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A new durable and high performance platinum supported on Ag-Ni-porous coordination polymer as an anodic DMFC nano-electrocatalyst: DFT and experimental investigation

机译:以Ag-Ni-多孔配位聚合物为载体的新型耐用高性能铂作为阳极DMFC纳米电催化剂:DFT和实验研究

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Due to the poor performance and intermediates poisoning of available catalysts in direct methanol fuel cells (DMFC), the researcher is confronted with a considerable challenge for obtaining modified electrocatalyst. Ag-Ni porous coordination polymer (ANP) as a new electrocatalyst supporter was synthesized by a hydrothermal method. To achieve favorable electrocatalyst for DMFC systems, platinum nanoparticles was deposited upon ANP by an electrochemical method and platinum supported on Ag-Ni porous coordination polymer (Pt-ANP) was formed. Fourier transform infrared spectroscopy (FTIR) analysis ensured correct synthesized of ANP and Pt-ANP. In addition, the morphologies investigation of ANP and Pt-ANP were carried out by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). The FE-SEM images indicate that the platinum nanoparticles have been greatly deposited on ANP surface. Electrochemical behaviors of prepared catalyst for methanol oxidation were evaluated by cyclic voltammetry (CV), linear sweep voltammetry (LSV), and chronoamperometry (CA) techniques. Electrochemical cyclic voltammetry tests (CV) indicate that the forward peak current density of Pt-ANP is about 105 mA/cm(2) which it is 33% more than the forward peak current density of pure Pt catalyst (70.21 mA/cm(2)). Moreover, electrochemical surface area (ECSA) of Pt-ANP is 26.42 m(2)/g(Pt). In addition, density functional theory (DFT) computations show that with the deposition of Pt upon ANP, the HOMO-LOMO energy gap of ANP has been decreased which they are suitable for electrochemical reactions. Theoretical results are greatly in accordance with the experiments. Based on the results, Pt-ANP could be a superior electrocatalyst for methanol oxidation. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:由于直接甲醇燃料电池(DMFC)中可用催化剂的不良性能和中间体中毒,研究人员面临着获得改性电催化剂的巨大挑战。采用水热法合成了Ag-Ni多孔配位聚合物(ANP)作为新型电催化剂载体。为了获得适合DMFC系统的电催化剂,通过电化学方法将铂纳米颗粒沉积在ANP上,并形成负载在Ag-Ni多孔配位聚合物(Pt-ANP)上的铂。傅里叶变换红外光谱(FTIR)分析确保正确合成ANP和Pt-ANP。另外,通过X射线衍射(XRD),场发射扫描电子显微镜(FE-SEM)和透射电子显微镜(TEM)进行了ANP和Pt-ANP的形态研究。 FE-SEM图像表明铂纳米颗粒已经大量沉积在ANP表面上。制备的甲醇氧化催化剂的电化学行为通过循环伏安法(CV),线性扫描伏安法(LSV)和计时安培法(CA)进行评估。电化学循环伏安测试(CV)表明,Pt-ANP的正向峰值电流密度约为105 mA / cm(2),比纯Pt催化剂的正向峰值电流密度(70.21 mA / cm(2)高33% ))。此外,Pt-ANP的电化学表面积(ECSA)为26.42 m(2)/ g(Pt)。此外,密度泛函理论(DFT)计算表明,随着Pt在ANP上的沉积,ANP的HOMO-LOMO能隙减小,适合电化学反应。理论结果与实验结果基本吻合。根据结果​​,Pt-ANP可能是甲醇氧化的优良电催化剂。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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