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A sponge-like Li(4)Ti(5)O(12)/graphene composite was prepared via sequential hydrothermal process and solid-state heat treatment process for the application to high-power lithium ion batteries. The as-prepared electrode showed outstanding Li electroactivities with a rapid and reversible Li insertion/ extraction of up to 10 C-rate (1.75 A/g). It delivered a discharge capacity of 174 mAh/g at 0.5 C, near the theoretical capacity of Li(4)Ti(5)O(12), with good rate capability and cyclic stability. First-principles calculations revealed the intimate interaction of the Li(4)Ti(5)O(12) and graphene, which implies that graphene functions as an ‘electron tunnel.’ Electrochemical impedance spectroscopy also proved that the graphene-hybridization and the unique structure of the Li(4)Ti(5)O(12) material significantly reduce the resistive behavior of electrodes. The 3D structured Li(4)Ti(5)O(12)/graphene hybrid reported herein could be a promising candidate for a safe, low-cost, high-power anode for lithium ion batteries, and our seeding-growth-sintering method for decorating graphene with active material will offer an effective upgrade on highly insulating Li(4)Ti(5)O(12) materials.

Although little is known about the behavior of engineered nanomaterials after exposure to terrestrial areas, recent studies indicate that silver nanoparticles (AgNPs) can perturb the soil environment due to their biocidal and catalytic properties. The fundamental evaluation of the environmental fate of AgNPs would be a significant step toward a comprehensive understanding of the harmful effects of such particles on ecosystems. Therefore, from an eco-toxicological perspective, the estimation of AgNP behavior in soil should be investigated. Among the various environmental characteristics, the deposition of nanoparticles in the soil constitute is a critical step in their migration into surface or groundwater and interaction with organisms, which is determined by the stability of aqueous dispersions in a soil micro-environment. In the present study, we observed the aggregation and deposition of AgNPs to natural soil surfaces by comparing the partitioning of AgNPs in a soil/water interface with that of Ag + ion. Both AgNPs and Ag + ion were selectively quantified by means of inductively coupled plasma (ICP) spectrometry and an ion-selective electrode (ISE). We interpreted the partitioning of AgNPs and Ag + ion using the Freundlich isotherm and the findings indicate that AgNPs with reduced dispersion stability in a soil micro-environment were aggregated and deposited on the surface of natural soil. This study provides a fundamental basis for understanding the deposition of AgNPs, which will enable their accumulation and mobility in a soil environment to be predicted.