posted on 2025-01-06, 13:20authored byJae Hyo Han, Mansoo Park, Jung-uk Lee, Changhoon Choi, Jung Been Park, Yongjun Lim, Gooreum Kim, Jaemog Jung, Dominik Lungerich, Chul-Ho Jun, Dong-Wan Kim, Jinwoo Cheon
Perpendicular nanochannel creation of two-dimensional
(2D) nanostructures
requires highly controlled anisotropic drilling processes of the entire
structure via void formation. However, chemical approaches for the
creation of porosity and defects of 2D nanostructures have been challenging
due to the strong basal plane chemical stability and the use of harsh
reactants, tending to give randomly corroded 2D structures. In this
study, we introduce Lewis acid–base conjugates (LABCs) as molecular
drillers with attenuated chemical reactivity which results in the
well-defined perpendicular nanochannel formation of 2D TiS2 nanoplates. With the treatment of LABCs, tris(trimethylsilyl)pnictogens
(TMS3P or TMS3As), high resolution perforation
of TiS2 nanoplates was achieved while maintaining their
initial shape and structures. Such perforated TiS2 nanoplates
are tunable in their channel diameter between 4 and 10 nm with 2 nm
resolution. With their increased surface area and enhanced adsorption
of Li2Sx, perforated TiS2 nanoplates served as a diffusion barrier of lithium–sulfur
(Li–S) cells, leading to a 2.5-fold improvement in cell performance
compared to pristine TiS2 nanoplates. Our molecular design
concept for attenuated reactivity of LABCs is simple and could serve
as a new approach for chemical drilling processes of 2D metal chalcogenides.