TY - JOUR
T1 - A dual-functional organic p-n bilayer catalyst comprising a perylene derivative and cobalt phthalocyanine working under illumination and in the dark
AU - Abe, Toshiyuki
AU - Okumura, Masato
AU - Kikuchi, Yuko
AU - Itoh, Takashi
AU - Nagai, Keiji
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - In this study, we show dual-functional catalysis for down-hill reaction by an organic p-n bilayer with and without irradiation. The organic p-n bilayer, composed of 3,4,9,10-perylenetetracarboxylic-bis-benzimidazole (PTCBI, n-type) and cobalt phthalocyanine (CoPc, p-type), is employed as a photocatalyst in the presence of 2-mercaptoethanol. The PTCBI/CoPc bilayer can induce the photocatalytic oxidation of thiol along with the reduction of H+ to H2 by oxidizing and reducing powers generated at CoPc and PTCBI surfaces, respectively, through a series of photophysical events within the organic bilayer. Moreover, the aforementioned reaction can also be found to occur in the dark, due to the catalysis of the bilayer. The distinct oxidation states of CoPc (i.e. CoIIPc in the dark and CoIIIPc under illumination) are responsible for thiol oxidation, where the reducing power for H2 evolution can consist of the electrons released from thiol in the dark and the electron carriers generated under illumination. In this paper, photoelectrochemical and photocatalytic results have been presented to discuss the details of the two types of catalyses by the PTCBI/CoPc bilayer.
AB - In this study, we show dual-functional catalysis for down-hill reaction by an organic p-n bilayer with and without irradiation. The organic p-n bilayer, composed of 3,4,9,10-perylenetetracarboxylic-bis-benzimidazole (PTCBI, n-type) and cobalt phthalocyanine (CoPc, p-type), is employed as a photocatalyst in the presence of 2-mercaptoethanol. The PTCBI/CoPc bilayer can induce the photocatalytic oxidation of thiol along with the reduction of H+ to H2 by oxidizing and reducing powers generated at CoPc and PTCBI surfaces, respectively, through a series of photophysical events within the organic bilayer. Moreover, the aforementioned reaction can also be found to occur in the dark, due to the catalysis of the bilayer. The distinct oxidation states of CoPc (i.e. CoIIPc in the dark and CoIIIPc under illumination) are responsible for thiol oxidation, where the reducing power for H2 evolution can consist of the electrons released from thiol in the dark and the electron carriers generated under illumination. In this paper, photoelectrochemical and photocatalytic results have been presented to discuss the details of the two types of catalyses by the PTCBI/CoPc bilayer.
UR - http://www.scopus.com/inward/record.url?scp=85018521141&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85018521141&partnerID=8YFLogxK
U2 - 10.1039/c7ta00174f
DO - 10.1039/c7ta00174f
M3 - Article
AN - SCOPUS:85018521141
SN - 2050-7488
VL - 5
SP - 7445
EP - 7450
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 16
ER -