Micron-Scale Fabrication of Ultrathin Amorphous Copper Nanosheets Templated by DNA Scaffolds.
Xiangyuan OuyangYongli WuYanjing GaoLingyun LiLe LiTing LiuXinxin JingYue FuJing LuoGang XieSisi JiaMingqiang LiQian LiChun-Hai FanXiaoguo LiuPublished in: Journal of the American Chemical Society (2023)
Two-dimensional (2D) amorphous materials could outperform their crystalline counterparts toward various applications because they have more defects and reactive sites and thus could exhibit a unique surface chemical state and provide an advanced electron/ion transport path. Nevertheless, it is challenging to fabricate ultrathin and large-sized 2D amorphous metallic nanomaterials in a mild and controllable manner due to the strong metallic bonds between metal atoms. Here, we reported a simple yet fast (10 min) DNA nanosheet (DNS)-templated method to synthesize micron-scale amorphous copper nanosheets (CuNSs) with a thickness of 1.9 ± 0.4 nm in aqueous solution at room temperature. We demonstrated the amorphous feature of the DNS/CuNSs by transmission electron microscopy (TEM) and X-ray diffraction (XRD). Interestingly, we found that they could transform to crystalline forms under continuous electron beam irradiation. Of note, the amorphous DNS/CuNSs exhibited much stronger photoemission (∼62-fold) and photostability than dsDNA-templated discrete Cu nanoclusters due to the elevation of both the conduction band (CB) and valence band (VB). Such ultrathin amorphous DNS/CuNSs hold great potential for practical applications in biosensing, nanodevices, and photodevices.
Keyphrases
- room temperature
- electron microscopy
- ionic liquid
- aqueous solution
- circulating tumor
- cell free
- single molecule
- machine learning
- high resolution
- photodynamic therapy
- quantum dots
- gold nanoparticles
- risk assessment
- magnetic resonance
- nucleic acid
- optical coherence tomography
- highly efficient
- tissue engineering
- deep learning
- transition metal
- sensitive detection
- oxide nanoparticles
- solar cells
- human health
- circulating tumor cells
- electron transfer