摘要
The facet-dependent photocatalytic performance of TiO_2 nanocrystals has been extensively investigated due to their promising applications in renewable energy and environmental fields. However, the intrinsic distinction in the photocatalytic oxidation activities between the {001}and {101} facets of anatase TiO_2 nanocrystals is still unclear and under debate. In this work, a simple photoelectrochemical method was employed to meaningfully quantify the intrinsic photocatalytic activities of {001} and{101} faceted TiO_2 nanocrystal photoanodes. The effective surface areas of photoanodes with different facets were measured based on the monolayer adsorption of phthalic acid on TiO_2 photoanode surface by an ex situ photoelectrochemical method, which were used to normalize the photocurrents obtained from different faceted photoanodes for meaningful comparison of their photocatalytic activities. The results demonstrated that the {001} facets of anatase TiO_2 nanocrystals exhibited much better photocatalytic activity than that of {101} facets of anatase TiO_2 nanocrystals toward photocatalytic oxidation of water and organic compounds with different functional groups(e.g.,–OH, –CHO, –COOH). Furthermore, the instantaneous kinetic constants of photocatalytic oxidation of pre-adsorbates on {001} faceted anatase TiO_2 photoanode are obviously greater than those obtained at {101} faceted anatase TiO_2 photoanode, further verifying the higher photocatalytic activity of {001} facets of anatase TiO_2.This work provided a facile photoelectrochemical method to quantitatively determine the photocatalytic oxidation activity of specific exposed crystal facets of a photocatalyst, which would be helpful to uncover and meaningfully compare the intrinsic photocatalytic activities of different exposed crystal facets of a photocatalyst.
The facet-dependent photocatalytic performance of TiO2 nanocrystals has been extensively investigated due to their promising applications in renewable energy and environmental fields. However, the intrinsic distinction in the photocatalytic oxidation activities between the {001 } and {101} facets of anatase TiO2 nanocrystals is still unclear and under debate. In this work, a simple photo- electrochemical method was employed to meaningfully quantify the intrinsic photocatalytic activities of {001 } and { 101 } faceted TiO2 nanocrystal photoanodes. The effective surface areas of photoanodes with different facets were measured based on the monolayer adsorption of phthalic acid on TiO2 photoanode surface by an ex situ photoelectrochemical method, which were used to normalize the photocurrents obtained from different faceted photoanodes for meaningful comparison of their photocatalytic activities. The results demonstrated that the { 001 } facets of anatase TiO2 nanocrystals exhibited much better photo- catalytic activity than that of { 101 } facets of anatase TiO2 nanocrystals toward photocatalytic oxidation of water and organic compounds with different functional groups （e.g., -OH, -CHO, -COOH）. Furthermore, the instantaneous kinetic constants of photocatalytic oxidation of pre-adsor- bates on {001} faceted anatase TiO2 photoanode are obviously greater than those obtained at {101} faceted anatase TiO2 photoanode, further verifying the higher photocatalytic activity of {001} facets of anatase TiO2. This work provided a facile photoelectrochemical method to quantitatively determine the photocatalytic oxidation activity of specific exposed crystal facets of a photocata- lyst, which would be helpful to uncover and meaningfully compare the intrinsic photocatalytic activities of different exposed crystal facets of a photocatalyst.
基金
supported by the National Natural Science Foundation of China (51372248, 51432009 and 51272255)
the CAS/SAFEA International Partnership Program for Creative Research Teams of Chinese Academy of Sciences, China
the CAS Pioneer Hundred Talents Program
