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微乳液介导合成钴(纯面心立方相和六方相)及钴镍合金纳米颗粒。

Microemulsion-mediated synthesis of cobalt (pure fcc and hexagonal phases) and cobalt-nickel alloy nanoparticles.

作者信息

Ahmed Jahangeer, Sharma Shudhanshu, Ramanujachary Kandalam V, Lofland Samuel E, Ganguli Ashok K

机构信息

Department of Chemistry, Indian Institute of Technology, Hauz Khas, New Delhi 110 016, India.

出版信息

J Colloid Interface Sci. 2009 Aug 15;336(2):814-9. doi: 10.1016/j.jcis.2009.04.062. Epub 2009 May 3.

Abstract

By choosing appropriate microemulsion systems, hexagonal cobalt (Co) and cobalt-nickel (1:1) alloy nanoparticles have been obtained with cetyltrimethylammonium bromide as a cationic surfactant at 500 degrees C. This method thus stabilizes the hcp cobalt even at sizes (<10 nm) at which normally fcc cobalt is predicted to be stable. On annealing the hcp cobalt nanoparticles in H(2) at 700 degrees C we could transform them to fcc cobalt nanoparticles. Microscopy studies show the formation of spherical nanoparticles of hexagonal and cubic forms of cobalt and Co-Ni (1:1) alloy nanoparticles with the average size of 4, 8 and 20 nm, respectively. Electrochemical studies show that the catalytic property towards oxygen evolution is dependent on the applied voltage. At low voltage (less than 0.65 V) the Co (hexagonal) nanoparticles are superior to the alloy (Co-Ni) nanoparticles while above this voltage the alloy nanoparticles are more efficient catalysts. The nanoparticles of cobalt (hcp and fcc) and alloy (Co-Ni) nanoparticles show ferromagnetism. The saturation magnetization of Co-Ni nanoparticles is reduced compared to the bulk possibly due to surface oxidation.

摘要

通过选择合适的微乳液体系,以十六烷基三甲基溴化铵作为阳离子表面活性剂,在500℃下制备出了六方钴(Co)和钴镍(1:1)合金纳米颗粒。该方法能够稳定hcp钴,即使在尺寸小于10nm时,通常预计稳定的是fcc钴。在700℃的氢气中对hcp钴纳米颗粒进行退火处理后,我们能够将它们转变为fcc钴纳米颗粒。显微镜研究表明,形成了六方和立方形式的钴以及Co-Ni(1:1)合金纳米颗粒的球形纳米颗粒,平均尺寸分别为4nm、8nm和20nm。电化学研究表明,对析氧的催化性能取决于施加的电压。在低电压(小于0.65V)下,Co(六方)纳米颗粒优于合金(Co-Ni)纳米颗粒,而高于该电压时,合金纳米颗粒是更高效的催化剂。钴(hcp和fcc)以及合金(Co-Ni)纳米颗粒表现出铁磁性。与块状材料相比,Co-Ni纳米颗粒的饱和磁化强度降低,这可能是由于表面氧化所致。

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