Bottom-up Synthesis of Nanosheets at Various Interfaces.

Nanostructured materials with high aspect ratios have been widely studied for their unique properties. In particular, nanosheets have safety, dispersibility, and nanosized effects, and nanosheets with exceptionally small thicknesses exhibit unique properties. For non-exfoliable materials, the bottom-up nanosheet growth using various interfaces as templates have been investigated. This review article presents the synthesis of nanosheets at the interfaces and layered structure; it explains the features of each interface type, its advantages, and its uniqueness. The interfaces work as templates for nanosheet synthesis. We can easily use the liquid-liquid and gas-liquid interfaces as the templates; however, the thickness of nanosheets usually becomes thick because it allows materials to grow in thickness. The solid-gas and solid-liquid interfaces can prevent nanosheets from growing in thickness. However, the removal of template solids is required after the synthesis. The layered structures of various materials provide two-dimensional reaction fields between the layers. These methods have high versatility, and the nanosheets synthesized by these methods are thin. Finally, this review examines the key challenges and opportunities associated with scalable nanosheet synthesis methods for industrial production.

Detection of alkali and alkaline earth metal ions using birefringence of hyperswollen lamellar phase.

Chemical sensors have targeted various substances. Most sensors electrically amplify signals. Here, we propose a visual detection system that uses a hyperswollen lamellar phase and detects targets in a solution without electric amplification. Amphiphiles with an oligo(ethylene glycol) chain can catch alkali and alkaline earth metal ions and amplify to macroscopic birefringence.

Amorphous Aluminosilicate Nanosheets as Universal Precursors for the Synthesis of Diverse Zeolite Nanosheets for Polymer-Cracking Reactions.

Zeolites catalyze some reactions in their molecular-sized pores, but large molecules can react only on their external surface. Zeolite-nanosheets (NSs) have been developed as catalysts for large molecules. The previously reported methods to synthesize zeolite-NSs are specialized for each zeolite type. Here we propose a new method to synthesize various zeolite-NSs from the same amorphous aluminosilicate NSs (AAS-NSs) as a universal precursor. We successfully synthesized the unprecedented AAS-NSs in the hydrophilic space of the stable hyperswollen lyotropic lamellar (HL) phase. The four zeolite types could be obtained from the single-species AAS-NSs. These results imply that this method enables us to synthesize almost all types of zeolite-NSs. Moreover, the synthesized CHA-NSs have great potential for various applications because of their thickness and large external surface area.

Thin ZIF-8 nanosheets synthesized in hydrophilic TRAPs.

The preparation method of nanosheets using hyperswollen lyotropic lamellar phases, the 'two-dimensional reactor in amphiphilic phases (TRAP) method', has successfully provided nanosheets of various non-layered materials. Previously reported examples started from a single hydrophobic or hydrophilic precursor and multiple hydrophobic precursors. Here, we propose a synthesis method of nanosheets of ZIF-8, zinc 2-methylimidazolate, with a sodalite-like framework. They grow up to a few nanometers of thickness and several hundred nanometers of width with neither aggregation nor impurities from multiple hydrophilic precursors in the stoichiometric ratio inside the hydrophilic TRAPs consisting of the amphiphile Brij L4. The thin nanosheets of ZIF-8 doped with Co2+ (Co-ZIF-8) synthesized by the same method maintained a high specific surface area after calcination. Therefore, the oxygen reduction reaction (ORR) activity of the calcined Co-ZIF-8 NSs for fuel cells becomes higher than that of the calcined conventional Co-ZIF-8 crystals.

Lateral Growth of Uniformly Thin Gold Nanosheets Facilitated by Two-Dimensional Precursor Supply.

The nanosheets of highly symmetric materials with a face-centered cubic lattice such as gold have been synthesized by adsorbing the precursors on a flat surface, whose chemical specificity induces the anisotropy of growth rates. We have succeeded in the fabrication of gold nanosheets in a hydrophilic space inside highly separated bilayers, which work as two-dimensional hydrophilic reactors, in a hyperswollen lamellar liquid crystalline phase of an amphiphile solution. One of the physical properties, amphiphilicity, confines the ingredients therein. The nanosheets can only grow in the in-plane direction due to the inhibition of the out-of-plane growth rather than the anisotropy of growth rates probably. Thus, the synthesis can be accelerated; the particles can be completed within 15 min. As not relying on chemical specificity, silver nanosheets could also be synthesized in the same way. The suspension of gold and silver nanosheets without any amphiphiles could be obtained, and the solvent is replaceable. We found that the width of the obtained gold nanosheets is proportional to the Reynolds number of the solution because the area of the bilayer in the hyperswollen lamellar phase depends on shear stress. This implies that the areas of gold nanosheets depend on the areas of the bilayers, and it can be controlled by changing the Reynolds number. This method could be widely used to continuously obtain large-area nanosheets of various materials in a roll-to-roll manufacturing process.