Monocrystalline materials are essential for optoelectronic devices such as solar cells, LEDs, lasers, and transistors to reach the highest performance. Advances in synthetic chemistry now allow for high quality monocrystalline nanomaterials to be grown at low temperature in solution for many materials; however, the realization of extended structures with control over the final 3D geometry still remains elusive. Here, a new paradigm is presented, which relies on epitaxy between monocrystalline nanocube building blocks. The nanocubes are assembled in a predefined pattern and then epitaxially connected at the atomic level by chemical growth in solution, to form monocrystalline nanopatterns on arbitrary substrates. As a first demonstration, it is shown that monocrystalline silver structures obtained with such a process have optical properties and conductivity comparable to single-crystalline silver. This flexible multiscale process may ultimately enable the implementation of monocrystalline materials in optoelectronic devices, raising performance to the ultimate limit.@en

The emergence of two-dimensional transition metal dichalcogenide materials has sparked intense activity in valleytronics, as their valley information can be encoded and detected with the spin angular momentum of light. We demonstrate the valley-dependent directional coupling of light using a plasmonic nanowire-tungsten disulfide (WS2) layers system. We show that the valley pseudospin in WS2 couples to transverse optical spin of the same handedness with a directional coupling efficiency of 90 ± 1%. Our results provide a platform for controlling, detecting, and processing valley and spin information with precise optical control at the nanoscale.@en

The chiral interaction between transverse optical spin and circularly polarized emitters provides a novel way to manipulate spin information at the nanoscale. Here, we demonstrate the valley(spin)-dependent directional emission of transition metal chalcogenides (TMDs) into plasmonic eigenstates of a silver nanowire. Due to the spin-path locking of the plasmonic eigenstates, the emission from the two different valleys of TMDs material will couple to the guided modes propagating in opposite directions. The high valley polarization of TMDs and high density of the transverse optical spin of the plasmonic wire together offer a novel platform for a chiral network even at room temperature without any magnetic fields.@en