Jang Kwang-Suk, Kim Jong-Duk
Department of Chemical and Biomolecular Engineering (BK21 Graduate Program), KAIST, Daejeon 305-701, Republic of Korea.
J Nanosci Nanotechnol. 2011 May;11(5):4496-500. doi: 10.1166/jnn.2011.3622.
CuO nanosheets approximately 0.8 nm thick were synthesized under ambient conditions within a few hours using a surfactant lamellar mesophase as a soft template. In aqueous media, metal ions and anionic surfactants form a lamellar mesophase. In the lamellar layers, metal ions can crystallize without structural collapse. Highly ordered CuO nanosheet/surfactant lamellar layers formed in an aqueous solution can be easily delaminated by washing with water. The use of the delaminated CuO nanosheet catalyst instead of traditional metallic catalysts resulted in a reduction reaction of 4-nitrophenol with NaBH4 that obeyed zero-order kinetics. This indicates in situ conversion of CuO to Cu in the reaction solution. Cu in situ reduced by BH4- acted as a catalyst relaying electrons for the reduction of 4-NP. The catalytic reaction was investigated by UV-vis spectroscopy, and the reduction and crystalline structures of the nanosheets were analyzed by UV-vis spectroscopy and X-ray diffraction. These results indicate CuO nanosheets to be an attractive alternative to metal catalysts in reactions involving hydrogen.
使用表面活性剂层状中间相作为软模板,在环境条件下于数小时内合成了厚度约为0.8纳米的氧化铜纳米片。在水介质中,金属离子和阴离子表面活性剂形成层状中间相。在层状层中,金属离子可以结晶而不会发生结构崩塌。在水溶液中形成的高度有序的氧化铜纳米片/表面活性剂层状层可以通过水洗轻松分层。使用分层的氧化铜纳米片催化剂代替传统金属催化剂,导致4-硝基苯酚与硼氢化钠的还原反应遵循零级动力学。这表明在反应溶液中氧化铜原位转化为铜。被硼氢化根原位还原的铜充当了还原4-硝基苯酚的电子中继催化剂。通过紫外可见光谱研究了催化反应,并通过紫外可见光谱和X射线衍射分析了纳米片的还原和晶体结构。这些结果表明,在涉及氢的反应中,氧化铜纳米片是金属催化剂的有吸引力的替代品。