Poly(1,4-Diethynylbenzene) Gradient Homojunction with Enhanced Charge Carrier Separation for Photoelectrochemical Water Reduction.
basic_science · Level V
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- Record sourced from PubMed, PMID 30919520.
- Also identified by DOI 10.1002/adma.201900961.
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Abstract
As appealing photoelectrode materials for photoeletrochemical hydrogen evolution reaction (PEC HER), conjugated polymers still show poor PEC HER performance as a result of their serious recombination of photogenerated electrons and holes. Herein, a novel design of gradient homojunction is demonstrated by controlled copolymerization of 1,4-diethynylbenzene (DEB) and 1,3,5-triethynylbenzene (TEB). The as-built gradient distribution of TEB monomer in poly(1,4-diethynylbenzene) (pDEB) leads to continuous band bending engineering, which constitutes a gradient homojunction. Under AM 1.5G irradiation and in 0.1 m Na<sub>2</sub> SO<sub>4</sub> aqueous solution, the as-fabricated pDEB gradient homojunction exhibits a charge separation efficiency of 0.27% at 0.3 V versus reversible hydrogen electrode (RHE), which is 3.4 and 1.7 times higher than those for pure pDEB and the traditionally designed pDEB homojunction. As a result, the photocurrent of the pDEB gradient homojunction unprecedentedly reaches 55 µA cm<sup>-2</sup> at 0.3 V versus RHE, which is much higher than 19 µA cm<sup>-2</sup> for pure pDEB, 32 µA cm<sup>-2</sup> for the pDEB homojunction, and state-of-the-art organic photocathodes, e.g., g-C<sub>3</sub> N<sub>4</sub> (≈1-32 µA cm<sup>-2</sup> ). This work opens up a new window for the design of gradient homojunctions and will advance the exploration of high-performance organic photoelectrodes.