Catalytic and Electrochemical Properties of Doped Lanthanum Chromites as New Anode Materials for Solid Oxide Fuel Cells

Defective perovskites contained in the general formula La(Sr)Cr(Ru,Mn)O_3–δ are successfully synthesized by spray pyrolysis. Powders of high phase purity are obtained after annealing, and they are used to prepare homogeneous films by spray printing. From a catalytic point of view for the methane steam reforming, these powdered perovskites do not generate a carbon deposit. Catalytic results, focused on doped ruthenium perovskites, confirm that the insertion of ruthenium in the structure of the lanthanum chromite presents a real benefit for the methane steam reforming. The electrochemical properties of La(Sr)CrO_3–δ, either pure and doped with manganese, show that the perovskite films can be potential electrodes, depending on their doping, for hydrogen anodic oxidation in solid oxide fuel cells.     

Recent Advances in Counter Electrodes for Thiolate-mediated Dye-sensitized Solar Cells

Dye-sensitized solar cells (DSSCs) based on disulfide/thiolate (T₂/T⁻) redox couples have attracted remarkable attention due to their high efficiency and low cost. As an indispensible part of DSSCs, counter electrode (CE) design plays a crucial role in high efficiency DSSCs. This mini-review paper selectively reviews the recent advances in T-mediated DSSCs using novel CE (namely cathode) materials, mainly including noble metal platinum (Pt), carbon materials, transition metal compounds (TMCs), polymers, and hybrids, thus highlighting the merits and demerits of alternative Pt catalysts, and the prospects and challenges of Pt-free CEs for the development of high-performance and low-cost DSSCs.     

Optical,electrochemical, and photovoltaic properties of conjugated polymers with dithiafulvalene as side chains

Three conjugated polymers, P1–P3, with dithiafulvalene (DTF) as side chains have been synthesized. All polymers have good thermal stabilities. The DTF unit could be oxidized to DTF?⁺ which was observed from cyclic voltammetry and ultraviolet–visible (UV–vis) spectra, and the oxidation process was independent of the conjugated backbone of the polymer. The strong π–π* transition absorbing band of the three polymers decreases gradually as increasing oxidation, and the resulting DTF?⁺ species give rise to an additional band at 750–1100 nm, which can be assigned to a distinguishing feature of the cation radical species. Photovoltaic device based on the blend of P2 and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PC₆₁BM) showed the power conversion efficiency of 1.05% with a fill factor of 42.8%. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41508.     

Fullerene-like Re-Doped MoS2 Nanoparticles as an Intercalation Host with Fast Kinetics for Sodium Ion Batteries

Sodium ion batteries (SIBs) are considered as a promising alternative to threaten the reign of lithium ion batteries (LIBs) among various next-generation rechargeable energy storage systems, including magnesium ion, metal air, and metal sulfur batteries. Since both sodium and lithium are located in Group 1 of the periodic table, they share similar (electro)chemical properties with regard to ionization pattern, electronegativity, and electronic configuration; thus the vast number of compounds developed from LIBs can provide guidance to design electrode materials for SIBs. However, the larger ionic radius of the sodium cation and unique (de)sodiation processes may also lead to uncertainties in terms of thermodynamic or kinetic properties. Herein, we present the first construction of SIBs based on inorganic fullerene-like (IF) MoS₂ nanoparticles. Closed-shell-type structures, represented by C₆₀ fullerene, have largely been neglected for studies of alkali-metal hosting materials due to their inaccessibility for intercalating ions into the inner spaces. However, IF-MoS₂, with faceted surfaces, can diffuse sodium ions through the defective channels, thereby allowing reversible sodium ion intercalation/deintercalation. Interestingly, Re-doped MoS₂ showed good electrochemical performances with fast kinetics (ca. 74 mA h g⁻¹ at 20 C). N-type doping caused by Re substitution of Mo in IF-MoS₂ revealed enhanced electrical conductivity and an increased number of diffusion defect sites. Thus, chemical modification of fullerene-like structures through doping is proven to be a promising synthetic strategy to prepare improved electrodes.     

煤层气发电高温NO_x烟气SCR处理技术及其应用

煤层气发电是煤层气利用的重要途径之一,但煤层气发电排放的高温尾气中含有大量的氮氧化物(NO_x),会对环境造成污染,需要对其进行脱硝处理,而高温烟气(约500℃)又不宜用V_2O_5/TiO_2蜂窝式催化剂进行直接脱硝处理。为此,在分析比较煤层气发电高温烟气与燃煤发电烟气差别的基础上,应用纳米组装和灌注法研制了GJ-HC-5型催化剂,并通过室内实验确定了脱除NO_x的最佳温度窗口(400~600℃)。之后,在某煤层气电厂进行中间试验,将发电机组高温烟气直接通入到SCR一体化装置进行脱硝处理,在SCR反应器进出口处连续监测,进口NO_x浓度约为620 mg/m~3,出口监测浓度约为20 mg/m~3,对烟气中的NO_x的脱除率始终保持在90%以上。试验结果表明,所研制的高温SCR催化剂符合实际烟气温度条件,且制备方法简单,是一种可行的煤层气发电高温烟气的脱硝方法。     

