College of Chemistry and Life Science, College of Geography and Environmental Science, Zhejiang Normal University, Jinhua 321004, China.
College of Chemistry and Life Science, College of Geography and Environmental Science, Zhejiang Normal University, Jinhua 321004, China.
J Colloid Interface Sci. 2017 May 15;494:15-21. doi: 10.1016/j.jcis.2017.01.030. Epub 2017 Jan 10.
In this work, solid-core@porous-shell alloyed PtAg nanocrystals (PtAg NCs) were fabricated via a simple one-pot co-reduction wet-chemical method on a large scale. Diprophylline (DPP) was employed as the stabilizing agent and shape-directing agent, without any surfactant, polymer, seed or template. The products were mainly analyzed by a series of characterization technique. The hierarchical architectures had enhanced stability and improved electrocatalytic activity for hydrogen evolution reaction (HER) and glycerol oxidation reaction (GOR) in contrast with commercial available Pt/C and Pt black catalysts. For the prepared PtAg NCs catalyst, the Tafel slope is 40mVdec toward HER in 0.5M HSO, coupled with the specific activity and mass activity of 77.91mAcm and 1303mAmg toward GOR, respectively.
在这项工作中,通过简单的一锅共还原湿化学方法在大规模上制备了实心核@多孔壳合金化 PtAg 纳米晶体 (PtAg NCs)。二羟丙茶碱 (DPP) 被用作稳定剂和形状导向剂,而无需使用任何表面活性剂、聚合物、种子或模板。通过一系列的表征技术对产物进行了主要分析。与商业 Pt/C 和 Pt 黑催化剂相比,分层结构提高了稳定性,并提高了析氢反应 (HER) 和甘油氧化反应 (GOR) 的电催化活性。对于所制备的 PtAg NCs 催化剂,在 0.5M HSO 中 HER 的 Tafel 斜率为 40mVdec,分别对应于 GOR 的 77.91mAcm 的比活性和 1303mAmg 的质量活性。