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Title: Assessing Carbon-Based Anodes for Lithium-Ion Batteries: A Universal Description of Charge-Transfer Binding

Journal Article · · Physical Review Letters
 [1];  [2];  [1];  [3]
  1. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Quantum Simulations Group; Rice Univ., Houston, TX (United States). Dept. of Materials Science and NanoEngineering, Chemistry, and Smalley Inst. for Nanoscale Science and Technology
  2. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Nanoscale Synthesis and Characterization Lab.
  3. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Quantum Simulations Group

Many key performance characteristics of carbon-based lithium-ion battery anodes are largely determined by the strength of binding between lithium (Li) and sp2 carbon (C), which can vary significantly with subtle changes in substrate structure, chemistry, and morphology. We use density functional theory calculations to investigate the interactions of Li with a wide variety of sp2 C substrates, including pristine, defective, and strained graphene, planar C clusters, nanotubes, C edges, and multilayer stacks. In almost all cases, we find a universal linear relation between the Li-C binding energy and the work required to fill previously unoccupied electronic states within the substrate. This suggests that Li capacity is predominantly determined by two key factors—namely, intrinsic quantum capacitance limitations and the absolute placement of the Fermi level. This simple descriptor allows for straightforward prediction of the Li-C binding energy and related battery characteristics in candidate C materials based solely on the substrate electronic structure. It further suggests specific guidelines for designing more effective C-based anodes. Furthermore, this method should be broadly applicable to charge-transfer adsorption on planar substrates, and provides a phenomenological connection to established principles in supercapacitor and catalyst design.

Research Organization:
Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC52-07NA27344
OSTI ID:
1325867
Report Number(s):
LLNL-JRNL-652098; PRLTAO
Journal Information:
Physical Review Letters, Vol. 113, Issue 2; ISSN 0031-9007
Publisher:
American Physical Society (APS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 76 works
Citation information provided by
Web of Science

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Cited By (13)

Activating Basal Planes of NiPS 3 for Hydrogen Evolution by Nonmetal Heteroatom Doping journal February 2020
High-Performance Hydrogen Evolution from MoS 2(1- x ) P x Solid Solution journal December 2015
Oxygen-Vacancy Abundant Ultrafine Co 3 O 4 /Graphene Composites for High-Rate Supercapacitor Electrodes journal January 2018
Impact of Interfacial Electron Transfer on Electrochemical CO 2 Reduction on Graphitic Carbon Nitride/Doped Graphene journal February 2019
Rational Design of Transition Metal-Based Materials for Highly Efficient Electrocatalysis journal September 2018
Self-optimizing, highly surface-active layered metal dichalcogenide catalysts for hydrogen evolution journal July 2017
Defect-enriched iron fluoride-oxide nanoporous thin films bifunctional catalyst for water splitting journal May 2018
Lithium adsorption and migration in group IV–VI compounds and GeS/graphene heterostructures: a comparative study journal January 2018
Mechanistic insight into electroreduction of carbon dioxide on FeN x ( x = 0–4) embedded graphene journal January 2019
Interactions of ions across carbon nanotubes journal January 2020
Enhancing hydrogen evolution activity by doping and tuning the curvature of manganese-embedded carbon nanotubes journal January 2019
Computational screening of transition metal-doped phthalocyanine monolayers for oxygen evolution and reduction journal January 2020
Origin of low sodium capacity in graphite and generally weak substrate binding of Na and Mg among alkali and alkaline earth metals journal March 2016

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