Guo Lulu, Xin Chen, Gao Jian, Zhu Jianxun, Hu Yiming, Zhang Ying, Li Junpeng, Fan Xiulin, Li Yutao, Li Hong, Qiu Jieshan, Zhou Weidong
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, China.
School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310058, China.
Angew Chem Int Ed Engl. 2021 Jun 1;60(23):13013-13020. doi: 10.1002/anie.202102605. Epub 2021 Apr 28.
Anti-perovskite type Li OHCl was previously studied as a solid-state Li conductor. Here, we report that the Li OHCl can be electrolyzed at 3.3 V or 4.0 V, with the creation of O /HCl gases and the release of 2 equiv. Li via two different decomposition routes, depending on the acidity of electrolyte. In the electrolyte with trace acid, the Li OHCl is oxidized at a constant voltage of 3.3 V. In neutral electrolyte, the oxidization of Li OHCl starts at 4.0 V, but the produced HCl will increase the acidity of electrolyte and lead to a voltage drop to 3.3 V for the electrolysis of Li OHCl. The electrolysis of Li OHCl delivers a lithium releasing capacity as high as 810 mAh g , with an equivalent Li-deposition or Li-intercalation on anode, making it a promising candidate as a Li reservoir for prelithiation of anode. Using Li OHCl as the lithium source, silicon-carbon (Si@C) composite anode can be effectively prelithiated. The full cells composed of LiNi Mn Co O (NMC811) cathode and prelithiated Si@C anode exhibited increased capacities with the increment of prelithiation dosages.
反钙钛矿型LiOHCl此前被作为一种固态锂导体进行研究。在此,我们报道LiOHCl可在3.3 V或4.0 V下进行电解,会产生O₂/HCl气体并通过两种不同的分解途径释放出2当量的Li,这取决于电解质的酸度。在含有微量酸的电解质中,LiOHCl在3.3 V的恒定电压下被氧化。在中性电解质中,LiOHCl的氧化始于4.0 V,但生成的HCl会增加电解质的酸度,并导致LiOHCl电解的电压降至3.3 V。LiOHCl的电解具有高达810 mAh g⁻¹的锂释放容量,在阳极上有等效的锂沉积或锂嵌入,这使其成为阳极预锂化锂储存库的有前途的候选材料。使用LiOHCl作为锂源,可以有效地对硅碳(Si@C)复合阳极进行预锂化。由LiNi₀.₈Mn₀.₁Co₀.₁O₂(NMC811)阴极和预锂化Si@C阳极组成的全电池随着预锂化剂量的增加容量增加。