Hwan Kim, Dan Na, Dohyeon Yu, Yoonseob So, Byeonghun Oh, Young-Kwon Kim, Dong Ick Son, Inseok Seo
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The developed cell exhibits remarkable electrochemical performance, achieving a high full-depth discharge capacity of 35,502 mAh g<sup>-1</sup>, stable cycling for over 1000<!-- --> <!-- -->h at 100<!-- --> <!-- -->mA<!-- --> <!-- -->g<sup>-1</sup>, and substantially reduced polarization. These results are attributed to the synergistic interactions of the cathode components, with the δ-MnO<sub>2</sub> facilitating the CO<sub>2</sub> adsorption, γ-MnO<sub>2</sub> promoting the Li-ion diffusion, and the conductive MWCNT network boosting the electronic conductivity. Additionally, the high density and robust microstructure of the LATP electrolyte ensures reliable long-term operation and contributes to the high capacity by enabling a wider stable electrochemical window compared to liquid electrolytes. Comprehensive post-cycle analyses confirmed the improved performance, effective Li<sub>2</sub>CO<sub>3</sub> formation/decomposition, and catalyst structural integrity. 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引用次数: 0
摘要
锂-二氧化碳电池(lcb)在能量储存和二氧化碳利用方面具有巨大的前景,但其实际应用受到有限的可逆性、高极化和与液体电解质相关的安全问题的阻碍。为了解决这些问题,我们引入了一种包含nasicon型磷酸铝钛锂(LATP)固体电解质和新型MWCNT/δ&;γ-MnO2复合阴极的全固态LCB,系统地研究了MnO2相的不同作用,δ&;γ-MnO2增强二氧化碳吸附,γ-MnO2促进锂离子扩散。该电池具有优异的电化学性能,可实现35502 mAh g-1的高全深度放电容量,在100 mA g-1下稳定循环1000小时以上,并且大大降低了极化。这些结果归因于阴极组分的协同作用,δ-MnO2促进CO2吸附,γ-MnO2促进li离子扩散,导电MWCNT网络提高电子导电性。此外,与液体电解质相比,LATP电解质的高密度和坚固的微观结构确保了可靠的长期运行,并通过提供更宽的稳定电化学窗口来实现高容量。综合循环后分析证实了该催化剂的性能、Li2CO3的有效形成/分解以及催化剂结构的完整性。这些发现提供了一种可行的策略,基于明确的协同催化机制,可以克服关键挑战,实现更安全、更高效的lcb。
Stable, Hierarchical MWCNT/δ&γ-MnO2 Composite Cathode for High-Performance Solid-State Li–CO2 Batteries
Li–CO2 batteries (LCBs) hold great promise for energy storage and CO2 utilization, yet their practical use is hindered by limited reversibility, high polarization, and safety concerns associated with liquid electrolytes. To address these issues, we introduced an all-solid-state LCB incorporating a NASICON-type lithium aluminum titanium phosphate (LATP) solid electrolyte and a novel MWCNT/δ&γ-MnO2 composite cathode, where the distinct roles of the MnO2 phases were systematically investigated, with δ-MnO2 enhancing CO2 adsorption and γ-MnO2 improving Li-ion diffusion. The developed cell exhibits remarkable electrochemical performance, achieving a high full-depth discharge capacity of 35,502 mAh g-1, stable cycling for over 1000 h at 100 mA g-1, and substantially reduced polarization. These results are attributed to the synergistic interactions of the cathode components, with the δ-MnO2 facilitating the CO2 adsorption, γ-MnO2 promoting the Li-ion diffusion, and the conductive MWCNT network boosting the electronic conductivity. Additionally, the high density and robust microstructure of the LATP electrolyte ensures reliable long-term operation and contributes to the high capacity by enabling a wider stable electrochemical window compared to liquid electrolytes. Comprehensive post-cycle analyses confirmed the improved performance, effective Li2CO3 formation/decomposition, and catalyst structural integrity. These findings offer a viable strategy, rooted in a well-defined synergistic catalytic mechanism, to overcome critical challenges, enabling safer and more efficient LCBs.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.