Higher-ordered architectures self-assembly of nanomaterials have recently attracted increasing attention. In this work, we report a spontaneous and efficient route to simultaneous synthesis and self-assembly of 3D layered beta-FeOOH nanorods depending on a pH-induced strategy, in which the continuous change of pH is achieved by hydrolysis of FeCl(3).6H(2)O in the presence of urea under hydrothermal conditions. The electron microscopy observations reveal that the square-prismic beta-FeOOH nanorods are self-assembled in a side-by-side fashion to form highly oriented 2D nanorod arrays, and the 2D nanorod arrays are further stacked in a face-to-face fashion to form the final 3D layered architectures. On the basis of time-dependent experiments, a multistage reaction mechanism for the formation of the 3D layered beta-FeOOH nanorods architecture is presented, involving the fast growth and synchronous self-assembly of the nanorods toward 1D, 2D, and 3D spontaneously. The experimental evidence further demonstrates that the urea-decomposition-dependent pH continuously changing in the solution, spontaneously altering the driving force competition between the electrostatic repulsive force and the attractive van der Waals force among the nanorods building blocks, is the essential factor to influence the self-assembly of the beta-FeOOH nanorods from 1D to 3D.
We used a low energy electron irradiation technique to prepare graphene sheets embedded carbon (GSEC) film based on electron cyclotron resonance plasma. The particular π electronic structure of the GSEC film similar to bilayer graphene was verified by Raman spectra 2D band analyzing. The phase transition from amorphous carbon to GSEC was initiated when electron irradiation energy reached 40 eV, and the growth mechanism of GSEC was interpreted as inelastic scattering of low energy electrons. This finding indicates that the GSEC film obtained by low energy electron irradiation can be excepted for widely applications with outstanding electric properties.
Pincer-type ruthenium complexes incorporating an asymmetric negatively charged imidazolylidene were prepared and capable to oxidize water chemically and photo-chemically with high stability.
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