Qiu Chuang, Li Ang, Qiu Daping, Wu Yawen, Jiang Zhijie, Zhang Jiapeng, Xiao Jianqi, Yuan Renlu, Jiang Zipeng, Liu Xuewei, Chen Xiaohong, Song Huaihe
State Key Laboratory of Chemical Resources Engineering, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029, P. R. China.
Hubei Provincial Collaborative Innovation Center for New Energy Microgrid, College of Electrical Engineering & New Energy, China Three Gorges University, Yichang 443002, Hubei, China.
ACS Nano. 2024 May 7;18(18):11941-11954. doi: 10.1021/acsnano.4c02046. Epub 2024 Apr 23.
Closed pores play a crucial role in improving the low-voltage (<0.1 V) plateau capacity of hard carbon anodes for sodium-ion batteries (SIBs). However, the lack of simple and effective closed-pore construction strategies, as well as the unclear closed-pore formation mechanism, has severely hindered the development of high plateau capacity hard carbon anodes. Herein, we present an effective closed-pore construction strategy by one-step pyrolysis of zinc gluconate (ZG) and elucidate the corresponding mechanism of closed-pore formation. The closed-pore formation mechanism during the pyrolysis of ZG mainly involves (i) the precipitation of ZnO nanoparticles and the ZnO etching on carbon under 1100 °C to generate open pores of 0.45-4 nm and (ii) the development of graphitic domains and the shrinkage of the partial open pores at 1100-1500 °C to convert the open pores to closed pores. Benefiting from the considerable closed-pore content and suitable microstructure, the optimized hard carbon achieves an ultrahigh reversible specific capacity of 481.5 mA h g and an extraordinary plateau capacity of 389 mA h g for use as the anode of SIBs. Additionally, some in situ and ex situ characterizations demonstrate that the high-voltage slope capacity and the low-voltage plateau capacity stem from the adsorption of Na at the defect sites and Na-cluster formation in closed pores, respectively.
封闭孔在提高钠离子电池(SIBs)硬碳负极的低电压(<0.1 V)平台容量方面起着至关重要的作用。然而,缺乏简单有效的封闭孔构建策略以及封闭孔形成机制不明确,严重阻碍了高平台容量硬碳负极的发展。在此,我们通过葡萄糖酸锌(ZG)的一步热解提出了一种有效的封闭孔构建策略,并阐明了相应的封闭孔形成机制。ZG热解过程中的封闭孔形成机制主要包括:(i)在1100℃下ZnO纳米颗粒的沉淀以及ZnO对碳的蚀刻,以产生0.45-4nm的开孔;(ii)在1100-1500℃下石墨域的发展以及部分开孔的收缩,将开孔转化为封闭孔。受益于大量的封闭孔含量和合适的微观结构,优化后的硬碳作为SIBs的负极实现了481.5 mA h g的超高可逆比容量和389 mA h g的非凡平台容量。此外,一些原位和非原位表征表明,高电压斜率容量和低电压平台容量分别源于缺陷位点处Na的吸附和封闭孔中Na团簇的形成。