Ramesh Gubbala V, Kodiyath Rajesh, Tanabe Toyokazu, Manikandan Maidhily, Fujita Takeshi, Umezawa Naoto, Ueda Shigenori, Ishihara Shinsuke, Ariga Katsuhiko, Abe Hideki
National Institute for Materials Science , 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
ACS Appl Mater Interfaces. 2014 Sep 24;6(18):16124-30. doi: 10.1021/am504147q. Epub 2014 Sep 12.
Although compositional tuning of metal nanoparticles (NPs) has been extensively investigated, possible control of the catalytic performance through bulk-structure tuning is surprisingly overlooked. Here we report that the bulk structure of intermetallic ZrPt3 NPs can be engineered by controlled annealing and their catalytic performance is significantly enhanced as the result of bulk-structural transformation. Chemical reduction of organometallic precursors yielded the desired ZrPt3 NPs with a cubic FCC-type structure (c-ZrPt3 NPs). The c-ZrPt3 NPs were then transformed to a different phase of ZrPt3 with a hexagonal structure (h-ZrPt3 NPs) by annealing at temperatures between 900 and 1000 °C. The h-ZrPt3 NPs exhibited higher catalytic activity and long-term stability than either the c-ZrPt3 NPs or commercial Pt/C NPs toward the electro-oxidation of ethanol. Theoretical calculations have elucidated that the enhanced activity of the h-ZrPt3 NPs is attributed to the increased surface energy, whereas the stability of the catalyst is retained by the lowered bulk-free-energy.
尽管对金属纳米颗粒(NPs)的成分调控已进行了广泛研究,但通过体相结构调控来控制催化性能却出人意料地被忽视了。在此,我们报告金属间化合物ZrPt3 NPs的体相结构可通过控制退火来设计,并且由于体相结构转变,其催化性能得到显著增强。有机金属前驱体的化学还原产生了具有立方FCC型结构的所需ZrPt3 NPs(c-ZrPt3 NPs)。然后,通过在900至1000°C之间的温度下退火,c-ZrPt3 NPs转变为具有六方结构的不同相的ZrPt3(h-ZrPt3 NPs)。h-ZrPt3 NPs对乙醇的电氧化表现出比c-ZrPt3 NPs或商业Pt/C NPs更高的催化活性和长期稳定性。理论计算表明,h-ZrPt3 NPs活性增强归因于表面能增加,而催化剂的稳定性则通过降低的体相自由能得以保持。