TY - JOUR
T1 - Role of CoOx cocatalyst on Ta3N5 photocatalysts studied by transient visible to mid-infrared absorption spectroscopy
AU - Vequizo, Junie Jhon M.
AU - Hojamberdiev, Mirabbos
AU - Teshima, Katsuya
AU - Yamakata, Akira
N1 - Funding Information:
This work was supported by the PRESTO/JST program “Chemical Conversion of Light Energy” , the Grant-in-Aid for Basic Research (B) (No. 16H04188 ) and Scientific Research on Innovative Areas (Soft Molecular Systems: 16H00852 and Mixed Anion: 17H05491 ), and the Str ategic Research Infrastructure Project of MEXT .
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Tantalum nitride (Ta3N5) photocatalysts attract considerable attention owing to their visible light absorption below 600 nm and suitable band structures for reduction and oxidation of water to generate hydrogen and oxygen gas. Herein, we investigated the effects of CoOx on the dynamics of photogenerated charge carriers in Ta3N5 powder photocatalysts by using microsecond to millisecond transient visible to mid-IR absorption spectroscopy. Transient absorption measurements revealed that most of the electrons in Ta3N5 are deeply trapped at the defects, most likely originating from oxygen vacancies and reduced Ta species. Two important roles of CoOx were elucidated: effective capture of holes to prolong electron lifetime and reduction of defects as recombination centers, which further elongates the lifetime of both electrons and holes.
AB - Tantalum nitride (Ta3N5) photocatalysts attract considerable attention owing to their visible light absorption below 600 nm and suitable band structures for reduction and oxidation of water to generate hydrogen and oxygen gas. Herein, we investigated the effects of CoOx on the dynamics of photogenerated charge carriers in Ta3N5 powder photocatalysts by using microsecond to millisecond transient visible to mid-IR absorption spectroscopy. Transient absorption measurements revealed that most of the electrons in Ta3N5 are deeply trapped at the defects, most likely originating from oxygen vacancies and reduced Ta species. Two important roles of CoOx were elucidated: effective capture of holes to prolong electron lifetime and reduction of defects as recombination centers, which further elongates the lifetime of both electrons and holes.
KW - Charge separation
KW - Co-catalysts
KW - Defects
KW - Photocatalysts
KW - Time-resolved measurements
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U2 - 10.1016/j.jphotochem.2017.09.005
DO - 10.1016/j.jphotochem.2017.09.005
M3 - Article
AN - SCOPUS:85029539181
SN - 1010-6030
VL - 358
SP - 315
EP - 319
JO - Journal of Photochemistry and Photobiology A: Chemistry
JF - Journal of Photochemistry and Photobiology A: Chemistry
ER -