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Science. 2016 May 06;352(6286):667. doi: 10.1126/science.aaf1399.

Comment on "Cycling Li-O₂ batteries via LiOH formation and decomposition".

Science (New York, N.Y.)

Yue Shen, Wang Zhang, Shu-Lei Chou, Shi-Xue Dou

Affiliations

  1. State Key Laboratory of Material Processing and Die and Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China. [email protected] [email protected].
  2. State Key Laboratory of Material Processing and Die and Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.
  3. Institute for Superconducting and Electronic Materials, Australian Institute for Innovative Materials, University of Wollongong, Innovation Campus, Squires Way, North Wollongong NSW 2522, Australia. [email protected] [email protected].
  4. Institute for Superconducting and Electronic Materials, Australian Institute for Innovative Materials, University of Wollongong, Innovation Campus, Squires Way, North Wollongong NSW 2522, Australia.

PMID: 27151858 DOI: 10.1126/science.aaf1399

Abstract

Liu et al (Research Article, 30 October 2015, p. 530) described a lithium-oxygen (Li-O2) battery based on lithium iodide (LiI)-assisted lithium hydroxide (LiOH) formation and decomposition. We argue that LiOH cannot be oxidized by triiodide (I3 (-)). The charge capacity is from the oxidation of I(-) instead of LiOH. The limited-capacity cycling test is misleading when the electrolyte contributes considerable parasitic reaction capacity.

Copyright © 2016, American Association for the Advancement of Science.

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