The high-efficiency coupling of a Ni2+ coordinated/uncoordinated pyridine N-COF self-supporting nanofilm as an asymmetric supercapacitor.

A large-area COFTAPB-BPY film with a pore size of 3.9 nm was prepared on a gas-liquid interface by the virtue of the limiting and guiding functions of sodium dodecylbenzene sulfonate, followed by modification by Ni2+ ions with the reversible redox reaction of Ni(II/III), where Ni2+ was evidently anchored on the N in BPY. The obtained COFTAPB-BPY and Ni-COFTAPB-BPY nanofilms could avoid the inevitable aggregation and stacking of bulk COFTAPB-BPY, which facilitated a high specific capacitance of 0.26 mF cm-2 for the COFTAPB-BPY nanofilm and 0.38 mF cm-2 for the Ni-COFTAPB-BPY nanofilm at 0.001 mA cm-2. Considering the pseudocapacitance and double-layer capacitance traits of Ni-COFTAPB-BPY and COFTAPB-BPY nanofilms, the asymmetric Ni-COFTAPB-BPY//COFTAPB-BPY film supercapacitor was assembled with a symmetric COFTAPB-BPY//COFTAPB-BPY film device as a control. The asymmetric Ni-COFTAPB-BPY//COFTAPB-BPY film supercapacitor could enhance the energy density of 273.9 mW h cm-3 at 14.09 W cm-3 from 85.2 mW h cm-3 at 4.38 W cm-3 for the symmetric COFTAPB-BPY//COFTAPB-BPY film device. This work provides a new perspective on the application of self-supporting COF nanofilms as film asymmetric supercapacitors.

Two Birds with One Stone: Micro/Nanostructured SiOx Cy Composites for Stable Li-Ion and Li Metal Anodes.

Developing stable silicon-based and lithium metal anodes still faces many challenges. Designing new highly practical silicon-based anodes with low-volume expansion and high electrical conductivity, and inhibiting lithium dendrite growth are avenues for developing silicon-based and lithium metal anodes, respectively. In this study, SiOx Cy microtubes are synthesized using a chemical vapor deposition method. As Li-ion battery anodes, the as-prepared SiOx Cy not only combines the advantages of nanomaterials and the practical properties of micromaterials, but also exhibits high initial Coulombic efficiency (80.3%), low volume fluctuations (20.4%), and high cyclability (98% capacity retention after 1000 cycles). Furthermore, SiOx Cy , as a lithium deposition substrate, can effectively promote the uniform deposition of metallic lithium. As a result, low nucleation overpotential (only 6.0 mV) and high Coulombic efficiency (≈98.9% after 650 cycles, 1.0 mA cm-2 and 1.0 mAh cm-2 ) are obtained on half cells, as well as small voltage hysteresis (only 9.5 mV, at 1.0 mA cm-2 ) on symmetric cells based on SiOx Cy . Full batteries based on both SiOx Cy and SiOx Cy @Li anodes demonstrate great practicality. This work provides a new perspective for the simultaneous development of practical SiOx Cy and dendrite-free lithium metal anodes.

SiOxCy Microspheres with Homogeneous Atom Distribution for a High-Performance Li-Ion Battery.

The broad application of silicon-based materials is limited by large volume fluctuation, high preparation costs, and complicated preparation processes. Here, we synthesized SiOxCy microspheres on 3D copper foams by a simple chemical vapor deposition method using a low-cost silane coupling agent (KH560) as precursors. The SiOxCy microspheres are available with a large mass loading (>3 mg/cm2) on collectors and can be directly used as the electrode without any binders or extra conductive agents. As a result, the as-prepared SiOxCy shows a high reversible capacity of ∼1240 mAh g-1 and can be cycled more than 1900 times without decay. Ex situ characterizations show that the volume change of the microspheres is only 55% and the spherical morphology as well as the 3D structure remain intact after cycles. Full-cell electrochemical tests paired with LiFePO4 as cathodes show 87% capacity retention after 500 cycles, better than most reported results, thus showing the commercial potential of the material.

Practical and Sustainable Modification Method on Activated Carbon to Improve the Decolorization Process in the Acetaminophen Pharmaceutical Industry.

