A Versatile Synthesis Platform Based on Polymer Cubosomes for a Library of Highly Ordered Nanoporous Metal Oxides Particles.

Abstract

Polymer cubosomes (PCs) have well-defined inverse bicontinuous cubic mesophases formed by amphiphilic block copolymer bilayers. The open hydrophilic channels, large periods, and robust physical properties of PCs are advantageous to many host-guest interactions and yet not fully exploited, especially in the fields of functional nanomaterials. Here, the self-assembly of poly(ethylene oxide)-block-polystyrene block copolymers is systematically investigated and a series of robust PCs is developed via a cosolvent method. Ordered nanoporous metal oxide particles are obtained by selectively filling the hydrophilic channels of PCs via an impregnation strategy, followed by a two-step thermal treatment. Based on this versatile PC platform, the general synthesis of a library of ordered porous particles with different pore structures <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics><mover><mn>3</mn> <mo>¯</mo></mover> <annotation>$\bar{3}$</annotation></semantics> </math> <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics><mover><mn>3</mn> <mo>¯</mo></mover> <annotation>$\bar{3}$</annotation></semantics> </math> , tunable large pore size (18-78 nm), high specific surface areas (up to 123.3 m² g^-1 for WO₃) and diverse framework compositions, such as transition and non-transition metal oxides, rare earth chloride oxides, perovskite, pyrochlore, and high-entropy metal oxides is demonstrated. As typical materials obtained via this method, ordered porous WO₃ particles have the advantages of open continuous structure and semiconducting properties, thus showing superior gas sensing performances toward hydrogen sulfide.