Syngas production via coal char-CO2 fluidized bed gasification and the effect on the performance of LSCFN//LSGM//LSCFN solid oxide fuel cell

Fluidized bed reactor is widely used in coal char-CO_2 gasification. In this work, the production of syngas by using a fluidized bed gasification technique was first investigated and then the effect of the produced syngas on the performance of the solid oxide fuel cell with a configuration of La_(0.4)Sr_(0.6) Co_(0.2)Fe_(0.7)Nb_(0.1)O_(3-δ)//La_(0.8)Sr_(0.2)Ga_(0.83)Mg_(0.17)O_(3-δ)//La_(0.4)Sr_(0.6) Co_(0.2)Fe_(0.7)Nb_(0.1)O_(3-δ)(LSCFN//LSGM//LSCFN)was studied. During the syngas production, we found that the volume fraction of CO increased with the increment of gasification temperature, and it reached a maximum value of 88.8%, corresponding to a composition of 0.76% H_2, 88.8% CO, and 10.44% CO_2, when the ratio of oxygen mass flow rate to that of coal char(MO2/Mchar) increased to 0.29. In the following utilization of the produced syngas in solid oxide fuel cells, it was found that the increasing CO volume fraction in the syngas results in a gradual increase of the peak power density of the LSCFN//LSGM//LSCFN cell. The maximum peak power density of 410 m W/cm~2 was achieved for the syngas produced at 0.29 of M_(O2)/M_(char). In the stability test, the cell voltage decreased by 4% at a constant current density of 0.475 A/cm~2 after 54 h when fueled with the syngas with the composition of 0.76% H2, 88.8% CO, and 10.44% CO_2.It reveals that a carbon deposition with the content of 13.66% in the anode is attributed to the cell performance degradation.     

Polyethylene Oxide-Coated Electrospun Polyimide Fibrous Seperator for High-Performance Lithium-Ion Battery

A polyethylene oxide(PEO)-coated polyimide(PI) membrane was prepared by electrospinning method followed by a dip-coating and drying process for high-performance lithium-ion batteries(LIB). Semicrystal PEO was covered on the surface of the fibers and partially enmeshed in PI matrix, which formed unique porous structures. The pores with an average size of 4.1 μm and a porosity of 90% served as ion transport channels. Compared with the cell with Celgard 2400 membrane, the half-cell using PEO-coated PI membrane as a separator exhibits excellent electrochemical performance both at room temperature and at low temperature. The electrolyte uptaking rate of PEO-coated PI membrane was 170% and the ionic conductivity was 3.83 × 10~(–3)S cm~(–1). PEO-coated PI membrane possessed 5.3 V electrochemical window.The electrode–electrolyte interfacial resistance was 62.4 Ω. The capacity retention ratios with PEOcoated PI membrane were 86.4% at 5 C and 73.5% at 10 C at 25 ℃ and 75% at 5 C at 0 ℃. Furthermore,the cell using the separator demonstrates excellent capacity retention over cycling. These advanced characteristics would boost the application of the PEO-coated PI membrane for high-power lithium ion battery.     

High-performance asymmetric supercapacitors based on reduced graphene oxide/polyaniline composite electrodes with sandwich-like structure

The sandwich-like structure of reduced graphene oxide/polyaniline(RGO/PANI) hybrid electrode was prepared by electrochemical deposition. Both the voltage windows and electrolytes for electrochemical deposition of PANI and RGO were optimized. In the composites, PANI nanofibers were anchored on the surface of the RGO sheets, which avoids the re-stacking of neighboring sheets. The RGO/PANI composite electrode shows a high specific capacitance of 466 F/g at 2 m A/cm~2 than that of previously reported RGO/PANI composites. Asymmetric flexible supercapacitors applying RGO/PANI as positive electrode and carbon fiber cloth as negative electrode can be cycled reversibly in the high-voltage region of 0–1.6 V and displays intriguing performance with a maximum specific capacitance of 35.5 m F cm~(-2). Also, it delivers a high energy density of 45.5 m W h cm~(-2) at power density of 1250 m W cm~(-2). Furthermore, the asymmetric device exhibits an excellent long cycle life with 97.6% initial capacitance retention after 5000 cycles.Such composite electrode has a great potential for applications in flexible electronics, roll-up display,and wearable devices.     

