The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Influence of Li2O2 morphology on oxygen reduction and evolution kinetics in Li–O2 batteries
Abstract
Understanding the origins of high overpotentials required for Li2O2 oxidation in Li–O2 batteries is critical for developing practical devices with improved round-trip efficiency. While a number of studies have reported different Li2O2 morphologies formed during discharge, the influence of the morphology and structure of Li2O2 on the oxygen evolution reaction (OER) kinetics and pathways is not known. Here, we show that two characteristic Li2O2 morphologies are formed in carbon nanotube (CNT) electrodes in a 1,2-dimethoxyethane (DME) electrolyte: discs/toroids (50–200 nm) at low rates/overpotentials (10 mA gC−1 or E > 2.7 V vs. Li), or small particles (<20 nm) at higher rates/overpotentials. Upon galvanostatic charging, small particles exhibit a sloping profile with low overpotential (<4 V) while discs exhibit a two-stage process involving an initially sloping region followed by a voltage plateau. Potentiostatic intermittent titration technique (PITT) measurements reveal that charging in the sloping region corresponds to solid solution-like delithiation, whereas the voltage plateau (E = 3.4 V vs. Li) corresponds to two-phase oxidation. The marked differences in charging profiles are attributed to differences in surface structure, as supported by X-ray absorption near edge structure (XANES) data showing that oxygen anions on disc surfaces have LiO2-like electronic features while those on the particle surfaces are more bulk Li2O2-like with modified electronic structure compared to commercial Li2O2. Such an integrated structural, chemical, and morphological approach to understanding the OER kinetics provides new insights into the desirable discharge product structure for charging at lower overpotentials.
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Cites
Li-O2 and Li-S batteries with high energy storage
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An improved high-performance lithium–air battery
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Twin Problems of Interfacial Carbonate Formation in Nonaqueous Li–O2 Batteries
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Lithium–oxygen batteries: bridging mechanistic understanding and battery performance
Lu, Y.-C., Gallant, B. M., Kwabi, D. G., Harding, J. R., Mitchell, R. R., Whittingham, M. S., & Shao-Horn, Y. (2013) · Energy & Environmental Science · doi:10.1039/c3ee23966g · Cited by 927
Self-citation
Cited by
Mechanism and Kinetics of Li2S Precipitation in Lithium–Sulfur Batteries
Fan, F. Y., Carter, W. C., & Chiang, Y. (2015) · Advanced Materials · doi:10.1002/adma.201501559 · Cited by 987
A review of cathode materials and structures for rechargeable lithium–air batteries
Ma, Z., Yuan, X., Li, L., Ma, Z.-F., Wilkinson, D. P., Zhang, L., & Zhang, J. (2015) · Energy & Environmental Science · doi:10.1039/c5ee00838g · Cited by 485
Artificial Protection Film on Lithium Metal Anode toward Long‐Cycle‐Life Lithium–Oxygen Batteries
Liu, Q., Xu, J., Yuan, S., Chang, Z., Xu, D., Yin, Y., Li, L., Zhong, H., Jiang, Y., Yan, J., et al. (2015) · Advanced Materials · doi:10.1002/adma.201501490 · Cited by 482
Lyu, Z., Zhou, Y., Dai, W., Cui, X., Lai, M., Wang, L., Huo, F., Huang, W., Hu, Z., & Chen, W. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00255f · Cited by 408
Shu, C., Wang, J., Long, J., Liu, H., & Dou, S. (2019) · Advanced Materials · doi:10.1002/adma.201804587 · Cited by 388
Metadata
- Authors
- Gallant, B. M., Kwabi, D. G., Mitchell, R. R., Zhou, J., Thompson, C. V., & Shao-Horn, Y.
- Venue
- Energy & Environmental Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2013
- Volume
- 6
- Issue
- 8
- Pages
- 2518
- ISSN
- 1754-5692 (ISSN-L)
- 1754-5706
- OpenAlex
- W1967751239
- Cited by
- 447
- References
- 36
- FWCI
- 37.94
- Type
- journal article
- Language
- en
- Open access
- closed
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