High performance asymmetric supercapacitor based on 3D microsphere-like 1T-MoS2 with high 1T phase content

1T phase molybdenum disulfide (1T-MoS₂) has aroused extensive concern in energy storage devices such as supercapacitors due to its large interlayer spacing, high conductivity and good hydrophilicity. However, it is struggle to synthesize 1T-MoS₂ with stable 1T phase with high content. Herein, Ammonium ion intercalation molybdenum disulfide (A-MoS₂) with high 1T content and stable 3D microsphere structure was successfully synthesized using a facile hydrothermal method. We explained the feasibility of ammonium ion (NH₄⁺) intercalation through density functional theory (DFT) calculations and proved the successful intercalation of NH₄⁺ by XRD and XPS. Through XPS fitting, the 1T phase content is calculated as high as 83.1%. The as-prepared A-MoS₂ presents a stable 3D microsphere structure with the interlayer spacing expanded to 0.93 nm, which provides a wide ion diffusion channel that allows ions to pass through quickly. Moreover, the high 1T content increases the hydrophilicity of MoS₂, thereby improving the wettability of the electrode, which contributes to the interaction between the electrolyte and electrode. In 1 M Na₂SO₄, A-MoS₂ electrode material displays high specific capacitance of 228 F g^?1 at 5 mV s^?1 and retains 127 F g^?1 at 80 mV s^?1, which proves the good rate capability. Furthermore, the assembled α-MnO₂//A-MoS₂ asymmetric supercapacitor (ASC) displayed a wide operating voltage of 2.1 V. The assembled ASC displays a high energy density of 35.8 Wh?kg^?1 at a power density of 525.0 W kg^?1, which indicates excellent energy storage performance.     

Facile synthesis of black phosphorus directly grown on carbon paper as an efficient OER Electrocatalyst: Role of Interfacial charge transfer and induced local charge distribution

Black phosphorus (BP), as a new 2D material, is normally synthesized by a high-pressure and high-temperature (HPHT) method from white and red phosphorus, which severely hinders the further development of BP for any potential applications and leads to search for other potential applications of BP with big challenge. Herein, we develop a facile and efficient Thermal-Vaporization-Transformation (TVT) approach to prepare a highly active BP directly grown on carbon paper as the electrode for Oxygen evolution reaction (OER), showing a low onset potential of 1.45 V versus RHE. Simultaneously, the current density of BP-CP illustrates the excellent electro-catalysis stability only decreases by 3.4% after continuous operation for 10000 s. Meanwhile, the density functional theory (DFT) calculations further illustrates the P-doped carbon layer in the upper side of BP layer is actually responsible for its enhanced OER property, and the adjacent carbon atoms of the embedded P atoms are actually the active sites due to the induced local change distribution by intramolecular change transfer. Considering the facile, but efficient and scalable, TVT approach can directly synthesize BP-CP with excellent OER performance, which is promising for BP electrocatalysts used for OER in metal-air batteries, fuel cells, water-splitting devices, even other key renewable energy.     

Rapid preparation of Palygorskite/Al2O3 composite aerogels with superhydrophobicity,high-temperature thermal insulation and improved mechanical properties

Al₂O₃ aerogels are widely employed in heat insulation and flame retardancy because of their unique combination of low thermal conductivity and exceptional high-temperature stability. However, the mechanical properties of Al₂O₃ aerogel are poor, and the preparation time is considerably long. In this study, we present a simple and scalable approach to construct monolithic Pal/Al₂O₃ composite aerogels using solvothermal treatment instead of traditional solvent replacement, which remarkably shortened the preparation time. Subsequently, to obtain stable superhydrophobicity (θ > 152°), the Pal/Al₂O₃ aerogel was modified by gas-phase modification method. The obtained Pal/Al₂O₃ composite aerogels demonstrate the integrated properties of low density (0.078–0.106 g/cm³), low thermal conductivity (1000 °C, 0.143 W/(m·K)), good mechanical properties (Young's modulus, 1.6 MPa), and good heat resistance. The monolithic Pal/Al₂O₃ composite aerogels with improved mechanical performance and improved thermal stability can show great potential in the field of thermal insulation.     

