2026
Microtron-induced surface defects and phase transformations in anatase TiO2 colloidal nanoparticles
THELAPPURATH, Aiswarya Vijayakumar; Zuzana SISKA; Sanjay Gopal ULLATTIL; Lucie ŠIMONÍKOVÁ; Nadezda PIZUROVA et al.Základní údaje
Originální název
Microtron-induced surface defects and phase transformations in anatase TiO2 colloidal nanoparticles
Autoři
THELAPPURATH, Aiswarya Vijayakumar; Zuzana SISKA; Sanjay Gopal ULLATTIL; Lucie ŠIMONÍKOVÁ a Nadezda PIZUROVA
Vydání
SURFACES AND INTERFACES, AMSTERDAM, ELSEVIER, 2026, 2468-0230
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10403 Physical chemistry
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 6.300 v roce 2024
Označené pro přenos do RIV
Ano
Organizační jednotka
Přírodovědecká fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Ligand pair strategy; Oleic acid-oleylamine capping; Microtron irradiation; Surface defects; Phase transformation; TiO2 colloidal nanoparticles
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 19. 3. 2026 13:12, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Ultrasmall TiO2 colloidal nanoparticles (2-5 nm) were synthesized by ligand-assisted thermal decomposition and subsequently exposed to extreme-dose 16.5 MeV microtron electrons for 0-80 min, delivering absorbed doses of 23-171 MGy. Despite the unusually high irradiation levels, high-resolution TEM showed that the crystalline core size remained constant at 3.0-3.6 nm, while rutile nanodomains nucleated after >= 10 min, evidencing a localized anatase -> rutile transformation decoupled from particle growth. X-ray photoelectron spectroscopy recorded a transient increase and eventual depletion of Ti3+ surface species (0.074 -> < 0.005), accompanied by an indirect band-gap contraction from 3.30 to 2.50 eV. Dynamic light scattering revealed only minor aggregation, and the dispersions possessed promising colloidal stability. These findings demonstrate that multi-MGy microtron irradiation can simultaneously engineer defects and trigger phase change in sub-5 nm oxide colloids without sintering - an irradiation window that, to the best of our knowledge, has not been systematically explored for TiO2 nanomaterials, where published electron-beam studies rarely exceed 1 MGy. The approach offers a single-step, post-synthetic route to tune the redox activity and optical properties of oxide nanomaterials while preserving their ultrasmall dimension.