Lattach Youssef, Deronzier Alain, Moutet Jean-Claude
Université Joseph Fourier Grenoble 1, Département de Chimie Moléculaire, UMR CNRS-5250, Institut de Chimie Moléculaire de Grenoble, FR CNRS-2607, BP 53, 38041 Cedex 9, Grenoble, France.
ACS Appl Mater Interfaces. 2015 Jul 29;7(29):15866-75. doi: 10.1021/acsami.5b03188. Epub 2015 Jul 17.
The design of more efficient catalytic electrodes remains an important objective for the development of water splitting electrolyzers. In this context a structured composite cathode material has been synthesized by electrodeposition of molybdenum sulfide (MoSx) into a poly(pyrrole-alkylammonium) matrix, previously coated onto carbon electrodes by oxidative electropolymerization of a pyrrole-alkylammonium monomer. The composite material showed an efficient electrocatalytic activity toward proton reduction and the hydrogen evolution reaction (HER). Data from Tafel plots have demonstrated that the electron transfer rate in the composite films is fast, in agreement with the high catalytic activity of this cathode material. Bulk electrolysis of acidic water at carbon foam electrodes modified with the composite have shown that the cathodes display a high catalytic activity and a reasonable operational stability, largely exceeding that of regular amorphous MoSx electrodeposited on naked carbon foam. The enhanced catalytic performances of the composite electrode material were attributed to the structuration of the composite, which led to a homogeneous distribution of the catalyst on the carbon foam network, as shown by SEM characterizations.
设计更高效的催化电极仍然是水电解槽发展的一个重要目标。在此背景下,通过将硫化钼(MoSx)电沉积到聚(吡咯 - 烷基铵)基体中合成了一种结构化复合阴极材料,该基体先前通过吡咯 - 烷基铵单体的氧化电聚合涂覆在碳电极上。该复合材料对质子还原和析氢反应(HER)表现出高效的电催化活性。塔菲尔曲线数据表明复合膜中的电子转移速率很快,这与该阴极材料的高催化活性一致。用该复合材料修饰的碳泡沫电极对酸性水进行批量电解表明,阴极显示出高催化活性和合理的操作稳定性,大大超过了沉积在裸碳泡沫上的普通非晶态MoSx。复合电极材料催化性能的增强归因于复合材料的结构化,如扫描电子显微镜表征所示,这导致催化剂在碳泡沫网络上均匀分布。