Cobalt-free Composite Ba_(0.5)Sr_(0.5)Fe_(0.9)Ni_(0.1)O_(3-δ)-Ce_(0.8)Sm_(0.2)O_(2-δ) as Cathode for Intermediate-Temperature Solid Oxide Fuel Cell

New cobalt-free composites consisting of Ba0.5Sr0.5Fe0.9Ni0.1O3-δ(BSFN) and Ce0.8Sm0.2O2-δ(SDC) were investigated as possible cathode materials for intermediate-temperature solid oxide fuel cell (IT-SOFC). BSFN, which was synthesized by auto ignition process, was chemically compatible with SDC up to 1100℃ as indicated by X-ray diffraction analysis. The electrical conductivity of BSFN reached the maximum value of 57 S·cm-1 at 450℃. The thermal expansion coefficient (TEC) value of BSFN was 30.9×10-6K-1 , much higher than that of typical electrolytes. The electrochemical behavior of the composites was analyzed via electrochemical impedance spectroscopy with symmetrical cells BSFN-SDC/SDC/BSFN-SDC. The area specific interfacial polarization resistance (ASR) decreased with increasing SDC content of the composite. The area specific interfacial polarization resistance (ASR) at 700℃ is only 0.49, 0.34 and 0.31 Ω·cm2 when 30, 40, and 50 wt% SDC was cooperated to BSFN, respectively. These results suggest that BSFN-SDC is a possible candidate for IT-SOFC cathode.     

Electrochemical Properties of Tubular SOFC Based on a Porous Ceramic Support Fabricated by Phase-Inversion Method

In this work, a tubular ceramic-supported solid oxide fuel cell(SOFC) was successfully fabricated by a low cost and simple process involving phase-inversion, brush coating and co-sintering. Properties including sintering behavior, microstructure of the tubular support as well as the electrochemical properties of single cell were investigated. The results show that a porous tubular support with ?nger-like pores and macrovoids was obtained after phase-inversion process. The tubular support is proved to be gaspermeable after sintering at 1400 °C with shrinkage of about 34%. The maximum power density of single tubular SOFC is 100 mW /cm~2 and 122 mW /cm~2 at 850 °C when fed with wet methane and hydrogen, respectively. The current collection, thickness of electrolyte and gas permeability of tubular support should account for the large total resistance. The present tubular design could be expected to deliver a higher voltage for longer support with several segmented-in-series cell stacks.     

Cu3(PO4)2: Novel Anion Convertor for Aqueous Dual‑Ion Battery

Electrode materials which can reversibly react with anions are of interest for aqueous dual-ion batteries.Herein,we propose a novel anion electrode,Cu3(PO4)2,for constructing an aqueous dual-ion cell.The Cu3(PO4)2 electrode can operate in a quasi-neutral condition and deliver a reversible capacity of 115.6 mAh g^−1 with a well-defined plateau at−0.17 V versus Ag/AgCl.Its reaction mechanism shows that Cu3(PO4)2 decomposes into Cu2O and subsequently is converted into Cu during the initial discharge process.In the following charge process,Cu is oxidized into Cu2O.It suggests Cu3(PO4)2 reacts with OH−ions instead of PO43−ions after the initial discharge process and its potential thereby depends upon the OH−ions concentration in electrolyte.Additionally,an aqueous dual-ion cell is built by using pretreated Cu3(PO4)2 and Na0.44MnO2 as anode and cathode,respectively.During cycling,OH−ions and Na^+ions in electrolyte can be stored and released.Such a cell can provide a discharge capacity of 52.6 mAh g^−1 with plateaus at 0.70 and 0.45 V,exhibiting the potential of application.This work presents an available aqueous dual-ion cell and provides new insights into renewable energy storage and adjustment of the OH−ions concentration in aqueous buffer solution.     

Stable controlled growth of 3D CuO/Cu nanoflowers by surfactant-free method for non-enzymatic hydrogen peroxide detection

Sensitive, convenient and rapid detection of hydrogen peroxide(H_2 O_2) is highly desirable in fields like fundamental biological research, food industries, and clinical environmental analysis. Herein, a hierarchical porous CuO/Cu flower-like active electrode material for non-enzymatic H_2 O_2 sensor was synthesized via a low-cost and one-step chemical oxidation of Cu powder in water bath without surfactants. In order to discuss the growth mechanism of the product, products with different growth time length were fabricated. The electro-catalysis of all products were first exhibited by cyclic-voltammetry,and the product under 6 h reaction shows the best result. The detailed electro-catalytic behaviors of the best product(under 6 h reaction) are characterized by cyclic-voltammetry and amperometry under alkaline conditions. The materials have high sensitivity of 103 μA mM~(-1) cm~(-2)(R~2= 0.9979), low detection limit of 2 μmol/L and wide concentration range(from 2 μmol/L to 19.4 mmol/L). Large specific surface area and stabled nanostructure enabled good features, such as stability and sensitivity for the H_2 O_2 determination.     

