Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity
- Autores
- Fu, Chengyin; Oviedo, María Belén; Zhu, Yihan; von Wald Cresce, Arthur; Xu, Kang; Li, Guanghui; Itkis, Mikhail E.; Haddon, Robert C.; Chi, Miaofang; Han, Yu; Wong, Bryan M.; Guo, Juchen
- Año de publicación
- 2018
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We demonstrate an unusual electrochemical reaction of sulfur with lithium upon encapsulation in narrow-diameter (subnanometer) single-walled carbon nanotubes (SWNTs). Our study provides mechanistic insight on the synergistic effects of sulfur confinement and Li+ ion solvation properties that culminate in a new mechanism of these sub-nanoscale-enabled reactions (which cannot be solely attributed to the lithiation-delithiation of conventional sulfur). Two types of SWNTs with distinct diameters, produced by electric arc (EA-SWNTs, average diameter 1.55 nm) or high-pressure carbon monoxide (HiPco-SWNTs, average diameter 1.0 nm), are investigated with two comparable electrolyte systems based on tetraethylene glycol dimethyl ether (TEGDME) and 1,4,7,10,13-pentaoxacyclopentadecane (15-crown-5). Electrochemical analyses indicate that a conventional solution-phase Li-S reaction occurs in EA-SWNTs, which can be attributed to the smaller solvated [Li(TEGDME)]+ and [Li(15-crown-5)]+ ions within the EA-SWNT diameter. In stark contrast, the Li-S confined in narrower diameter HiPco-SWNTs exhibits unusual electrochemical behavior that can be attributed to a solid-state reaction enabled by the smaller HiPco-SWNT diameter compared to the size of solvated Li+ ions. Our results of the electrochemical analyses are corroborated and supported with various spectroscopic analyses including operando Raman, X-ray photoelectron spectroscopy, and first-principles calculations from density functional theory. Taken together, our findings demonstrate that the controlled solid-state lithiation-delithiation of sulfur and an enhanced electrochemical reactivity can be achieved by sub-nanoscale encapsulation and one-dimensional confinement in narrow-diameter SWNTs.
Fil: Fu, Chengyin. University Of California Riverside; Estados Unidos
Fil: Oviedo, María Belén. University Of California Riverside; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Zhu, Yihan. Zhejiang University Of Technology; China
Fil: von Wald Cresce, Arthur. U. S. Army Research Laboratory; Estados Unidos
Fil: Xu, Kang. U. S. Army Research Laboratory; Estados Unidos
Fil: Li, Guanghui. University Of California Riverside; Estados Unidos
Fil: Itkis, Mikhail E.. University Of California Riverside; Estados Unidos
Fil: Haddon, Robert C.. University Of California Riverside; Estados Unidos
Fil: Chi, Miaofang. Oak Ridge National Laboratory; Estados Unidos
Fil: Han, Yu. King Abdullah University Of Science And Technology; Arabia Saudita
Fil: Wong, Bryan M.. University Of California Riverside; Estados Unidos
Fil: Guo, Juchen. University Of California Riverside; Estados Unidos - Materia
-
CONTROLLED SOLID-STATE REACTIONS
ELECTROCHEMICAL SYSTEMS
LITHIUM-SULFUR BATTERY
SINGLE-WALLED CARBON NANOTUBES
SUB-NANOSCALE CONFINED SULFUR - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/88431
Ver los metadatos del registro completo
| id |
CONICETDig_32544e50de5ad6fe77556473ed722d2b |
|---|---|
| oai_identifier_str |
oai:ri.conicet.gov.ar:11336/88431 |
| network_acronym_str |
CONICETDig |
| repository_id_str |
3498 |
| network_name_str |
CONICET Digital (CONICET) |
| spelling |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivityFu, ChengyinOviedo, María BelénZhu, Yihanvon Wald Cresce, ArthurXu, KangLi, GuanghuiItkis, Mikhail E.Haddon, Robert C.Chi, MiaofangHan, YuWong, Bryan M.Guo, JuchenCONTROLLED SOLID-STATE REACTIONSELECTROCHEMICAL SYSTEMSLITHIUM-SULFUR BATTERYSINGLE-WALLED CARBON NANOTUBESSUB-NANOSCALE CONFINED SULFURhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1We demonstrate an unusual electrochemical reaction of sulfur with lithium upon encapsulation in narrow-diameter (subnanometer) single-walled carbon nanotubes (SWNTs). Our study provides mechanistic insight on the synergistic effects of sulfur confinement and Li+ ion solvation properties that culminate in a new mechanism of these sub-nanoscale-enabled reactions (which cannot be solely attributed to the lithiation-delithiation of conventional sulfur). Two types of SWNTs with distinct diameters, produced by electric arc (EA-SWNTs, average diameter 1.55 nm) or high-pressure carbon monoxide (HiPco-SWNTs, average diameter 1.0 nm), are investigated with two comparable electrolyte systems based on tetraethylene glycol dimethyl ether (TEGDME) and 1,4,7,10,13-pentaoxacyclopentadecane (15-crown-5). Electrochemical analyses indicate that a conventional solution-phase Li-S reaction occurs in EA-SWNTs, which can be attributed to the smaller solvated [Li(TEGDME)]+ and [Li(15-crown-5)]+ ions within