Synergy ascension of SnS/MoS2 binary metal sulfides on initial coulombic efficiency and stable capacity for lithium storage.

Numerous efforts have been devoted to capability improvement and cycling stability in the past decades, and these performances have been significantly enhanced. Low initial coulombic efficiency is still a problem in the metal sulfide-based anode materials. This study developed a strategy to achieve high initial coulombic efficiency and superior capacity retention by interpenetrating binary metal sulfides of SnS and MoS2 in a conductive carbon matrix. The synergy ascension of electrochemical performances for the metal sulfides is attributed to their mutual impeding effects on coarsening of metal grains and the capsule-shaped coating structure embedded in the carbon sheet architecture. The SnS/MoS2/C composite was prepared by a simple NaCl template-assisted ball milling method, and showed excellent electrochemical performances in terms of a high initial coulombic efficiency up to 90.2% and highly stable reversibility with a specific capacity of 515.4 mA h g-1 after 300 cycles at 1.0 A g-1. All of these characteristics suggest that the proposed materials are superior among the previously reported metal sulfide-based anode materials for lithium-ion batteries.

A sensitive surface-enhanced Raman scattering method for chondroitin sulfate with Victoria blue 4R molecular probes in nanogold sol substrate.

Using silver nanoparticles (AgNPs) as the nanocatalyst, l-cysteine rapidly reduced HAuCl4 to make a stable gold nanoparticle sol (Ag/AuNP) that had a high surface-enhanced Raman scattering (SERS) activity in the presence of Victoria blue 4R (VB4r) molecular probes. Under the selected conditions, chondroitin sulfate (Chs) reacted with the VB4r probes to form associated complexes that caused the SERS effect to decrease to 1618 cm-1 . The decreased SERS intensity was linear to the Chs concentration in the range 3.1-500 ng/ml, with a detection limit of 1.0 ng/ml Chs. Accordingly, we established a simple and sensitive SERS quantitative analysis method to determine Chs in real samples, with a relative standard deviation of 1.47-3.16% and a recovery rate of 97.6-104.2%.

Resonance scattering spectral detection of trace Hg2+ using aptamer-modified nanogold as probe and nanocatalyst.

Single-strand DNA (ssDNA) was used to modify 10 nm nanogold to obtain an aptamer-modified nanogold resonance scattering (RS) probe (AussDNA) for detection of Hg(2+). In the presence of NaCl, Hg(2+) interacts with AussDNA to form very stable double-strand T-Hg(2+)-T mismatches and release nanogold particles that aggregate to large nanogold clusters causing the RS intensity at 540 nm to be enhanced linearly. On those grounds, 1.3-1667 nM Hg(2+) can be detected rapidly by the aptamer-modified nanogold RS assay, with a detection limit of 0.7 nM Hg(2+). If the large nanogold clusters were removed by membrane filtration, the excess AussDNA in the filtrate solution exhibits a catalytic effect on the new Cu(2)O particle reaction between NH(2)OH and Cu(2+)-EDTA complex at 60 degrees C. The excess AussDNA decreased with the addition of Hg(2+), which led the Cu(2)O particle RS intensity at 602 nm to decrease. The decreased RS intensity (DeltaI(602nm)) had a linear response to Hg(2+) concentration in the range of 0.1-400 nM, with a detection limit of 0.03 nM Hg(2+). This aptamer-modified nanogold catalytic RS method was applied for the detection of Hg(2+) in water samples, with sensitivity, selectivity, and simplicity.

A norsesquiterpene lactone and a benzoic acid derivative from the leaves of Cyclocarya paliurus and their glucosidase and glycogen phosphorylase inhibiting activities.

