Selectivity of a Copper Oxide CO2 Reduction Electrocatalyst Shifted by a Bioinspired pH-Sensitive Polymer
A bioinspired polymeric membrane capable of shifting the selectivity of a copper oxide electrocatalyst in the CO2 reduction reaction is described. The membrane is deposited on top of copper oxide thin films from wet deposition techniques under controlled conditions of humidity and self-assembles int...
| Autores: | , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2072/537804 |
| Acceso en línea: | http://hdl.handle.net/2072/537804 https://doi.org/10.1021/acsami.4c11927 |
| Access Level: | acceso abierto |
| Palabra clave: | Química 54 - Química |
| Sumario: | A bioinspired polymeric membrane capable of shifting the selectivity of a copper oxide electrocatalyst in the CO2 reduction reaction is described. The membrane is deposited on top of copper oxide thin films from wet deposition techniques under controlled conditions of humidity and self-assembles into an arranged network of micrometer-sized pores throughout the polymer cross-section. The membrane was composed of a block copolymer with a precisely controlled ratio of poly-4-vinylpyridine and poly(methyl methacrylate) blocks (PMMA-b-P4VP). The intrinsic hydrophobicity, together with the porous nature of the membrane’s surface, induces a Cassie–Baxter wetting transition above neutral pH, resulting in water repulsion from the catalyst surface. As a consequence, the catalyst’s surface is shielded from surrounding water molecules under CO2 electroreduction reaction conditions, and CO2 molecules are preferentially located in the vicinity of the catalytically active area. The CO2 reduction reaction is therefore kinetically favored over the hydrogen evolution reaction (HER). |
|---|