Lee Sang-Yup, Gao Xueyun, Matsui Hiroshi
Department of Chemistry, Hunter College, and The Graduate Center, The City University of New York, 695 Park Avenue, New York, New York 10021, USA.
J Am Chem Soc. 2007 Mar 14;129(10):2954-8. doi: 10.1021/ja0677057. Epub 2007 Feb 16.
The room-temperature synthesis of beta-Ga2O3 nanocrystal was examined by coupling two biomimetic crystallization techniques, enzymatic peptide nanoassembly templating and aggregation-driven crystallization. The catalytic template of peptide assembly nucleated and mineralized primary beta-Ga2O3 crystals and then fused them to grow single-crystalline and monodisperse nanoparticles in the cavity of the peptide assembly at room temperature. In this work, the peptide assembly was exploited as a nanoreactor with an enzymatic functionality catalyzing the hydrolysis of gallium precursors. In addition, the characteristic ring structure of peptide assembly is expected to provide an efficient dehydration pathway and crystallization control over the surface tension, which are advantageous for beta-Ga2O3 crystal growth. This multifunctional peptide assembly could be applied for syntheses of a variety of nanomaterials that are kinetically difficult to grow at room temperature.
通过结合两种仿生结晶技术,即酶促肽纳米组装模板法和聚集驱动结晶法,研究了β-Ga2O3纳米晶体的室温合成。肽组装的催化模板使初级β-Ga2O3晶体成核并矿化,然后在室温下将它们融合,在肽组装的腔内生长出单晶且单分散的纳米颗粒。在这项工作中,肽组装被用作具有催化镓前体水解的酶功能的纳米反应器。此外,肽组装的特征性环结构有望提供一条有效的脱水途径,并通过表面张力控制结晶,这有利于β-Ga2O3晶体的生长。这种多功能肽组装可应用于合成各种在室温下动力学上难以生长的纳米材料。