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Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range

[Image: see text] The electrochemical performance of Ge, an alloying anode in the form of directly grown nanowires (NWs), in Li-ion full cells (vs LiCoO(2)) was analyzed over a wide temperature range (−40 to 40 °C). LiCoO(2)||Ge cells in a standard electrolyte exhibited specific capacities 30× and 5...

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Autores principales: Collins, Gearoid A., McNamara, Karrina, Kilian, Seamus, Geaney, Hugh, Ryan, Kevin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288911/
https://www.ncbi.nlm.nih.gov/pubmed/34296064
http://dx.doi.org/10.1021/acsaem.0c02928
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author Collins, Gearoid A.
McNamara, Karrina
Kilian, Seamus
Geaney, Hugh
Ryan, Kevin M.
author_facet Collins, Gearoid A.
McNamara, Karrina
Kilian, Seamus
Geaney, Hugh
Ryan, Kevin M.
author_sort Collins, Gearoid A.
collection PubMed
description [Image: see text] The electrochemical performance of Ge, an alloying anode in the form of directly grown nanowires (NWs), in Li-ion full cells (vs LiCoO(2)) was analyzed over a wide temperature range (−40 to 40 °C). LiCoO(2)||Ge cells in a standard electrolyte exhibited specific capacities 30× and 50× those of LiCoO(2)||C cells at −20 and −40 °C, respectively. We further show that propylene carbonate addition further improved the low-temperature performance of LiCoO(2)||Ge cells, achieving a specific capacity of 1091 mA h g(–1) after 400 cycles when charged/discharged at −20 °C. At 40 °C, an additive mixture of ethyl methyl carbonate and lithium bis(oxalato)borate stabilized the capacity fade from 0.22 to 0.07% cycle(–1). Similar electrolyte additives in LiCoO(2)||C cells did not allow for any gains in performance. Interestingly, the capacity retention of LiCoO(2)||Ge improved at low temperatures due to delayed amorphization of crystalline NWs, suppressing complete lithiation and high-order Li(15)Ge(4) phase formation. The results show that alloying anodes in suitably configured electrolytes can deliver high performance at the extremes of temperature ranges where electric vehicles operate, conditions that are currently not viable for commercial batteries without energy-inefficient temperature regulation.
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spelling pubmed-82889112021-07-20 Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range Collins, Gearoid A. McNamara, Karrina Kilian, Seamus Geaney, Hugh Ryan, Kevin M. ACS Appl Energy Mater [Image: see text] The electrochemical performance of Ge, an alloying anode in the form of directly grown nanowires (NWs), in Li-ion full cells (vs LiCoO(2)) was analyzed over a wide temperature range (−40 to 40 °C). LiCoO(2)||Ge cells in a standard electrolyte exhibited specific capacities 30× and 50× those of LiCoO(2)||C cells at −20 and −40 °C, respectively. We further show that propylene carbonate addition further improved the low-temperature performance of LiCoO(2)||Ge cells, achieving a specific capacity of 1091 mA h g(–1) after 400 cycles when charged/discharged at −20 °C. At 40 °C, an additive mixture of ethyl methyl carbonate and lithium bis(oxalato)borate stabilized the capacity fade from 0.22 to 0.07% cycle(–1). Similar electrolyte additives in LiCoO(2)||C cells did not allow for any gains in performance. Interestingly, the capacity retention of LiCoO(2)||Ge improved at low temperatures due to delayed amorphization of crystalline NWs, suppressing complete lithiation and high-order Li(15)Ge(4) phase formation. The results show that alloying anodes in suitably configured electrolytes can deliver high performance at the extremes of temperature ranges where electric vehicles operate, conditions that are currently not viable for commercial batteries without energy-inefficient temperature regulation. American Chemical Society 2021-02-02 2021-02-22 /pmc/articles/PMC8288911/ /pubmed/34296064 http://dx.doi.org/10.1021/acsaem.0c02928 Text en © 2021 American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Collins, Gearoid A.
McNamara, Karrina
Kilian, Seamus
Geaney, Hugh
Ryan, Kevin M.
Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title_full Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title_fullStr Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title_full_unstemmed Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title_short Alloying Germanium Nanowire Anodes Dramatically Outperform Graphite Anodes in Full-Cell Chemistries over a Wide Temperature Range
title_sort alloying germanium nanowire anodes dramatically outperform graphite anodes in full-cell chemistries over a wide temperature range
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288911/
https://www.ncbi.nlm.nih.gov/pubmed/34296064
http://dx.doi.org/10.1021/acsaem.0c02928
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