Hauck John G, McGinn Paul J
Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
ACS Comb Sci. 2015 Jun 8;17(6):355-64. doi: 10.1021/acscombsci.5b00030. Epub 2015 May 21.
A combinatorial synthesis and high-throughput screening process was developed for the investigation of potential oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) catalysts for use as Li-air battery cathode materials. Libraries of discrete ternary metal alloy compositions were deposited via thin-film sputtering. The samples were electrochemically tested in parallel using cyclic voltammetry in O2-saturated KOH electrolyte. Compositions were ranked by ORR and OER onset potentials with respect to an internal Pt reference. Results from the Pt-Mn-Co, Cr-Mn-Co, Pd-Mn-Co, and Pd-Mn-Ru systems are reported. Many alloy compositions showed marked improvement in catalytic activity compared to pure Pt. Among the systems considered, Pt12Mn44Co44, Pd43Co57 and Pd36Mn28Ru36 in particular exhibited lower overpotentials for oxygen reactions, which occur at the cathode in Li-air batteries.
开发了一种组合合成和高通量筛选方法,用于研究用作锂空气电池阴极材料的潜在氧还原反应(ORR)和析氧反应(OER)催化剂。通过薄膜溅射沉积离散三元金属合金成分库。使用循环伏安法在O2饱和的KOH电解质中对样品进行并行电化学测试。相对于内部Pt参比,根据ORR和OER起始电位对成分进行排名。报告了Pt-Mn-Co、Cr-Mn-Co、Pd-Mn-Co和Pd-Mn-Ru体系的结果。与纯Pt相比,许多合金成分的催化活性有显著提高。在所考虑的体系中,特别是Pt12Mn44Co44、Pd43Co57和Pd36Mn28Ru36在锂空气电池阴极发生的氧反应中表现出较低的过电位。