Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries

Anode-less batteries are a promising innovation in energy storage technology, eliminating the need for traditional anodes and offering potential improvements in efficiency and capacity. Here, we have fabricated and tested two types of anode-less pouch cells, the first using solely a copper negative...

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Main Authors: Manuela C. Baptista, Beatriz Moura Gomes, Diana Capela, Miguel F. S. Ferreira, Diana Guimarães, Nuno A. Silva, Pedro A. S. Jorge, José J. Silva, Maria Helena Braga
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Batteries
Subjects:
Online Access:https://www.mdpi.com/2313-0105/9/8/402
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author Manuela C. Baptista
Beatriz Moura Gomes
Diana Capela
Miguel F. S. Ferreira
Diana Guimarães
Nuno A. Silva
Pedro A. S. Jorge
José J. Silva
Maria Helena Braga
author_facet Manuela C. Baptista
Beatriz Moura Gomes
Diana Capela
Miguel F. S. Ferreira
Diana Guimarães
Nuno A. Silva
Pedro A. S. Jorge
José J. Silva
Maria Helena Braga
author_sort Manuela C. Baptista
collection DOAJ
description Anode-less batteries are a promising innovation in energy storage technology, eliminating the need for traditional anodes and offering potential improvements in efficiency and capacity. Here, we have fabricated and tested two types of anode-less pouch cells, the first using solely a copper negative current collector and the other the same current collector but coated with a nucleation seed ZnO layer. Both types of cells used the same all-solid-state electrolyte, Li<sub>2.99</sub>Ba<sub>0.005</sub>ClO composite, in a cellulose matrix and a LiFePO<sub>4</sub> cathode. Direct and indirect methods confirmed Li metal anode plating after charging the cells. The direct methods are X-ray photoelectron spectroscopy (XPS) and laser-induced breakdown spectroscopy (LIBS), a technique not divulged in the battery world but friendly to study the surface of the negative current collector, as it detects lithium. The indirect methods used were electrochemical cycling and impedance and scanning electron microscopy (SEM). It became evident the presence of plated Li on the surface of the current collector in contact with the electrolyte upon charging, both directly and indirectly. A maximum average lithium plating thickness of 2.9 µm was charged, and 0.13 µm was discharged. The discharge initiates from a maximum potential of 3.2 V, solely possible if an anode-like high chemical potential phase, such as Li, would form while plating. Although the ratings and energy densities are minor in this study, it was concluded that a layer of ZnO, even at 25 °C, allows for higher discharge power for more hours than plain Cu. It was observed that where Li plates on ZnO, Zn is not detected or barely detected by XPS. The present anode-less cells discharge quickly initially at higher potentials but may hold a discharge potential for many hours, likely due to the ferroelectric character of the electrolyte.
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spelling doaj.art-ad6d59df6f9e44438fa0c8cbeb5f3b862023-11-19T00:15:41ZengMDPI AGBatteries2313-01052023-08-019840210.3390/batteries9080402Conditioning Solid-State Anode-Less Cells for the Next Generation of BatteriesManuela C. Baptista0Beatriz Moura Gomes1Diana Capela2Miguel F. S. Ferreira3Diana Guimarães4Nuno A. Silva5Pedro A. S. Jorge6José J. Silva7Maria Helena Braga8Engineering Physics Department, Engineering Faculty, University of Porto, 4200-465 Porto, PortugalEngineering Physics Department, Engineering Faculty, University of Porto, 4200-465 Porto, PortugalPhysics and Astronomy Department, Sciences Faculty, University of Porto, 4169-007 Porto, PortugalPhysics and Astronomy Department, Sciences Faculty, University of Porto, 4169-007 Porto, PortugalPhysics and Astronomy Department, Sciences Faculty, University of Porto, 4169-007 Porto, PortugalPhysics and Astronomy Department, Sciences Faculty, University of Porto, 4169-007 Porto, PortugalPhysics and Astronomy Department, Sciences Faculty, University of Porto, 4169-007 Porto, PortugalMota Ceramic Solutions Portugal, Apartado 8, Meirinhas, 3106-601 Pombal, PortugalEngineering Physics Department, Engineering Faculty, University of Porto, 4200-465 Porto, PortugalAnode-less batteries are a promising innovation in energy storage technology, eliminating the need for traditional anodes and offering potential improvements in efficiency and capacity. Here, we have fabricated and tested two types of anode-less pouch cells, the first using solely a copper negative current collector and the other the same current collector but coated with a nucleation seed ZnO layer. Both types of cells used the same all-solid-state electrolyte, Li<sub>2.99</sub>Ba<sub>0.005</sub>ClO composite, in a cellulose matrix and a LiFePO<sub>4</sub> cathode. Direct and indirect methods confirmed Li metal anode plating after charging the cells. The direct methods are X-ray photoelectron spectroscopy (XPS) and laser-induced breakdown spectroscopy (LIBS), a technique not divulged in the battery world but friendly to study the surface of the negative current collector, as it detects lithium. The indirect methods used were electrochemical cycling and impedance and scanning electron microscopy (SEM). It became evident the presence of plated Li on the surface of the current collector in contact with the electrolyte upon charging, both directly and indirectly. A maximum average lithium plating thickness of 2.9 µm was charged, and 0.13 µm was discharged. The discharge initiates from a maximum potential of 3.2 V, solely possible if an anode-like high chemical potential phase, such as Li, would form while plating. Although the ratings and energy densities are minor in this study, it was concluded that a layer of ZnO, even at 25 °C, allows for higher discharge power for more hours than plain Cu. It was observed that where Li plates on ZnO, Zn is not detected or barely detected by XPS. The present anode-less cells discharge quickly initially at higher potentials but may hold a discharge potential for many hours, likely due to the ferroelectric character of the electrolyte.https://www.mdpi.com/2313-0105/9/8/402anode-less batterysolid-state electrolytelithium batterybattery conditioningLiFePO<sub>4</sub>
spellingShingle Manuela C. Baptista
Beatriz Moura Gomes
Diana Capela
Miguel F. S. Ferreira
Diana Guimarães
Nuno A. Silva
Pedro A. S. Jorge
José J. Silva
Maria Helena Braga
Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
Batteries
anode-less battery
solid-state electrolyte
lithium battery
battery conditioning
LiFePO<sub>4</sub>
title Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
title_full Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
title_fullStr Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
title_full_unstemmed Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
title_short Conditioning Solid-State Anode-Less Cells for the Next Generation of Batteries
title_sort conditioning solid state anode less cells for the next generation of batteries
topic anode-less battery
solid-state electrolyte
lithium battery
battery conditioning
LiFePO<sub>4</sub>
url https://www.mdpi.com/2313-0105/9/8/402
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