Precise
morphological control over anisotropic noble metal nanoparticles
(ANPs) is one of the key issues in the nano-research field owing to
their unique optoelectronic, magnetic, mechanical, and catalytic properties.
Although nanostructures fabricated by the directed assembly of adsorbate
have been widely demonstrated recently, facile yet universal synthesis
of nanocrystal with tunable morphologies, green templates, no seeds,
and high yield remains challenging. Herein, we develop a versatile
method, allowing for the rapid, one-step, seedless, surfactant-free
synthesis of a noble metal nanostructure with tunable anisotropy on
MXene in a sequence-dependent manner through a single-DNA molecular
regulator. Based on the mild reducibility of MXene and the selective
affinity of the DNA to the specific facets in the crystals, oriented
aggregations and the growth of ANPs (Au, Pt, Pd) can be achieved and
the resulting asymmetric morphology from polyhedrons, or flowers,
or nanoplates to dendrites is observed. The ability to align such
ANPs on the MXene surface is expected to lead to improved photothermal
effect and surface-enhanced Raman scattering. Furthermore, our work
makes the fabrication of the ANPs or ANP-MXene heterostructure easier,
stimulating further explorations of physical, chemical, and biological
applications.