the EA-SWNT diameter. In stark contrast, the Li-S confined in narrower diameter HiPco-SWNTs exhibits unusual electrochemical behavior that can be attributed to a solid-state reaction enabled by the smaller HiPco-SWNT diameter compared to the size of solvated Li+ ions. Our results of the electrochemical analyses are corroborated and supported with various spectroscopic analyses including operando Raman, X-ray photoelectron spectroscopy, and first-principles calculations from density functional theory. Taken together, our findings demonstrate that the controlled solid-state lithiation-delithiation of sulfur and an enhanced electrochemical reactivity can be achieved by sub-nanoscale encapsulation and one-dimensional confinement in narrow-diameter SWNTs.Fil: Fu, Chengyin. University Of California Riverside; Estados UnidosFil: Oviedo, María Belén. University Of California Riverside; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Zhu, Yihan. Zhejiang University Of Technology; ChinaFil: von Wald Cresce, Arthur. U. S. Army Research Laboratory; Estados UnidosFil: Xu, Kang. U. S. Army Research Laboratory; Estados UnidosFil: Li, Guanghui. University Of California Riverside; Estados UnidosFil: Itkis, Mikhail E.. University Of California Riverside; Estados UnidosFil: Haddon, Robert C.. University Of California Riverside; Estados UnidosFil: Chi, Miaofang. Oak Ridge National Laboratory; Estados UnidosFil: Han, Yu. King Abdullah University Of Science And Technology; Arabia SauditaFil: Wong, Bryan M.. University Of California Riverside; Estados UnidosFil: Guo, Juchen. University Of California Riverside; Estados UnidosAmerican Chemical Society2018-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/88431Fu, Chengyin; Oviedo, María Belén; Zhu, Yihan; von Wald Cresce, Arthur; Xu, Kang; et al.; Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity; American Chemical Society; ACS Nano; 12; 10; 10-2018; 9775-97841936-08511936-086XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acsnano.7b08778info:eu-repo/semantics/altIdentifier/doi/10.1021/acsnano.7b08778info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:06:22Zoai:ri.conicet.gov.ar:11336/88431instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 12:06:22.626CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| title |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| spellingShingle |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity Fu, Chengyin CONTROLLED SOLID-STATE REACTIONS ELECTROCHEMICAL SYSTEMS LITHIUM-SULFUR BATTERY SINGLE-WALLED CARBON NANOTUBES SUB-NANOSCALE CONFINED SULFUR |
| title_short |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| title_full |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| title_fullStr |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| title_full_unstemmed |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| title_sort |
Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity |
| dc.creator.none.fl_str_mv |
Fu, Chengyin Oviedo, María Belén Zhu, Yihan von Wald Cresce, Arthur Xu, Kang Li, Guanghui Itkis, Mikhail E. Haddon, Robert C. Chi, Miaofang Han, Yu Wong, Bryan M. Guo, Juchen |
| author |
Fu, Chengyin |
| author_facet |
Fu, Chengyin Oviedo, María Belén Zhu, Yihan von Wald Cresce, Arthur Xu, Kang Li, Guanghui Itkis, Mikhail E. Haddon, Robert C. Chi, Miaofang Han, Yu Wong, Bryan M. Guo, Juchen |
| author_role |
author |
| author2 |
Oviedo, María Belén Zhu, Yihan von Wald Cresce, Arthur Xu, Kang Li, Guanghui Itkis, Mikhail E. Haddon, Robert C. Chi, Miaofang Han, Yu Wong, Bryan M. Guo, Juchen |
| author2_role |
author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
CONTROLLED SOLID-STATE REACTIONS ELECTROCHEMICAL SYSTEMS LITHIUM-SULFUR BATTERY SINGLE-WALLED CARBON NANOTUBES SUB-NANOSCALE CONFINED SULFUR |
| topic |
CONTROLLED SOLID-STATE REACTIONS ELECTROCHEMICAL SYSTEMS LITHIUM-SULFUR BATTERY SINGLE-WALLED CARBON NANOTUBES SUB-NANOSCALE CONFINED SULFUR |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
We demonstrate an unusual electrochemical reaction of sulfur with lithium upon encapsulation in narrow-diameter (subnanometer) single-walled carbon nanotubes (SWNTs). Our study provides mechanistic insight on the synergistic effects of sulfur confinement and Li+ ion solvation properties that culminate in a new mechanism of these sub-nanoscale-enabled reactions (which cannot be solely attributed to the lithiation-delithiation of conventional sulfur). Two types of SWNTs with distinct diameters, produced by electric arc (EA-SWNTs, average diameter 1.55 nm) or high-pressure carbon monoxide (HiPco-SWNTs, average diameter 1.0 nm), are investigated with two comparable electrolyte systems based on tetraethylene glycol dimethyl ether (TEGDME) and 1,4,7,10,13-pentaoxacyclopentadecane (15-crown-5). Electrochemical analyses indicate that a conventional solution-phase Li-S reaction