{"title":"Overhauser Dynamic Nuclear Polarization of Lithiated Graphite Anodes: Probing Bulk and Surface Structures.","authors":"Teresa Insinna, Anne-Laure Barra, Clare P Grey","doi":"10.1021/acs.chemmater.5c00845","DOIUrl":null,"url":null,"abstract":"<p><p>Graphite is used, almost ubiquitously, as an anode material in today's high energy density Li-ion batteries. Both artificial and natural graphites are widely used, and there are large differences in the production methods, cost, particle morphologies, sizes, and percentage of defects in their structures, all these parameters affecting use and performance. The success of graphite as an anode depends on the formation of a Li-ion-conducting passivation layer (the solid electrolyte interphase (SEI)) on the first cycle, with the nature of this layer still being under investigation with a range of approaches. During lithiation (charge in a full cell), graphite is lithiated in stages and becomes electronically conductive. The conduction electrons of lithiated graphite anodes are exploited in this work to enhance the nuclear magnetic resonance (NMR) signal of bulk and surface nuclei via Overhauser dynamic nuclear polarization (DNP). The parameters directly affecting the enhancement factor (leakage factor, saturation factor, and coupling factor) are examined in detail for an artificial graphite at different lithiation stages. Four additional (natural and artificial) graphites are then studied to explore the effects of particle size and morphology, electron relaxation times, and conductivity on the observed DNP enhancements. Finally, the polarization transfer between bulk and surface (SEI) species is explored through <sup>6,7</sup>Li, <sup>1</sup>H, and <sup>13</sup>C DNP NMR experiments.</p>","PeriodicalId":33,"journal":{"name":"Chemistry of Materials","volume":"37 14","pages":"5167-5182"},"PeriodicalIF":7.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12287998/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.chemmater.5c00845","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/22 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Graphite is used, almost ubiquitously, as an anode material in today's high energy density Li-ion batteries. Both artificial and natural graphites are widely used, and there are large differences in the production methods, cost, particle morphologies, sizes, and percentage of defects in their structures, all these parameters affecting use and performance. The success of graphite as an anode depends on the formation of a Li-ion-conducting passivation layer (the solid electrolyte interphase (SEI)) on the first cycle, with the nature of this layer still being under investigation with a range of approaches. During lithiation (charge in a full cell), graphite is lithiated in stages and becomes electronically conductive. The conduction electrons of lithiated graphite anodes are exploited in this work to enhance the nuclear magnetic resonance (NMR) signal of bulk and surface nuclei via Overhauser dynamic nuclear polarization (DNP). The parameters directly affecting the enhancement factor (leakage factor, saturation factor, and coupling factor) are examined in detail for an artificial graphite at different lithiation stages. Four additional (natural and artificial) graphites are then studied to explore the effects of particle size and morphology, electron relaxation times, and conductivity on the observed DNP enhancements. Finally, the polarization transfer between bulk and surface (SEI) species is explored through 6,7Li, 1H, and 13C DNP NMR experiments.
期刊介绍:
The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.