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首页> 外文期刊>Bulletin of Materials Science >Chemical nature of catalysts of oxide nanoparticles in environment prevailing during growth of carbon nanostructures by CCVD
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Chemical nature of catalysts of oxide nanoparticles in environment prevailing during growth of carbon nanostructures by CCVD

机译:CCVD在碳纳米结构生长过程中普遍存在的环境中氧化物纳米颗粒催化剂的化学性质

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摘要

Carbon nanostructures (CNS) are often grown using oxide nanoparticles as catalyst in chemical vapour deposition and these oxides are not expected to survive as such during growth. In the present study, the catalysts of cobalt- and nickel oxide-based nanoparticles of sizes varying over a range have been reduced at 575(A degrees)C under environment resulting from the introduction of C2H2 + NH3 during growth of CNS as well as under introduction of C2H2 and NH3 separately. The structure of the reduced nanoparticles is often different from the equilibrium structure of the bulk. Nanoparticles of cobalt oxide with and without doping by copper oxide are reduced to cobalt alloy or cobalt nanoparticles having fcc structure, but the rate of reduction is relatively less in NH3 environment. However, reduced nickel oxide nanoparticles with and without doping shows a mix of fcc and hcp phases. The presence of hydrogen and nitrogen in the environment appears to discourage the formation of hcp nickel as inferred from the results in NH3 environment. Cobalt carbide forms when the 10 wt.% or less doped cobalt oxide is reduced in C2H2 + NH3 environment. At higher level of doping of 20 wt.%, separate metallic phase of copper appears and carbide formation gets suppressed.
机译:碳纳米结构(CNS)通常在化学气相沉积中使用氧化物纳米颗粒作为催化剂来生长,预计这些氧化物不会在生长过程中原样存活。在本研究中,在中枢神经系统(CNS)生长期间以及在低温条件下引入C2H2 + NH3导致的环境下,在575(A°C)的条件下,尺寸变化范围大的钴和镍氧化物基纳米颗粒的催化剂被还原。分别引入C2H2和NH3。还原的纳米颗粒的结构通常不同于本体的平衡结构。具有和不具有由氧化铜掺杂的氧化钴的纳米颗粒被还原成钴合金或具有fcc结构的钴纳米颗粒,但是在NH 3环境中还原速率相对较小。然而,具有和不具有掺杂的还原的氧化镍纳米颗粒显示出fcc和hcp相的混合。从NH3环境的结果推断,环境中氢和氮的存在似乎会阻止hcp镍的形成。当在C2H2 + NH3环境中还原10 wt%或更少的掺杂氧化钴时,会形成碳化钴。在20wt。%的较高掺杂水平下,铜的分离的金属相出现并且碳化物的形成得到抑制。

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