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Heteroatom‐Modulated Switching of Photocatalytic Hydrogen and Oxygen Evolution Preferences of Anatase TiO 2 Microspheres
Author(s) -
Liu Gang,
Pan Jian,
Yin Lichang,
Irvine John TS,
Li Feng,
Tan Jun,
Wormald Philip,
Cheng HuiMing
Publication year - 2012
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201200414
Subject(s) - photocatalysis , heteroatom , materials science , anatase , water splitting , oxygen , hydrogen , chemical engineering , photochemistry , oxygen evolution , boron , nanotechnology , catalysis , electrochemistry , chemistry , organic chemistry , ring (chemistry) , electrode , engineering
Understanding and manipulating the two half‐reactions of photoinduced electron reduction and hole oxidation are key to designing and constructing efficient photocatalysts. Here, how the spatial distribution of the heteroatom modulates photocatalytic reduction (hydrogen evolution) and oxidation (oxygen evolution) reaction preferences is investigated by moving boron from the core to the shell of an anatase TiO 2 microsphere along [001] via thermal diffusion control. The preference towards photocatalytic hydrogen and oxygen producing reactions from splitting water can be switched by creating a shell with an interstitial B σ + ( σ ≤ 3) gradient in the TiO 2 microsphere. This switching stems from the downward shift of electronic band edges of the shell by a band bending effect that originates from the extra electrons coming from the interstitial B σ+ . These results create new opportunities for designing and constructing efficient photocatalysts by spatial heteroatom engineering.