An interactive organic-inorganic composite interface enables fast ion-transport, low self-discharge and stable storage of lithium battery.

Lithium batteries have been widely used in various fields, however, further research needs to be conducted to improve their stability and long-term storage performance for the highly active lithium metal anode. Herein, an organic-inorganic composite film composed of polypropylene carbonate (PPC), lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) and LiLaZrNbO (LLZNO) is fabricated on the lithium foil surface by spin-coating technique to passivate the lithium anode and regulate the ion transport behavior. The Li/CF battery with the optimized composite film coated lithium anode exhibits excellent discharge capacity (1006.

Solvation Structure Tuning Induces LiF/Li N-Rich CEI and SEI Interfaces for Superior Li/CF Batteries.

The electrode/electrolyte interfaces play an important role in the electrochemical reaction kinetics to alleviate the severe polarization and voltage hysteresis in lithium primary batteries. Herein, C F N is proposed as an electrolyte additive to tune the characteristics of the electrode/electrolyte interfaces. The Li/CF primary battery with C F N additive exhibits an excellent discharge-specific capacity of 981.

Depletion of florfenicol and florfenicol amine in eggs of laying hens and growing pullets after oral administration.

In this study, we carried out two experiments to evaluate depletion of florfenicol (FF) and its metabolite florfenicol amine (FFA) in eggs from growing pullets and laying hens. Eggs were collected, and the egg white and yolk were separated. FF and FFA were analysed by liquid chromatography-tandem mass spectrometry.

Determination of Lactoferrin in Camel Milk by Ultrahigh-Performance Liquid Chromatography-Tandem Mass Spectrometry Using an Isotope-Labeled Winged Peptide as Internal Standard.

An ultrahigh-performance liquid chromatography-tandem mass spectrometry method was developed and validated for the determination of lactoferrin in camel milk based on the signature peptide. The camel lactoferrin was purified by heparin affinity chromatography and then used to screen tryptic signature peptides. The signature peptide was selected on the basis of sequence database search and identified from the tryptic hydrolysates of purified camel lactoferrin by ultrahigh-performance liquid chromatography and quadrupole time-of-flight tandem mass spectrometry.