AlCl<Subscript>3</Subscript>/amide ionic liquids for electrodeposition of aluminum

AlCl₃/amide (acetamide, propionamide, butyramide) ionic liquids were used as the electrolytes to study the electrodeposition behavior of aluminum on a tungsten electrode. Cyclic voltammograms on the tungsten electrode indicate that Al(III) ions can be reduced to aluminum only within the molar ratio range of 1.1 to 1.5 and the reduction potentials of Al(III) ions strongly depend on the molar ratio of AlCl₃/amide. Raman spectra results reveal that the electroactive specie of AlCl₃/amide ionic liquids is Al₂Cl₇ ^?. Aluminum coatings were prepared at ?0.25 V (vs. Al/Al³⁺) and at 313 K in AlCl₃/amide ionic liquids with the molar ratio of 1.3. The SEM and cross-sectional SEM images show that all the obtained aluminum films are silver-colored, thick, and adherent. The EDS and XRD analysis confirm that the obtained deposits are pure aluminum. The present results can provide a new route for aluminum electrodeposition under ambient conditions.     

Understanding the accumulated cycle capacity fade caused by the secondary particle fracture of LiNi<Subscript>1-x-y</Subscript>Co<Subscript>x</Subscript>Mn<Subscript>y</Subscript>O<Subscript>2</Subscript> cathode for lithium ion batteries

Effect of secondary particle fracture on the accumulated cycle capacity fade of LiNi_1-x-yCo_xMn_yO₂ cathode is difficult to evaluate since performance degradation of electrode material is always caused by several factors simultaneously. Herein, LiNi_0.5Co_0.2Mn_0.3O₂ single particles (Sin-P) are prepared and introduced as a reference to understand the accumulated cycle capacity fade caused by the secondary particle fracture of LiNi_0.5Co_0.2Mn_0.3O₂ secondary particles (Sec-P). Sec-P exhibited accumulated cycle capacity fade compared to Sin-P when cycled at high rate, high voltage, and high temperature. The accumulated cycle capacity fade was mainly caused by the secondary particle fracture of Sec-P, which was confirmed by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscope (SEM) analysis. Further, XPS and electrochemical impedance spectroscopy (EIS) analysis indicated that the surface property changes and resistance rise were responsible for the accumulated cycle capacity fade. The study provides a novel way to analyze the accumulated cycle capacity fade caused by the secondary particle fracture and is helpful for understanding the performance degradation mechanism of electrode material.     

Ultra-high surface area and mesoporous N-doped carbon derived from sheep bones with high electrocatalytic performance toward the oxygen reduction reaction

A nitrogen (N)-doped mesoporous carbon material exhibiting ultra-high surface area was successfully synthesized from sheep bones via a facile and low-cost method. The obtained carbon material had an ultra-high specific surface area of 1961 m² g^?1 and provided rich active sites for the oxygen reduction reaction (ORR), which in turn resulted in high electrocatalytic activity. It was found that the pore size distribution for the newly prepared carbonaceous material fell in the range of 1–4 nm. Benefiting from its high surface area and the presence of pyridine-N and quaternary-N species, the as-prepared carbon material exhibited excellent ORR activity in an oxygen-saturated 0.1 M KOH solution, compared to commercial Pt/C (10 wt%). Due to its high ORR catalytic activity, stability and low-cost, using sheep bone as C and N precursors to produce N-doped carbon provides an encouraging step toward the goal of replacing commercial Pt/C as fuel cell cathode electrocatalyst.     

Na3V2(PO4)3/C nanofiber bifunction as anode and cathode materials for sodium-ion batteries

Journal of Solid State Electrochemistry - Na3V2(PO4)3/C composite nanofibers are prepared successfully through a coaxial electrospinning technique and subsequent calcination. The diameter of the...     

Tea-leaves based nitrogen-doped porous carbons for high-performance supercapacitors electrode

Journal of Solid State Electrochemistry - Nitrogen-doped porous activated carbons have been fabricated through a simple and efficient carbonization method at 700&nbsp;°C with the waste...     