Capacitor Applications of Nanocomposite Films for Poly(3,4-ethylenedioxythiophene-co-pyrrole)/Multi-Walled Carbon Nanotubes and Poly(3,4-ethylenedioxythiophene-co-pyrrole)/Copper Oxide

Polypyrrole/multi-walled carbon nanotube, poly(3,4-ethylenedioxythiophene)/multi-walled carbon nanotube and their nanocomposites P(EDOT-co-Py)/multi-walled carbon nanotube and P(EDOT-co-Py)/copper (II) oxide, (CuO) in the initial feed ratio of [EDOT]₀/[Py]₀ = 1/5 were electrosynthesized on glassy carbon electrode by cyclic voltammetric method. Their characterizations were performed by cyclic voltammetric, Fourier transform infrared-attenuated total reflectance, scanning electron microscopy, energy dispersion X-ray analysis, and electrochemical impedance spectroscopy. To the best of authors’ knowledge, the first report on polypyrrole/multi-walled carbon nanotube, PEDOT/multi-walled carbon nanotube, P(EDOT-co-Py)/multi-walled carbon nanotube and P(EDOT-co-Py)/CuO nanocomposite films were comparatively examined in 0.1 M NaClO₄/CH₃CN and in 0.1 M sodium dodecyl sulfate solutions. The highest specific capacitance for PEDOT/multi-walled carbon nanotube and polypyrrole/multi-walled carbon nanotube composite films were obtained as C_sp = 306 mF × cm^?2 for 3% multi-walled carbon nanotube and C_sp = 804 mF × cm^?2 for 1% multi-walled carbon nanotube, respectively. The highest specific capacitances were obtained as C_sp = 27.40 mF × cm^?2 and C_sp = 26.90 mF × cm^?2 for P(EDOT-co-Py)/multi-walled carbon nanotube includes the wt percent of 1% multi-walled carbon nanotube and P(EDOT-co-Py)/CuO includes the wt percent of 3% CuO, respectively. The C_sp of P(EDOT-co-Py)/CNT composite films were calculated as 9.43 and 11.49 mF × cm^?2 for 3 and 5% multi-walled carbon nanotube, respectively. In addition, The EIS results were simulated with the equivalent circuit model of R_s(C_dl1(R₁(QR₂)))(C_dl2R₃).     

Laccase‐catalyzed synthesis of polypyrrole‐multiwalled carbon nanotube composites as energy storage materials for capacitors

Multiwalled carbon nanotubes (MWNTs) were coated with polypyrrole (PPy) using in situ enzymatic polymerization of pyrrole catalyzed by a laccase (benzenediol:oxygen oxidoreductase, EC 1.10.3.2) from Trametes versicolor. Transmission electron microscopy revealed that the MWNTs were uniformly coated with very thin layers of PPy without any indication of globular polymer aggregate formations. The enzymatic synthesis of the MWNTs/PPy composites was quite simple being performed in a one‐pot aqueous solution (pH 4.0) under mild reaction conditions. The potential of the composites with respect to the development of energy storage devices was demonstrated by fabricating a two‐electrode coin cell capacitor (diameter 20 mm, thickness 1.6 mm) utilizing the composites as electrode materials. The capacitance of the cell was 28.0 F g^?1 for the electrode material as measured by a galvanostatic charge–discharge method. The energy density and power density were 2.55 and 805 W kg^?1, respectively, which were close to those of the capacitors classified as ultracapacitors. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43307.     

Structure,thermal stability,electrochemical behaviors,and mechanical properties of organosoluble polyimide with pyrimidine ring in the main chain

A novel organosoluble polyimide (PI) with pyrimidine ring in the main chain was synthesized by chemical and thermal imidization, respectively, from 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride and 2,4‐diamino‐6‐chloropyrimidine as raw materials and its molecular structure, solubility, UV–visible absorption characteristic, crystallinity, thermal stability, electrochemical behaviors, and mechanical properties were also studied. It was found that the introduction of pyrimidine ring in the main chain could increase the solubility of PI in polar aprotic solvents at room temperature and 60 °C, respectively, because of its molecular main chain with asymmetric structure and two polar N atoms in pyrimidine ring. Furthermore, PI had strong optical absorption peak intensity, excellent thermal stability, good redox reversibility, especially outstanding mechanical properties, which were conductive to its potential applications in adhesives, polyelectrolyte, separation membrane, and so on. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43680.