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Dual-Function Alloying Nitrate Additives Stabilize Fast-Charging Lithium Metal Batteries
Lithium metal is regarded as the “holy grail” of lithium-ion battery anodes due to its exceptionally high theoretical capacity (3800 mAh g–1) and lowest possible electrochemical potential (−3.04 V vs Li/Li+); however, lithium suffers from the dendritic formation that leads to parasitic reactions and...
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Published in: | ACS applied materials & interfaces 2024-07, Vol.16 (30), p.39341-39348 |
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creator | Paul-Orecchio, Austin G. Stockton, Lucas Barichello, Neel Petersen, Andrew Dolocan, Andrei Wang, Yixian Mitlin, David Mullins, C. Buddie |
description | Lithium metal is regarded as the “holy grail” of lithium-ion battery anodes due to its exceptionally high theoretical capacity (3800 mAh g–1) and lowest possible electrochemical potential (−3.04 V vs Li/Li+); however, lithium suffers from the dendritic formation that leads to parasitic reactions and cell failure. In this work, we stabilize fast-charging lithium metal plating/stripping with dual-function alloying M-nitrate additives (M: Ag, Bi, Ga, In, and Zn). First, lithium metal reduces M, forming lithiophilic alloys for dense Li nucleation. Additionally, nitrates form ionically conductive and mechanically stable Li3N and LiN x O y , enhancing Li-ion diffusion through the passivation layer. Notably, Zn-protected cells demonstrate electrochemically stable Li||Li cycling for 750+ cycles (2.0 mA cm–2) and 140 cycles (10.0 mA cm–2). Moreover, Zn-protected Li||Lithium Iron Phosphate full-cells achieve 134 mAh g–1 (89.2% capacity retention) after 400 cycles (C/2). This work investigates a promising solution to stabilize lithium metal plating/stripping for fast-charging lithium metal batteries. |
doi_str_mv | 10.1021/acsami.4c06385 |
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Buddie</creator><creatorcontrib>Paul-Orecchio, Austin G. ; Stockton, Lucas ; Barichello, Neel ; Petersen, Andrew ; Dolocan, Andrei ; Wang, Yixian ; Mitlin, David ; Mullins, C. Buddie</creatorcontrib><description>Lithium metal is regarded as the “holy grail” of lithium-ion battery anodes due to its exceptionally high theoretical capacity (3800 mAh g–1) and lowest possible electrochemical potential (−3.04 V vs Li/Li+); however, lithium suffers from the dendritic formation that leads to parasitic reactions and cell failure. In this work, we stabilize fast-charging lithium metal plating/stripping with dual-function alloying M-nitrate additives (M: Ag, Bi, Ga, In, and Zn). First, lithium metal reduces M, forming lithiophilic alloys for dense Li nucleation. Additionally, nitrates form ionically conductive and mechanically stable Li3N and LiN x O y , enhancing Li-ion diffusion through the passivation layer. Notably, Zn-protected cells demonstrate electrochemically stable Li||Li cycling for 750+ cycles (2.0 mA cm–2) and 140 cycles (10.0 mA cm–2). Moreover, Zn-protected Li||Lithium Iron Phosphate full-cells achieve 134 mAh g–1 (89.2% capacity retention) after 400 cycles (C/2). 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Buddie</creatorcontrib><title>Dual-Function Alloying Nitrate Additives Stabilize Fast-Charging Lithium Metal Batteries</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>Lithium metal is regarded as the “holy grail” of lithium-ion battery anodes due to its exceptionally high theoretical capacity (3800 mAh g–1) and lowest possible electrochemical potential (−3.04 V vs Li/Li+); however, lithium suffers from the dendritic formation that leads to parasitic reactions and cell failure. In this work, we stabilize fast-charging lithium metal plating/stripping with dual-function alloying M-nitrate additives (M: Ag, Bi, Ga, In, and Zn). First, lithium metal reduces M, forming lithiophilic alloys for dense Li nucleation. Additionally, nitrates form ionically conductive and mechanically stable Li3N and LiN x O y , enhancing Li-ion diffusion through the passivation layer. Notably, Zn-protected cells demonstrate electrochemically stable Li||Li cycling for 750+ cycles (2.0 mA cm–2) and 140 cycles (10.0 mA cm–2). Moreover, Zn-protected Li||Lithium Iron Phosphate full-cells achieve 134 mAh g–1 (89.2% capacity retention) after 400 cycles (C/2). 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Buddie</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paul-Orecchio, Austin G.</au><au>Stockton, Lucas</au><au>Barichello, Neel</au><au>Petersen, Andrew</au><au>Dolocan, Andrei</au><au>Wang, Yixian</au><au>Mitlin, David</au><au>Mullins, C. Buddie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dual-Function Alloying Nitrate Additives Stabilize Fast-Charging Lithium Metal Batteries</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. 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Notably, Zn-protected cells demonstrate electrochemically stable Li||Li cycling for 750+ cycles (2.0 mA cm–2) and 140 cycles (10.0 mA cm–2). Moreover, Zn-protected Li||Lithium Iron Phosphate full-cells achieve 134 mAh g–1 (89.2% capacity retention) after 400 cycles (C/2). This work investigates a promising solution to stabilize lithium metal plating/stripping for fast-charging lithium metal batteries.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39016522</pmid><doi>10.1021/acsami.4c06385</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6107-8352</orcidid><orcidid>https://orcid.org/0000-0003-1030-4801</orcidid><orcidid>https://orcid.org/0000-0001-5653-0439</orcidid><orcidid>https://orcid.org/0000-0001-6967-2153</orcidid></addata></record> |
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subjects | electrochemistry Energy, Environmental, and Catalysis Applications iron phosphates lithium lithium batteries nitrates |
title | Dual-Function Alloying Nitrate Additives Stabilize Fast-Charging Lithium Metal Batteries |
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