Vine Shoots‐Derived Hard Carbons as Anodes for Sodium‐Ion Batteries: Role of Annealing Temperature in Regulating Their Structure and Morphology

Author:

Alvira Darío12,Antorán Daniel12,Vidal Mariano3,Sebastian Victor2456ORCID,Manyà Joan J.12

Affiliation:

1. Aragón Institute of Engineering Research (I3 A) Thermochemical Processes Group University of Zaragoza, Escuela Politécnica Superior Crta. de Cuarte s/n 22071 Huesca Spain

2. Department of Chemical Engineering and Environmental Technologies University of Zaragoza, Campus Río Ebro María de Luna 3 50018 Zaragoza Spain

3. Department of Mechanical Engineering and Environmental Technologies University of Zaragoza, Escuela Politécnica Superior Crta. de Cuarte s/n 22071 Huesca Spain

4. Instituto de Nanociencia y Materiales de Aragón (INMA) CSIC-Universidad de Zaragoza, Campus Río Ebro Mariano Esquillor, s/n 50018 Zaragoza Spain

5. Networking Research Center on Bioengineering Biomaterials and Nanomedicine CIBER-BBN 28029 Madrid Spain

6. Laboratorio de Microscopías Avanzadas Universidad de Zaragoza, Campus Río Ebro Mariano Esquillor, s/n 50018 Zaragoza Spain

Abstract

AbstractSodium‐ion batteries (SIBs) are considered one of the most promising large‐scale and low‐cost energy storage systems due to the abundance and low price of sodium. Herein, hard carbons from a sustainable biomass feedstock (vine shoots) were synthesized via a simple two‐step carbonization process at different highest temperatures to be used as anodes in SIBs. The hard carbon produced at 1200 °C delivered the highest reversible capacity (270 mAh g−1 at 0.03 A g−1, with an acceptable initial coulombic efficiency of 71 %) since a suitable balance between the pseudographitic domains growth and the retention of microporosity, defects, and functional groups was achieved. A prominent cycling stability with a capacity retention of 97 % over 315 cycles was also attained. Comprehensive characterization unraveled a three‐stage sodium storage mechanism based on adsorption, intercalation, and filling of pores. A remarkable specific capacity underestimation of up to 38 % was also found when a two‐electrode half‐cell configuration was employed to measure the rate performance. To avoid this systematic error caused by the counter/reference electrode polarization, we strongly recommend the use of a three‐electrode setup or a full‐cell configuration to correctly evaluate the anode response at moderate and high current rates.

Publisher

Wiley

Subject

Electrochemistry,Electrical and Electronic Engineering,Energy Engineering and Power Technology

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