Decolorization plays an important part in the industrial production of acetaminophen (APAP) drugs. The impurities generated from the APAP pharmaceutical industry decolorization refining process were primarily separated and purified, and their structures were determined by MS and 1H NMR technology. Then the catalytic effects of three samples of modified powdered activated carbon (PAC) on APAP in heterogeneous solution systems and the adsorption catalysis system were systematically investigated, which indicated that PAC catalyzed the APAP oxidative coupling side reaction and thus increased the impurities in the APAP product. The M-T-RAC (thermal regeneration PAC modified by ammonium sulfate) possessing more acidic surface groups can effectively inhibit this side reaction. Furthermore, according to the different catalytic results of O-T-RAC (thermal regeneration PAC modified by hydrogen peroxide) in solid-liquid catalytic and adsorption catalytic systems, we speculated that the multimer impurities were generated by the oxidative coupling reaction of APAP being oxidized to rated N-acetyl-p-benzoquinone (NAPQI) during decolorization, while free radical polymerization of APAP mainly occurred in the pores of the spent PAC. The pore textural structure and chemical properties of M-T-RAC were further characterized to ensure its feasibility of industrial application. The process of simulating industrial decolorization substantiated the excellent ability of M-T-RAC to inhibit side reactions. This study contributes to the development of green materials for sustainable recycling of activated carbon to reduce pollution and costs, and provides an effective advice for the pharmaceutical process.

Influence of Acid Treatment on the Loading and Release Behavior of Halloysite with 2-Mercaptobenzothiazole.

Halloysite nanotubes (HNTs) are natural clay minerals with a tubular structure. They have attracted considerable attention as a potential nanocontainer due to their abundance, biocompatibility and nontoxicity. In this study, HNTs were handled with H2SO4 at 70 °C. The morphology and structure of these acid-treated and original HNTs were investigated by scanning electron microscopy (SEM), energy dispersion spectrum (EDS), transmission electron microscope (TEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR), and their specific surface area was determined by automatic gas adsorption analyzer. The loading efficiency and release behavior of acid-treated HNTs for 2-Mercaptobenzothiazole (MBT) were investigated by UV-vis spectrophotometer. Results show that acid-treated HNTs retained their tubular structure, but their internal diameter expanded by 35-37 nm after 32 h of acid treatment. After 72 h of acid treatment, HNTs can be transferred into amorphous silica nanotubes. Moreover, the specific surface area of these HNTs samples initially increased with the increase in acid treatment time but then started to decrease after 32 h. The specific surface area of acid-treated HNTs at 32 h can reach 251.6 m2/g, which was much higher than that for untreated HNTs (55.3 m2/g). In addition, the loading capacity of acid-treated HNTs can reach 32.1% for HNTs-32, which is about three times higher than that of original HNTs. The acid treatment has slight effect on the release behavior.

Corrosion behavior of X65 steel in seawater containing sulfate reducing bacteria under aerobic conditions.

The corrosion behavior of X65 steel was investigated in the seawater inoculated with sulfate reducing bacteria (SRB) under the aerobic environment by electrochemical impedance techniques and immersion tests. The corroded morphologies and the composition of the corrosion products were investigated. The variation of the solution parameters including the bacterium number, the pH value and the soluble iron concentration were also investigated. The results indicated that in the SRB-containing system, the impedance responses presented a depressed semi-circle in the initial period, which then turned into the blocked electrode characteristic during the later immersion. The biofilm, mainly composed of extracellular polymeric substances, Fe(OH)3, γ-FeOOH and α-Fe2O3, formed and degraded with the SRB growth. The soluble iron concentration initially increased, then rapidly decreased and later slowly increased. In the SRB-containing seawater under the aerobic environment, the X65 steel was corroded in the initial immersion. The corrosion became inhibited with the forming of the biofilm during the subsequent immersion. The inhibition efficiency rapidly increased in the logarithmic phase, remained stable in the stationary phase and then decreased in the declination phase. In the corrosion process, the biofilm metabolized by SRB played a key role in the corrosion inhibition of X65 steel.