Huang Zheng, Wang Wei, Song Wei-Li, Wang Mingyong, Chen Haosen, Jiao Shuqiang, Fang Daining
State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
Institute of Advanced Structure Technology, Beijing Institute of Technology, Beijing, 100081, P. R. China.
Angew Chem Int Ed Engl. 2022 Jun 13;61(24):e202202696. doi: 10.1002/anie.202202696. Epub 2022 Apr 20.
Aluminum-sulfur (Al-S) batteries of ultrahigh energy-to-price ratios are a promising energy storage technology, while they suffer from a large voltage gap and short lifespan. Herein, we propose an electrocatalyst-boosting quasi-solid-state Al-S battery, which involves a sulfur-anchored cobalt/nitrogen co-doped graphene (S@CoNG) positive electrode and an ionic-liquid-impregnated metal-organic framework (IL@MOF) electrolyte. The Co-N sites in CoNG continuously catalyze the breaking of Al-Cl and S-S bonds and accelerate the sulfur conversion, endowing the Al-S battery with a shortened voltage gap of 0.43 V and a high discharge voltage plateau of 0.9 V. In the quasi-solid-state IL@MOF electrolytes, the shuttle effect of polysulfides has been inhibited, which stabilizes the reversible sulfur reaction, enabling the Al-S battery to deliver 820 mAh g specific capacity and 78 % capacity retention after 300 cycles. This finding offers novel insights to design Al-S batteries for stable energy storage.
超高能量价格比的铝硫(Al-S)电池是一种很有前途的储能技术,但它们存在较大的电压差和较短的寿命。在此,我们提出了一种电催化剂增强的准固态Al-S电池,它包括硫锚定的钴/氮共掺杂石墨烯(S@CoNG)正极和离子液体浸渍的金属有机框架(IL@MOF)电解质。CoNG中的Co-N位点持续催化Al-Cl键和S-S键的断裂并加速硫转化,使Al-S电池的电压差缩短至0.43 V,放电电压平台高达0.9 V。在准固态IL@MOF电解质中,多硫化物的穿梭效应受到抑制,稳定了可逆硫反应,使Al-S电池在300次循环后具有820 mAh g的比容量和78%的容量保持率。这一发现为设计用于稳定储能的Al-S电池提供了新的见解。