长江经济带城市生态效率演变及驱动因素分析

城市生态文明建设依托于生态效率的改善，基于2005—2016年长江经济带107座城市面板数据，采用超效率SBM（slacks-based measure)模型测算生态效率，并结合探索性空间分析与空间马尔科夫链等探讨生态效率时空演化格局的内在规律， 实证分析生态效率驱动因素的影响效果。研究表明：2005—2016年经济带生态效率总体呈平稳态势，上、中、下游呈现“阶梯型”分布，下游依次优于中游和上游地区，部分地区生态效率呈“两级型”分化趋势；城市间生态效率发展存在空间联动效应，与生态效率高的城市为邻，其正向溢出作用促进城市状态向高水平跃迁，而与生态效率低的城市为邻，其负向作用拉动城市状态向低水平发展；人口规模与产业升级对经济带不同流域具有异质性作用，其提升下游生态效率而抑制中游和上游生态效率，产业升级与生态效率存在“U”型关联，意味着产业升级在短期内并不能使生态效率状态改善，而经济发展有利于促进生态效率向高水平状态演变。     

Porous Si3N4 ceramics prepared by aqueous gelcasting using low–toxicity DMAA system: Regulatable microstructure and properties by monomer content

In this study, the low–toxicity monomer N, N–dimethylacrylamide (DMAA), serving as both gelling agent and pore–forming agent, was adopted to fabricate porous Si₃N₄ ceramics with a regulatable microstructure and property by aqueous gelcasting. Results indicate that monomer content played an important role in regulating and optimizing the properties of sintered bodies. With increasing monomer content (5.94–30.69?wt%), both slurry viscosity (maximum 0.14?Pa?s at 95.40 s^?1) and green body strength (11.35–49.23?MPa) exhibited monotonic increasing trends, demonstrating superior mechanical properties to those obtained using the neurovirulent acrylamide (AM) gelling system. The increased monomer content not only improved porosity, but also promoted α→β–Si₃N₄ transformation as well as β–Si₃N₄ grain growth through enhancing the connectivity of interlocking pores and accelerating the vapor phase transport during liquid–phase sintering. These variations in phase composition and microstructure derived from the varied monomer content further resulted in monotonic changes in porosity (40.32–51.50%), mean pore size (0.27–0.38?μm), flexural strength (202.77–132.15?MPa), fracture toughness (2.93–2.32?MPa?m^1/2), dielectric constant (3.48–2.78) and loss (3.52–3.09?×?10^?3) at 10?GHz for sintered bodies, displaying an excellent comprehensive properties. This study suggests a promising prospect for DMAA in preparation of high–performance porous Si₃N₄ ceramics by aqueous gelcasting.     

In Situ Anchoring Ultra Small Au Nanoparticles by Conformal Coating of Carbon Layer within the Micro-Environments of Mesoporous Silica for Highly Efficient Catalytic Reduction of 4-nitrophenol

Catalysis Letters - For the noble-metal based catalysts, the metal dispersion and sinter resistance of the metal nanoparticles (NPs) are the most vital factors for their application in series...     

Co-substitution of zirconium and neodymium on hyperfine interactions and AC susceptibility of SrFe_(12)O_(19) nanohexaferrites

This study presents the influence of Zn and Nd co-substitution on structure,morphology,AC susceptibility and ZFC-FC magnetizations of Sr nanohexaferrites(NHFs),SrFe_(12-x)(Zn,Nd)_xO_(19)(0.0≤x≤1.0),which was produced by sol-gel approach.XRD powder patterns,scanning electron microscopy(SEM) and high-resolution transmission electron spectroscopy(HR-TEM) approve the synthesis of Sr M-type hexaferrite.Mossbauer spectra show that Zn~(2+)ions occupy 2 b and 4f_1 sites while Nd~(3+)ions locate at 2 a,4f_2 and 12 k sites.The magnetic properties of the produced Sr-NHFs were investigated also by ZFC-FC magnetizations and AC susceptibility.According to the M_(FC)-M_(ZFC) results(between 2 and 400 K),no blocking temperature was detected which indicates the ferromagnetic(FM) behavior of NHFs.At lower temperatures,a super-spin glass like behavior is discerned.The AC susceptibility indicates that the magnetic interactions are improved due to the inclusion of low content(x=0.1) of Nd~(3+)and Zn~(2+)ions into the Sr-NHFs.However,with further increasing the Nd~(3+)and Zn~(2+)contents(x=0.9),the magnetic interactions are weakened.     

