Sun Zhaohong, Pham Ngoc, Derakhshan Shahab, Brutchey Richard L
Department of Chemistry, University of Southern California Los Angeles California 90089 USA
Department of Chemistry and Biochemistry, California State University Long Beach California 90840 USA
Chem Sci. 2025 Sep 12. doi: 10.1039/d5sc04592d.
Design of one-dimensional (1D) nanomaterials based on non-van der Waals (non-vdW) 1D chain structures is emerging as a new materials frontier, owing to their strong intrinsic anisotropy and broad compositional diversity. However, achieving ultrathin 1D morphology in such systems remains a significant challenge. In this work, we report the colloidal synthesis of ultrathin KFeS and RbFeS nanowires-representing the first fabrication of ultrathin 1D nanomaterials driven by non-vdW 1D crystal structures. The nanowires exhibit diameters of ∼5 nm and lengths of microns, with anisotropic growth directed by covalent [FeS] chains. Magnetic characterization reveals significantly reduced antiferromagnetic transition temperatures and suppressed interchain ferromagnetic interactions, demonstrating pronounced size and morphology effects. Control experiments on structurally related materials indicate that direct nucleation of the 1D phase is essential for achieving the nanowire morphology. These findings establish a new synthetic pathway to an understudied family of non-vdW 1D nanomaterials, enabling exploration of their emergent quantum and magnetic properties.
基于非范德华(non-vdW)一维链结构的一维(1D)纳米材料设计正成为一个新的材料前沿领域,这归因于其强大的固有各向异性和广泛的成分多样性。然而,在这类体系中实现超薄一维形态仍然是一项重大挑战。在这项工作中,我们报告了超薄KFeS和RbFeS纳米线的胶体合成——这代表了由非vdW一维晶体结构驱动的超薄一维纳米材料的首次制备。这些纳米线直径约为5纳米,长度达微米级,具有由共价[FeS]链引导的各向异性生长。磁性表征显示反铁磁转变温度显著降低,链间铁磁相互作用受到抑制,表明了明显的尺寸和形态效应。对结构相关材料的对照实验表明,一维相的直接成核对于实现纳米线形态至关重要。这些发现为一个研究较少的非vdW一维纳米材料家族建立了一条新的合成途径,有助于探索其新出现的量子和磁性特性。