Component modulation strategy of waste camellia shells via hydrogen-bond competition within neutral deep eutectic solvents to construct hard carbon as a high-performance sodium-ion battery anode
Jiaying Chen , Xi Yu , Yuejin Zhan , Jing Huang , Hanlin Hu , Bi Luo , Hui Li , Ping Gao , Yefeng Zhou
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引用次数: 0
Abstract
Deep eutectic solvents (DESs) pretreatment is a key strategy for modulating the three major components of waste biomass (cellulose, hemicellulose, and lignin). However, it is still a challenge to regulate the biomass components via DESs to construct a multi-closed-pore structure within hard carbon. This work presents a novel neutral DES pretreatment approach based on hydrogen-bond competition for waste camellia shells to construct a hard-carbon anode for high-performance sodium-ion batteries. DES pretreatment selectively dissolves and removes amorphous components (partial lignin, hemicellulose, and amorphous cellulose), allowing cellulose chains to rearrange into a more ordered structure, thereby increasing cellulose crystallinity. A higher cellulose-to-lignin ratio in the precursor favors an increase in the closed-pore proportion and promotes the formation of closed-pore walls of the hard-carbon. By optimizing the DES treatment time to 0.5 h, the hard-carbon material (HC-0.50) pyrolyzed from the pretreated biomass exhibits a high closed-pore volume and abundant defect sites, which is beneficial for enhancing sodium storage capacity. Furthermore, the flake-like structure and the large interlayer spacing (0.378 nm) favor diffusion kinetics. Consequently, HC-0.50 achieves a reversible capacity of 304.2 mAh g−1 at 0.1 C, which is 72 mAh g−1 higher than that of the untreated sample (HC-0). Additionally, HC-0.5 delivers an initial coulombic efficiency of 81.52%. This work reports a preparation method for a high-performance sodium-storage hard-carbon anode by precisely controlling the composition of waste camellia shells.
深度共晶溶剂(DESs)预处理是调节废生物质(纤维素、半纤维素和木质素)三种主要成分的关键策略。然而,如何通过DESs调控生物质组分,在硬碳内部构建多闭孔结构仍然是一个挑战。本文提出了一种基于废弃茶花壳氢键竞争的中性DES预处理方法,用于构建高性能钠离子电池的硬碳阳极。DES预处理选择性地溶解和去除无定形成分(部分木质素、半纤维素和无定形纤维素),使纤维素链重新排列成更有序的结构,从而提高纤维素的结晶度。前驱体中纤维素与木质素的比例越高,有利于增加闭孔比例,促进硬炭闭孔壁的形成。通过优化DES处理时间至0.5 h,预处理后的生物质热解后的硬碳材料(HC-0.50)具有较高的闭孔体积和丰富的缺陷位点,有利于提高钠的存储容量。片状结构和较大的层间距(0.378 nm)有利于扩散动力学。因此,HC-0.50在0.1℃下达到304.2 mAh g - 1的可逆容量,比未经处理的样品(HC-0)高72 mAh g - 1。此外,HC-0.5的初始库仑效率为81.52%。本文报道了一种通过精确控制废茶花壳的组成来制备高性能储钠硬碳阳极的方法。
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.