Abstract

Hard carbon attracts wide attentions as the anode for high-energy rechargeable batteries due to its low cost and high theoretical capacities. However, the intrinsically disordered microstructure gives it poor electrical conductivity and unsatisfactory rate performance. Here we report a facile synthesis of N-doped graphitized hard carbon via a simple carbonization and activation of a urea-soaked self-crosslinked Co-alginate for the high-performance anode of lithium/sodium-ion batteries. Owing to the catalytic graphitization of Co and the introduction of nitrogen-functional groups, the hard carbon shows structural merits of ordered expanded graphitic layers, hierarchical porous channels, and large surface area. Applying in the anode of lithium/sodium-ion batteries, the large surface area and the existence of nitrogen functional groups can improve the specific capacity by surface adsorption and faradic reaction, while the hierarchical porous channels and expanded graphitic layers can provide facilitate pathways for electrolyte and improve the rate performance. In this way, our hard carbon provides its feasibility to serve as an advanced anode material for high-energy rechargeable lithium/sodium-ion batteries.

Highlights

  • In the past two decades, lithium-ion batteries (LIBs) have occupied the main market of energy storage devices owing to their light weight, high energy density and long cycle life[1,2,3,4,5]

  • We present a facile solution to improve the electrochemical performance of hard carbon by an in-suit catalytic graphitization and N-doping method

  • The N-doped graphitized hard carbon (N-GHC) was synthesized by carbonization and activation of a ureasoaked catalytical metal-alginate precursor

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Summary

Introduction

In the past two decades, lithium-ion batteries (LIBs) have occupied the main market of energy storage devices owing to their light weight, high energy density and long cycle life[1,2,3,4,5]. Hard carbon consists mainly of single graphene layers randomly packed in a disordered arrangement[18,19,20,21,22,23,24] This structure usually provides broad parallel carbon layers and numerous nanopores for Li+/Na+ intercalation, giving larger specific capacities[25,26,27]. When applied in the anode of LIBs and SIBs, the large surface area and abundant nitrogen and oxygen functional groups can help generate high lithium and sodium storage capacity through surface adsorption and faradic reaction[31,32,33,34,35,36], while the expanded graphitic layers and hierarchical porous channels can accelerate the transportation of electrolyte and improve the rate performance

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