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Enzyme-Metal Oxide Composite as Catalysts for Enzymatic Oxygen Reduction

机译:Enzyme-Metal氧化物复合催化剂酶氧还原

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摘要

The immobilization of laccase on metal oxide nanoparticles was achieved using a silane coupling agent and a homobifuntional cross-linking agent. The metal oxide nanoparticles studied were TiO2, ZnO and SnO2. The coupling agent was silane and the crosslinking agents was 1,5-Difluoro-2,4-dinitrobenzene (DFDNB). The resulting laccase-metal oxide bio-nanocomposites were deposited onto screen printed carbon electrode and tested as electrocatalysts for oxygen reduction in an electrochemical cell using 0.2 M pH 4.5 sodium acetate buffer as the electrolyte. The bio-nanocomposite modified electrode showed an open circuit potential as high as 0.61 V vs Ag/AgCl. Cyclic voltammograms showed a clear difference between unmodified and laccase modified metal oxide nanoparticles in the oxygen reduction region with an onset potential of ~ 0.57 V. In comparison, the laccase physisorbed onto the metal oxide nanoparticles without the molecu crosslinkers showed no obvious electrocatalytic activity. The work adds significant value to the bio-electrochemistry literature, as a new class of support material with photocatalytic properties have been found to serve as excellent enzyme immobilization support that has potential applications in biosensors and biological fuel cells.
机译:漆酶的固定化金属氧化物使用硅烷纳米颗粒实现偶联剂和homobifuntional交联剂。纳米颗粒研究二氧化钛、氧化锌和SnO2。和硅烷偶联剂交联剂是1、5-Difluoro-2 4-dinitrobenzene (DFDNB)。结果氧化laccase-metal bio-nanocomposites被放置在屏幕上打印碳呢作为electrocatalysts电极和测试氧气减少一个电化电池使用0.2米pH值4.5醋酸钠缓冲的电解液。电极显示一个开放的电路的潜力高为0.61 V和Ag / AgCl。修改的和显示一个明确的区别漆酶改性金属氧化物纳米颗粒氧气减少地区爆发潜力~ 0.57 V。physisorbed到金属氧化物纳米颗粒没有molecu交联剂显示没有明显的electrocatalytic活动。bio-electrochemistry重要的价值文学,作为一个新类的支持材料具有光催化特性已经被发现作为优秀的酶固定化的支持潜在的应用在生物传感器和生物燃料电池。

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