Nitrogen doping of materials with melamine for proton exchange membrane fuel cells: Pre-treatment of carbon support or post treatment of the electrocatalyst

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Pınar Çelik, Ayşe Bayrakçeken
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Abstract

In this study, two different routes were followed for nitrogen doping and compared with each other. In the first route, carbon support was nitrogen doped (Method 1). In the second route, firstly, carbon supported Pt catalysts were synthesized, and then these electrocatalysts were nitrogen doped (Method 2). Physical characterizations including elemental analysis, inductively coupled plasma mass spectrometer (ICP-MS), Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy, Brunauer–Emmett–Teller (BET) analysis, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), transmission electron microscopy (TEM), contact angle measurement, and PEM fuel cell performance tests were performed. In Method 1, Pt/C:M-4:1/Pre catalyst showed the current density of 235.5 mA/cm2 @0.6 V and a max. power density of 160.5 mW/cm2. In Method 2, Pt/C:M-1:1/Post electrocatalyst had the current density of 626.0 mA/cm2 @0.6 V and a max. power density of 374.3 mW/cm2. Maximum power density obtained for Method 2 was 2.3 times higher than the electrocatalyst prepared with Method 1. Overall, it was observed that nitrogen doping of the electrocatalyst gave better result than nitrogen doping of the support material.

质子交换膜燃料电池用三聚氰胺氮掺杂材料:碳载体的前处理或电催化剂的后处理
本研究采用两种不同的途径进行氮掺杂,并进行比较。在第一种途径中,碳载体被氮掺杂(方法1)。在第二种途径中,首先合成碳负载Pt催化剂,然后对这些电催化剂进行氮掺杂(方法二)。物理表征包括元素分析、电感耦合等离子体质谱(ICP-MS)、傅里叶变换红外(FT-IR)光谱、拉曼光谱、布鲁诺尔-埃米特-泰勒(BET)分析、x射线光电子能谱(XPS)、x射线衍射(XRD)、透射电子显微镜(TEM)、接触角测量和PEM燃料电池性能测试。方法1中,Pt/C:M-4:1/预催化剂的电流密度为235.5 mA/cm2 @0.6 V。功率密度为160.5 mW/cm2。在方法2中,Pt/C:M-1:1/Post电催化剂的电流密度为626.0 mA/cm2 @0.6 V,最大电流密度为626.0 mA/cm2。功率密度为374.3 mW/cm2。方法2得到的最大功率密度比方法1制备的电催化剂高2.3倍。综上所述,电催化剂的氮掺杂比载体材料的氮掺杂效果更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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