Abstract:
Rechargeable lithium-ion batteries (LIBs) are the most essential inventions that have driven
the development of electronic devices over the decades. Scientists are currently working hard
to develop rechargeable sodium-ion batteries (SIBs) to replace expensive LIBs. One of the
most difficult challenges in developing SIBs is selecting the most appropriate anode material
for Na+ intercalation. Hard carbon as an anode material for SIBs has sparked a lot of interest
in recent years. Biomass waste is one of the most exciting, readily available, and cost-effective
sources of hard carbon (HC). In this study, biomass waste from Palmyrah kernel shells were
studied as potential precursors for the preparation of HC employing a pyrolysis approach
followed by acid washing, which helps to eliminate inorganic impurities. Palmyrah kernel
shells are impregnated with phosphoric acid (H3PO4
) and pyrolyzed at 1100 ℃ after washing
away the acid with deionized water to prepare the HC material. In this research study,
Scanning Electron Microscopy (SEM) was used to analyze the carbon morphology of the HC,
and Fourier-transform infrared spectroscopy (FTIR) was used to analyze the functional groups
contained in the HC. According to recorded SEM images, the derived HC has a fibrous
structure with high porosity and large cavities, as well as an irregular structure that is more
conducive to Na+ intercalation through the inter-atomic layers in HC. Furthermore, the
prominent band at 1733 𝑐𝑚−1
in the FTIR spectrum indicates the presence of C=O stretching
frequency caused by the hemicellulose carboxyl functional groups in the HC.
