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In this work, we demonstrated an accessible and facile method to prepare hierarchically porous carbon (HPC)/Co 3 O 4 nanocomposites (HPCC). Biomaterials-derived HPC was used as the appropriate carrier to load Co 3 O 4 nanoparticles due to its hierarchically porous structure and high surface area of 163 m 2 g −1 . The HPCC nanocomposites were used as an anode material for lithium-ion batteries (LIBs) and showed good electrochemical performance, delivering an initial discharge of 1566 and charge capacity of 1314 mA h g −1 with a initial coulombic efficiency of 83.9%. Additionally, it could still maintain a high reversible capacity of 1215 mA h g −1 after 100 cycles at a specific current of 100 mA g −1 , which is much better than that of HPC, and Co 3 O 4 and some Co 3 O 4 -based nanocomposites. The good electrochemical performance was mainly attributed to the good distribution of small Co 3 O 4 on HPC, the high surface area and hierarchical pores of HPC to effectively load a number of small Co 3 O 4 , alleviate the severe volume expansion during cycling and improve the electrical conductivity of nanocomposites, and the synergistic effects from the HPC and Co 3 O 4 . Therefore, the HPCC nanocomposites were expected to be an advanced anode material for LIBs. [ABSTRACT FROM AUTHOR]

The silver loaded adsorbents has been demonstrated to be an exciting approach towards Hg 0 removal from natural gas streams, its Hg 0 removal efficiency and capacity is closely related to the valence state, particle size and dispersity of silver particles. This study focused on chemical reduction methods in aqueous solutions to synthesize Ag/4A zeolite, and the influences of ultrasonic and protective additives were investigated to reduce the size of silver particles. The characterization results showed that silver particles are loaded on the surface of 4A zeolite with highly dispersed elemental form, ultrasonic and addition of stearic acid as protective additives are the effective ways to produce small nano-scale silver particles close to 15 nm. Meanwhile, the silver particles on the surface of Ag/4A zeolite are the active sites for Hg 0 adsorption which can react with Hg 0 to form Ag-Hg amalgam alloy. The silver lattices disappeared from the outer boundary to the interior of the particles after Hg 0 adsorption, which indicated that the Hg 0 firstly reacts with the nano-scale silver on the surfaces and then gradually penetrates into the interior of silver particles. The Hg 0 removal efficiency of prepared Ag/4A zeolite adsorbents was higher than 96% after 200 min adsorption at 30 °C, and adsorption capacity reached to 5.985 mg/g. Furthermore, the regeneration and reutilization results indicated that the Hg 0 adsorption performance remained stable after 5 reuse cycles. [ABSTRACT FROM AUTHOR]

Hollow multicomponent transition metal oxide nanostructures have caused extensive attention due to their enhanced performances in lithium-ion batteries (LIBs). Herein, a hybrid of multicomponent 3NiO·2Ni 3/2 Co 1/2 ZnO 4 nanocomposite with porous hollow dodecahedron nanostructures (3NiO·2Ni 3/2 Co 1/2 ZnO 4 -HD) was fabricated by carbonization of NiCoZn-layered double hydroxides which were derived from multimetallic zeolitic imidazolate frameworks (Zn/Co-ZIFs) as both self-sacrificial template and precursors. The 3NiO·2Ni 3/2 Co 1/2 ZnO 4 -HD nanocomposites were carefully characterized by various techniques including scanning electron microscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis, N 2 adsorption/desorption, transmission electron microscopy, Four-Point Probes and electrochemical techniques. When the 3NiO·2Ni 3/2 Co 1/2 ZnO 4 -HD nanocomposites were acted as anode materials for LIBs, a capacity of about 1337 mA h g −1 could be obtained after 100 cycles. The improved electrochemical performances might originate from synergistic effect of multicomponents, enhanced electrical conductivity and porous hollow dodecahedron nanostructures which could effectively alleviate volume deformation in the process of discharge/charge, accelerate mass transfer and increase the active sites for Li + storage. [ABSTRACT FROM AUTHOR]