Photocatalytic hydrogen production using twinned nanocrystals and an unanchored NiSx co-catalyst
Maochang Liu (),
Yubin Chen,
Jinzhan Su,
Jinwen Shi,
Xixi Wang and
Liejin Guo ()
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Maochang Liu: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Yubin Chen: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Jinzhan Su: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Jinwen Shi: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Xixi Wang: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Liejin Guo: International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an
Nature Energy, 2016, vol. 1, issue 11, 1-8
Abstract:
Abstract Facilitating charge separation as well as surface redox reactions is considered to be central to improving semiconductor-catalysed solar hydrogen generation. To that end, photocatalysts comprising intimately interfaced photo absorbers and co-catalysts have gained much attention. Here, we combine an efficient Cd0.5Zn0.5S (CZS) nanotwinned photocatalyst with a NiSx co-catalyst for photogeneration of hydrogen. We find that an internal quantum efficiency approaching 100% at 425 nm can be achieved for photocatalytic H2 production from water with Na2S/Na2SO3 as hole scavengers. Our results indicate that the NiSx co-catalyst is not anchored on the surface of the host CZS nanotwins and instead exists in the reaction solution as freestanding subnanometre clusters. We propose that charge transfer is accomplished via collisions between the CZS and NiSx clusters, which aids charge separation and inhibits back reaction, leading to high water reduction rates in the suspension.
Date: 2016
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DOI: 10.1038/nenergy.2016.151
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