Structural changes and thermal stability of charged LiNixMnyCozO₂ cathode materials studied by combined in situ time-resolved XRD and mass spectroscopy
Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heatin...
Saved in:
Published in | ACS applied materials & interfaces Vol. 6; no. 24; pp. 22594 - 22601 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
24.12.2014
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3̅m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3̅m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. This systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density. |
---|---|
AbstractList | Thermal stability of charged LiNiₓMnyCozO₂ (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3̅m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3̅m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. This systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density. Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3̅m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3̅m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. This systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density. Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time- resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3¯m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3¯m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. As a result, this systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density. Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3̅m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3̅m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. This systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density.Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode materials is systematically studied using combined in situ time-resolved X-ray diffraction and mass spectroscopy (TR-XRD/MS) techniques upon heating up to 600 °C. The TR-XRD/MS results indicate that the content of Ni, Co, and Mn significantly affects both the structural changes and the oxygen release features during heating: the more Ni and less Co and Mn, the lower the onset temperature of the phase transition (i.e., thermal decomposition) and the larger amount of oxygen release. Interestingly, the NMC532 seems to be the optimized composition to maintain a reasonably good thermal stability, comparable to the low-nickel-content materials (e.g., NMC333 and NMC433), while having a high capacity close to the high-nickel-content materials (e.g., NMC811 and NMC622). The origin of the thermal decomposition of NMC cathode materials was elucidated by the changes in the oxidation states of each transition metal (TM) cations (i.e., Ni, Co, and Mn) and their site preferences during thermal decomposition. It is revealed that Mn ions mainly occupy the 3a octahedral sites of a layered structure (R3̅m) but Co ions prefer to migrate to the 8a tetrahedral sites of a spinel structure (Fd3̅m) during the thermal decomposition. Such element-dependent cation migration plays a very important role in the thermal stability of NMC cathode materials. The reasonably good thermal stability and high capacity characteristics of the NMC532 composition is originated from the well-balanced ratio of nickel content to manganese and cobalt contents. This systematic study provides insight into the rational design of NMC-based cathode materials with a desired balance between thermal stability and high energy density. |
