A High Capacity Gas Diffusion Electrode for Li–O2 Batteries

Author:

Jenkins Max1,Dewar Daniel1ORCID,Lagnoni Marco12ORCID,Yang Sixie1,Rees Gregory J.1ORCID,Bertei Antonio2ORCID,Johnson Lee R.3ORCID,Gao Xiangwen4ORCID,Bruce Peter G.15ORCID

Affiliation:

1. Department of Materials University of Oxford Parks Road Oxford OX1 3PH UK

2. Department of Civil and Industrial Engineering University of Pisa Pisa 56122 Italy

3. Nottingham Applied Materials and Interfaces Group School of Chemistry University of Nottingham Nottingham NG7 2RD UK

4. Future Battery Research Centre Global institute of Future Technology Shanghai Jiao Tong University Shanghai 200240 China

5. Department of Chemistry University of Oxford Oxford OX1 3TA UK

Abstract

AbstractThe very high theoretical specific energy of the lithium–air (Li–O2) battery (3500 Wh kg−1) compared with other batteries makes it potentially attractive, especially for the electrification of flight. While progress has been made in realizing the Li–air battery, several challenges remain. One such challenge is achieving a high capacity to store charge at the positive electrode at practical current densities, without which Li–air batteries will not outperform lithium‐ion. The capacity is limited by the mass transport of O2 throughout the porous carbon positive electrode. Here it is shown that by replacing the binder in the electrode by a polymer with the intrinsic ability to transport O2, it is possible to reach capacities as high as 31 mAh cm−2 at 1 mA cm−2 in a 300 µm thick electrode. This corresponds to a positive electrode energy density of 2650 Wh L−1 and specific energy of 1716 Wh kg−1, exceeding significantly Li‐ion batteries and previously reported Li–O2 cells. Due to the enhanced oxygen diffusion imparted by the gas diffusion polymer, Li2O2 (the product of O2 reduction on discharge) fills a greater volume fraction of the electrode and is more homogeneously distributed.

Funder

Engineering and Physical Sciences Research Council

Publisher

Wiley

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