Abstract

As attractive materials for photoeletrochemical hydrogen evolution reaction (PEC HER), conjugated polymers (e.g., conjugated acetylenic polymers [CAPs]) still show poor PEC HER performance due to the associated serious recombination of photogenerated electrons and holes. Herein, taking advantage of the in situ conversion of nanocopper into Cu2 O on copper cellulose paper during catalyzing of the Glaser coupling reaction, a general strategy for the construction of a CAPs/Cu2 O Z-scheme heterojunction for PEC water reduction is demonstrated. The as-fabricated poly(2,5-diethynylthieno[3,2-b]thiophene) (pDET)/Cu2 O Z-scheme heterojunction exhibits a carrier separation efficiency of 16.1% at 0.3V versus reversible hydrogen electrode (RHE), which is 6.7 and 1.4-times higher respectively than those for pDET and Cu2 O under AM 1.5G irradiation (100mW cm-2 ) in the 0.1 m Na2 SO4 aqueous solution. Consequently, the photocurrent of the pDET/Cu2 O Z-scheme heterojunction reaches ≈520 µA cm-2 at 0.3V versus RHE, which is much higher than pDET (≈80 µA cm-2 ), Cu2 O (≈100 µA cm-2 ), and the state-of-the-art cocatalyst-free organic or organic-semiconductor-based heterojunctions/homojunctions photocathodes (1-370 µA cm-2 ). This work advances the design of polymer-based Z-scheme heterojunctions and high-performance organic photoelectrodes.

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