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纳米尺度上氧还原/析氧反应的测量。

Measuring oxygen reduction/evolution reactions on the nanoscale.

机构信息

The Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.

出版信息

Nat Chem. 2011 Aug 14;3(9):707-13. doi: 10.1038/nchem.1112.

Abstract

The efficiency of fuel cells and metal-air batteries is significantly limited by the activation of oxygen reduction and evolution reactions. Despite the well-recognized role of oxygen reaction kinetics on the viability of energy technologies, the governing mechanisms remain elusive and until now have been addressable only by macroscopic studies. This lack of nanoscale understanding precludes optimization of material architecture. Here, we report direct measurements of oxygen reduction/evolution reactions and oxygen vacancy diffusion on oxygen-ion conductive solid surfaces with sub-10 nm resolution. In electrochemical strain microscopy, the biased scanning probe microscopy tip acts as a moving, electrocatalytically active probe exploring local electrochemical activity. The probe concentrates an electric field in a nanometre-scale volume of material, and bias-induced, picometre-level surface displacements provide information on local electrochemical processes. Systematic mapping of oxygen activity on bare and platinum-functionalized yttria-stabilized zirconia surfaces is demonstrated. This approach allows direct visualization of the oxygen reduction/evolution reaction activation process at the triple-phase boundary, and can be extended to a broad spectrum of oxygen-conductive and electrocatalytic materials.

摘要

燃料电池和金属空气电池的效率受到氧还原和氧析出反应的活化的显著限制。尽管氧反应动力学对能源技术的可行性起着公认的作用,但控制机制仍然难以捉摸,到目前为止,只能通过宏观研究来解决。这种缺乏纳米级理解的情况排除了材料结构的优化。在这里,我们报告了对氧离子导电固体表面上的氧还原/氧析出反应和氧空位扩散的直接测量,分辨率达到了亚 10nm。在电化学应变显微镜中,受偏压的扫描探针显微镜尖端充当移动的、电催化活性探针,用于探测局部电化学活性。探针在纳米级材料体积中集中电场,而偏压诱导的皮米级表面位移提供了关于局部电化学过程的信息。在裸露和铂功能化的氧化钇稳定氧化锆表面上对氧活性进行了系统的映射。这种方法可以直接观察三相边界处的氧还原/氧析出反应活化过程,并且可以扩展到广泛的氧导电和电催化材料。

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