggish kinetics and high overpotential due to its complex 4‐electron/proton transfer mechanism.Thus,developing efficient electrocatalysts is particularly urgent to accelerate OER catalysis but still remains a great challenge.Herein,we have synthesized the novel cobalt molybdate nanoflakes(CoMoO_(4)‐O_(v)‐n@GF)with adjustable oxygen vacancies contents by in situ constructing CoMoO_(4) nanoflakes on graphite felt(GF)and annealing treatment under the reduction atmosphere.The best‐performing CoMoO_(4)‐O_(v)‐2@GF with optimal oxygen vacancies content shows splendid electrocatalytic performance with the low overpotential(296 mV at 10 mA cm^(‒2))and also small Tafel slope(62.4 mV dec^(‒1))in alkaline solution,which are comparable to those of the RuO_(2)@GF.The experimental and the density functional theory calculations results reveal that the construction of optimal oxygen vacancies in CoMoO_(4) can expose more active sites,narrow the band‐gap to increase the electrical conductivity,and modulate the free energy of the OER‐related intermediates to accelerate OER kinetics,thus improving its intrinsic activity.

Enhanced coercivity and remanence of PrCo_5 nanoflakes prepared by surfactant-assisted ball milling with heat-treated starting powder

PrCo5 nanoflakes with strong texture and high coercivity of 8.15 kOe were prepared by surfactant-assisted ball milling with heat-treated starting powder. The thickness and length of the as-milled nanoflakes are mainly in the ranges of 50–100 nm and 0.5–3 μm, respectively. The x-ray diffraction patterns demonstrate that the heat treatment can increase the single phase and crystallinity of the PrCo5 compound, and combined with the demagnetization curves, indicate that the single phase and crystallinity are important for preparing high-coercivity and strong-textured rare earth permanent magnetic nanoflakes. In addition, the coercivity mechanism of the as-milled PrCo5 nanoflakes is studied by the angle dependence of coercivity for an aligned sample and the field dependence of coercivity, isothermal（IRM） and dc demagnetizing（DCD）remanence curves for an unaligned sample. The results indicate that the coercivity is dominated by co-existing mechanisms of pinning and nucleation. Furthermore, exchange coupling and dipolar coupling also co-exist in the sample.

Quantum plasmon enhanced nonlinear wave mixing in graphene nanoflakes

A distant-neighbor quantum-mechanical method is used to study the nonlinear optical wave mixing in graphene nanoflakes(GNFs),including sum-and difference-frequency generation,as well as four-wave mixing.Our analysis shows that molecular-scale GNFs support quantum plasmons in the visible spectrum region,and significant enhancement of nonlinear optical wave mixing is achieved.Specifically,the second-and third-order wave-mixing polarizabilities of GNFs are dramatically enhanced,provided that one(or more) of the input or output frequencies coincide with a quantum plasmon resonance.Moreover,by embedding a cavity into hexagonal GNFs,we show that one can break the structural inversion symmetry and enable otherwise forbidden second-order wave mixing,which is found to be enhanced by the quantum plasmon resonance too.This study reveals that the molecular-sized graphene could be used in the quantum regime for nanoscale nonlinear optical devices and ultrasensitive molecular sensors.

Adsorption of 1,3,5-Triphenylbenzene Molecules and Growth of Graphene Nanoflakes on Cu(100)Surface

Adsorption of 1,3,5-triphenylbenzene （TPB） molecules on Cu（100） surface is studied using ultraviolet photo- electron spectroscopy （UPS） and density functional theory （DFT） calculations. Researches on the bottom-up fabrication of graphene nanoflakes （GNFs） with TPB as a precursor on the Cu（100） surface are carried out based on UPS and DFT calculations. Three emission features d, e and f originating from the TPB molecules are located at 3.095, 7.326 and 9.349 eV below the Fermi level, respectively. With the increase of TPB coverage on the Cu（100） substrate, the work function decreases due to the formation of interfacial dipoles and charge （electron） rearrangement at the TPB/Cu（100） interface. Upon the formation of GNFs, five emission characteristic peaks of g, h, i, j and k originating from the GNFs are located at 1.100, 3.529, 6.984, 8.465 and 9.606eV below the Fermi level, respectively. Angle resolved ultraviolet photoelectron spectroscopy （ARUPS） and DFT calculations indicate that TPB molecules adopt a lying-down configuration with their molecular plane nearly parallel to the Cu（100） substrate at the monolayer stage. At the same time, the lying-down configuration for the GNFs on the Cu（100） surface is also unveiled by ARUPS and DFT calculations.

