High Capacity All-Solid-State Lithium Batteries Enabled by Pyrite-Sulfur Composites

2018 ◽  
Vol 8 (26) ◽  
pp. 1801462 ◽  
Author(s):  
Ulderico Ulissi ◽  
Seitaro Ito ◽  
Seyed Milad Hosseini ◽  
Alberto Varzi ◽  
Yuichi Aihara ◽  
...  
2012 ◽  
Vol 159 (7) ◽  
pp. A1019-A1022 ◽  
Author(s):  
James E. Trevey ◽  
Jeremy R. Gilsdorf ◽  
Conrad R. Stoldt ◽  
Se-Hee Lee ◽  
Ping Liu

2021 ◽  
Author(s):  
Luise Bloi ◽  
Felix Hippauf ◽  
Tom Boenke ◽  
Marcus Rauche ◽  
Silvia Paasch ◽  
...  

<p>For decades graphite has been used as the anode material of choice for lithium batteries since porous carbons were believed to be inappropriate because of their high potential slope during lithiation as well as capacity losses due to intense formation of solid electrolyte interphase (SEI).</p> However, in this work we demonstrate a microporous carbide-derived carbon material (HCmicro) to provide a high-capacity anode framework for lithium storage in all solid-state batteries. Half-cell measurements of HCmicro exhibit exceptionally high and reversible lithiation capacities of 1000 mAh g<sup>-1</sup><sub>carbon</sub> utilizing an extremely long voltage plateau near 0 V vs. Li/Li<sup>+</sup>. The defined microporosity of the HCmicro combined well with the argyrodite-type electrolyte (Li<sub>6</sub>PS<sub>5</sub>Cl) suppressing extensive SEI formation to deliver high coulombic efficiencies. Preliminary full-cell measurements vs. NMC-cathodes (LiNi<sub>0.9</sub>Co<sub>0.05</sub>Mn<sub>0.05</sub>O<sub>2</sub>) obtained a considerably improved average potential of 3.76 V leading to a projected energy density as high as 443 Wh kg<sup>-1</sup>. <sup>7</sup>Li Nuclear Magnetic Resonance spectroscopy was combined with ex-situ Small Angle X-ray Scattering and further electrochemical investigations to elucidate the storage mechanism of lithium inside the carbon matrix revealing the formation of extended quasi-metallic lithium clusters.


2018 ◽  
Vol 10 (12) ◽  
pp. 10029-10035 ◽  
Author(s):  
Yibo Zhang ◽  
Rujun Chen ◽  
Ting Liu ◽  
Bingqing Xu ◽  
Xue Zhang ◽  
...  

2018 ◽  
Vol 10 (26) ◽  
pp. 22329-22339 ◽  
Author(s):  
Martin Finsterbusch ◽  
Timo Danner ◽  
Chih-Long Tsai ◽  
Sven Uhlenbruck ◽  
Arnulf Latz ◽  
...  

2012 ◽  
Vol 41 (9) ◽  
pp. 886-888 ◽  
Author(s):  
Akitoshi Hayashi ◽  
Takuya Matsuyama ◽  
Atsushi Sakuda ◽  
Masahiro Tatsumisago

2015 ◽  
Vol 112 (25) ◽  
pp. 7650-7655 ◽  
Author(s):  
Naoaki Yabuuchi ◽  
Mitsue Takeuchi ◽  
Masanobu Nakayama ◽  
Hiromasa Shiiba ◽  
Masahiro Ogawa ◽  
...  

Rechargeable lithium batteries have rapidly risen to prominence as fundamental devices for green and sustainable energy development. Lithium batteries are now used as power sources for electric vehicles. However, materials innovations are still needed to satisfy the growing demand for increasing energy density of lithium batteries. In the past decade, lithium-excess compounds, Li2MeO3 (Me = Mn4+, Ru4+, etc.), have been extensively studied as high-capacity positive electrode materials. Although the origin as the high reversible capacity has been a debatable subject for a long time, recently it has been confirmed that charge compensation is partly achieved by solid-state redox of nonmetal anions (i.e., oxide ions), coupled with solid-state redox of transition metals, which is the basic theory used for classic lithium insertion materials, such as LiMeO2 (Me = Co3+, Ni3+, etc.). Herein, as a compound with further excess lithium contents, a cation-ordered rocksalt phase with lithium and pentavalent niobium ions, Li3NbO4, is first examined as the host structure of a new series of high-capacity positive electrode materials for rechargeable lithium batteries. Approximately 300 mAh⋅g−1 of high-reversible capacity at 50 °C is experimentally observed, which partly originates from charge compensation by solid-state redox of oxide ions. It is proposed that such a charge compensation process by oxide ions is effectively stabilized by the presence of electrochemically inactive niobium ions. These results will contribute to the development of a new class of high-capacity electrode materials, potentially with further lithium enrichment (and fewer transition metals) in the close-packed framework structure with oxide ions.


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