Utilizing the capacity below 0 V to maximize lithium storage of hard carbon anodes

A team of researchers has systematically explored the true reversibility of hard carbon anodes below 0 V that works identify the lithiation boundary parameters that control the reversible capacity of hard carbon anodes. The lithium storage capacity of hard carbon has been almost doubled. Meanwhile, the lithium storage mechanism of hard carbons is revealed. This work enables insights of the potentially low-voltage performance of hard carbons in lithium-ion batteries.

 

The team of Chinese researchers from Chinese Academy of Sciences published their work in the journal Particuology (Utilizing the capacity below 0 V to maximize lithium storage of hard carbon anodes) on March 17, 2023.

 

Hard carbons (HCs) have been emerging as promising anode materials for lithium-ion batteries because of their low redox potential and high reversible capacities. HCs consist of plentiful randomly oriented graphene nanosheets as described by the ‘house of cards’ model. Such a nanoarchitecture endows HCs with large interlayer spacing (0.37-0.4 nm) and abundant amorphous microstructures (defects, short-range microcrystalline, and rich pore structures), which makes more than half of the total capacity of HCs comes from the plateau area (below 0 V). Utilizing the plateau capacity of HCs actually enhances the operating voltage as well as the energy density when coupled with cathodes. However, limited by the experience gained from graphite anode, considerable reports on HCs have mainly focused on the lithium storage capacity above 0 V.

 

In order to utilize the lithium storage capacity of HCs below 0 V effectively, the research team investigated the following issues: 1) How much capacity is endurable for long-term cycling, 2) What is the kinetic performance of this part of the capacity, 3) What is the lithium storage mechanism of hard carbon? Next, using the commercial HCs as anodes, the limit of reversible lithium storage capacity of hard carbon was systematically investigated. The cells are lithiated to a series of depths (V-0, C-400, C-500 and C-600). The V-0 exhibits a capacity of 209 mAh g^-1 and the voltage of C-400, C-500, C-600 is -0.028, -0.032 and -0.038 V, respectively.

 

The team observed the surface morphology of electrodes at different lithiation depths. A large number of lithium dendrites appeared on the surface of high lithiation depths (C-500 and C-600). No dendrites were found on the surface of V-0 and C-400.

 

The research team further tested the rate (25, 50 and 100 mA g^-1) and cycle performance of hard carbons at different lithiation depths. The results show that the C-400 exhibits a high average CE of above 99.5% at 50 mA g^-1 and operate 172 cycles with a capacity of 80%. Compared with discharging to 0 V, C-400 provides a nearly twice reversible capacity. C-500 and C-600 were prone to failure during cycles due to increased cell polarization caused by lithium dendrites.

 

The research team finally analyzed lithium storage behavior of hard carbon below 0 V. The results of characterization and finite element model reveal that the large reversible capacity below 0 V of hard carbon anodes is mainly benefited from the dual effect of lithium intercalation and reversible lithium film.

 

“This work enables insights of the potentially low-voltage performance of hard carbons in lithium-ion batteries,” said Cheng-meng Chen at Chinese Academy of Sciences.Because utilizing the capacity below 0 V can make the hard carbon capacity fully to release and increase the anode gram capacity, it can make full cells higher energy density.

 

“In the next step, our research team will explore more suitable electrolytes for enhancing the performance of hard carbon below 0 V,” said Liu. In this way, the researchers might expand the application hard carbons and also improve the potential for practical applications. “Our ultimate goal is to provide the hard carbon anode for lithium-ion batteries that can be used in a variety of environments with high capacity and long cycle performance,” said Liu.

 

The research team includes Qianlei Liu, Liqin Dai, Lijing Xie, Zonglin Yi, Mingxin Song, Yafeng Fan, Guohua Sun, Fangyuan Su and Cheng-Meng Chen from CAS Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences.

 

The research is funded by National Key Research and Development (R&D) Program of China, National Science Foundation for Excellent Young Scholars of China, the Youth Innovation Promotion Association of CAS, Research and Development Project of Key Core and Common Technology of Shanxi Province, Key Research and Development (R&D) Projects of Shanxi Province.

 

Particuology (IF=3.251) is an interdisciplinary journal that publishes frontier research articles and critical reviews on the discovery, formulation and engineering of particulate materials, processes and systems. Topics are broadly relevant to the production of materials, pharmaceuticals and food, the conversion of energy resources, and protection of the environment. For more information, please visit: https://www.journals.elsevier.com/particuology.

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