Abstract

Designing and fabricating semiconductor photoanodes with efficient charge separation and appropriate active sites for solar energy conversion is indubitably a promising alternative to overcome the environmental crisis and energy shortage. Herein, we report a heterojunction WO3/ZnIn2S4 (WO3/ZIS) grafting silane molecule (N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, AESI) as photoanode with boosted photoelectrochemical (PEC) efficiency toward highly efficient water splitting. The type Ⅱ WO3/ZIS heterostructure are firstly synthesized by hydrothermal growth of WO3 nanosheets on the surface of fluorine-doped tine oxide (FTO)-coated glass, followed by depositing ZIS onto WO3 surface. After that, silane molecules are anchored on WO3/ZIS via chemical water bath method. It is demonstrated that forming WO3/ZIS heterostructure and grafting silane molecules would greatly enhance the charge separation efficiency and transfer mobility. In addition, silane molecules would offer enough reactive sites for water oxidization reaction. As a result, the obtained WO3/ZIS/AESI photoanode exhibits a photocurrent density of 1.51 mA cm−2 under simulated solar light irradiation, to be 74.6% enhanced than that of WO3. Moreover, the incident photon-to-current conversion efficiency (IPCE) at 365 nm increases from 39.1% to 50.6% for WO3 and WO3/ZIS/AESI, respectively. The present strategy provides inspiration for preparation of photoelectrode materials in water splitting.

Full Text
Paper version not known

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.