Preparation and electrochemical lithium storage performance of porous silicon microsphere composite with metal modification and carbon coating

This work adopts a multi⁃step etching⁃heat treatment strategy to prepare porous silicon microsphere com⁃posite with Sb⁃Sn surface modification and carbon coating(pSi/Sb⁃Sn@C),using industrial grade SiAl alloy micro⁃spheres as a precursor.pSi/Sb⁃Sn@C had a 3D structure with bimetallic(Sb⁃Sn)modified porous silicon micro⁃spheres(pSi/Sb⁃Sn)as the core and carbon coating as the shell.Carbon shells can improve the electronic conductivi⁃ty and mechanical stability of porous silicon microspheres,which is beneficial for obtaining a stable solid electrolyte interface(SEI)film.The 3D porous core promotes the diffusion of lithium ions,increases the intercalation/delithia⁃tion active sites,and buffers the volume expansion during the intercalation process.The introduction of active met⁃als(Sb⁃Sn)can improve the conductivity of the composite and contribute to a certain amount of lithium storage ca⁃pacity.Due to its unique composition and microstructure,pSi/Sb⁃Sn@C showed a reversible capacity of 1247.4 mAh·g^(-1) after 300 charge/discharge cycles at a current density of 1.0 A·g^(-1),demonstrating excellent rate lithium storage performance and enhanced electrochemical cycling stability.

高超声速飞机机载作动系统发展分析

吸气式高超声速飞机面临严酷的高动压、大热流飞行环境,要求机载系统既要兼具高功率、高效能与高耐热能力,又要满足严苛的体积、重量(质量)与能量约束,给飞控作动系统设计带来了极大的技术挑战。本文通过对高超声速飞机任务和平台动力特点的分析,系统地论述了其飞控作动系统面临的挑战,包括能源、结构和热管理等问题。基于已有高速飞机的公开资料,对作动技术发展现状进行了梳理,结合热管理与机载能源的发展趋势,展望了高超声速飞机作动系统的重点发展方向,并给出了具有可行性的发展路线。

Nanostructured electrocatalytic materials and porous electrodes for direct methanol fuel cells

Direct methanol fuel cells （DMFCs） are promising for use in portable devices because of advantages such as high fuel energy density, low working temperature and low emission of pollutants. Nanotechnology has been used to improve the performance of DMFCs. Catalytic materials composed of small, metallic particles with unique nanostructure supparted on carbons or metal oxides have been widely investigated for use in DMFCs. Despite our increased understanding of this type of fuel cell, many challenges still remain. This paper reviews the current developments of nanostructured elec- trocatalytic materials and porous electrodes for use in DMFCs. In particular, this review focuses on the synthesis and characterization of nanostructured catalysts and supporting materials. Both computational and experimental approaches to optimize mass transportation in porous electrodes of DMFCs, such as theoretical modeling of internal transfer processes and preparation of functional structures in membrane electrode assemblies, are introduced.

A 1.25Gb/s InP-Based Vertical Monolithic Integration of an MQW Laser Diode and an HBT Driver witha Lateral Buffer Mes a Structure

A novel fabrication process related to a smoothly wet chemical etching profile o f InP-based epitaxial layers in the crystal direction of [01for an InP-based monol ithic vertically integrated transmitter with an MQW laser diode and a heterojunction bipolar tran sistors driver circuit is described.A clear eye output diagram via an O/E converter is demonstrat ed und er a 1.25Gb/s non-return-zero pseudorandom code with a pattern length of 2 the integrated transmitter has a power dissipation of about 120mW with an optical output of 2dBm.

Configuration optimization model of multi-energy distributed generation system

To integrate different renewable energy resources effectively in a microgrid, a configuration optimization model of a multi-energy distributed generation（DG） system and its auxiliary equipment is proposed. The model mainly consists of two parts, the determination of initial configuration schemes according to user preference and the selection of the optimal scheme. The comprehensive evaluation index（CEI）, which is acquired through the analytic hierarchy process（AHP） weight calculation method, is adopted as the evaluation criterion to rank the initial schemes. The optimal scheme is obtained according to the ranking results. The proposed model takes the diversity of different equipment parameters and investment cost into consideration and can give relatively suitable and economical suggestions for system configuration.Additionally, unlike Homer Pro, the proposed model considers the complementation of different renewable energy resources, and thus the rationality of the multi-energy DG system is improved compared with the single evaluation criterion method which only considers the total cost.

