Recent Advances in Scalable, High‐Mass Loaded Electrodes for Grid‐Scale Energy Storage

M Makena White (Department of Materials Science and Engineering University of California Los Angeles CA 90095 USA) M Minseok Choi B Bintao Hu (Department of Materials Science and Engineering University of California Los Angeles CA 90095 USA) S Swetha Chandrasekaran (Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550, United States) X Xinzhe Xue (Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, California 95064, United States) M Marcus Worsley (Lawrence Livermore National Laboratory Livermore CA 94550 USA) Y Yat Li (Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, California 95064, United States) B Bruce Dunn (Department of Materials Science and Engineering)

Abstract

Abstract The increasing electrification of daily life as well as the intermittent characteristic of renewable energy sources require viable solutions for grid‐scale energy storage. Critical considerations for grid storage applications are electrode mass loading and electrode thickness as these features govern battery pack energy density, an important factor in determining manufacturing costs. For this reason, there is increased interest in finding new ways of creating electrodes with high mass loading. In this review, various high‐mass loading fabrication approaches are considered for positive electrode materials used in batteries. The benchmark used for high mass loading is above 20 mg cm −2 , which is higher than the practical limit of conventional tape‐cast electrodes. Several different electrode approaches are described including templating, laser patterning, direct ink writing, and electrodeposition. A variety of materials are covered with the most prominent being LiFe(PO 4 ) (LFP), LiCoO 2 (LCO), and MnO 2 . In research to date, scalable electrochemical performance has been achieved with mass loadings over 100 mg cm −2 . Areal capacities as high as 14.7 mAh cm −2 at 1.82 mA cm −2 have been achieved in non‐aqueous electrolytes and 9.8 mAh cm −2 at 10 mA cm −2 in aqueous electrolytes. These results establish that the mass loading of electrodes can be scaled up without compromising their electrochemical properties.

Article Details

Volume / Issue Vol. 37, Issue 46
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (8)

M

Makena White

Department of Materials Science and Engineering University of California Los Angeles CA 90095 USA

M

Minseok Choi

B

Bintao Hu

Department of Materials Science and Engineering University of California Los Angeles CA 90095 USA

S

Swetha Chandrasekaran

Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550, United States

X

Xinzhe Xue

Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, California 95064, United States

M

Marcus Worsley

Lawrence Livermore National Laboratory Livermore CA 94550 USA

Y

Yat Li

Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, California 95064, United States

B

Bruce Dunn

Department of Materials Science and Engineering