Artículo

Surface Stabilization of High-Pressure TiO 2 Polymorph via High-Energy Ball Milling: Boosting Noble-Metal-Free CO 2 Photoreduction

Mufari, Abigail Icon; Capelupi, Thiago ; Saleta, Martin Eduardo Icon; Zelaya, Maria Eugenia Icon; Furlong, Octavio Javier Icon; Boldrin Zanoni, Maria Valnice ; Cadus, Luis Eduardo Icon; Ferreira de Brito, Juliana ; Larregola, Sebastian Alberto Icon

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Fecha

03/2026

Editorial

American Chemical Society

Revista

ACS Omega

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Institución organizadora

ISSN

2470-1343

eISSN

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Inglés

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Resumen

High-energy ball milling (HEBM) is employed to stabilize the high-pressure TiO2−II polymorph as nanocrystallites anchored to anatase surfaces, producing a controllable polymorphic mixture that markedly enhances CO2 photoreduction to CH3OH in aqueous media without noble metals or cocatalysts. The resulting architecture features TiO2−II intimately interfaced with strained anatase and a high density of extended defects (grain boundaries, phase interfaces, and dislocation terminations) hosting reactive surface species with modified electronic properties. This defect-rich configuration provides high-affinity CO2 adsorption and activation sites. Both bulk and surface are profoundly restructured under the extreme nonequilibrium conditions of HEBM, which reproduce high-pressure transformation pathways at ambient conditions. These results highlight a green, scalable strategy for defect and polymorph engineering in TiO2, enabling targeted surface chemistry design to improve photocatalytic CO2 conversion. High-energy ball milling (HEBM) is employed to stabilize the high-pressure TiO2−II polymorph as nanocrystallites anchored to anatase surfaces, producing a controllable polymorphic mixture that markedly enhances CO2 photoreduction to CH3OH in aqueous media without noble metals or cocatalysts. The resulting architecture features TiO2−II intimately interfaced with strained anatase and a high density of extended defects (grain boundaries, phase interfaces, and dislocation terminations) hosting reactive surface species with modified electronic properties. This defect-rich configuration provides high-affinity CO2 adsorption and activation sites. Both bulk and surface are profoundly restructured under the extreme nonequilibrium conditions of HEBM, which reproduce high-pressure transformation pathways at ambient conditions. These results highlight a green, scalable strategy for defect and polymorph engineering in TiO2, enabling targeted surface chemistry design to improve photocatalytic CO2 conversion.

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