Approach to High Performance Electrode Catalysts for DMFC

DMFC 高性能电极催化剂的研究方法

基本信息

项目摘要

The mesoporous carbons were synthesized by using mesoporous silica materials such as MCM-48 and SBA-15 as a template, respectively. Typically, the templates were impregnated with sucrose as a carbon source and sulfuric acid as an acid catalyst. Following dehydration-condensation of the carbon source, the carbonization was carried out mainly at 900℃ under flowing argon. The silica was removed from the silica-carbon composite by treating it with hydrofluoric acid, producing mesoprpus carbons CMK-1, CMK-3, and CMK-5. Another type of carbon has been also synthesized by using petroleum pitch. MCF carbons can be synthesized by using MCF silica as a template. A carbon structure composed of spherical hollows with closed walls with mesopores of around 4 nm in diameter is prepared by the two-step impregnation of sucrose followed by carbonization. The mesoporous structure was maintained up to 1400℃. Platinum is loaded on these mesoporous carbons. TEM observations revealed the presence of metal particles of below 2 nm in the mesoporous material treated at 1100℃. The metal dispersion is highly dependent not only on the carbon structures but also on the temperature for thermal treatments in inert gas atmosphere. The latter is interpreted in terms of the change in the surface functional groups and their density, which probably affect the interaction of the surface and Pt sources. Oxygen reduction activity of the Pt-loaded electrode on CMK-1 was higher than that of the acetylene derived carbon. The performance of Pt catalyst was affected not only by the Pt dispersion but also by their distribution in the carbon electrode.
分别以MCM-48和SBA-15等介孔二氧化硅材料为模板,以蔗糖为碳源,以硫酸为酸催化剂,然后进行脱水缩合,合成介孔碳。碳源主要在900℃、流动氩气下进行碳化,从硅碳复合材料中除去二氧化硅。通过用氢氟酸对其进行处理,可以通过使用MCF二氧化硅作为模板来合成另一种类型的碳CMK-1、CMK-3和CMK-5。通过蔗糖的两步浸渍和碳化制备了由具有封闭壁的球形空心和直径约为4 nm的中孔组成的碳结构。介孔结构在高达 1400℃ 的温度下仍保持不变。TEM 观察表明,在 1100℃ 处理的介孔材料中存在 2 nm 以下的金属颗粒。金属分散度不仅取决于碳结构。还涉及惰性气体气氛中热处理的温度,后者根据表面官能团及其密度的变化来解释,这可能会影响表面和 Pt 的相互作用。 CMK-1上负载Pt的电极的氧还原活性高于乙炔衍生的碳。Pt催化剂的性能不仅受到Pt分散的影响,而且还受到它们在碳电极中的分布的影响。

项目成果

期刊论文数量(36)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Synthesis of Cubic Ia3d-like Mesostructure at Low Temperature Using an Oligomeric Nonionic Surfactant
使用低聚非离子表面活性剂低温合成立方 Ia3d 介观结构
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  • 发表时间:
    2005
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    0
  • 作者:
    SungHyun Lim;Hideaki Yoshitake;Takashi Tatsumi
  • 通讯作者:
    Takashi Tatsumi
Katsutoshi Yamamoto, Takashi Tatsumi: "Remarkable Improvement in Hydrothermal Stability of MCM-41 by Surface Modification with Grignard Reagent"Microporous Mesporous Mater.. 44-45. 459-464 (2001)
Katsutoshi Yamamoto、Takashi Tatsumi:“通过格氏试剂表面改性显着改善 MCM-41 的水热稳定性”微孔介孔材料.. 44-45。
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    0
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Satoshi Kamiya, Osamu Terasaki, Takashi Tatsumi: "The Formation of Cubic Pm3n Mesostructure by an Epitaxial Phase Transformation from Hexagonal p6mm Mesophase"J.Am.Chem.. Soc.,123. 12089-12090 (2001)
Satoshi Kamiya、Osamu Terasaki、Takashi Tatsumi:“通过六方 p6mm 中间相的外延相变形成立方 Pm3n 介观结构”J.Am.Chem.. Soc.,123。
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    0
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Hideaki Yoshitake, Tae Sugihara, Takashi Tatsumi: "Synthesis of Wormhole-like Titania Mesoporous Molecular Sieve with Extremely High Surface Area"Chem.Mater.. (in press). (2002)
Hideaki Yoshitake、Tae Sugihara、Takashi Tatsumi:“具有极高表面积的虫孔状二氧化钛介孔分子筛的合成”Chem.Mater..(印刷中)。
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    0
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Bozhi Tian, Shunai Che, Zheng Liu, Weibin Fan, Takashi Tatsumi: "Novel Approaches to Synthesize Self-Supported Ultrathin Carbon Nanowire Arrays Templated by MCM-41"Chem Commun.. 2726-2727 (2003)
田博智、车树乃、刘峥、范伟斌、辰巳隆:“以MCM-41为模板合成自支撑超薄碳纳米线阵列的新方法”Chem Commun.. 2726-2727 (2003)
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    0
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TATSUMI Takashi其他文献

TATSUMI Takashi的其他文献

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{{ truncateString('TATSUMI Takashi', 18)}}的其他基金

Creation and diversification of novel porous materials with controllable nanospaces and sophisticated molecular recognition functions
具有可控纳米空间和复杂分子识别功能的新型多孔材料的创造和多样化
  • 批准号:
    19106015
  • 财政年份:
    2007
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for Scientific Research (S)
DESIGN OF HIGHLY EFFICIENT LIQUID-PHASE OXIDATION CATALYSTS OF TITANOSILICATES THROUGH PRECISE CONTROL OF ZEOLITE STRCUTURES
通过精确控制沸石结构设计高效钛硅酸盐液相氧化催化剂
  • 批准号:
    13305056
  • 财政年份:
    2001
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Development of Novel Methods for Synthesizing Hydrophobic Metallosilicates
疏水性金属硅酸盐合成新方法的开发
  • 批准号:
    11555212
  • 财政年份:
    1999
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B).
Hydrodesulfurization catalyzed by zeolite-supported
沸石负载催化加氢脱硫
  • 批准号:
    08455370
  • 财政年份:
    1996
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Development of liquid-phase oxidation processes by use of highly dispersed metal-metal oxide catalysts
使用高度分散的金属-金属氧化物催化剂开发液相氧化工艺
  • 批准号:
    07555247
  • 财政年份:
    1995
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Oxidation Catalyzed by Polyoxometalate-Anion-Intercalated Layred Compounds
多金属氧酸盐阴离子插层层状化合物催化的氧化
  • 批准号:
    05453106
  • 财政年份:
    1993
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Study on Shape Selectivity in Hydrocarbon Oxidation catalyzed by Zedites
沸石催化烃氧化的择形研究
  • 批准号:
    03453081
  • 财政年份:
    1991
  • 资助金额:
    $ 47.1万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)

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