Influence of Lithium Oxide Addition on the Sintering Behavior and Electrical Conductivity of Gadolinia Doped Ceria

Ceria-based electrolytes have been widely researched in intermediate-temperature solid oxide fuel cell (SOFC), which might be operated at 500-600?C. Sintering behavior with lithium oxide as sintering additive and electrical conductivity of gadolinia doped ceria (Gd0.1Ce0.9O2δ, GDC10) electrolyte was studied in this paper by X-ray di?raction (XRD), scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). As the results, the fully dense GDC10 electrolytes are obtained at a low temperature of 800?C with 2.5 mol% Li2O as sintering additive (called 5LiGDC800). During sintering process, lithium oxides adsorbed by around GDC10 surface help to sinter at 800?C and are kept at the grain boundary of GDC10 in the end. The fine grains of 100-400 nm and high electrical conductivity of 0.014 S/cm at 6000C in 5LiGDC800 were achieved, which contributed to the lower sintering temperature and enhanced grain boundary conductivity, respectively. Lithium, staying at grain boundary, reduces the depletion of oxygen vacancies in the space charge layers and increases the oxygen vacancy concentration in the grain boundary, which leads to improve the total electrical conductivity of 5LiGDC800.     

Construction of hierarchical three-dimensional interspersed flower-like nickel hydroxide for asymmetric supercapacitors

Low-cost and easily obtainable electrode materials are crucial for the application of supercapacitors.Nickel hydroxides have recently attracted intensive attention owning to their high theoretical specific capacitance,high redox activity,low cost,and eco-friendliness.In this study,novel three-dimensional (3D) interspersed flower-like nickel hydroxide was assembled under mild conditions.When ammonia was used as the precipitant and inhibitor and CTAB was used as an exfoliation agent,the obtained exfoliated ultrathin Ni(OH)2 nanosheets were assembled into 3D interspersed flower-like nickel hydroxide.In this novel 3D structure,the ultrathin Ni(OH)2 nanosheets not only provided a large contact area with the electrolyte,reducing the polarization of the electrochemical reaction and providing more active sites,but also reduced the concentration polarization in the electrode solution interface.Consequently,the utilization efficiency of the active material was improved,yielding a high capacitance.The electrochemical performance was improved via promoting the electrical conductivity by mixing the as-synthesized Ni(OH)2 with carbon tubes (N-4-CNT electrode),yielding excellent specific capacitances of 2,225.1 F·g-1 at 0.5 A·g-1 in a three-electrode system and 722.0 F·g-1 at 0.2 A·g-1 in a two-electrode system.The N-4-CNT//active carbon (AC) device exhibited long-term cycling performance (capacitance-retention ratio of 111.4％ after 10,000 cycles at 5 A·g-1) and a high specific capacitance of 180.5 F·g-1 with a high energy density of 33.5 W·h·kg-1 and a power density of 2,251.6 W·kg-1.     

Preparation of Ceramic Composite Pipes Through Paste Extrusion

An experimental investigation was carried out in order to prepare ceramic composite pipes used for tubular solid oxide fuel cells by using a multi-billet extrusion technique. Particular emphasis was given to the forming possibility and extrusion behavior of a two-layer pipe consisting of NiO-YSZ(PSZ) (anode) and YSZ (electrolyte). It is shown that the extrusion pressure and binder content required decrease with increasing the fraction of nickel oxide in the anode layers. The porosity in the anode layers depends on the binder content in pastes. It is feasible to prepare anode/electrolyte composite pipes by means of co-extrusion of different pastes.Furthermore, it is possible to obtain sound sintered pipes even under pressureless sintering conditions.     

Thermal Stability of Amorphous Hydride Mg_(50)Ni_(50)H_(54) and Mg_(30)Ni_(70)H_(45)

The thermal stability of amorphous ternary hydrides Mg_(50)Ni_(50)H_(54) and Mg_(30)Ni_(70)H_(45) and their corre-sponding amorphous binary alloys Mg_(50)Ni_(50) and Mg_(30)Ni_(70) were studied with X-ray diffraction(XRD) and differential scanning calorimetry(DSC). Samples of the amorphous alloys were preparedby mechanical alloying and the amorphous hydrides were obtained by charging the alloys with gas-eous hydrogen at 3.0 MPa and 423 K. It was found that the amorphous hydrides released most oftheir hydrogen before the crystallization of the essentially hydrogen depleted amorphous alloy. Thecrystallization temperature of amorphous Mg_(50)Ni_(50)H_(54) elevated and that of amorphousMg_(30)Ni_(70)H_(45) did not change in relation to the original binary amorphous alloy. This is very excep-tional for amorphous hydrides. The reason for the effects of hydrogen absorption/desorption on thecrystallization of amorphous alloys was discussed.     

