Enhancing cycle life of nickel-rich LiNi0.9Co0.05Mn0.05O2 via a highly fluorinated electrolyte additive - pentafluoropyridine

A highly fluorinated additive, pentafluoropyridine (PFP), is used here to enhance the interfacial stability of the Ni-rich LiNi0.9Co0.05Mn0.05O2 (NCM90) cathode at a cut-off voltage of 4.3 V vs. Li/Li+ at 30 °C. The capacity retention of the NCM90||Li cell is obviously improved from 72.3% to 80.3% after 200 cycles at 1C (1C = 180 mA g-1) when 0.2% PFP is introduced into the baseline electrolyte (1 mol L-1 LiPF6 in ethylene carbonate/diethyl carbonate). The improvement in electrochemical performance could be attributed to the formation of a compact and uniform cathode electrolyte interphase (CEI) layer enriched with F-containing polypyridine moieties and LiF species on the NCM90 particles. This CEI prevents side reactions between the electrode and electrolyte and hinders the corrosion of the cathode caused by HF attack. In addition, the formation of internal particle cracks is somewhat suppressed by the robust CEI, thus prohibiting the irreversible phase transformation and better maintaining the superior lithium-ion diffusion kinetics

The influence of acute ammonia stress on intestinal oxidative stress, histology, digestive enzymatic activities and PepT1 activity of grass carp (Ctenopharyngodon idella)

This study was conducted to evaluate the effect of acute ammonia stress on intestinal oxidative stress levels, histology, and activity of digestive enzymes and oligopeptide transporter 1 (PepT1) in grass carp. Three concentrations of ammonia nitrogen: 0 mg/L total ammonia nitrogen (TAN) (the control group), 1.7 mg/L TAN were used in the present study. Fish were sampled at 0 h, 12 h, 24 h, and 48 h after exposure to ammonia. The results showed that the activities of reactive oxygen species (ROS), superoxide dismutase (SOD), catalase (CAT) and the content of cortisol were all increased in fish exposed to the two concentrations of TAN. Compared with the control group, the activities of intestinal trypsin and chymotrypsin significantly increased in the 1.7 mg/L TAN group, while amylase activity was significantly suppressed in the 50 mg/L TAN group. After ammonia exposure, the expression of intestinal Nrf2 gene significantly increased in the 1.7 mg/L TAN group while the expression of Keap1 gene significantly increased in the 50 mg/L TAN group. Moreover, the expression of intestinal PepT1, Sp1 and CDX2 significantly increased after fish exposed to 1.7 mg/L TAN. The width of mid-intestine villi of fish from the 50 mg/L TAN group was significantly higher than fish from the other two groups. Meanwhile, the area density of PepT1 in the 50 mg/L TAN group was significantly smaller than that in the control and 1.7 mg/L TAN groups. The results suggested that ammonia stress induces intestinal oxidative stress, and 1.7 mg/L TAN increased the expressions of PepT1-related genes and the activities of the intestinal trypsin and chymotrypsin. This conclusion indicates that ammonia nitrogen stress affects the intestinal digestion and absorption performance of aquatic animals, and reducing ammonia nitrogen to a suitable level can improve the protein digestion ability of animals