Beniwal Amisha, Bhalothia Dinesh, Yeh Wei, Cheng Mingxing, Yan Che, Chen Po-Chun, Wang Kuan-Wen, Chen Tsan-Yao
Department of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan.
Department of Materials and Mineral Resources Engineering, National Taipei University of Technology, Taipei 10608, Taiwan.
Nanomaterials (Basel). 2022 Aug 17;12(16):2824. doi: 10.3390/nano12162824.
An effective approach for increasing the Noble metal-utilization by decorating the atomic Pt clusters (1 wt.%) on the CoO@SnPd nanoparticle (denoted as CSPP) for oxygen reduction reaction (ORR) is demonstrated in this study. For the optimum case when the impregnation temperature for Co-crystal growth is 50 °C (denoted as CSPP-50), the CoPt nanoalloys and Pt-clusters decoration with multiple metal-to-metal oxide interfaces are formed. Such a nanocatalyst (NC) outperforms the commercial Johnson Matthey-Pt/C (J.M.-Pt/C; 20 wt.% Pt) catalyst by 78-folds with an outstanding mass activity (MA) of 4330 mA mg at 0.85 V vs. RHE in an alkaline medium (0.1 M KOH). The results of physical structure inspections along with electrochemical analysis suggest that such a remarkable ORR performance is dominated by the potential synergism between the surface anchored Pt-clusters, CoPt-nanoalloys, and adjacent SnPd domain, where Pt-clusters offer ideal adsorption energy for O splitting and CoPt-nanoalloys along with SnPd domain boost the subsequent desorption of hydroxide ions (OH).
本研究展示了一种通过在CoO@SnPd纳米颗粒(记为CSPP)上装饰原子级Pt簇(1 wt.%)来提高贵金属利用率以用于氧还原反应(ORR)的有效方法。对于Co晶体生长的浸渍温度为50°C的最佳情况(记为CSPP-50),形成了具有多个金属-金属氧化物界面的CoPt纳米合金和Pt簇装饰。在碱性介质(0.1 M KOH)中,相对于可逆氢电极(RHE),在0.85 V时,这种纳米催化剂(NC)的质量活性(MA)高达4330 mA mg,比商业的庄信万丰Pt/C(J.M.-Pt/C;20 wt.% Pt)催化剂高出78倍。物理结构检查和电化学分析结果表明,这种卓越的ORR性能主要由表面锚定的Pt簇、CoPt纳米合金和相邻的SnPd域之间潜在的协同作用决定,其中Pt簇为O分裂提供了理想的吸附能,而CoPt纳米合金与SnPd域促进了随后氢氧根离子(OH)的解吸。