Cathode‐Electrolyte Interphase Engineering toward Fast‐Charging LiFePO4 Cathodes by Flash Carbon Coating

Author:

Chen Jinhang1ORCID,Onah Obinna E.12,Cheng Yi1ORCID,Silva Karla J.1ORCID,Choi Chi Hun (Will)13ORCID,Chen Weiyin1ORCID,Xu Shichen1,Eddy Lucas12ORCID,Han Yimo4ORCID,Yakobson Boris I.4ORCID,Zhao Yufeng56,Tour James M.1345ORCID

Affiliation:

1. Department of Chemistry Rice University 6100 Main Street Houston TX 77005 USA

2. Applied Physics Program and Smalley‐Curl Institute Rice University 6100 Main Street Houston TX 77005 USA

3. Department of Materials Science & Nanoengineering 6100 Main Street Houston TX 77005 USA

4. Smalley‐Curl Institute Rice University 6100 Main Street Houston TX 77005 USA

5. Nanocarbon Center and the Rice Advanced Materials Institute Rice University 6100 Main Street Houston TX 77005 USA

6. Corban University 5000 Deer Park Drive SE Salem Oregon 97317 USA

Abstract

AbstractLithium iron phosphate (LiFePO4, LFP) batteries are widely used in electric vehicles and energy storage systems due to their excellent cycling stability, affordability and safety. However, the rate performance of LFP remains limited due to its low intrinsic electronic and ionic conductivities. In this work, an ex situ flash carbon coating method is developed to enhance the interfacial properties for fast charging. A continuous, amorphous carbon layer is achieved by rapidly decomposing the precursors and depositing carbon species in a confined space within 10 s. Simultaneously, different heteroatoms can be introduced into the surface carbon matrix, which regulates the irregular growth of cathode‐electrolyte interphase (CEI) and selectively facilitates the inorganic region formation. The inorganic‐rich, hybrid conductive CEI not only promotes electron and ion transport but also restricts parasitic side reactions. Consequently, LFP cathodes with fluorinated carbon coatings exhibited the highest capacity of 151 mAh g−1 at 0.2 C and 96 mAh g−1 at 10 C, indicating their excellent rate capability over commercial LFP (58 mAh g−1 at 10 C). This solvent‐free, versatile surface modification is shown for other electrode materials, providing an efficient platform for electrode‐electrolyte interphase engineering through a surface post‐treatment.

Funder

U.S. Department of Energy

Welch Foundation

Air Force Office of Scientific Research

American Chemical Society Petroleum Research Fund

Publisher

Wiley

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