Structural Changes and Reversibility Upon Deintercalation of Li from LiCoPO4 Derivatives.

In an effort to improve the cycle life and rate capability of olivine LiCoPO4, Cr, Fe, and Si were added to produce nominal Li1.025Co0.84Fe0.10Cr0.05Si0.01(PO4)1.025. This cathode material has an energy density comparable to LiCoPO4, with markedly improved electrochemical performance. Here, we apply operando X-ray diffraction to gain an understanding of the crystallographic delithiation mechanism of this new substituted electrode material, compared to both LiCo0.75Fe0.25PO4 and LiCo0.75Fe0.25PO4. Throughout charging, the extent of solid-solution domains was significantly increased in Li1.025Co0.84Fe0.10Cr0.05Si0.01(PO4)1.025 and LiCo0.75Fe0.25PO4 compared to LiCoPO4. These domains reduce the mechanical strain during electrode function, providing a clear explanation for the high durability with Co substitution. Li1.025Co0.84Fe0.10Cr0.05Si0.01(PO4)1.025 operated at notably higher average potential than LiCo0.75Fe0.25PO4, which would increase the energy density of the cell. Ex situ measurements reveal the persistence of structural irreversibilities in the substituted phase after the first cycle, identifying avenues for further improvement in durability. This finding sheds light on the strategies for judicious cation substitution in LiCoPO4 electrodes to maximize the cycle life while preserving high energy density, especially compared to LiFePO4.

Variation in the susceptibility of the forest tent caterpillar (Lepidoptera: Lasiocampidae) to Bacillus thuringiensis variety kurstaki HD-1: effect of the host plant.

Host-mediated effect on the efficacy of Bacillus thuringiensis Berliner against larvae of the forest tent caterpillar. Malacosoma disstria Hübner, was investigated under controlled conditions. Host plants used in this study were quaking aspen, Populus tremuloides Michx., a preferred host, and sugar maple, Acer saccharum Marsh., a secondary host. Larvae were reared in the laboratory on leaves of these hosts, and upon reaching the third, fourth, and fifth instar, they were fed leaves treated with one of a range of concentrations of B. thuringiensis variety kurstaki HD-1 suspensions. Larvae were tested on the host on which they were feeding before the 4-d bioassays. The estimated LC50s were 100-fold greater on quaking aspen than on sugar maple. Also, there was a decrease in efficacy over the whole ranges of concentrations with larval age on both hosts. LC50s varied approximately two-fold between third and fifth instar. These results indicate that host-mediated effects on B. thuringiensis efficacy warrant more interest. In particular, they strongly indicate that the host plant modifies the interaction between B. thuringiensis and a target insect, and offer the opportunity to investigate the mechanism(s) that may be involved in the enhancement of B. thuringiensis toxicity.

Arbitrary primer polymerase chain reaction, a powerful method to identify Bacillus thuringiensis serovars and strains.

Arbitrary primer polymerase chain reaction technology has been applied to the identification of commercial strains of Bacillus thuringiensis by using total DNAs extracted from single bacterial colonies as templates. Characteristic DNA banding patterns can be readily and reproducibly obtained by agarose gel electrophoresis. This method has been used to distinguish commercial products containing B. thuringiensis serovar kurstaki (3a3b). When a single primer was used this method was capable of producing discriminating DNA fingerprints for 33 known serovars. Differentiation from the closely related species Bacillus cereus is also readily achieved. This technique should prove to be a powerful tool for identification and discrimination of individual B. thuringiensis strains.