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首页> 外文期刊>ACS catalysis >Palladium Nanoparticle-Graphitic Carbon Nitride Porous Synergistic Catalyst for Hydrogen Evolution/Oxidation Reactions over a Broad Range of pH and Correlation of Its Catalytic Activity with Measured Hydrogen Binding Energy
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Palladium Nanoparticle-Graphitic Carbon Nitride Porous Synergistic Catalyst for Hydrogen Evolution/Oxidation Reactions over a Broad Range of pH and Correlation of Its Catalytic Activity with Measured Hydrogen Binding Energy

机译:钯纳米粒子-碳氮化碳多孔协同催化剂,用于宽pH范围内的氢释放/氧化反应以及其催化活性与测得的氢键能的相关性

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摘要

The hydrogen evolution reaction (HER) and hydrogen oxidation reaction (HOR) in aqueous medium are two fundamental reactions for the development of non-fossil energy storage and conversion devices. In the polymer electrolyte membrane fuel cell (PEMFC) carbon supported platinum (Pt/C) based catalysts are universally used in cathodes and anodes; however, the poor durability of Pt/C due to degradation of the catalyst in the strongly oxidizing environment prevents its widespread applications. It remains a great challenge to develop new electrocatalysts with superior activity and very high durability for the HER/HOR. Here, we report the synthesis of a porous palladium nanoparticle- carbon nitride composite (Pd-CNx) for its superior activity and high durability toward the HER/HOR in acidic and alkaline media. The Pd-CNx composites exhibited high catalytic activity for hydrogen evolution in acidic media with a small onset potential of -12 mV and a Tafel slope of 35 mV dec(-1). At a small Pd loading of 0.043 mg cm(-2), this catalyst also exhibits a current density of 10 mA cm(-2) at a low overpotential of -55 mV with an excellent stability. The HER activity on Pd-CNx composite is comparable to that of commercial Pt/C in acid media. The stability tests of this catalyst were done through a large number of repeated potential cycles and long-term electrolysis. These confirm the exceptional durability of this catalyst, which is much better than that of Pt/C catalysts. Furthermore, this catalyst has also displayed superior HOR activity, measured by a rotating-disk experiment with a broad range of pH (0-14) in different buffer solutions. The HER/HOR activities of porous Pd-CNx composite in different buffer solutions were correlated with the hydrogen binding energy (HBE) of the catalyst surface. The HER/HOR activity gradually decreases with an increase in the HBE as the solution pH increases. The superior HER/HOR activities and very high durability at porous Pd-CNx composite are due to strong bonding between Pd and carbon (Pd-C bond), the porous morphology, and synergistic interactions between Pd-NPs and the carbon nitride (CNx) support.
机译:水性介质中的析氢反应(HER)和氢氧化反应(HOR)是开发非化石能量存储和转化装置的两个基本反应。在聚合物电解质膜燃料电池(PEMFC)中,碳负载的铂(Pt / C)基催化剂普遍用于阴极和阳极。然而,由于在强氧化环境中催化剂的降解,Pt / C的耐久性差,阻碍了其的广泛应用。为HER / HOR开发具有优异活性和极高耐久性的新型电催化剂仍然是一个巨大的挑战。在这里,我们报告了多孔钯纳米颗粒-氮化碳复合物(Pd-CNx)的合成,因为它在酸性和碱性介质中具有出色的活性和对HER / HOR的高耐久性。 Pd-CNx复合材料对酸性介质中的氢气释放具有高催化活性,其起始电位为-12 mV,Tafel斜率为35 mV dec(-1)。在0.043 mg cm(-2)的小Pd负载下,该催化剂在-55 mV的低过电势下还具有10 mA cm(-2)的电流密度,具有出色的稳定性。在酸性介质中,Pd-CNx复合材料的HER活性与市售Pt / C相当。通过大量重复的电势循环和长期电解,对该催化剂进行了稳定性测试。这些证实了该催化剂的优异耐久性,这比Pt / C催化剂的耐久性好得多。此外,该催化剂还显示出优异的HOR活性,通过转盘实验在不同的缓冲溶液中在宽pH(0-14)范围内进行测量。多孔Pd-CNx复合材料在不同缓冲溶液中的HER / HOR活性与催化剂表面的氢键能(HBE)相关。随着溶液pH值的增加,HER / HOR活性随着HBE的增加而逐渐降低。多孔Pd-CNx复合材料具有优异的HER / HOR活性和极高的耐久性,这归因于Pd和碳之间的牢固键合(Pd-C键),多孔形貌以及Pd-NP与氮化碳(CNx)之间的协同作用支持。

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