A Novel Method to Improve the Electrochemical Performance of LiMn_2O_4 Cathode Active Material by CaCO_3 Surface Coating

Spinel LiMn2O4 was synthesized by glycine-nitrate method and coated with CaCO3 in order to enhance the electrochemical performance at room temperature (250C) and 550C. The uncoated and CaCO3-coated LiMn2O4 materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrochemical tests. XRD and SEM results indicated that CaCO3 particles encapsulated the surface of the LiMn2O4 without causing any structural change. The charge-discharge tests showed that the specific discharge capacity fade of pristine electrode at 25 and 550C were 25.5% and 52%, respectively. However, surface modified cathode shows 7.4% and 29.5% loss compared to initial specific discharge capacity at 70th cycle for 25 and 550C, respectively. The improvement of electrochemical performance is attributed to suppression of Mn2+ dissolution into electrolyte via CaCO3 layer.     

H2O/CO2 co-electrolysis in solid oxide electrolysis cells

A solid oxide electrolysis cell (SOEC) is an environmental-friendly device which can convert electric energy into chemical energy with high efficiency. In this paper,the progress on structure and operational principle of an SOEC for co-electrolyzing H2O and CO2 to generate syngas was reviewed. The recent development of high temperature H2O/CO2 co-electrolysis from solid oxide single electrolysis cell was introduced. Also investigated was H2O/CO2 co-electrolysis research using hydrogen electrode-supported nickel (Ni)-yttria-stabilized zirconia (YSZ)/YSZ/Sr-doped LaMnO3 (LSM)-YSZ cells in our group. With 50 % H2O,15.6 % H2 and 34.4 % CO2 inlet gas to Ni-YSZ electrode,polarization curves (I-U curves) and electrochemical impedance spectra (EIS) were measured at 800 ℃ and 900 ℃. Long-term durability of electrolysis was carried out with the same inlet gas at 900 ℃ and 0.2 A/cm2. In addition,the improvement of structure and development of novel materials for increasing the electrolysis efficiency of SOECs were put forward as well.     

Sodium Activity in Molten Aluminum Measured with a Solid Electrolyte

The sodium activities in aluminium in equilibrium with cryolite-alumina melt and during electrolysiswere determined by EMF with Naβ-Al_2O_3 solid electrolyte.With this sodium activities,we calculatethe activities of NaF and AIF_3 in the cryolite-alumina melt.The potential difference of discharge be-tween sodium ions and aluminum ions at cathode of Hall-Heroult cell was also obtained from thesodium activity in aluminum.     

Tungsten Doped Indium Oxide Thin Films Deposited at Room Temperature by Radio Frequency Magnetron Sputtering

Tungsten doped indium oxide(IWO) thin films were deposited on glass substrate at room temperature by radio frequency reactive magnetron sputtering.Chemical states analysis was carried out,indicating that valence states of element W in the films were W~(4+) and W~(6+).The effects of sputtering power and film thickness on the surface morphology,optical and electrical properties of IWO thin films were investigated.The IWO thin films had high transmittance in near infrared(NIR) spectral range.The resistivity,carrier mobility and carrier concentration owned their respective optimum values as sputtering power and thickness changed.The asdeposited IWO film with the minimum resistivity of 3.23 × 10~(-4) Ω cm was obtained at a sputtering power of50 W,with carrier mobility of 27.1 cm~2 V~(-1) s~(-1),carrier concentration of 7.15 × 10~(20) cm~(-3),average transmittance about 80%in visible region and above 75%in NIR region.It may meet the application requirement of high conductivity and transparency in NIR wavelength region.     

