Difference in Electrochemical Mechanism of SnO2 Conversion in Lithium-Ion and Sodium-Ion Batteries: Combined in Operando and Ex Situ XAS Investigations
Author(s) -
Ditty Dixon,
Marta Ávila,
Helmut Ehrenberg,
Aiswarya Bhaskar
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b00563
Subject(s) - x ray absorption spectroscopy , electrochemistry , lithium (medication) , electrode , materials science , sodium , ion , electrochemical cell , absorption (acoustics) , chemical engineering , absorption spectroscopy , inorganic chemistry , chemistry , metallurgy , composite material , medicine , physics , organic chemistry , engineering , endocrinology , quantum mechanics
Conversion and alloying type negative electrodes attracted huge attention in the present research on lithium/sodium-ion batteries (LIBs/SIBs) due to the high capacity delivered. Among these, SnO 2 is investigated intensively in LIBs due to high cyclability, low reaction potential, cost-effectiveness, and environmental friendliness. Most of the LIB electrodes are explored in SIBs too due to expected similar electrochemical performance. Though several LIB negative electrode materials successfully worked in SIBs, bare SnO 2 shows very poor electrochemical performance in SIB. The reason for this difference is investigated here through combined in operando and ex situ X-ray absorption spectroscopy (XAS). For this, the electrodes of SnO 2 (space group P 4 2 / mnm synthesized via one-pot hydrothermal method) were cycled in Na-ion and Li-ion half-cells. The Na/SnO 2 half-cell delivered a much lower discharge capacity than the Li/SnO 2 half-cell. In addition, higher irreversibility was observed for Na/SnO 2 half-cell during electrochemical investigations compared to that for Li/SnO 2 half-cell. In operando XAS investigations on the Na/SnO 2 half-cell confirms incomplete conversion and alloying reactions in the Na/SnO 2 half-cell, resulting in poor electrochemical performance. The difference in the lithiation and sodiation mechanisms of SnO 2 is discussed in detail.
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