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The high efficiencies of CO2 decrease and H2O oxidation in the synthetic system tend to be caused by both the direct Z-scheme electric structure of Cu2O-Pt/SiC/IrOx in addition to indirect Z-scheme spatially separated decrease and oxidation units, which considerably prolong lifetime of photogenerated electrons and holes and give a wide berth to the backward reaction of products. This work provides a very good and feasible technique to b
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