Prominent removal of trace lead(Ⅱ)ions from polluted water by terephthalic acid reformed Al/Zn metal organic nanoflakes

Terephthalic acid reformed Al/Zn metal organic nanoflake was prepared and functionalized with trie-thylamine(T-AlZn).Without adding terephthalic acid,there was no product of metal organic nanoflake.T-AlZn has a remarkable performance in removing trace lead(Ⅱ)ions(Pb^(2+)).The adsorption equipoise with the removal rate≥97%was reached within 35 min.The removal rates of T-AlZn for Pb^(2+)declined by only 16.73%after four regenerations.The adsorption of T-AlZn for Pb^(2+)follows the Langmuir isotherms model and pseudo-second-order dynamics model.The utmost adsorption competence was calculated as 215.27 mg g^(-1).The T-AlZn adsorbent exhibits a bright prospect in the adsorption for Pb^(2+)and is a considerable candidate in the disposal of industrial sewage.

Comment on“Chemical vapor deposition synthesis and Raman scattering investigation of quasi-one-dimensional ZrS_(3) nanoflakes”

A fundamentally crucial suggestion to rectify the fits to the high-resolution X-ray photoemission spectroscopy(XPS)raw data for the S 2p core level published by Chen et al.(Nano Res.2023,16,10567-10572)is presented herein.

Defect-modulated and heteroatom-functionalized Ti_(3−x)C_(2)T_(y)MXene 3D nanocavities induce growth of MoSe_(2)nanoflakes toward electrocatalytic hydrogen evolution in all pH electrolytes

Reducing kinetic energy barriers and developing accessible active sites are critical to deliver high hydrogen evolution reaction(HER)efficiency.In this paper,we synthesized defect-modulated and heteroatom(boron)-functionalized three-dimensional(3D)bowl-shaped Ti_(3−x)C_(2)T_(y)MXene(B-TCT)nanocavities coupled with the vertical growth of MoSe_(2)nanoflakes.The B-TCT@MoSe_(2)nanohybrids catalyst delivers the overpotentials of 49.9,52.7,and 67.8 mV to reach a HER current density of 10 mA·cm^(−2)under acidic,alkaline,and neutral conditions,respectively.Such outstanding HER activity is predominantly attributed to the heteroatom functionalization,self-adapting Ti vacancy(VTi)defect modulation,and spatial configuration design in the 3D B-TCT nanocavity,which synergistically regulate the electronic structure,activate the basal plane/edge unsaturated sites,and reduce the reaction energy barrier.Experimental and theoretical calculations demonstrate that strong heterogeneous interfacial bonding interactions between B-TCT and MoSe_(2)can dramatically reduce the free energy of hydrogen adsorption and facilitate efficient interfacial charge migration,thus essentially improving the HER kinetics.We used this 3D porous nanohybrid system assembled by defectrich lamellar structures to elucidate the advantageous synergistic effects of multiple mechanisms among defect structure,heteroatom functionalization,and interfacial coupling,which provided important insights for the development of efficient hybridtype catalysts.

纳米薄片状氯氧化铋的制备及其热解行为研究

本研究探讨了纳米薄片状氯氧化铋的制备方法及其在热解过程中的行为。采用室温下水解法制备氯氧化铋,形貌为近似圆角状的长方形结构。通过热重分析和X射线衍射分析,研究了氯氧化铋在不同温度下的热解行为,发现其在600℃开始分解,产物为BixCly、BixOyClz、Bi_(2)O_(3),于800℃分解结束,最终生成Bi_(3)O_(4)Cl。光催化性能评价结果表明,制备的氯氧化铋及其热解产物在降解有机染料甲基橙方面表现出优异的光催化性能。本研究为纳米薄片状氯氧化铋的制备与应用提供了重要的实验依据。

2D MOF Nanoflake-Assembled Spherical Microstructures for Enhanced Supercapacitor and Electrocatalysis Performances

Metal–organic frameworks(MOFs) are of great interest as potential electrochemically active materials.However, few studies have been conducted into understanding whether control of the shape and components of MOFs can optimize their electrochemical performances due to the rational realization of their shapes. Component control of MOFs remains a significant challenge. Herein, we demonstrate a solvothermal method to realize nanostructure engineering of 2D nanoflake MOFs. The hollow structures withNi/Co-and Ni-MOF(denoted as Ni/Co-MOF nanoflakes and Ni-MOF nanoflakes) were assembled for their electrochemical performance optimizations in supercapacitors and in the oxygen reduction reaction(ORR). As a result, the Ni/CoMOF nanoflakes exhibited remarkably enhanced performance with a specific capacitance of 530.4 F g^(-1)at 0.5 A g^(-1)in1 M LiO H aqueous solution, much higher than that of NiMOF(306.8 F g^(-1)) and ZIF-67(168.3 F g^(-1)), a good rate capability, and a robust cycling performance with no capacity fading after 2000 cycles. Ni/Co-MOF nanoflakes also showed improved electrocatalytic performance for the ORR compared to Ni-MOF and ZIF-67. The present work highlights the significant role of tuning 2D nanoflake ensembles of Ni/Co-MOF in accelerating electron and charge transportation for optimizing energy storage and conversion devices.