首页> 外文会议>Sixth European Space Power Conference (ESPC); May 6-10, 2002; Porto, Portugal >HYDROGEN PEROXIDE REDUCTION CATHODE UTILIZING ENZYME ELECTROCATALYSIS
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HYDROGEN PEROXIDE REDUCTION CATHODE UTILIZING ENZYME ELECTROCATALYSIS

机译:利用酶电解还原过氧化氢的阴极

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The electrochemical reduction of hydrogen peroxide on noble metal catalyst surfaces is hindered by the evolution of oxygen, as well as a reaction mechanism that involves an adsorption step, which decreases electrical potential and thermodynamic efficiency. The only way to overcome this loss is to produce a catalyst with an associated reaction mechanism that realizes the full reduction energy of hydrogen peroxide. Increasing reduction potential through a change in the properties of the reaction mechanism via properties of the catalyst, without a compromise in current density, would offer an enhancement. While it is still to be determined whether or not this actually does involve a change in the reaction mechanism of hydrogen peroxide reduction, changes in the half-reaction voltage may be realized by new catalytic methods. Following recent work on bioelectrocatalysis for the fabrication of biosensors, it is proposed that a fuel cell electrode be produced utilizing enzyme electrocatalysis. One effect of bioelectrocatalysis research has been the invention of enzyme immobilization methods such that the kinetic effectiveness is not hindered, while maintaining direct (mediatorless) transfer of electrons between the enzyme and the electrode. The properties of enzyme electrocatalysis result in an electrode that operates at a higher potential than previous noble-metal catalysed electrodes for hydrogen peroxide reduction, yet with sufficient current density to make its use worthwhile in a fuel cell for the production of power. In this paper, a number of oxido-reductases (enzymes that participate electro-catalytically in a reduction or oxidation reaction) are investigated for their suitability as an electrocatalyst for the electrochemical reduction of hydrogen peroxide. The criteria of suitability include a high reduction potential (not yet realized with noble metal catalyzed electrodes), a proper reaction mechanism that does not involve excessive oxygen evolution, and sufficient current density.
机译:氧气的放出以及涉及吸附步骤的反应机理阻碍了贵金属催化剂表面上过氧化氢的电化学还原,该反应机理降低了电势和热力学效率。克服这种损失的唯一方法是生产具有相关反应机理的催化剂,该催化剂可实现过氧化氢的完全还原能。通过在不损害电流密度的情况下通过催化剂的性质改变反应机理的性质来增加还原电位将提供增强作用。尽管仍要确定这是否确实涉及过氧化氢还原反应机理的改变,但是可以通过新的催化方法来实现半反应电压的改变。在关于用于制造生物传感器的生物电催化的最新工作之后,提出了利用酶电催化制备燃料电池电极。生物电催化研究的一种效果是发明了酶固定化方法,从而在保持酶与电极之间电子的直接(无介体)转移的同时,不妨碍动力学有效性。酶电催化的性质导致电极的工作电位比以前的贵金属催化的电极高,可减少过氧化氢,但电流密度足够大,值得在燃料电池中用于发电。在本文中,研究了多种氧化还原酶(以电催化方式参与还原或氧化反应的酶)是否适合用作过氧化氢电化学还原的电催化剂。适合性的标准包括高还原电位(贵金属催化电极尚未实现),不涉及过多氧气释放的适当反应机理以及足够的电流密度。

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