Vos Johannes G, Wezendonk Tim A, Jeremiasse Adriaan W, Koper Marc T M
Leiden Institute of Chemistry , Leiden University , PO Box 9502, 2300 RA Leiden , The Netherlands.
Delft University of Technology , Julianalaan 136 , 2628 BL Delft , The Netherlands.
J Am Chem Soc. 2018 Aug 15;140(32):10270-10281. doi: 10.1021/jacs.8b05382. Epub 2018 Aug 1.
The oxygen evolution reaction (OER) and chlorine evolution reaction (CER) are electrochemical processes with high relevance to water splitting for (solar) energy conversion and industrial production of commodity chemicals, respectively. Carrying out the two reactions separately is challenging, since the catalytic intermediates are linked by scaling relations. Optimizing the efficiency of OER over CER in acidic media has proven especially difficult. In this regard, we have investigated the OER versus CER selectivity of manganese oxide (MnO), a known OER catalyst. Thin films (∼5-20 nm) of MnO were electrodeposited on glassy carbon-supported hydrous iridium oxide (IrO/GC) in aqueous chloride solutions of pH ∼0.9. Using rotating ring-disk electrode voltammetry and online electrochemical mass spectrometry, it was found that deposition of MnO onto IrO decreases the CER selectivity of the system in the presence of 30 mM Cl from 86% to less than 7%, making it a highly OER-selective catalyst. Detailed studies of the CER mechanism and ex-situ structure studies using SEM, TEM, and XPS suggest that the MnO film is in fact not a catalytically active phase, but functions as a permeable overlayer that disfavors the transport of chloride ions.
析氧反应(OER)和析氯反应(CER)分别是与(太阳能)能量转换中的水分解以及商品化学品的工业生产高度相关的电化学过程。分别进行这两个反应具有挑战性,因为催化中间体通过比例关系相互关联。事实证明,在酸性介质中优化OER相对于CER的效率尤为困难。在这方面,我们研究了已知的OER催化剂氧化锰(MnO)的OER与CER选择性。在pH约为0.9的氯化物水溶液中,将MnO薄膜(约5 - 20纳米)电沉积在玻璃碳负载的水合氧化铱(IrO/GC)上。使用旋转环盘电极伏安法和在线电化学质谱法发现,在存在30 mM Cl的情况下,将MnO沉积到IrO上会使系统的CER选择性从86%降低到7%以下,使其成为一种高度OER选择性的催化剂。对CER机理的详细研究以及使用扫描电子显微镜(SEM)、透射电子显微镜(TEM)和X射线光电子能谱(XPS)进行的非原位结构研究表明,MnO薄膜实际上不是催化活性相,而是作为一种不利于氯离子传输的可渗透覆盖层发挥作用。