共查询到18条相似文献,搜索用时 85 毫秒
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分别以中孔炭(MPC)和VXC-72R炭黑作载体,制备了中孔炭载纳米Au粒子(Au/MPC)和VXC-72R炭黑载纳米Au粒子(Au/CB),并将其用作直接硼氢化钠燃料电池阳极电氧化催化剂.分别用X-射线衍射(XRD)、透射电镜(TEM)等比较了不同载体催化剂的结构和形貌.结果表明,纳米Au粒子均为面心立方结构,Au/MPC中纳米Au粒子的粒径为16nm左右比Au/CB中的纳米Au粒子的更小,且均匀分散在载体的表面.用循环伏安曲线和动电位极化曲线等比较了不同载体催化剂的电化学特性.结果表明,Au/CB的电流密度为38.10mA·cm-2,而Au/MPC的电流密度达到42.88mA·cm-2,比Au/CB的电流密度提高了12.5%. 相似文献
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直接甲醇燃料电池电催化剂载体碳纳米带的合成与表征 总被引:2,自引:0,他引:2
以间苯二酚和甲醛为碳前体,合成了一种新型碳纳米材料碳纳米带(CNRs), 并采用透射电镜(TEM)、 X射线衍射(XRD)及氮气吸附/脱附测试对CNRs进行了结构表征. 结果表明,所合成的CNRs具有很高的石墨化程度及较规则的带状结构,带宽约为8~20 nm, BET比表面积为283 m2/g, 氮气等温线为type-Ⅳ型,表明CNRs为中孔结构,平均孔径约为8.2 nm. 以CNRs为载体通过多元醇法制备了45%PtRu/CNRs电催化剂,该催化剂与以Vulcan XC-72R为载体的PtRu电催化剂相比,直接甲醇燃料电池单池性能得到明显提高. 相似文献
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直接甲酸燃料电池用碳载铁卟啉-Au复合阴极催化剂的性能 总被引:1,自引:0,他引:1
研究了用于直接甲酸燃料电池(DFAFC)的碳载铁卟啉(FeTPP/C)、金复合阴极催化剂(FeTPP-Au/C)对氧还原的电催化性能和抗甲酸能力。结果表明,FeTPP-Au/C催化剂对氧气还原反应的电催化活性要远优于碳载铁卟啉(FeTPP/C)和碳载Au(Au/C)催化剂。而且,FeTPP-Au/C催化剂对甲酸氧化没有催化活性,因此,FeTPP-Au/C催化剂也有很好的抗甲酸能力。所以,FeTPP-Au/C催化剂适合作为DFAFC的阴极催化剂。 相似文献
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反胶束法制备直接甲醇燃料电池Pt-Sn/C催化剂及其表征 总被引:3,自引:0,他引:3
在水/AOT/环己烷反胶束体系中, 制备了Pt-Sn/C催化剂, 研究了不同ω (反胶束溶液中水与表面活性剂的物质量之比)值对Pt-Sn粒径的影响. 并采用TEM, XRD, XPS, 循环伏安等技术对其进行表征. TEM结果表明合成的Pt-Sn纳米颗粒为球形, 在碳载体表面均匀分布, 粒径分布窄, 平均粒径为2.7 nm. Pt-Sn颗粒尺寸随着ω的增加而增大. XRD结果表明该催化剂中Pt具有面心立方结构且没有与Sn形成合金. XPS结果表明在该催化剂中, Pt主要以零价态存在. 在甲醇溶液中的循环伏安扫描结果表明, 甲醇氧化峰电位和峰电流随着ω的增加而减小, 说明反胶束方法可以通过控制颗粒尺寸, 从而影响催化剂的电氧化活性. 相对于商用Pt-Ru/Vulcan XC-72 (20 wt%, E-TEK公司), 该催化剂具有较低的峰电势以及较高的If/Ib (循环伏安曲线中正向扫描峰电流与反向扫描峰电流的比值), 这表明用此方法制备的Pt-Sn/C催化剂具有较好的抗中毒能力. 相似文献
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Prof. Dr. Yusuke Yamada Masaki Yoneda Prof. Dr. Shunichi Fukuzumi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(35):11733-11741
A robust one‐compartment H2O2 fuel cell, which operates without membranes at room temperature, has been constructed by using a series of polynuclear cyanide complexes that contain Fe, Co, Mn, and Cr as cathodes, in sharp contrast to conventional H2 and MeOH fuel cells, which require membranes and high temperatures. A high open‐circuit potential of 0.68 V was achieved by using Fe3[{CoIII(CN)6}2] on a carbon cloth as the cathode and a Ni mesh as the anode of a H2O2 fuel cell by using an aqueous solution of H2O2 (0.30 M , pH 3) with a maximum power density of 0.45 mW cm?2. The open‐circuit potential and maximum power density of the H2O2 fuel cell were further increased to 0.78 V and 1.2 mW cm?2, respectively, by operation under these conditions at pH 1. No catalytic activity of Co3[{CoIII(CN)6}2] and Co3[{FeIII(CN)6}2] towards H2O2 reduction suggests that the N‐bound Fe ions are active species for H2O2 reduction. H2O2 fuel cells that used Fe3[{MnIII(CN)6}2] and Fe3[{CrIII(CN)6}2] as the cathode exhibited lower performance compared with that using Fe3[{CoIII(CN)6}2] as a cathode, because ligand isomerization of Fe3[{MIII(CN)6}2] into (FeM2)[{FeII(CN)6}2] (M=Cr or Mn) occurred to form inactive Fe? C bonds under ambient conditions, whereas no ligand isomerization of Fe3[{CoIII(CN)6}2] occurred under the same reaction conditions. The importance of stable Fe2+? N bonds was further indicated by the high performance of the H2O2 fuel cells with Fe3[{IrIII(CN)6}2] and Fe3[{RhIII(CN)6}2], which also contained stable Fe2+? N bonds. The stable Fe2+? N bonds in Fe3[{CoIII(CN)6}2], which lead to high activity for the electrocatalytic reduction of H2O2, allow Fe3[{CoIII(CN)6}2] to act as a superior cathode in one‐compartment H2O2 fuel cells. 相似文献
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