Photoelectrochemical degradation of acetaminophen and valacyclovir using nanoporous titanium dioxide

Electrochemically treated nanoporous TiO2 was employed as a novel electrode to assist in the pho- toelectrochemical degradation of acetaminophen and valacyclovir. The prepared electrode was characterized by scanning electron microscopy （SEM） and energy dispersive spectroscopy （EDS）. Cyclic voltammetry （CV）, Mott-Schottky plots, ultraviolet-visible light （UV-vis） absorbance spec- troscopy, and a total organic carbon （TOC） analyzer were employed to investigate the photoelec- trochemical degradation of acetaminophen and valacyclovir. The results indicated no obvious re- moval of acetaminophen and valacyclovir over 3 h when separate photochemical degradation and electrochemical oxidation were employed. In contrast, acetaminophen and valacyclovir were rapid- ly eliminated via photoelectrochemical degradation. In addition, electrochemically treated nanopo~ rous TiO2 electrodes significantly enhanced the efficacy of the photoelectrochemical degradation of acetaminophen and valacyclovir, by 86.96% and 53.12%, respectively, when compared with un- treated nanoporous TiO2 electrodes. This enhanced performance may have been attributed to the formation of Ti3~, Ti2~, and oxygen vacancies, as well as an improvement in conductivity during the electrochemical reduction process. The effect of temperature was further investigated, where the activation energy of the photoelectrochemical degradation of acetaminophen and valacyclovir was determined to be 9.62 and 18.42 kJ/mol, respectively.

Synthesis of a novel hexagonal porous TT-Nb2O5 via solid state reaction for high-performance lithium ion battery anodes

Hexagonal porous Nb2O5 was synthesized for the first time via a facile solid-state reaction.The structure and electrochemical properties have been optimized through tuning heating temperature.X-ray diffraction results indicate that pseudo hexagonal Nb2O5(TT-Nb2O5)and orthorhombic Nb2O5 have been synthesized at different temperatures.Hexagonal sheet and porous structure of Nb2O5 were characterized by scanning electron microscopy and N2-adsorption-desorption isotherms.The as-prepared TT-Nb2O5(heated at 600℃)shows the best performance with a remarkable charge capacity of 178 mA∙h/g at 0.2C,which is higher than that of T-Nb2O5.Even at 20℃,TT-Nb2O5 offers unprecedented rate capability up to 86 mA∙h/g.The high rate capacity is due to pseudocapacitive Li+intercalation mechanism of TT-Nb2O5.The reported results demonstrate that Nb2O5 with good crystal structure and high specific surface area is a powerful composite design for high-rate and safe anode materials.

Rational construction of cross-linked porous nickel arrays for efficient oxygen evolution reaction

It is important but challenging to design and fabricate an efficient and cost-effective electrocatalyst for the oxygen evolution reaction(OER). Herein, we report free-standing 3 D nickel arrays with a cross-linked porous structure as interesting and high-performance electrocatalysts for OER via a facile one-step electrodeposition method. The 3 D nickel arrays are strongly anchored on the substrate, forming self-supported electrocatalysts with reinforced structural stability and high electrical conductivity. Because of their increased active surface area, abundant channels for electron/ion transportation and enhanced electronic conductivity, the designed 3 D nickel arrays exhibit superior electrocatalytic OER performance with a low overpotential(496 mV at 50 mA cm–2) and a small Tafel slope(43 mV dec–1) as well as long-term stability(no decay after 24 h) in alkaline solution. Our proposed rational design strategy may open up a new way to construct other advanced 3 D porous materials for widespread application in electrocatalysis.

AN ALLOZYME ELECTROPHORESIS STUDY ON ELEVEN SPECIES OF MEGOPHRYINAE IN CHINA

Allozymes of eleven species of Megophryinae in China were examined electrophoretically to investigate genetic diversity and phylogenetic relationships. Fourteen enzymes, presumptively coded by 24 loci were detected to be variable. Gene frequencies of each population at each locus were presented. The commonly used measure of genetic diversity, the average heterozygosity (H) were calculated based on gene frequencies. The results indicated that Megophryinae had a high level of genetic diversity in amphibians, an average H of 0.18, ranging from 0.058 to 0.28. Nei's (1978) genetic distances(Nei's D) were calculated for all possible population pairs. A dendrogram of 13 populations representing 11 species, 3 genera of Megophryinae were derived and presented by using UPGMA, based on Nei' s D. The assignment of Ophryophryne as a distinct genus were supported by an average Nei's D of 1.4067 which separated O. microstoma from all other populations.Subdivision of Brachytarsophrys from Megophrys was not supported by this study. Within Megophrys, three groups were recognized: (1)M. lateralis, M. giganticus and M. longipes; (2)M. palpebralespineosa, M. boettgeri and M. parva;(3) M. minor and M. kuatunensis. Three populations of M. omeimontis were closely related and share a clade independent from all other Megophrys, and B. feae as well.

