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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/88431

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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
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