乙二醇
过电位
塔菲尔方程
化学工程
材料科学
纳米材料
电催化剂
析氧
电化学
制氢
电极
纳米结构
分解水
催化作用
无机化学
纳米技术
化学
光催化
有机化学
工程类
物理化学
作者
S. Swathi,R. Yuvakkumar,P. Senthil Kumar,G. Ravi,Dhayalan Velauthapillai,Dai‐Viet N. Vo
出处
期刊:Fuel
[Elsevier]
日期:2021-07-04
卷期号:302: 121151-121151
被引量:6
标识
DOI:10.1016/j.fuel.2021.121151
摘要
In this research, manganese carbonate nanostructures were prepared employing simple co-precipitation route using ethylene glycol. Rhombohedral phase of MnCO3 nanostructures was determined by X-ray diffraction. MnCO3@15 ml EG electrode exhibited small Tafel slope value and significantly facilitating its OER performance. The fabricated electrode materials of MnCO3 nanostructure exhibited high 257 mA/g current density with low 184 mV overpotential. The prepared electrodes explored excellent OER performance and good stability over 16 h without degradation. Organic additive of ethylene glycol tuning its morphology to favor of OER activity and it enhanced the electrochemical performance of MnCO3 nanomaterial. MnCO3 material was also subjected to photocatalytic hydrogen production. There was no activity noticed in the pure water even after 3 h of experiments. The following factor may enhance the H2 evolution rate. They are introducing hetero-atoms in crystal lattice points, combination with carbon materials such as GO, g-C3N4 etc and composed of heterostructures with some other material such as TMDs, CdS, TiO2 and ZnS etc. Hence, mono metal carbonate of MnCO3 doesn't show any H2 activity and the fabricated electrode was suitable candidate for oxygen evolution reaction.
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