Multi-objective capacity allocation optimization method of photovoltaic EV charging station considering V2G

Large-scale electric vehicles(EVs) connected to the micro grid would cause many problems. In this paper, with the consideration of vehicle to grid(V2 G), two charging and discharging load modes of EVs were constructed. One was the disorderly charging and discharging mode based on travel habits, and the other was the orderly charging and discharging mode based on time-of-use(TOU) price;Monte Carlo method was used to verify the case. The scheme of the capacity optimization of photovoltaic charging station under two different charging and discharging modes with V2 G was proposed. The mathematical models of the objective function with the maximization of energy efficiency, the minimization of the investment and the operation cost of the charging system were established. The range of decision variables, constraints of the requirements of the power balance and the strategy of energy exchange were given. NSGA-Ⅱ and NSGA-SA algorithm were used to verify the cases, respectively. In both algorithms, by comparing with the simulation results of the two different modes, it shows that the orderly charging and discharging mode with V2 G is obviously better than the disorderly charging and discharging mode in the aspects of alleviating the pressure of power grid, reducing system investment and improving energy efficiency.

Synthesis of porous nano/micro structured LiFePO_4/C cathode materials for lithium-ion batteries by spray-drying method

In order to enhance electrochemical properties of LiFePO4 （LFP） cathode materials, spherical porous nano/micro structured LFP/C cathode materials were synthesized by spray drying, followed by calcination. The results show that the spherical precursors with the sizes of 0.5-5 μm can be completely converted to LFP/C when the calcination temperature is higher than 500 ℃. The LFP/C microspheres obtained at calcination temperature of 700 ℃ are composed of numerous particles with sizes of -20 nm, and have well-developed interconnected pore structure and large specific surface area of 28.77 mE/g. The specific discharge capacities of the LFP/C obtained at 700 ℃ are 162.43, 154.35 and 144.03 mA.h/g at 0.5C, 1C and 2C, respectively. Meanwhile, the capacity retentions can reach up to 100% after 50 cycles. The improved electrochemical properties of the materials are ascribed to a small Li＋ diffusion resistance and special structure of LFP/C microspheres.

Synthesis and Characterization of Supported CulnSe2 Nanorod Arrays on Rigid Substrates

Copper indium diselenide nanorod arrays were electrodeposited on tungsten/silicon rigid substrates using porous anodic alumina as growth template. The porous anodic alumina templates were prepared by anodizing aluminum films which were sputtered onto the tungsten/silicon substrates. A selective chemical etching was used to penetrate the barrier layer at the bottom of the alumina channels before electrodeposition, which enables direct electrical and chemical contact with the underside substrate electrode. The as-deposited samples were annealed at 450 ℃ in vacuum. Scanning electron microscopy revealed that the nanorods were dense and compact with diameter of about 100 nm, length of approximate 1 um, and the aspect ratio of 10. X-ray diffraction, micro-Raman spectroscopy, and high resolution transmission electron microscopy showed that chalcopyrite polycrystalline structure and high purity CuInSe2 nanorods were obtained. The grain size was large in the rod axial direction. Energy-dispersive X-ray spectroscopy showed the composition was nearly stoichiometric. The energy band gap of this nanorod arrays was analyzed by fundamental absorption spectrum and was evaluated to be 0.96 eV.

Preparation of dendritic bismuth film electrodes and their application for detection of trace Pb(Ⅱ)and Cd(Ⅱ)

In this paper,dendritic Bi film electrodes with porous structure had successfully been prepared on glassy carbon electrode using a constant current electrolysis method based on hydrogen bubble dynamic templates.The electrode prepared using a large applied current density showed an increased internal electroactive area and a significantly improved electrochemical performance.The analytical utility of the prepared dendritic Bi film electrodes for the determination of Pb(Ⅱ)and Cd(Ⅱ)in the range of 5–50 μg·L^(-1)were presented in combination with square wave stripping voltammetry in model solution.Compared with non-porous Bi film electrode,the dendritic Bi film electrode exhibited higher sensitivity and lower detection limit.The prepared Bi film electrode with dendritic structure was also successfully applied to real water sample analysis.