Author | Senanayake, Sanjaya D Zhou, Yongning Cho, Sung-Jin Yu, Xiqian Chung, Kyung Yoon Yang, Xiao-Qing Kim, Kwang-Bum Nam, Kyung-Wan Bak, Seong-Min Hu, Enyuan |
Author_xml | – sequence: 1 givenname: Seong-Min surname: Bak fullname: Bak, Seong-Min organization: Chemistry Department, Brookhaven National Laboratory , Upton, New York 11973, United States – sequence: 2 givenname: Enyuan surname: Hu fullname: Hu, Enyuan – sequence: 3 givenname: Yongning surname: Zhou fullname: Zhou, Yongning – sequence: 4 givenname: Xiqian surname: Yu fullname: Yu, Xiqian – sequence: 5 givenname: Sanjaya D surname: Senanayake fullname: Senanayake, Sanjaya D – sequence: 6 givenname: Sung-Jin surname: Cho fullname: Cho, Sung-Jin – sequence: 7 givenname: Kwang-Bum surname: Kim fullname: Kim, Kwang-Bum – sequence: 8 givenname: Kyung Yoon surname: Chung fullname: Chung, Kyung Yoon – sequence: 9 givenname: Xiao-Qing surname: Yang fullname: Yang, Xiao-Qing – sequence: 10 givenname: Kyung-Wan surname: Nam fullname: Nam, Kyung-Wan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25420188$$D View this record in MEDLINE/PubMed https://www.osti.gov/servlets/purl/1169557$$D View this record in Osti.gov |
BookMark | eNqFkctuFDEQRS0URB6wyA8gi1U2DX61x16iSUiQBiLxkNi1_OqMo7Y92O4ozTJ_we_xJRiSSOxY1dXVubdKqkOwF1N0ABxj9Bojgt-o0CO-wsQ8AQdYMtYJ0pO9f_Q-OCzlGiFOCeqfgX3SM4KwEAfg5-eaZ1PnrCZotipeuQJVtLBuXQ7NK1VpP_m6wDT-AfKVs3DjP_rbD3FZpx-Xv-7uoFF1m6yDQVWXvZpKi83WN1Iv0KSgfWzaR1h8nWH1wXXZlTTdNPfbp9O_C4MqLbZzpuZUTNotz8HTsVW5Fw_zCHx9d_ZlfdFtLs_fr99uumu6IrWTo9aMaEvxSLURGHPMpebKWCSI1ZRIh62TTDBpxYrhhnKpBO-poaM0hh6BV_e9qVQ_FOOrM1uTYmynDK1O9v2qQSf30C6n77MrdQi-GDdNKro0l4EghKikSLD_opgzxATlhDb05QM66-DssMs-qLwMj--hvwH5hJVn |
ContentType | Journal Article |
CorporateAuthor | Brookhaven National Laboratory (BNL), Upton, NY (United States) |
CorporateAuthor_xml | – name: Brookhaven National Laboratory (BNL), Upton, NY (United States) |
DBID | NPM 7X8 7S9 L.6 OIOZB OTOTI |
DOI | 10.1021/am506712c |
DatabaseName | PubMed MEDLINE - Academic AGRICOLA AGRICOLA - Academic OSTI.GOV - Hybrid OSTI.GOV |
DatabaseTitle | PubMed MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
DatabaseTitleList | AGRICOLA PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Engineering |
EISSN | 1944-8252 |
EndPage | 22601 |
ExternalDocumentID | 1169557 25420188 |
Genre | Research Support, U.S. Gov't, Non-P.H.S Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- .K2 23M 4.4 53G 55A 5GY 5VS 5ZA 6J9 7~N AABXI AAHBH ABJNI ABMVS ABQRX ABUCX ACGFS ACS ADHLV AEESW AENEX AFEFF AHGAQ ALMA_UNASSIGNED_HOLDINGS AQSVZ BAANH CUPRZ EBS ED~ EJD F5P GGK GNL IH9 JG~ LG6 NPM P2P RNS ROL UI2 VF5 VG9 W1F XKZ 7X8 ABBLG ABLBI 7S9 L.6 ABFRP OIOZB OTOTI |
ID | FETCH-LOGICAL-j372t-9fbb42bd31f3bc8116169b6acd082db329e1de94849d87412bd69a8653c3f9cc3 |
ISSN | 1944-8252 1944-8244 |
IngestDate | Mon Jul 03 03:59:58 EDT 2023 Fri Jul 11 10:34:14 EDT 2025 Thu Jul 10 22:36:34 EDT 2025 Thu Jan 02 22:16:47 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 24 |
Keywords | synchrotron X-ray diffraction energy storage Li-ion battery safety layered structure |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-j372t-9fbb42bd31f3bc8116169b6acd082db329e1de94849d87412bd69a8653c3f9cc3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 BNL-107164-2014-JA AC02-98CH10886; 2V03693 USDOE Office of Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (EE-3V) |
OpenAccessLink | https://www.osti.gov/servlets/purl/1169557 |
PMID | 25420188 |
