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A study around the improvement of electrochemical activity of MnO{sub}2 as cathodic material in alkaline batteries

机译:关于改善碱性电池中MnO {sub} 2作为阴极材料的电化学活性的研究

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摘要

An optimized combination of reduction by methane and sulfuric acid digestion was developed to improve the electrochemical activity of manganese dioxide at a battery set. Chemical manganese dioxide, CMD, and electrolytic manganese dioxide, EMD, which have been destroyed after discharge cycling process in potential window of 900-1650 mV versus Hg/HgO, were reduced in a furnace with a flow of methane at 300 and 250 ℃ correspondingly. Thereafter, the reduced samples, CMDr and EMDr, were digested in a solution of sulfuric acid with optimized concentration and temperature. It was found that digested samples, CMDro and EMDro, typically show more stability in cycling, higher capacity and more reversible redox reaction. Alternatively, we reported about the effect of digestion temperature on electrochemical and structural properties of the samples. Digestion at temperatures 60 and 98 ℃ in 1.5 M sulfuric acid as superior concentration was preferred after comparative experiments in the range 40-98 ℃. The samples which were digested in 60 ℃ (CMDro1 and EMDro1) showed superior electrochemical activity at the early stages of discharge cycling. By contrast, the samples which were obtained at 98 ℃ (CMDro2 and EMDro2) showed more stability and were superior to the former samples in final stages of discharge cycling process. Afterward, the electrochemical behavior of the pretreated samples was investigated by means of cyclic voltammetry technique and discharge cumulative capacity profiles. Also X-ray diffraction was employed to verify the responses of voltammetric methods. In XRD patterns, peak at 29 = 28.6° which is due to β-MnO{sub}2 type was the strongest signal as temperature 98 ℃ was selected for digestion. After digestion at 60 ℃, the characteristic peaks at 26 = 38° and 42° were amplified which are attributed to formation of γ-MnO{sub}2. Interestingly enough, the results according to the XRD patterns were in good agreement with the electrochemical approaches.
机译:开发了甲烷和硫酸消解还原的优化组合,以提高电池组中二氧化锰的电化学活性。化学式二氧化锰(CMD)和电解二氧化锰(EMD)在放电循环过程中在900-1650 mV(相对于Hg / HgO)的潜在窗口中被破坏,分别在300和250℃的甲烷流中还原。此后,将还原后的样品CMDr和EMDr在具有最佳浓度和温度的硫酸溶液中进行消解。发现消化后的样品CMDro和EMDro通常在循环中显示出更高的稳定性,更高的容量和更可逆的氧化还原反应。另外,我们报道了消化温度对样品的电化学和结构性质的影响。在40-98℃的范围内进行对比实验后,最好在1.5M硫酸中以60和98℃的温度进行消化。在60℃下消化的样品(CMDro1和EMDro1)在放电循环的早期显示出优异的电化学活性。相比之下,在放电循环过程的最后阶段,在98℃下获得的样品(CMDro2和EMDro2)显示出更高的稳定性,并且优于以前的样品。然后,通过循环伏安法和放电累积容量曲线研究了预处理样品的电化学行为。还使用X射线衍射来验证伏安法的响应。在X射线衍射图中,β-MnO{sub} 2型在29 = 28.6°处的峰是最强的信号,因为选择了98℃的温度进行消化。在60℃下消化后,在26 = 38°和42°处的特征峰被放大,这归因于γ-MnO{sub} 2的形成。有趣的是,根据XRD图谱得出的结果与电化学方法非常吻合。

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