煤制烯烃含盐废水近零排放技术的应用

与石油、天然气相比，我国煤炭资源更加丰富，发展新型煤化工产业是大势所趋。煤炭和水资源的逆向分布导致煤化工企业所在地水环境问题尤为突出。常规处理工艺难以实现废水达标排放和资源回用目标，需通过特定的近零排放技术工艺，将浓盐水进一步浓缩至盐结晶，产水全部回用，结晶盐外排作为固废处置。本文结合工程实例，介绍了某煤化工项目针对生产过程中产生的含盐废水所采取的近零排放处理工艺技术路线，其主要由含盐废水膜处理单元和浓盐水蒸发结晶单元组成。采用机械蒸汽压缩循环、强制循环降膜蒸发、高效传热和盐种等技术，同时对蒸发结晶近零排放系统进行改进和优化。装置实际运行结果表明：各项工艺参数指标及药剂和能源消耗量均达到设计要求，产水水质达到优质再生水回用标准，实现整套装置长周期稳定运行及废水近零排放目标。     

Photoluminescence and unique magnetoluminescence of transparent (Tb1-xYx)3Al5O12 ceramics

Luminescent transparent ceramics (Tb_1-xY_x)₃Al₅O₁₂ (x = 0, 0.2, 0.5, 0.8) are successfully prepared by a solid-state method with additional hot isostatic pressing (HIP) treatment, and the structure and properties are investigated by XRD, SEM, PL, UV–Vis spectrophotometry and ellipsometry. The Y-containing samples are shown to be solid solution phases between TAG and YAG. The PL intensity is 14 times stronger with the incorporation of 80 mol.% Y, and the ⁵D₄→⁷F₅ emission lifetime of Tb³⁺ is prolonged from 0.357 to 3.035 ms at room temperature. A unique magnetoluminescence emerges upon the incorporation of Y, showing an interesting emission decrease to 55% as the Y content reaches 80 mol.%. Remarkably, this magnetoluminesence can occur at room temperature without an intense magnetic field. Based on our work, transparent (Tb_1-xY_x)₃Al₅O₁₂ ceramics exhibit the potential for applications in green emitters, optical instruments and photoelectric devices. In particular, the magnetoluminescence provides a simple, noncontact and nondestructive route for probing magnetic fields.     

Effect of pyrolysis temperature on the mechanical evolution of SiCf/SiC composites fabricated by PIP

Three types of SiC_f/SiC composites with a four-step three-dimensional SiC fibre preform and pyrocarbon interface fabricated via precursor infiltration and pyrolysis at 1100 °C, 1300 °C, and 1500 °C were heat-treated at 1300 °C under argon atmosphere for 50 h. The effects of the pyrolysis temperature on the microstructural and mechanical properties of the SiC_f/SiC composites were studied. With an increase in the pyrolysis temperature, the SiC crystallite size of the as-fabricated composites increased from 3.4 to 6.4 nm, and the flexural strength decreased from 742 ± 45 to 467 ± 38 MPa. After heat treatment, all the samples exhibited lower mechanical properties, accompanied by grain growth, mass loss, and the formation of open pores. The degree of mechanical degradation decreased with an increase in the pyrolysis temperature. The composites fabricated at 1500 °C exhibited the highest property retention rates with 90% flexural strength and 98% flexural modulus retained. The mechanism of the mechanical evolution after heat treatment was revealed, which suggested that the thermal stability of the mechanical properties is enhanced by the high crystallinity of the SiC matrix after pyrolysis at higher temperatures.