Decorating Cu2O with Ni-doped metal organic frameworks as efficient photocathodes for solar water splitting
Severe photocorrosion and fast photoexcited charges recombination hinder the application of Cu2O in photoelectrochemical (PEC) water splitting. In this work, Ni-doped metal-organic frameworks is firstly applied to improve the performance of electrodeposited Cu2O. A decorative layer of Ni-doped Cu3(B...
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Published in | International journal of hydrogen energy Vol. 48; no. 45; pp. 17065 - 17073 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
26.05.2023
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Subjects | |
Online Access | Get full text |
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Summary: | Severe photocorrosion and fast photoexcited charges recombination hinder the application of Cu2O in photoelectrochemical (PEC) water splitting. In this work, Ni-doped metal-organic frameworks is firstly applied to improve the performance of electrodeposited Cu2O. A decorative layer of Ni-doped Cu3(BTC)2 (Ni-CuBTC) was in-suit constructed on Cu2O through solvothermal followed by ion-exchange. Cu2O/Ni-CuBTC photocathodes increase absorption edge to ∼800 nm, positive shift flat band position to 0.4 V, and decrease Tafel value to 74 mV/dec. These results confirm the decorative layer can extend light absorption, facilitate photoexcited charge separation and transfer, and enhance HER activity. A photocurrent density of −1.51 mA/cm2 at 0 VRHE is obtained with the decoration of Ni-CuBTC, which is 3.4 times of pristine Cu2O photocathode. Here, the PEC water splitting performance of electrodeposited Cu2O has been significantly improved with noble-metal-free decorations, which provides a new idea for solving the defects of Cu2O based photocathode.
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•Ni-CuBTC decorated Cu2O as HER photocathode by solvothermal and ion-exchange.•CuBTC can adjust the energy band structure and promote charges transfer.•HER kinetics can be improved with Ni doping.•Noble-metal-free Ni-CuBTC acts as co-catalyst, photosensitizer, and protector.•It exhibits 3.4 times current density of bare Cu2O with −1.51 mA/cm2 at 0 VRHE. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2023.01.145 |