Effect of Depth of Discharge on the Performance of Zn-Mn and Zn-Ni Battery

IF 0.2 Q4 ENERGY & FUELS Journal of The Japan Institute of Energy Pub Date : 2021-08-20 DOI:10.3775/jie.100.144
Nattaporn Chaba, Sutasinee Neramittagapong, Arthit Neramittagapong, N. Eua-anant, S. Theerakulpisut
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Abstract

In this communication, the zinc anode electrode was prepared by electroplating. MnO2 cathodes and Ni(OH)2 cathode electrodes were prepared by the pressing process. KOH 6 M with 40%ZnO were used as the electrolyte solution of a battery. X-ray diffraction (XRD) was used to study the complexation of cathode electrodes. The Fourier transform infrared spectroscopy (FTIR) analysis showed some peaks which ascertain chemical interlinking of ZnMnO2 and Zn-Ni(OH)2 on cathode electrodes. After performance testing, morphology characterization of zinc anode electrode was performed by scanning electron microscopy (SEM). The electrodes were tested for performance by a battery analyzer for 100 cycles with a depth of discharge (DOD) at 10%, 20%, 40%, and 80%. It was found that zinc electrodes had branching of a dendrite, which quickly grew at a high depth of discharge. The depth of discharge influenced dendrite growth and the battery performance during cell discharging at high DOD. The Zn anode was damaged due to the excessive dissolution of Zn+ in the electrolyte, causing the decay of the Zn anode. On the other hand, during cell charging, Zn+ was not uniformly deposited on the anode, resulting in dendrite branching. Zinc electrode in Zn-MnO2 cell had more dendrite than zinc electrode in Zn-Ni(OH)2 cell at 10%DOD. The results also showed higher efficiency of 99.08% and better stability for Zn-Ni(OH)2 than Zn-MnO2 cells in similar conditions. This was due to the fact that during cell discharge. Mn+ in the electrolyte continuously reacts with Zn+ to form other complex compounds. On the contrary, Ni(OH)2 cathode exhibited better recyclability than MnO2 cathode. Therefore, Ni(OH)2 cathode offers excellent potential for use as a cathode electrode because it can be used at high DOD. Another advantage of Ni(OH)2 cathode is that it can be prepared from a simple process by making use of readily available non-toxic materials.
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放电深度对锌锰和锌镍电池性能的影响
本通讯采用电镀法制备锌阳极电极。采用压制法制备了二氧化锰阴极和Ni(OH)2阴极电极。以KOH 6m和40%ZnO作为电池的电解液。采用x射线衍射(XRD)对阴极电极的络合进行了研究。傅里叶变换红外光谱(FTIR)分析显示,在阴极电极上发现了锌氧化锰和锌镍(OH)2的化学连接。经性能测试后,利用扫描电镜对锌阳极电极进行形貌表征。在放电深度(DOD)为10%、20%、40%和80%的情况下,通过电池分析仪测试电极的性能,进行100次循环。发现锌电极具有枝晶分支,在高放电深度下枝晶迅速生长。在高放电深度下,放电深度对电池枝晶生长和性能有影响。电解液中Zn+的过量溶解导致Zn阳极的损坏,导致Zn阳极的衰减。另一方面,在电池充电过程中,Zn+没有均匀沉积在阳极上,导致枝晶分支。在10%DOD下,Zn-MnO2电池中的锌电极比Zn-Ni(OH)2电池中的锌电极有更多的枝晶。结果还表明,在相同条件下,Zn-Ni(OH)2电池的效率比Zn-MnO2电池高99.08%,稳定性更好。这是由于在电池放电过程中。电解液中的Mn+不断与Zn+反应生成其他络合物。相反,Ni(OH)2阴极比MnO2阴极具有更好的可回收性。因此,Ni(OH)2阴极可以在高DOD下使用,具有很好的潜力作为阴极电极。镍(OH)2阴极的另一个优点是,它可以通过一个简单的过程,利用现成的无毒材料制备。
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CiteScore
0.60
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发文量
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