2022
DOI: 10.1016/j.ensm.2022.07.005
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Towards enhanced sodium storage of hard carbon anodes: Regulating the oxygen content in precursor by low-temperature hydrogen reduction

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Cited by 125 publications
(47 citation statements)
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“…As shown in Figure a, the G band gradually shifts toward lower wavenumbers upon discharging in the plateau region. This redshift phenomenon is related to elongation of the C–C bond length and weakness of the bond, , which is caused by the electron occupation in the π* antibonding band when Na + are embedded in the pseudographitic layer. This phenomenon indicates that the intercalation process occurred in the plateau rather than the slope region. Furthermore, the I D / I G values at various states of charge are also counted and displayed in the Figure b.…”
Section: Resultsmentioning
confidence: 99%
“…As shown in Figure a, the G band gradually shifts toward lower wavenumbers upon discharging in the plateau region. This redshift phenomenon is related to elongation of the C–C bond length and weakness of the bond, , which is caused by the electron occupation in the π* antibonding band when Na + are embedded in the pseudographitic layer. This phenomenon indicates that the intercalation process occurred in the plateau rather than the slope region. Furthermore, the I D / I G values at various states of charge are also counted and displayed in the Figure b.…”
Section: Resultsmentioning
confidence: 99%
“…The GITT curves of the N/S-HC electrode present high symmetry, which exhibits that the charging and discharging processes of electrode materials are reversible. Furthermore, according to Fick’s second law, D Na + is calculated by D normalN a + = 4 π τ true( m B V m M B s true) 2 true( normalΔ E s normalΔ E τ true) 2 Here, τ (s) is the pulse duration, M B is the molar mass of carbon, m B (g) and S (cm 2 ) are the active mass and surface area, respectively, V m (cm 3 mol –1 ) is the molar volume, and Δ E S (V) and Δ E τ (V) are the voltage changes caused by the current pulse and galvanostatic discharge, respectively. As shown in Figure h,i, the Na + diffusion kinetics of the N/S-HC electrodes are generally higher than those of HC and N-HC electrodes during the sodiation/desodiation process, demonstrating that the proper spacing between stable layers of the N/S-HC skeleton structure arising from the uniform heteroatom doping ensures smooth intercalation and removal of sodium ions.…”
Section: Resultsmentioning
confidence: 99%
“…S12 ). Because solid electrolyte interface (SEI) films are mainly formed on the surface of electrode materials [ 40 ], the low ICE is mainly caused by the high specific surface area (Fig. S13 ) and structural defects of the HC-1200 electrode.…”
Section: Resultsmentioning
confidence: 99%