Haoteng Wu , Haiwei Wu , Xuan Ren , Ruihua Li , Huan Wang , Wenhao Jia , Zhihua Lin , Hanbin Liu , Chuanyin Xiong , Lin Zhang
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引用次数: 0
摘要
穿梭效应和硫氧化还原动力学迟缓是影响锂硫电池循环寿命的主要因素。因此,研究具有大量活性位点和高活性的电催化剂来改善可溶性锂多硫化物(lip)的转化动力学是解决这些问题的关键。本研究以细菌纤维素(BNF)为载体,通过部分磷酸化制备了表面工程诱导的高分散性、多晶结构的磷酸镍氧化物(NiOPs)催化剂。具体而言,优化后的NiOP-1h(磷化1h)催化剂具有丰富的Ni2P/Ni5P4多晶结构,且与LiPS具有良好的相互作用,大大优于原始NiO、N2P等部分磷化NiOP的硫氧化还原性能。采用NiOP-1h纸基电极的锂电池在0.15℃下,即使硫负载为4 mg cm - 2,电解液为6.7 μ L mg -1,也能达到3.4 mAh cm - 2的最大容量。该方法具有制备高分散性和丰富活性位点的电催化剂的潜力,在其他领域具有广泛的应用前景。
Surface engineering-induced highly dispersed and polycrystalline structured nickel phosphide nano catalysts for lithium-sulfur batteries
The shuttle effect and sluggish sulfur redox kinetics are the primary factors that influence the cycle life of lithium-sulfur (Li-S) batteries. Therefore, investigating electrocatalysts with a large number of active sites and high activity to improve the conversion kinetics of soluble lithium polysulfides (LiPS) is quite critical to solve these problems. In this study, surface engineering induced highly dispersible and polycrystalline structured catalyst of phosphatized nickel oxides (NiOPs) was prepared using bacterial cellulose (BNF) as a carrier and followed by partial phosphorization. Specifically, the as optimized nano NiOP-1 h (phosphating for 1 h) catalyst show an abundant polycrystalline structure of Ni2P/Ni5P4 and also appropriate interaction with LiPS, which helps it greatly overperform the pristine NiO, N2P and other partially phosphorized NiOP for enhancing the sulfur redox. The Li-S cells with paper-based NiOP-1 h electrodes can achieve a maximum capacity of 3.4 mAh cm−2 at 0.15C, even with sulfur loading of 4 mg cm−2 and lean electrolyte of 6.7 µL mg−1. This method demonstrates the potential for preparing electrocatalysts characterized by high dispersibility and abundant active sites, offering applications in various other domains.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.