Cobalt phosphide nanocage@ferric-zinc mixed-metal phosphide nanotube hierarchical nanocomposites for enhanced overall water splitting

Hierarchical nanostructures have attracted widespread interest owing to their unique properties compared to their bulk counterparts. Thus, they are considered promising electrocatalytic materials. In this work, a novel hierarchical porous nanocomposite of cobalt phosphide nanocage@ferric-zinc mixed-metal phosphide nanotubes(denoted Co P@Zn Fe P) was fabricated using a self-assembly approach. Because of their structural and compositional merits, the as-prepared phosphide hybrids have abundant catalytic active sites and high porosity for facile mass diffusion. In an alkaline electrolyte, the CoP@ZnFeP flower-like hybrids displayed enhanced catalytic activity for the hydrogen evolution reaction and the oxygen evolution reaction compared with a mechanical mixture of Co P and Zn Fe P nanoparticles. The CoP@ZnFeP hierarchical nanocomposites also showed excellent activity for the overall water splitting reaction, yielding a water-splitting current of 10 mA/cm^2 on the application of just 1.6 V, as well as excellent durability(24-h long-term operation) in a two-electrode system. Our design methodology may create opportunities to search for highly efficient and robust non-precious metal catalysts with applications in high-performance energy conversion and storage devices.

In-situ hydrothermal synthesis of Ni−MoO_(2)heterostructure on porous bulk NiMo alloy for efficient hydrogen evolution reaction

The Ni−MoO_(2) heterostructure was synthesized in suit on porous bulk NiMo alloy by a facile powder metallurgy and hydrothermal method.The results of field emission scanning electron microscopy(SEM),field emission transmission electron microscopy(TEM)and X-ray photoelectron spectroscopy(XPS)reveal that the as-prepared electrode possesses the heterostructure and a layer of Ni(OH)_(2) nanosheets is formed on the surface of Ni−MoO_(2) electrode simultaneously after hydrothermal treatment,which provides abundant interface and much active sites,as well as much active specific surface area.The results of hydrogen evolution reaction indicate that the Ni−MoO_(2) heterostructure electrode exhibits excellent catalytic performance,requiring only 41 mV overpotential to reach the current density of 10 mA/cm^(2).It also possesses a small Tafel slope of 52.7 mV/dec and long-term stability of electrolysis in alkaline medium.

Catalytic effects of [Ag(H_2O)(H_3PW_(11)O_(39))]^(3-)on a TiO_2 anode for water oxidation

A[H3AgI(H2O)PW11O39]3?‐TiO2/ITO electrode was fabricated by immobilizing a molecular polyoxometalate‐based water oxidation catalyst,[H3AgI(H2O)PW11O39]3?(AgPW11),on a TiO2electrode.The resulting electrode was characterized by X‐ray powder diffraction,scanning electron microscopy,and energy dispersive X‐ray spectroscopy.Linear sweep voltammetry,chronoamperometry,and electrochemical impedance measurements were performed in aqueous Na2SO4solution(0.1molL?1).We found that a higher applied voltage led to better catalytic performance by AgPW11.The AgPW11‐TiO2/ITO electrode gave currents respectively10and2.5times as high as those of the TiO2/ITO and AgNO3‐TiO2/ITO electrodes at an applied voltage of1.5V vs Ag/AgCl.This result was attributed to the lower charge transfer resistance at the electrode‐electrolyte interface for the AgPW11‐TiO2/ITO electrode.Under illumination,the photocurrent was not obviously enhanced although the total anode current increased.The AgPW11‐TiO2/ITO electrode was relatively stable.Cyclic voltammetry of AgPW11was performed in phosphate buffer solution(0.1mol L?1).We found that oxidation of AgPW11was a quasi‐reversible process related to one‐electron and one‐proton transfer.We deduced that disproportionation of the oxidized[H2AgII(H2O)PW11O39]3?might have occurred and the resulting[H3AgIIIOPW11O39]3?oxidized water to O2.

Light alloying element‐regulated noble metal catalysts for energy‐related applications

Noble metals have been widely used as heterogeneous catalysts because they exhibit high activity and selectivity for many reactions of both academic and industrial interest.The introduction of light atomic species(e.g.,H,B,C,and N)into noble metal lattices plays an important role in optimizing catalytic performance by modulating structural and electronic properties.In this review,we present a general overview of the recent advances in the modification of noble metals with light alloying elements for various catalytic reactions,particularly for energy‐related applications.We summarize the types,location,concentration,and ordering degree of light atoms as major factors in the performance of noble metal‐based catalysts,with emphasis on how they can be rationally controlled to promote activity and selectivity.We then summarize the synthetic strategies developed to incorporate light elements and highlight the theoretical and experimental methods for understanding the alloying effects.We further focus on the wide usage of noble metal‐based catalysts modified with different light alloying atoms and attempt to correlate the structural features with their catalytic performances.Finally,we discuss current challenges and future perspectives regarding the development of highly efficient noble metal‐based catalysts modified with light elements.