Two novel compounds, 3-methoxypterolactone ( 1) and 2-amino-3,4-dihydroxy-5-methoxybenzoic acid ( 2), were isolated from leaves of Cyclocarya paliurus (Batal.) Iljinsk, together with nine known compounds: pterolactone ( 3), gallic acid ( 4), 4-hydroxy-3-methoxybenzoic acid ( 5), oleanolic acid ( 6), beta-boswellic acid ( 7), alpha-boswellic acid ( 8), beta-amyrin ( 9), beta-amyrone ( 10) and 3beta-O-trans-caffeoyl-morolic acid ( 11). The structure elucidation was based on spectroscopic methods, including two-dimensional NMR experiments ( (1)H- (1)H COSY, HMQC and HMBC). All isolated compounds were evaluated for their glycosidase and glycogen phosphorylase inhibitory activities. 2-Amino-3,4-dihydroxy-5-methoxybenzoic acid and gallic acid showed significant alpha-glucosidase and glycogen phosphorylase inhibitory activities.

Resonance scattering effect of rhodamine dye association nanoparticles and its application to respective determination of trace ClO2 and Cl2.

A new resonance scattering method, based on resonance scattering (RS) effect, for the respective determination of ClO2 and Cl2 in water samples was developed. In HCl-NaAc buffer solutions with the pH value of 1.42, chlorine dioxide, or chlorine, oxidizes I- to form 12, which then reacts with the excess I- to form I3-. The resulting 13- would combine, respectively, with four rhodamine(Rh) dyes, including rhodamine B (RhB), butyl rhodamine B (b-RhB), rhodamine 6G (RhG), and rhodamine S (RhS), to form association particles which exhibit a stronger resonance scattering (RS) effect at 420 nm. For four systems of RhB, bRhB, RhG, and RhS, chlorine dioxide was, respectively, determined in the concentration range of 0.0056 to approximately 0.787 mg/L, 0.0034 to approximately 0.396 mg/L, 0.0057 to approximately 0.795 mg/L, and 0.0052 to approximately 0.313 mg/L, with the detection limits of 0.0011 mg/L, 0.006 mg/L, 0.0054 mg/ L, and 0.0023 mg/L ClO2, respectively. At the same experimental conditions as those for the determination of ClO2, chlorine was, respectively, determined in the concentration range of 0.013 to approximately 0.784 mg/L, 0.0136 to approximately 0.522 mg/ L, 0.014 to approximately 0.81 mg/L, and 0.014 to approximately 0.42 mg/L, with the detection limits of 0.0016 mg/L, 0.0104 mg/L, 0.0079 mg/L, and 0.0037 mg/L Cl2, respectively. The total RS value originally from ClO2 and Cl2 was recorded in the buffer solution, while the RS value from ClO2 was obtained by using dimethyl sulfoxide to mask chlorine. Thus the RS value of chlorine was calculated by deducting the RS value of chlorine dioxide from the total RS value. The RhB RS method was chosen for the determination of ClO2 and Cl2 in drinking water, with advantages of high sensitivity, good selectivity, simplicity, rapidity, and convenience.

A novel, simple and sensitive resonance scattering spectral method for the determination of chlorite in water by means of rhodamine B.

A new resonance scattering method was proposed for the determination of chlorite, basing on the resonance scattering effect of rhodamine dye. In HCl-sodium acetate buffer solution, chlorite oxidizes I- into I2 and the reaction of I2 and excess I- results in I3- It is respectively combined with rhodamine dyes, including rhodamine B (RhB), butyl rhodamine B (b-RhB), rhodamine G (RhG) and rhodamine S (RhS), to form association complex particles, which exhibit stronger resonance scattering (RS) effect at 400 nm. The chlorite concentration of ClO2- in the range of 0.00726-0.218 microg/ml, 0.0102-0.292 microg/ml, 0.00726 0.145 microg/ml and 0.0290 0.174 microg/ml is respectively linear to the RS intensity of association complex particle systems at 400 nm for the RhB, b-RhB, RhG and RhS. The detection limits of the four systems were respectively 0.00436, 0.00652, 0.00580 and 0.01450 microg/ml ClO2-. In the four systems, the RhB system possesses good stability and high sensitivity. It has been applied to the analysis of chlorite in wastewater with satisfactory results.