Trapping a Silicon(I) Radical with Carbenes: A Cationic cAAC–Silicon(I) Radical and an NHC–Parent-Silyliumylidene Cation

The trapping of a silicon(I) radical with N-heterocyclic carbenes is described. The reaction of the cyclic (alkyl)(amino) carbene [cAAC_Me] (cAAC_Me=:C(CMe₂)₂(CH₂)NAr, Ar=2,6-iPr₂C₆H₃) with H₂SiI₂ in a 3:1 molar ratio in DME afforded a mixture of the separated ion pair [(cAAC_Me)₂Si:^.]⁺I⁻ ( 1 ), which features a cationic cAAC–silicon(I) radical, and [cAAC_Me−H]⁺I⁻. In addition, the reaction of the NHC–iodosilicon(I) dimer [I_Ar(I)Si:]₂ (I_Ar=:C{N(Ar)CH}₂) with 4 equiv of I_Me (:C{N(Me)CMe}₂), which proceeded through the formation of a silicon(I) radical intermediate, afforded [(I_Me)₂SiH]⁺I⁻ ( 2 ) comprising the first NHC–parent-silyliumylidene cation. Its further reaction with fluorobenzene afforded the C_Ar−H bond activation product [1-F-2-I_Me-C₆H₄]⁺I⁻ ( 3 ). The isolation of 2 and 3 confirmed the reaction mechanism for the formation of 1 . Compounds 1 – 3 were analyzed by EPR and NMR spectroscopy, DFT calculations, and X-ray crystallography.     

Phase-Selective Syntheses of Cobalt Telluride Nanofleeces for Efficient Oxygen Evolution Catalysts

Cobalt-based nanomaterials have been intensively explored as promising noble-metal-free oxygen evolution reaction (OER) electrocatalysts. Herein, we report phase-selective syntheses of novel hierarchical CoTe₂ and CoTe nanofleeces for efficient OER catalysts. The CoTe₂ nanofleeces exhibited excellent electrocatalytic activity and stablity for OER in alkaline media. The CoTe₂ catalyst exhibited superior OER activity compared to the CoTe catalyst, which is comparable to the state-of-the-art RuO₂ catalyst. Density functional theory calculations showed that the binding strength and lateral interaction of the reaction intermediates on CoTe₂ and CoTe are essential for determining the overpotential required under different conditions. This study provides valuable insights for the rational design of noble-metal-free OER catalysts with high performance and low cost by use of Co-based chalcogenides.     

Absolute Minimal Sampling of Homonuclear 2D NMR TOCSY Spectra for High-Throughput Applications of Complex Mixtures

Modern applications of 2D NMR spectroscopy to diagnostic screening, metabolomics, quality control, and other high-throughput applications are often limited by the time-consuming sampling requirements along the indirect time domain t₁. 2D total correlation spectroscopy (TOCSY) provides unique spin connectivity information for the analysis of a large number of compounds in complex mixtures, but standard methods typically require >100 t₁ increments for an accurate spectral reconstruction, rendering these experiments ineffective for high-throughput applications. For a complex metabolite mixture it is demonstrated that absolute minimal sampling (AMS), based on direct fitting of resonance frequencies and amplitudes in the time domain, yields an accurate spectral reconstruction of TOCSY spectra using as few as 16 t₁ points. This permits the rapid collection of homonuclear 2D NMR experiments at high resolution with measurement times that previously were only the realm of 1D experiments.     

Thioether‐derived Macrocycle for Peptide Secondary Structure Fixation

Recently, we developed methods to stabilize peptides into various secondary structures, including α‐helix, type III turn and β‐hairpin via proper thioether based macrocyclization. These conformationally constrained peptidomimetics confer enhanced biophysical properties and provide a valuable avenue towards clinically‐relevant therapeutic molecules. In this personal account, thioether‐derived macrocyclization methods developed by our group for stabilization of α‐helix, type‐III β turn and β‐hairpin conformations are discussed.     

Ruthenium‐Catalyzed Metathesis Cascade Reactions in Natural Products Synthesis

In this account, we provide a brief summary of recent developments in ruthenium‐catalyzed metathesis cascade reactions towards the total synthesis of natural products. We also highlight recent progress from our own laboratory regarding the synthesis of securinega alkaloids and humulanolides, which has resulted in the development of novel ruthenium‐catalyzed metathesis cascade reactions. Inspired and guided by the pioneering and elegant research conducted in this area, we developed a regio‐controlled relay dienyne metathesis cascade reaction and a cyclobutene‐promoted RCM/ROM/RCM cascade reaction for the synthesis of securinega alkaloids and humulanolides, respectively.