材料科学
石墨烯
阳极
插层(化学)
化学工程
硫黄
电化学
碳纤维
石墨烯纳米带
电池(电)
兴奋剂
纳米技术
无机化学
电极
复合材料
复合数
光电子学
物理化学
冶金
化学
工程类
功率(物理)
物理
量子力学
作者
Juhyung Choi,Aihua Jin,Hyun Dong Jung,Dongjin Ko,Ji Hyun Um,Yoon Jeong Choi,Sohee Kim,Seoin Back,Seung‐Ho Yu,Yuanzhe Piao
标识
DOI:10.1016/j.ensm.2022.03.041
摘要
Graphitic carbon materials, particularly few-layered graphene, exhibit great potentials as potassium-ion battery (PIBs) anodes. However, bulk graphene-based materials have the disordered structure owing to randomly stacked graphene layers, which causes the high migration barrier during K+ intercalation/deintercalation reactions and thus the surface-dominated capacitive response. Here, we present a novel nanoarchitecture of nitrogen and sulfur co-doped graphene nanoribbons with well-ordered stepped edges (NS–sGNR) via the electrochemical unzipping of multiwalled carbon nanotubes (MWCNTs) and the subsequent N/S co-doping process for high-performance PIB anodes. As an anode material for PIBs, the prepared sample exhibits high initial capacity (329.1 mAh g−1 at 50 mA g−1), superior rate capability (211.7 mAh g−1 at high current density, 2000 mA g−1), outstanding reversibility of K-staging, and stable long-term cyclability. Theoretical calculations were conducted to demonstrate that sGNRs with NS co-doping (NS–sGNR) exhibit much improved K+ intercalation properties, such as the K+ adsorption energy, charge transfer, and migration barriers, compared with the parallel-edged GNRs. Particularly, the migration barrier (the rate-determining step) can be substantially reduced at the stepped edges during K+ intercalation.
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