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Record W3210586630 · doi:10.1021/accountsmr.1c00137

All-Solid-State Lithium Metal Batteries with Sulfide Electrolytes: Understanding Interfacial Ion and Electron Transport

2021· article· en· W3210586630 on OpenAlexafffund
Changhong Wang, Keegan R. Adair, Xueliang Sun

Bibliographic record

VenueAccounts of Materials Research · 2021
Typearticle
Languageen
FieldEngineering
TopicAdvanced Battery Materials and Technologies
Canadian institutionsWestern University
FundersWestern UniversityNatural Sciences and Engineering Research Council of CanadaCanada Research ChairsCanada Foundation for InnovationOntario Research Foundation
KeywordsElectrolyteFast ion conductorMaterials scienceIonic conductivityAnodeLithium (medication)ElectrochemistryElectrochemical kineticsSulfideIonChemical engineeringNanotechnologyChemistryElectrodePhysical chemistryMetallurgyOrganic chemistry

Abstract

fetched live from OpenAlex

ConspectusWith the ever-growing demand for high energy density and high safety of energy storage technologies, all-solid-state lithium metal batteries (ASSLMBs) including all-solid-state lithium ion batteries (ASSLIBs) and all-solid-state lithium–sulfur batteries (ASSLSBs) have received considerable attention in recent years. To realize ASSLMBs, various solid-state electrolytes have been rapidly developed. Among them, sulfide electrolytes (SEs) demonstrate the highest ionic conductivity (>10 mS·cm–1) and the most favorable mechanical properties. However, the commercialization of SE-based ASSLMBs has been stymied by sluggish interfacial ion and electron transport kinetics, which arises from the detrimental interfacial reactions, poor interfacial solid–solid contact, and lithium dendrite growth. To overcome the interfacial challenges, an insightful understanding of the complex interfacial ion and electron transport processes in SE-based ASSLMBs is of the foremost importance. Although most of the previous review papers underscored the interfacial challenges and summarized the corresponding strategies, a fundamental understanding of the interfacial ions and electron-transport kinetics in SE-based ASSLMBs has not yet been presented. This Account therefore primarily summarizes our recent understanding of SE-based ASSLMBs from the perspectives of interfacial ion and electron transport, aiming to provide an insightful understanding of interfacial kinetics.We first compare various solid-state electrolytes including SEs, oxide electrolytes, halide electrolytes, polymer electrolytes, borohydride electrolytes in terms of their ionic conductivity, electrochemical stability windows, and mechanical properties, aiming to justify the advantages of SEs in ASSLMBs. Then, the interfacial challenges at both cathode and anode interfaces of SE-based ASSLIBs and SE-based ASSLSBs are presented, respectively. These interfacial challenges significantly hinder the interfacial ion and electron transport. To boost the interfacial charge transfer kinetics, our recent research advances related to the cathode interface between transition-metal oxides (TMOs) and SEs are then discussed. In parallel, our latest progress on SE-based ASSLSBs is also summarized from the perspective of interfacial kinetics. At the anode interface, our innovative strategies to enhance interfacial Li ion transport between Li metal and SEs are recapped. Finally, conclusions and our perspectives on SE-based ASSLMBs are presented. We believe that this specific Account provides an insightful understanding of interfacial ion and electron transport behavior in SE-based ASSLMBs.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.802

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.042
GPT teacher head0.314
Teacher spread0.272 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations98
Published2021
Admission routes2
Has abstractyes

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