PQID | 1640483623 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | osti_scitechconnect_1169557 proquest_miscellaneous_2000393084 proquest_miscellaneous_1640483623 pubmed_primary_25420188 |
PublicationCentury | 2000 |
PublicationDate | 2014-12-24 |
PublicationDateYYYYMMDD | 2014-12-24 |
PublicationDate_xml | – month: 12 year: 2014 text: 2014-12-24 day: 24 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | ACS applied materials & interfaces |
PublicationTitleAlternate | ACS Appl Mater Interfaces |
PublicationYear | 2014 |
Publisher | American Chemical Society |
Publisher_xml | – name: American Chemical Society |
SSID | ssj0063205 |
Score | 2.6302524 |
Snippet | Thermal stability of charged LiNixMnyCozO2 (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode... Thermal stability of charged LiNiₓMnyCozO₂ (NMC, with x + y + z = 1, x:y:z = 4:3:3 (NMC433), 5:3:2 (NMC532), 6:2:2 (NMC622), and 8:1:1 (NMC811)) cathode... |
SourceID | osti proquest pubmed |
SourceType | Open Access Repository Aggregation Database Index Database |
StartPage | 22594 |
SubjectTerms | cathode materials cathodes cations cobalt electrode material energy density ENERGY STORAGE manganese mass spectrometry nickel NSLS oxygen phase transition reaction mechanism sodium-ion battery temperature thermal degradation thermal stability transmission electron microscopy X-ray absorption spectroscopy X-ray diffraction |
Title | Structural changes and thermal stability of charged LiNixMnyCozO₂ cathode materials studied by combined in situ time-resolved XRD and mass spectroscopy |
URI | https://www.ncbi.nlm.nih.gov/pubmed/25420188 https://www.proquest.com/docview/1640483623 https://www.proquest.com/docview/2000393084 https://www.osti.gov/servlets/purl/1169557 |
Volume | 6 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1db9MwFLXKeIEHxDdlgIzEW5WROI4TP04VaEJ0PGyTCi9V7DgsiCaFpojucf-CH8Af45dwr-M0KVolQKqiynHrKOfo-p7E95iQF77yRcaDwGOQjXo8DZSXMpV6eZalihuVaoH1zpNjcXTG30yj6WDws7dqaVWrA31xZV3J_6AKbYArVsn-A7KbP4UG-A74whEQhuNfYXxizV-tcUZTwLtsF0RCuMU6kMaE275Et5ZIkF2-LY6L75NyPa4u3tmVDvgZoXtrZRez1s2FW99Zl57CpYN-NujSNFoW9cpuSO-BTq8-f4PWKchIHHYOefjIVm6iQ2a12HphfDg-GaUu4-0GQd6hYcXXHFeGdU9VbYg-MVX50ZsUZUc9G7nL9aqj9Ifzyra-h75lOw3bjcawdVp8aenvnmwE1j-xKag-ME00lpx7IGG3wrXosdL1drEXlBy_claAPAanvHkEU3PAdL8PALqYW3qAUoaLaPYY_MOCuz11jVxnoEZwowy4a-2EL0LmR61pFQtebsZBo2n3S5jwKwjZu2WMTWdOb5NbTofQw4ZUd8jAlHfJzZ475T3yo6MXdfSigDN19KIbetEqp45etE-vX5eX1BGLbjCnjlhUrWlLLFqUFIlFt4hFgVh2QCQW7RPrPjl7_ep0fOS5nTy8T2HMak_mSnGmsjDIQ6WTAGSGkEqkOoMMNFMhkybIjOQJl1kCOS50FTJNRBTqMJdahw_IXlmV5hGhvpJwu9PYxFxxGRrQL6ESPtexlozHyZDs452eQQKJLsgal4vpGoSukFEUD8nzFoAZxFF8OZaWplotZ4HguLsCqIHdfVhTyu4nfEgeNujNFo0pzKxF-vHOM_vkRsfyJ2QPMDRPIaOt1TPLp9-otqiF |
linkProvider | American Chemical Society |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Structural+changes+and+thermal+stability+of+charged+LiNixMnyCozO%E2%82%82+cathode+materials+studied+by+combined+in+situ+time-resolved+XRD+and+mass+spectroscopy&rft.jtitle=ACS+applied+materials+%26+interfaces&rft.au=Bak%2C+Seong-Min&rft.au=Hu%2C+Enyuan&rft.au=Zhou%2C+Yongning&rft.au=Yu%2C+Xiqian&rft.date=2014-12-24&rft.eissn=1944-8252&rft.volume=6&rft.issue=24&rft.spage=22594&rft_id=info:doi/10.1021%2Fam506712c&rft_id=info%3Apmid%2F25420188&rft.externalDocID=25420188 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1944-8252&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1944-8252&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1944-8252&client=summon |