Department of Mechanical and Aerospace Engineering and ‡Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology , Kowloon, Hong Kong.
ACS Appl Mater Interfaces. 2017 Oct 18;9(41):35829-35836. doi: 10.1021/acsami.7b10216. Epub 2017 Oct 9.
This article presents a facile and effective approach to activate the bifunctionality of calcium-manganese perovskites toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). We substituted Nb into the Mn site of CaMnO (CMO) and treated the material with H. The as-obtained CaMnNbO (H-CMNO) displays the same structure as that of CMO, and compared to that of CMO, H-CMNO exhibits significantly improved OER performance, including a lower overpotential, a reduced Tafel slope, a higher mass activity, and enhanced stability. In addition, the ORR performance of H-CMNO is also greatly enhanced, relative to CMO, with a higher ORR activity and a more efficient electron-transfer pathway. H-CMNO shows an even higher activity-per-catalyst cost and superior stability than that of state-of-the-art materials, such as IrO and Pt/C. This great enhancement in ORR and OER activity of H-CMNO is attributed to several factors, including phase stabilization, optimized e filling, better OH adsorption, and improved electrical conductivity.
本文提出了一种简便有效的方法,可激活钙锰钙钛矿的双功能特性,以实现氧还原反应(ORR)和氧析出反应(OER)。我们将 Nb 取代 CaMnO(CMO)中的 Mn 位,并对该材料进行 H 处理。所得到的 CaMnNbO(H-CMNO)具有与 CMO 相同的结构,与 CMO 相比,H-CMNO 表现出显著改善的 OER 性能,包括更低的过电势、更小的塔菲尔斜率、更高的质量活性和增强的稳定性。此外,H-CMNO 的 ORR 性能也得到了极大的提高,相对于 CMO,具有更高的 ORR 活性和更有效的电子转移途径。H-CMNO 的活性/催化剂成本甚至高于最先进的材料,如 IrO 和 Pt/C,且具有更好的稳定性。H-CMNO 的 ORR 和 OER 活性的这种巨大提高归因于几个因素,包括相稳定性、优化的电子填充、更好的 OH 吸附和提高的电导率。