Modification of NiCoCrAlY with Pt: Part Ⅱ. Application in TBC with pure metastable tetragonal(t’) phase YSZ and thermal cycling behavior

A thermal barrier coating system comprising Pt-modified NiCoCrAlY bond coating and nanostructured 4mol.% yttria stabilized zirconia(4YSZ, hereafter) top coat was fabricated on a second generation Ni-base superalloy. Thermal cycling behavior of NiCoCrAlY-4 YSZ thermal barrier coatings(TBCs) with and without Pt modification was evaluated in ambient air at 1100?C up to 1000 cycles, aiming to investigate the effect of Pt on formation of thermally grown oxide(TGO) and oxidation resistance. Results indicated that a dual layered TGO, which consisted of top(Ni,Co)(Cr,Al)_2O_4 spinel and underlying α-Al_2O_3, was formed at the NiCoCrAlY/4 YSZ interface with thickness of 8.4μm, accompanying with visible cracks at the interface. In contrast, a single-layer and adherent α-Al_2O_3 scale with thickness of 5.6μm was formed at the interface of Pt-modified NiCoCrAlY and 4 YSZ top coating. The modification of Pt on NiCoCrAlY favored the exclusive formation of α-Al_2O_3 and the reduction of TGO growth rate, and thus could effectively improve overall oxidation performance and extend service life of TBCs. Oxidation and degradation mechanisms of the TBCs with/without Pt-modification were discussed.     

New Developed Welding Electrode for Improving the Fatigue Strength of Welded Joints

A new welding electrode, low transformation temperature electrode (LTTE), was introduced in this paper. It was described in design principle, mechanics, chemical compositions of their deposited metal and manufacturing methods. It was proved that the best transformation starting temperature from austenite to martensite of the deposited metal of LTTE was at about 191℃ and it was obtained by adding alloying elements such as Cr, Ni, Mn and Mo. The microstructure of the weld metal of the LTTE was low carbon martensite and residual austenite. The compressive residual stress was induced around the weld of the LTTE and the -145 MPa in compression could be obtained in middle of weld metal. The fatigue tests showed that the fatigue strength of the longitudinal welded joints welded with the LTTE at 2×106 cycles was improved by 59% compared with that of the same type of welded joints welded with conventional E5015 and the fatigue life was increased by 47 times at 162 MPa. It is a very valuable method to improve th     

国家能源太阳能发电研发(实验)中心（英文）

正Introduction Approved by NEA,the National Solar Energy Center(the Center for short)was established in 2009,serving as the world’s first solar energy generation research and test center at the national level.The center is designed with the capabilities of solar power generation integration research,grid integration test of key components,and on-site test of photovoltaic power plants.     

Investigation on the Tribology of Co Implanted Stainless Steel Using Metal Vapor Vacuum Arc Ion Source

AISI 304 stainless steel was ion implanted with Co, and the tribological property on the surface of the stainless steelwas investigated. The Co ion implantation was carried out using a metal vapor vacuum arc (Mevva) broad-beam ionsource with an extraction voltage of 40 kV, implantation doses of 3×10~(17)/cm~2 and 5×10~(17)/cm~2, and ion currentdensities of 13, 22 and 32μA/cm~2. The results showed that the near-surface hardness of Co-implanted stainless steelsample was increased by 50% or more, and it increased with increasing ion current density at first and then declined.The friction coefficient decreased from 0.74 to 0.20 after Co implantation. The wear rate after Co implantationreduced by 25% or more as compared to the unimplanted sample. The wear rate initially decreased with increasingion current density and then an increase was observed. Within the range of experimental parameters, there existsa critical ion current density for the Co-implanted stainless steel, at which the wear rate decreased     

Stabilising Cobalt Sulphide Nanocapsules with Nitrogen-Doped Carbon for High-Performance Sodium-Ion Storage

Conversion-type anode materials with a high charge storage capability generally su er from large volume expansion, poor electron conductivity, and sluggish metal ion transport kinetics. The electrode material described in this paper, namely cobalt sulphide nanoparticles encapsulated in carbon cages(Co9S8@NC), can circumvent these problems. This electrode material exhibited a reversible sodium-ion storage capacity of 705 mAh g^-1 at 100 mA g^-1 with an extraordinary rate capability and good cycling stability. Mechanistic study using the in situ transmission electron microscope technique revealed that the volumetric expansion of the Co9S8 nanoparticles is bu ered by the carbon cages, enabling a stable electrode–electrolyte interface. In addition, the carbon shell with high-content doped nitrogen significantly enhances the electron conductivity of the Co9S8@NC electrode material and provides doping-induced active sites to accommodate sodium ions. By integrating the Co9S8@NC as negative electrode with a cellulose-derived porous hard carbon/graphene oxide composite as positive electrode and 1 M NaPF6 in diglyme as the electrolyte, the sodium-ion capacitor full cell can achieve energy densities of 101.4 and 45.8 Wh kg^-1 at power densities of 200 and 10,000 W kg^-1, respectively.