• Park, Jonghyun
• Patel, Rajankumar L.
• Liang, Xinhua
• He, Yufang
• Gao, Yan
• Pham, Hiep

Abstract

<jats:title>Abstract</jats:title><jats:p>The degree of metal dissolution of cathode materials is a critical parameter in determining the performance of lithium‐ion batteries (LIBs). Ultra‐thin coated cathode particles, fabricated via atomic layer deposition (ALD), exhibit superior battery performance over that of bare particles. Therefore, it is generally believed that a coating layer protects the particles from metal dissolution of active materials, which is a critical cathode degradation mechanism. However, it is observed that ultra‐thin CeO<jats:sub>2</jats:sub> coating intensified the Mn dissolution of LiMn<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub> (LMO) during cycling of LIBs, whereas ultra‐thin Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> coating tended to inhibit Mn dissolution. A detailed density functional theory (DFT) study is carried out to explain these experimental observations by analyzing interaction of Mn atoms with neighboring electrode atoms in terms of energetic and structural aspect. All atomic and electronic analyses are consistent with the experimental observations. Several common materials are investigated as possible ALD coatings for LIBs to provide general insight, and it is found that Mn dissolution can be suppressed or accelerated depending on the material selection. This is the first report finding that depending on the coating material, metal dissolution can be accelerated, providing new insights into the impact of ALD coating materials on metal dissolution in cathode materials.</jats:p>

Topics

• density
• impedance spectroscopy
• theory
• density functional theory
• Lithium
• atomic layer deposition