Synthesis of MnO2 Carbon nanotubes catalyst with enhanced Oxygen Reduction Reaction for Polymer Electrolyte Membrane Fuel Cell

IF 0.1 Q4 ENGINEERING, CHEMICAL
Muhammad Sadiq, M. Arif, A. Ullah, A. Naveed, S. Afridi, M. Humayun, M. Naeem Khan, M. Asif
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Abstract

Polymer Electrolyte Membrane Fuel Cell (PEMFC), an electrochemical power generating technology, uses a precious metal Platinum (Pt) catalyst for Oxygen Reduction Reaction (ORR), which is a major hindrance in its commercialization. Using a non-precious group metal (NPGM) instead of Pt will reduces the cost of PEMFCs. Herein MnO2 carbon nanotubes (CNTs) were synthesized by impregnating the transition metal in large surface carbonaceous material CNTs by hydrothermal synthesis techniques. To enhance the catalytic reaction and increase the volumetric current density, the sample was pyrolyzed at 800 0C temperature under nitrogen atmosphere. During pyrolysis, the nitrogen was also doped in the framework of carbonaceous materials. The materials were then treated with acid, removing the unreacted metals and adding oxygen functional group to the CNT framework due to which the activity of the catalyst is amplified. The catalysts have been characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), Catalyst activity has been calculated by Rotating Disc Electrode (RDE) experiment. The resulting materials are stronger in experimental conditions in alkaline environment and have high electro catalytic activity for oxygen reduction reaction (ORR). Linear Sweep Voltammetry (LSV) depicts a current density of - 4.0 mA/cm2 and over potential of -0.3V vs. Standard Calomel Electrode (SCE) in 0.1M KOH electrolyte. Rotating Disk Electrode (RDE) was conducted at 400, 800, 1200, and 1600 rpm. The results of MnO2CNT show a desirable future aspect in fuel cell commercialization.
聚合物电解质膜燃料电池用增强氧还原反应合成MnO2碳纳米管催化剂
聚合物电解质膜燃料电池(PEMFC)是一种电化学发电技术,其氧还原反应(ORR)使用贵金属铂(Pt)催化剂,这是其商业化的主要障碍。使用非贵重族金属(NPGM)代替Pt将降低pemfc的成本。本文采用水热合成技术将过渡金属浸渍在大表面碳质材料碳纳米管中,制备了二氧化锰碳纳米管。为了加强催化反应,提高体积电流密度,在氮气气氛下,在800℃温度下对样品进行热解。在热解过程中,氮也掺杂在碳质材料的框架中。然后用酸处理这些材料,去除未反应的金属,并在碳纳米管框架上添加氧官能团,因此催化剂的活性被放大。用扫描电镜(SEM)、x射线衍射(XRD)对催化剂进行了表征,用旋转圆盘电极(RDE)实验计算了催化剂的活度。所得材料在实验条件下在碱性环境下较强,对氧还原反应(ORR)具有较高的电催化活性。线性扫描伏安法(LSV)描述了在0.1M KOH电解质中,与标准甘汞电极(SCE)相比,电流密度为- 4.0 mA/cm2,过电位为-0.3 v。旋转圆盘电极(RDE)在400、800、1200和1600 rpm下进行。MnO2CNT的结果显示了燃料电池商业化的一个理想的未来方面。
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