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  1. Abstract

    An effective strategy to tackle the twin crises of global deforestation and fossil fuel depletion is to recycle biomass materials for energy storage devices. This study reports a unique and innovative solution to capitalize on a currently overlooked resource to produce high‐performance lithium–sulfur (Li–S) batteries from recycled paper. The recycled paper fibers are creatively composited with graphene oxide sheets via a capillary adsorption method. The recycled paper/graphene oxide hybrid is then converted to activated paper carbon/reduced graphene oxide (APC/graphene) scaffold for sulfur infiltration. The assembled Li–APC/graphene/S battery exhibits a superior lifespan of 620 cycles with an excellent capacity retention rate of 60.5%. An APC interlayer is sandwiched between the Li anode and the separator to suppress the degradation of Li anode by preventing the nonhomogeneous growth of mossy Li whiskers, stretching the battery lifespan up to 1000 cycles with a capacitance retention rate of 52.3%. The capillary adsorption method coupled with the porous carbonaceous anode interlayer configuration creates a new opportunity for the development of batteries derived from porous biomass materials.

     
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  2. Abstract

    The lithium–sulfur (Li–S) battery is a promising candidate for next‐generation high‐density energy storage devices because of its ultrahigh theoretical energy density and the natural abundance of sulfur. However, the practical performance of the sulfur cathode is plagued by fast capacity decay and poor cycle life, both of which can be attributed to the intrinsic dissolution/shuttling of lithium polysulfides. Here, a new built‐in magnetic field–enhanced polysulfide trapping mechanism is discovered by introducing ferromagnetic iron/iron carbide (Fe/Fe3C) nanoparticles with a graphene shell (Fe/Fe3C/graphene) onto a flexible activated cotton textile (ACT) fiber to prepare the ACT@Fe/Fe3C/graphene sulfur host. The novel trapping mechanism is demonstrated by significant differences in the diffusion behavior of polysulfides in a custom‐designed liquid cell compared to a pure ACT/S cathode. Furthermore, a cell assembled using the ACT@Fe/Fe3C/S cathode exhibits a high initial discharge capacity of ≈764 mAh g−1, excellent rate performance, and a remarkably long lifespan of 600 cycles using ACT@Fe/Fe3C/S (whereas only 100 cycles can be achieved using pure ACT/S). The new magnetic field–enhanced trapping mechanism provides not only novel insight but unveils new possibilities for mitigating the “shuttle effect” of polysulfides thereby promoting the practical applications of Li–S batteries.

     
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