3D Yolk@Shell TiO_2–<i>x</i>/LDH Architecture: Tailored Structure for Visible Light CO₂ Conversion

Abstract

CO₂ photoconversion into hydrocarbon solar fuels by engineered semiconductors is considered as a feasible plan to address global energy requirements in times of global warming. In this regard, three-dimensional yolk@shell hydrogenated TiO₂/Co-Al layered double hydroxide (3D Y@S TiO_{2- x}/LDH) architecture was successfully assembled by sequential solvothermal, hydrogen treatment, and hydrothermal preparation steps. This architecture revealed a high efficiency for the photoreduction of CO₂ to solar fuels, without a noble metal cocatalyst. The time-dependent experiment indicated that the production of CH₃OH was almost selective until 2 h (up to 251 μmol/g_cat. h), whereas CH₄ was produced gradually by increasing the time of reaction to 12 h (up to 63 μmol/g_cat. h). This significant efficiency can be ascribed to the engineering of 3D Y@S TiO_{2- x}/LDH architecture with considerable CO₂ sorption ability in mesoporous yolk@shell structure and LDH interlayer spaces. Also, oxygen vacancies in TiO_{2- x} could provide excess sites for sorption, activation, and conversion of CO₂. Furthermore, the generated Ti³⁺ ions in the Y@S TiO₂ structure as well as connecting of structure with LDH plates can facilitate the charge separation and decrease the band gap of nanoarchitecture to the visible region.