Progress of electrochemical CO_(2)reduction reactions over polyoxometalate-based materials

Electrochemical CO_(2)reduction to value-added fuels and chemicals is recognized as a promising strategy to alleviate energy shortages and global warming owing to its high efficiency and economic feasibility.Recently,understanding the activity origin,selectivity regulation,and reaction mechanisms of CO_(2)reduction reactions(CO_(2)RRs)has become the focus of efficient electrocatalyst design.Polyoxometalates(POMs),a unique class of nanosized metal-oxo clusters,are promising candidates for the development of efficient CO_(2)RR electrocatalysts and,owing to their well-defined structure,remarkable electron/proton storage and transfer ability,and capacities for adsorption and activation of CO_(2),are ideal models for investigating the activity origin and reaction mechanisms of CO_(2)RR electrocatalysts.In this review,we focus on the activity origin and mechanism of CO_(2)RRs and survey recent advances that were achieved by employing POMs in electrocatalytic CO_(2)RRs.We highlight the significant roles of POMs in the electrocatalytic CO_(2)RR process and the main factors influencing selectivity regulation and catalytic CO_(2)RR performance,including the electrolyte,electron-transfer process,and surface characteristics.Finally,we offer a perspective of the advantages and future challenges of POM-based materials in electrocatalytic CO_(2)reduction that could inform new advancements in this promising research field.

Photophysical Property of Photoactive Molecules with Multibranched Push-Pull Structures

The structure-property characteristics of a series of newly synthesized intramolecular charge- transfer （ICT） compounds, single-branch monomer with triphenylmethane as electron donor and 2,1,3-benzothiadiazole as acceptor, the corresponding two-branch dimer and three- branch trimer, have been investigated by means of steady-state and femtosecond time- resolved stimulated emission fluorescence depletion （FS TR-SEP FD） techniques in different polar solvents. The TD-DFT calculations are further performed to explain the observed ICT properties. The interpretation of the experimental results is based on the comparative studies of the series of compounds which have increased amount of identical branch moiety. The similarity of the absorption and fluorescence spectra as well as strong solvent-dependence of the spectral properties for the three compounds reveal that the excited state of the dimer and trimer are nearly the same with that of the monomer, which may localize on one branch. It is found that polar excited state emerged through multidimensional intramolecular charge transfer from the donating moiety to the acceptor upon excitation, and quickly relaxed to one branch before emission. Even so, the red-shift in the absorption and emission spectra and decreased fluorescence radiative lifetime with respect to their monomer counterpart still suggest some extent delocalization of excited state in the dimer and trimer upon excitation. The similar behavior of their excited ICT state is demonstrated by FS TR-SEP FD measurements, and shows that the trimer has the largest charge-separate extent in all studied three samples. Finally, steady-state excitation anisotropy measurements has further been carried out to estimate the nature of the optical excitation and the mechanism of energy redistribution among the branches, where no plateau through the ICT band suggests the intramolecular excitation transfer process between the branches in dimer and trimer.

Metal-organic frameworks for highly efficient oxygen electrocatalysis

Metal‐organic frameworks(MOFs)are a series of highly porous crystalline materials,which are built from inorganic metal nodes and organic linkers through coordination bonds.Their unique porous structural features(such as high porosity,high surface areas,and highly ordered nanoporous structures)and designable structures and compositions have facilitated their use in gas capture,separation,catalysis,and energy storage and conversion.Recently,the design and synthesis of pure MOFs and their derivatives have opened new routes to develop highly efficient electrocatalysts toward oxygen reduction reactions(ORR)and oxygen evolution reactions(OER),which are the core electrode reactions in many energy storage and conversion techniques,such as metal‐air batteries and fuel cells.This review first discusses recent progress in the synthesis and the electrocatalytic applications of pure MOF‐based electrocatalysts toward ORR or OER,including pure MOFs,MOFs decorated with active species,and MOFs incorporated with conductive materials.The following section focuses on the advancements of the design and preparation of various MOF‐derived materials-such as inorganic nano‐(or micro‐)structures/porous carbon composites,pure porous carbons,pure inorganic nano‐(or micro‐)structured materials,and single‐atom electrocatalysts-and their applications in oxygen electrocatalysis.Finally,we present a conclusion and an outlook for some general design strategies and future research directions of MOF‐based oxygen electrocatalysts.