TY - JOUR
T1 - Iron-based energy storage materials from carbon dioxide and scrap metal
AU - Yeoh, Joyce S.
AU - Di Bernardo, Iolanda
AU - White, Nicholas G.
AU - Otieno-Alego, Vincent
AU - Tsuzuki, Takuya
AU - Lowe, Adrian
N1 - Funding Information:
The authors thank Associate Prof. Yuerui Lu for the use of the tube furnace (SKGL-1200), and Kun Liang and Jian Zhang for their assistance with its operation. The authors also thank Prof. David Nisbet for the use of the Bruker Alpha Platinum-ATR unit, and Stephen Boyer at London Metropolitan University for carrying out CHN elemental analysis. The authors acknowledge the facilities and the scientific and technical assistance of Microscopy Australia at the Advanced Imaging Precinct, Australian National University, a facility that is funded by the University, State and Federal Governments. The authors acknowledge use of facilities within the Monash X-ray Platform. I. D. B. supported by the FLEET Centre of Excellence, ARC Grant No. CE170100039.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021
Y1 - 2021
N2 - The need for sustainable energy storage materials is extremely relevant today, given the increase in demand for energy storage and net zero carbon commitments made recently by multiple countries. In this study, scrap mild steel and carbon dioxide were utilised to synthesise ferrous oxalates, and the feasibility of using ferrous oxalate to store energy and carbon was investigated. Since transition metal oxalates are commonly used as precursors to oxides in the context of energy storage materials, the properties and performance of anhydrous ferrous oxalate were compared with those of iron oxides synthesised from ferrous oxalate. Hydrated ferrous oxalate was synthesised electrochemically from carbon dioxide and scrap mild steel. Subsequent heat treatment of the hydrated material at different temperatures, in both N2 and air, produced anhydrous ferrous oxalate and iron oxides. The products were characterised, carbon content analysed, and their electrochemical performances as negative electrode materials in lithium-ion batteries were investigated. Results indicated that anhydrous ferrous oxalate exhibited the highest gravimetric discharge capacities (810 mA h g-1), and the highest carbon content (0.28 g A h-1) when cycled at 100 mA g-1. Although the carbon content is low relative to graphite, this study demonstrates that there may be value in further investigating transition metal oxalates as sustainable energy storage materials. This journal is
AB - The need for sustainable energy storage materials is extremely relevant today, given the increase in demand for energy storage and net zero carbon commitments made recently by multiple countries. In this study, scrap mild steel and carbon dioxide were utilised to synthesise ferrous oxalates, and the feasibility of using ferrous oxalate to store energy and carbon was investigated. Since transition metal oxalates are commonly used as precursors to oxides in the context of energy storage materials, the properties and performance of anhydrous ferrous oxalate were compared with those of iron oxides synthesised from ferrous oxalate. Hydrated ferrous oxalate was synthesised electrochemically from carbon dioxide and scrap mild steel. Subsequent heat treatment of the hydrated material at different temperatures, in both N2 and air, produced anhydrous ferrous oxalate and iron oxides. The products were characterised, carbon content analysed, and their electrochemical performances as negative electrode materials in lithium-ion batteries were investigated. Results indicated that anhydrous ferrous oxalate exhibited the highest gravimetric discharge capacities (810 mA h g-1), and the highest carbon content (0.28 g A h-1) when cycled at 100 mA g-1. Although the carbon content is low relative to graphite, this study demonstrates that there may be value in further investigating transition metal oxalates as sustainable energy storage materials. This journal is
UR - http://www.scopus.com/inward/record.url?scp=85112824258&partnerID=8YFLogxK
U2 - 10.1039/d0ma00588f
DO - 10.1039/d0ma00588f
M3 - Article
AN - SCOPUS:85112824258
SN - 2633-5409
VL - 2
SP - 292
EP - 302
JO - Materials Advances
JF - Materials Advances
IS - 1
ER -