Enabling high-performance lithium iron phosphate cathodes through an interconnected carbon network for practical and high-energy lithium-ion batteries.

The olivine lithium iron phosphate (LFP) cathode has gained significant utilization in commercial lithium-ion batteries (LIBs) with graphite anodes. However, the actual capacity and rate performance of LFP still require further enhancement when combined with high-capacity anodes, such as silicon (Si) anodes, to achieve high-energy LIBs. In this study, we introduce a gelatin-derived carbon network into a nanosized LFP cathode without the need for additional binding and conductive agents, employing a simple and cost-effective method.

N,S-Doped Porous Carbon Nanobelts Embedded with MoS Nanosheets as a Self-Standing Host for Dendrite-Free Li Metal Anodes.

Metallic Li is one of the most promising anodes for high-energy secondary batteries. However, the enormous volume changes and severe dendrite formation during the Li plating/stripping process hinder the practical application of Li metal anodes (LMAs). We have developed a sulfate-assisted strategy to synthesize a self-standing host composed of N,S-doped porous carbon nanobelts embedded with MoS nanosheets (MoS @NSPCB) for use in LMAs.

Determination of hexabromocyclododecanes in sediments from the Haihe River in China by an optimized HPLC-MS-MS method.

Hexabromocyclododecanes (HBCDs), a new type of persistent organic pollutants widely used as brominated flame retardants, have attracted wide attention due to their increasing level and toxicity. A method based on high-performance liquid chromatography mass spectrometry (HPLC-MS-MS) in electrospray ionization mode has been developed by optimization of various parameters, which effectively improved the separation degree and responsive intensity of α-, β- and γ-HBCD isomers. The concentrations and distribution profiles of three HBCD isomers were investigated in sediments from the Haihe River in China.

[Development of Self-assembled Dumbbell-like Fe3O4 Micro/nanomaterial for Application in Thermocatalytic Degradation of Polybrominated Biphenyls].

Polybrominated biphenyls (PBBs) are a group of new persistent organic pollutants, which have high toxicity and long-term bioaccumulation, and cause potential risks to human beings and aquatic ecosystem. Self-assembled dumbbell-like Fe3O4 was synthesized via ethylene-glycol mediated method to degrade PBBs, using BB209 as a model compound. The results showed that the growth process of dumbbell-like Fe3O4 precursor had two stages involving a fast nucleation of amorphous primary particles followed by a slow aggregation and crystallization of primary particles.

Synergetic inhibition of PCDD/F formation from pentachlorophenol by mixtures of urea and calcium oxide.

Chlorophenols are structurally similar to PCDD/Fs and have been considered as highly potential precursors for PCDD/Fs formation. The suppressing effects of PCDD/F formation from pentachlorophenol (PCP) were investigated on various mass ratios of CaO and urea. The total concentration of 2,3,7,8-PCDD/Fs, mostly dominated by OCDD, was determined to be 48.

Thermal degradation of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) over synthesized Fe-Al composite oxide.

A series of Fe-Al composite oxides were synthesized by the hydrothermal method using different urea dosages and examined towards the degradation of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) at 300 °C. The as-prepared oxides were characterized by field-emission scanning electron microscopy, X-ray diffraction and energy-dispersive X-ray spectroscopy. The morphology and composition of the prepared materials could be regulated by controlling the urea concentration.