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首页> 外文期刊>Journal of power sources >Activity and stability studies of titanates and titanate-carbon nanotubes supported Ag anode catalysts for direct methanol fuel cell
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Activity and stability studies of titanates and titanate-carbon nanotubes supported Ag anode catalysts for direct methanol fuel cell

机译:钛酸酯和钛酸酯-碳纳米管负载的直接甲醇燃料电池用Ag阳极催化剂的活性和稳定性研究

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摘要

Titanate-SWCNT; synthesized via exploiting the interaction between TiO2 anatase with oxygen functionalized SWCNT, supported Ag nanoparticles and Ag/titanate are characterized using XRD, TEM-EDX-SAED, N-2 adsorption, Photoluminescence, Raman and FTIR spectroscopy. These samples are tested for methanol electrooxidation via using cyclic voltammetry (CV) and impedance measurements. It is shown that Ag/titanate nanotubes exhibited superior electrocatalytic performance for methanol oxidation (4.2 mA cm(-2)) than titanate-SWCNT, Ag/titanate-SWCNT and titanate. This study reveals the existence of a strong metal support interaction in Ag/titanate as explored via formation of Ti-O-Ag bond at 896 cm(-1) and increasing surface area and pore volume (103 m(2) g(-1), 0.21 cm(3) g(-1)) compared to Ag/titanate-SWCNT (71 m(2) g(-1), 0.175 cm(3) g(-1)) that suffers perturbation and defects following incorporation of SWCNT and Ag. Embedding Ag preferably in SWCNT rather than titanate in Ag/titanate-SWCNT disturbs the electron transfer compared to Ag/titanate. Charge transfer resistance depicted from Nyquist impedance plots is found in the order of titanate > Ag/titanate-SWCNT > titanate-SWCNT > Ag/titanate. Accordingly, Ag/titanate indicates a slower current degradation over time compared to rest of catalysts. Conductivity measurements indicate that it follows the order Ag/titanate > Ag/titanate-SWCNT > titanate > titanate-SWCNT declaring that SWCNT affects seriously the conductivity of Ag(titanate) due to perturbations caused in titanate and sinking of electrons committed by Ag through SWCNT. (C) 2015 Elsevier B.V. All rights reserved.
机译:钛酸酯-SWCNT;利用XRD,TEM-EDX-SAED,N-2吸附,光致发光,拉曼光谱和FTIR光谱对通过利用TiO2锐钛矿与氧官能化的SWCNT之间的相互作用合成的纳米级负载的Ag纳米颗粒和Ag /钛酸酯进行了表征。使用循环伏安法(CV)和阻抗测量测试了这些样品的甲醇电氧化作用。结果表明,Ag /钛酸酯纳米管对甲醇氧化表现出优异的电催化性能(4.2 mA cm(-2)),优于钛酸酯-SWCNT,Ag /钛酸酯-SWCNT和钛酸酯。这项研究揭示了通过在896 cm(-1)处形成Ti-O-Ag键并增加表面积和孔体积(103 m(2)g(-1)来探索的在Ag /钛酸酯中存在强金属支持相互作用的方法),0.21 cm(3)g(-1))与Ag /钛酸酯-SWCNT(71 m(2)g(-1),0.175 cm(3)g(-1))相比,掺入后会遭受微扰和缺陷SWCNT和Ag。与Ag /钛酸盐相比,优选将Ag优选地嵌入SWCNT中而不是将钛酸盐嵌入Ag /钛酸盐-SWCNT中。由奈奎斯特阻抗图描绘的电荷转移电阻按钛酸酯> Ag /钛酸酯-SWCNT>钛酸酯-SWCNT> Ag /钛酸酯的顺序找到。因此,与其余催化剂相比,Ag /钛酸酯表明电流随时间的流逝变慢。电导率测量表明,其遵循的顺序为:Ag /钛酸酯> Ag /钛酸酯-SWCNT>钛酸酯>钛酸酯-SWCNT,这表明SWCNT严重影响了Ag(钛酸酯)的电导率,这是由于钛酸酯产生的扰动和Ag通过SWCNT释放电子所致。 。 (C)2015 Elsevier B.V.保留所有权利。

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