Abstract

It is rather challenging to develop photocatalysts based on narrow-band-gap semiconductors for water splitting under solar irradiation. Herein, we synthesized the Cu2O/Cu2Se multilayer heterostructure nanowires exposing {111} crystal facets by a hydrothermal reaction of Se with Cu and KBH4 in ethanol amine aqueous solution and subsequent annealing in air. The photocatalytic H2 production activity of Cu2O/Cu2Se multilayer heterostructure nanowires is dramatically improved, with an increase on the texture coefficient of Cu2O(111) and Cu2Se(111) planes, and thus the exposed {111} facets may be the active surfaces for photocatalytic H2 production. On the basis of the polar structure of Cu2O {111} and Cu2Se {111} surfaces, we presented a model of charge separation between the Cu-Cu2Se(111) and O-Cu2O(1̅ 1̅ 1̅) polar surfaces. An internal electric field is created between Cu-Cu2Se(111) and O-Cu2O(1̅ 1̅ 1̅) polar surfaces, because of spontaneous polarization. As a result, this internal electric field drives the photocreated charge separation. The oxidation and reduction reactions selectively occur at the negative O-Cu2O(1̅ 1̅ 1̅) and the positive Cu-Cu2Se(111) surfaces. The polar surface-engineering may be a general strategy for enhancing the photocatalytic H2-production activity of semiconductor photocatalysts. The charge separation mechanism not only can deepen the understanding of photocatalytic H2 production mechanism but also provides a novel insight into the design of advanced photocatalysts, other photoelectric devices, and solar cells.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.