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.
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November 2024
Physical & Computational Science Directorate, Pacific Northwest National Laboratory, Richland, Washington, 99354, United States.
Investigating the structural evolution and phase transformation of iron oxides is crucial for gaining a deeper understanding of geological changes on diverse planets and preparing oxide materials suitable for industrial applications. In this study, in-situ heating techniques are employed in conjunction with transmission electron microscopy (TEM) observations and ex-situ characterization to thoroughly analyze the thermal solid-phase transformation of akaganéite 1D nanostructures with varying diameters. These findings offer compelling evidence for a size-dependent morphology evolution in akaganéite 1D nanostructures, which can be attributed to the transformation from akaganéite to maghemite (γ-FeO) and subsequent crystal growth.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2024
Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China. Electronic address:
Photocatalytic degradation is considered as the most energy-efficient, environmentally benign, and effective method for treating low fraction organic contaminants. However, the photocatalysts still suffer from low utilization efficiency of visible-light and severe carrier recombination. Heterojunctions can resolve these two main problems in some extent but still be restrained by the low quality of hetero-interface.
View Article and Find Full Text PDFNanotechnology
October 2023
School of Medicine, Jiangsu University, Zhenjiang 212013, People's Republic of China.
-FeOOH nanorods were prepared via the urea hydrolysis process with the average length of 289.1 nm and average diameter of 61.2 nm, while magnetic-FeO/FeOheterostructure nanorods were prepared via the urea calcination process with-FeOOH nanorods as precursor, and the optimum conditions were the calcination temperature of 400 °C, the calcination time of 2 h, the-FeOOH/urea mass ratio of 1:6.
View Article and Find Full Text PDFSoft Matter
August 2023
Soft and Active Matter group, Department of Physics, Indian Institute of Science Education and Research (IISER), Tirupati, Andhra Pradesh, 517507, India.
Pluronic F127 (PF127) is a copolymer with an amphiphilic nature and can self-assemble to form micelles and, beyond 20% (w/v), form a thermoresponsive physical gel state. However, they are mechanically weak and easily dissolve in physiological environments, which limits their use in load-bearing in specific biomedical applications. Therefore, we propose a pluronic-based hydrogel with enhanced stability by incorporating small amounts of paramagnetic nanorods, akaganeite (β-FeOOH) nanorods (NRs) of aspect ratio ∼7, with PF127.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2023
Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA 99352.
Iron-based redox-active minerals are ubiquitous in soils, sediments, and aquatic systems. Their dissolution is of great importance for microbial impacts on carbon cycling and the biogeochemistry of the lithosphere and hydrosphere. Despite its widespread significance and extensive prior study, the atomic-to-nanoscale mechanisms of dissolution remain poorly understood, particularly the interplay between acidic and reductive processes.
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