Michael A. Hernandez Bertran, Diana Zapata Dominguez, Christopher L. Berhaut, Samuel Tardif, Alessandro Longo, Christoph J. Sahle, Chiara Cavallari, Emmanuelle de Clermont Gallerande, Ivan Marri, Nathalie Herlin-Boime, Elisa Molinari, Stéphanie Pouget, Deborah Prezzi* and Sandrine Lyonnard*,
{"title":"用多边x射线散射分析了解硅阳极中不可逆锂的损耗","authors":"Michael A. Hernandez Bertran, Diana Zapata Dominguez, Christopher L. Berhaut, Samuel Tardif, Alessandro Longo, Christoph J. Sahle, Chiara Cavallari, Emmanuelle de Clermont Gallerande, Ivan Marri, Nathalie Herlin-Boime, Elisa Molinari, Stéphanie Pouget, Deborah Prezzi* and Sandrine Lyonnard*, ","doi":"10.1021/acs.chemmater.4c0336610.1021/acs.chemmater.4c03366","DOIUrl":null,"url":null,"abstract":"<p >During the first charge–discharge cycle, silicon-based batteries show an important capacity loss not only due to the formation of the solid electrolyte interphase (SEI) but also other effects taking place during the expansion-contraction sequence upon (de)alloying, such as electrochemical reduction of native oxide, Li trapping, and loss of active material. To understand this first-cycle irreversibility, quantitative methods are needed to characterize the chemical environment of silicon and lithium in the bulk of the cycled electrodes. Here, a methodology based on multiedge X-ray Raman scattering is reported, as applied to model silicon electrodes prepared in fully lithiated and delithiated states after the first cycle. The spectra are recorded at the C, O, F, and Li K-edges, as well as Si L<sub>2,3</sub> edge, and are analyzed using linear combinations of both experimental and computed reference spectra. Prototypical SEI compounds such as Li<sub>2</sub>CO<sub>3</sub>, LiF, and LiPF<sub>6</sub>, as well as electrode constituents such as binder and conductive carbon, crystalline Si, native SiO<sub>2</sub>, and Li<sub><i>x</i></sub>Si phases (<i>x</i> being the lithiation index) are taken into account to identify the main species, isolate their relative contributions, and quantitatively evaluate the proportions of organic and inorganic products. This analysis shows that 35% of the carbonates formed in the SEI during the lithiation are dissolved upon delithiation and that part of the Li<sub><i>x</i></sub>Si alloys remains present after delithiation. Moreover, in combination with electrochemical data, it enables the quantification of the lithium lost in the first cycle, 17% of which is trapped in disconnected silicon particles, while 30% forms a fluorine-rich stable SEI and 53% a carbonate-rich partially dissolvable SEI. These results pave the way to systematic, reference data-informed and modeling-assisted studies of SEI characteristics in the bulk of electrodes prepared under controlled state-of-charge and state-of-health conditions.</p>","PeriodicalId":33,"journal":{"name":"Chemistry of Materials","volume":"37 10","pages":"3648–3660 3648–3660"},"PeriodicalIF":7.0000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Understanding the Irreversible Lithium Loss in Silicon Anodes Using Multi-edge X-ray Scattering Analysis\",\"authors\":\"Michael A. Hernandez Bertran, Diana Zapata Dominguez, Christopher L. Berhaut, Samuel Tardif, Alessandro Longo, Christoph J. Sahle, Chiara Cavallari, Emmanuelle de Clermont Gallerande, Ivan Marri, Nathalie Herlin-Boime, Elisa Molinari, Stéphanie Pouget, Deborah Prezzi* and Sandrine Lyonnard*, \",\"doi\":\"10.1021/acs.chemmater.4c0336610.1021/acs.chemmater.4c03366\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >During the first charge–discharge cycle, silicon-based batteries show an important capacity loss not only due to the formation of the solid electrolyte interphase (SEI) but also other effects taking place during the expansion-contraction sequence upon (de)alloying, such as electrochemical reduction of native oxide, Li trapping, and loss of active material. To understand this first-cycle irreversibility, quantitative methods are needed to characterize the chemical environment of silicon and lithium in the bulk of the cycled electrodes. Here, a methodology based on multiedge X-ray Raman scattering is reported, as applied to model silicon electrodes prepared in fully lithiated and delithiated states after the first cycle. The spectra are recorded at the C, O, F, and Li K-edges, as well as Si L<sub>2,3</sub> edge, and are analyzed using linear combinations of both experimental and computed reference spectra. Prototypical SEI compounds such as Li<sub>2</sub>CO<sub>3</sub>, LiF, and LiPF<sub>6</sub>, as well as electrode constituents such as binder and conductive carbon, crystalline Si, native SiO<sub>2</sub>, and Li<sub><i>x</i></sub>Si phases (<i>x</i> being the lithiation index) are taken into account to identify the main species, isolate their relative contributions, and quantitatively evaluate the proportions of organic and inorganic products. This analysis shows that 35% of the carbonates formed in the SEI during the lithiation are dissolved upon delithiation and that part of the Li<sub><i>x</i></sub>Si alloys remains present after delithiation. Moreover, in combination with electrochemical data, it enables the quantification of the lithium lost in the first cycle, 17% of which is trapped in disconnected silicon particles, while 30% forms a fluorine-rich stable SEI and 53% a carbonate-rich partially dissolvable SEI. 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Understanding the Irreversible Lithium Loss in Silicon Anodes Using Multi-edge X-ray Scattering Analysis
During the first charge–discharge cycle, silicon-based batteries show an important capacity loss not only due to the formation of the solid electrolyte interphase (SEI) but also other effects taking place during the expansion-contraction sequence upon (de)alloying, such as electrochemical reduction of native oxide, Li trapping, and loss of active material. To understand this first-cycle irreversibility, quantitative methods are needed to characterize the chemical environment of silicon and lithium in the bulk of the cycled electrodes. Here, a methodology based on multiedge X-ray Raman scattering is reported, as applied to model silicon electrodes prepared in fully lithiated and delithiated states after the first cycle. The spectra are recorded at the C, O, F, and Li K-edges, as well as Si L2,3 edge, and are analyzed using linear combinations of both experimental and computed reference spectra. Prototypical SEI compounds such as Li2CO3, LiF, and LiPF6, as well as electrode constituents such as binder and conductive carbon, crystalline Si, native SiO2, and LixSi phases (x being the lithiation index) are taken into account to identify the main species, isolate their relative contributions, and quantitatively evaluate the proportions of organic and inorganic products. This analysis shows that 35% of the carbonates formed in the SEI during the lithiation are dissolved upon delithiation and that part of the LixSi alloys remains present after delithiation. Moreover, in combination with electrochemical data, it enables the quantification of the lithium lost in the first cycle, 17% of which is trapped in disconnected silicon particles, while 30% forms a fluorine-rich stable SEI and 53% a carbonate-rich partially dissolvable SEI. These results pave the way to systematic, reference data-informed and modeling-assisted studies of SEI characteristics in the bulk of electrodes prepared under controlled state-of-charge and state-of-health conditions.
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.