A lightweight nitrogen/oxygen dual-doping carbon nanofiber interlayer with meso-/micropores for high-performance lithium-sulfur batteries

Lithium-sulfur(Li-S) batteries are promising energy-storage devices for future generations of portable electronics and electric vehicles because of the outstanding energy density,low cost,and nontoxic nature of S.In the past decades,various novel electrodes and electrolytes have been studied to improve the performance of Li-S batteries.However,the very limited lifespan and rate performance of Li-S batteries originating from the dissolution and diffusion of long-chain polysulfides in liquid electrolytes,and the intrinsic poor conductivity of S severely hinder their practical application.Herein,an electrospinning method was developed to fabricate a thin conductive interlayer consisting of meso-/microporous N/O dual-doping carbon nanofiber(CNF).The freestanding 3 D interwoven structure with conductive pathways for electrons and ions can enhance the contact between polysulfides and N/O atoms to realize the highly robust trapping of polysulfides via the extremely polar interaction.Consequently,combining the meso-microporous N/O dual-doping CNF interlayer with a monodispersed S nanoparticle cathode results in a superior electrochemical performance of 862.5 mAh/g after 200 cycles at 0.2 C and a cycle decay as low as 0.08% per cycle.An area specific capacity of 5.22 mAh/cm^(2) can be obtained after 100 cycles at 0.1 C with a high S loading of 7.5 mg/cm^(2).

Synthesis of a chabazite-supported copper catalyst with full mesopores for selective catalytic reduction of nitrogen oxides at low temperature

A series of meso‐microporous copper‐supporting chabazite molecular sieve（CuSAPO‐34） catalysts with excellent performance in low‐temperature ammonia selective catalytic reduction（NH3‐SCR）have been synthesized via a one‐pot hydrothermal crystallization method. The physicochemical properties of the catalysts were characterized by scanning electron microscopy, transmission electron microscopy, N2 adsorption‐desorption measurements, X‐ray diffraction, 27 Al magic angle spinning nuclear magnetic resonance, diffuse reflectance ultraviolet‐visible spectroscopy, inductively coupled plasma‐atomic emission spectroscopy, X‐ray photoelectron spectroscopy, temperature‐programmed reduction measurements, and electron paramagnetic resonance analysis. The formation of micro‐mesopores in the Cu‐SAPO‐34 catalysts decreases diffusion resistance and greatly improves the accessibility of reactants to catalytic active sites. The main active sites for NH3‐SCR reaction are the isolated Cu^2＋ species displaced into the ellipsoidal cavity of the Cu‐SAPO‐34 catalysts.