提高溶解度的LiBOB细粉的合成

E. M. Wigayati, T. Lestariningsih, C. Ratri, I. Purawiardi, B. Prihandoko
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引用次数: 6

摘要

双(草酸)硼酸锂(LiBOB)化合物因其在锂离子电池系统中作为电解质盐具有潜在的可行性而引起了研究人员的兴趣。该化合物易于合成,由于不含光晕元素,与传统的电解质盐相比,被认为是更环保的。本文主要研究了LiBOB纳米粉体的合成,其主要目的是提高LiBOB在液态电解质溶液中的溶解度。这将有助于电极之间的i - on传递,从而提高电解质的性能。本实验采用固相反应。以二水合草酸、一水合氢氧化锂和硼酸为原料,合成了LiBOB化合物。然后用球磨技术将得到的粉末在不同的球磨时间(0、6、10和13)h内加工成细粉。然后分析样品的微观结构,以获得有关相形成,官能团,谷物表面形貌,表面积,孔隙体积,溶解度和离子电导率的信息。分析表明,反应过程中形成了lib0和LiBOB水合物相,磨矿过程中现有相没有变化,结晶度指数下降,但官能团没有变化。在10小时的钻削过程中,比表面积最大值为83.11 m /g,孔隙体积为1.21311e+02 A。粉末粒度越小,溶解度越高,但离子电导率降低。
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Synthesis of LiBOB Fine Powder to Increase Solubility
Lithium bis (oxalate) borate or LiBOB compound has c ptured interest of researchers, because it is pot entially viable to be used as electrolyte salt in lithium-ion battery system. This compound is easy to synthesize and con sidered to be more environmentally friendly compared to conventional e lectrolyte salt because LiBOB does not contain halo gen element. This research focused on the synthesis of LiBOB fin e powder, which main purpose is improving LiBOB sal t solubility in liquid electrolyte solution. This will aid the i on transfer between electrodes which in turn will i ncrease the electrolyte performance. Solid state reaction was employed in t his experiment. Synthesis of LiBOB compound was per formed by reacting oxalic acid dihydrate, lithium hydroxide m onohydrate, and boric acid. The resulting powder wa s then processed into fine powder using ball milling techn ique with varying milling time (0, 6, 10, and 13) h our. Microstructure of the sample was then analyzed to obtain informati on regarding phase formation, functional groups, gr ain surface morphology, surface area, pore volume, solubility, and ionic conductivity. The analysis shown that LiB O and LiBOB hydrate phase was formed during the reaction, there was no changed in existing phase during milling pr ocess, crystallinity index was shifted to lower value but there was no difference in functional groups. Highe st value in surface area was found to be 83.11 m /g, with pore volume of 1.21311e+02 A at 10 hours m illing. Smaller powder size resulted in higher solubility, unfortunately the ionic condu ctivity was found to be decreased.
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