z-logo
Premium
Lignin‐Derived Hard Carbon Microspheres Synthesized via Emulsion‐Solvent Evaporation as Anode for Sodium Storage
Author(s) -
Zhang Jie,
Yu Baojun,
Zhang Yang,
Wang Chengyang
Publication year - 2020
Publication title -
energy technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 44
eISSN - 2194-4296
pISSN - 2194-4288
DOI - 10.1002/ente.201901423
Subject(s) - thermogravimetric analysis , materials science , carbonization , chemical engineering , fourier transform infrared spectroscopy , faraday efficiency , carbon fibers , graphite , emulsion , thermal stability , anode , lignin , evaporation , chemistry , organic chemistry , composite material , scanning electron microscope , electrode , physics , composite number , engineering , thermodynamics
Lignin‐derived hard carbon microspheres with different amphiphilic carbonaceous material (ACM) contents are synthesized through a facile emulsion‐solvent evaporation process and subsequent thermal treatment. The influence of lignin/ACM mass ratio on morphology, microstructure, thermal stability, and electrochemical properties of carbon microspheres is studied in detail. Combined with Fourier‐transform infrared spectroscopy (FT‐IR) and thermogravimetric analysis, the interaction between lignin and ACM leads to enhanced thermal stability with a carbonization yield of 50.6%. Meanwhile, X‐ray diffraction (XRD) results indicate enlarged graphite‐like crystallite dimensions, L a and L c ,which contribute to electric conductivity. Due to ACM addition, the electrochemical performance is improved. When the mass ratio of lignin/ACM is 3:1, the sample exhibits a well‐balanced performance. The reversible capacity is 296.5 mAh g −1 with a high initial Coulombic efficiency of 82.0%. In the cycling test, the sample retains a capacity of 276.8 mAh g −1 after 100 cycles, corresponding to a capacity retention ratio of 90.8%.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here