occurs in EA-SWNTs, which can be attributed to the smaller solvated [Li(TEGDME)]+ and [Li(15-crown-5)]+ ions within the EA-SWNT diameter. In stark contrast, the Li-S confined in narrower diameter HiPco-SWNTs exhibits unusual electrochemical behavior that can be attributed to a solid-state reaction enabled by the smaller HiPco-SWNT diameter compared to the size of solvated Li+ ions. Our results of the electrochemical analyses are corroborated and supported with various spectroscopic analyses including operando Raman, X-ray photoelectron spectroscopy, and first-principles calculations from density functional theory. Taken together, our findings demonstrate that the controlled solid-state lithiation-delithiation of sulfur and an enhanced electrochemical reactivity can be achieved by sub-nanoscale encapsulation and one-dimensional confinement in narrow-diameter SWNTs. Fil: Fu, Chengyin. University Of California Riverside; Estados Unidos Fil: Oviedo, María Belén. University Of California Riverside; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Zhu, Yihan. Zhejiang University Of Technology; China Fil: von Wald Cresce, Arthur. U. S. Army Research Laboratory; Estados Unidos Fil: Xu, Kang. U. S. Army Research Laboratory; Estados Unidos Fil: Li, Guanghui. University Of California Riverside; Estados Unidos Fil: Itkis, Mikhail E.. University Of California Riverside; Estados Unidos Fil: Haddon, Robert C.. University Of California Riverside; Estados Unidos Fil: Chi, Miaofang. Oak Ridge National Laboratory; Estados Unidos Fil: Han, Yu. King Abdullah University Of Science And Technology; Arabia Saudita Fil: Wong, Bryan M.. University Of California Riverside; Estados Unidos Fil: Guo, Juchen. University Of California Riverside; Estados Unidos |
| description |
We demonstrate an unusual electrochemical reaction of sulfur with lithium upon encapsulation in narrow-diameter (subnanometer) single-walled carbon nanotubes (SWNTs). Our study provides mechanistic insight on the synergistic effects of sulfur confinement and Li+ ion solvation properties that culminate in a new mechanism of these sub-nanoscale-enabled reactions (which cannot be solely attributed to the lithiation-delithiation of conventional sulfur). Two types of SWNTs with distinct diameters, produced by electric arc (EA-SWNTs, average diameter 1.55 nm) or high-pressure carbon monoxide (HiPco-SWNTs, average diameter 1.0 nm), are investigated with two comparable electrolyte systems based on tetraethylene glycol dimethyl ether (TEGDME) and 1,4,7,10,13-pentaoxacyclopentadecane (15-crown-5). Electrochemical analyses indicate that a conventional solution-phase Li-S reaction occurs in EA-SWNTs, which can be attributed to the smaller solvated [Li(TEGDME)]+ and [Li(15-crown-5)]+ ions within the EA-SWNT diameter. In stark contrast, the Li-S confined in narrower diameter HiPco-SWNTs exhibits unusual electrochemical behavior that can be attributed to a solid-state reaction enabled by the smaller HiPco-SWNT diameter compared to the size of solvated Li+ ions. Our results of the electrochemical analyses are corroborated and supported with various spectroscopic analyses including operando Raman, X-ray photoelectron spectroscopy, and first-principles calculations from density functional theory. Taken together, our findings demonstrate that the controlled solid-state lithiation-delithiation of sulfur and an enhanced electrochemical reactivity can be achieved by sub-nanoscale encapsulation and one-dimensional confinement in narrow-diameter SWNTs. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018-10 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/88431 Fu, Chengyin; Oviedo, María Belén; Zhu, Yihan; von Wald Cresce, Arthur; Xu, Kang; et al.; Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity; American Chemical Society; ACS Nano; 12; 10; 10-2018; 9775-9784 1936-0851 1936-086X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/88431 |
| identifier_str_mv |
Fu, Chengyin; Oviedo, María Belén; Zhu, Yihan; von Wald Cresce, Arthur; Xu, Kang; et al.; Confined lithium–sulfur reactions in narrow-diameter carbon nanotubes reveal enhanced electrochemical reactivity; American Chemical Society; ACS Nano; 12; 10; 10-2018; 9775-9784 1936-0851 1936-086X CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acsnano.7b08778 info:eu-repo/semantics/altIdentifier/doi/10.1021/acsnano.7b08778 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| dc.format.none.fl_str_mv |
application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
American Chemical Society |
| publisher.none.fl_str_mv |
American Chemical Society |
| dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
| reponame_str |
CONICET Digital (CONICET) |
| collection |
CONICET Digital (CONICET) |
| instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
| _version_ |
1846782420452376576 |
| score |
12.982451 |