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Interfacial electric field of BiVO4/WO3 photoanode-induced S-scheme charge transfer for enhanced photoelectrochemical performance

机译:Interfacial electric field of BiVO4/WO3 photoanode-induced S-scheme charge transfer for enhanced photoelectrochemical performance

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Type-II heterojunction films are widely applied as photoanodes for photoelectrochemical (PEC) water splitting. However, type-II heterojunctions are disadvantaged by drawbacks such as reduced redox ability and the occurrence of repulsion against photogenerated charge transfer. Herein, it is first proposed that an S-scheme heterojunction be used as a photoanode in the PEC field. The proposed S-scheme BiVO4/WO3 photoanode (S-BiVO4/WO3) is inverse to the typical type-II WO3/BiVO4 heterojunction photoanode (IIWO3/ BiVO4) and shows significantly better PEC performance. The photocurrent density reaches 3.22 mA cm-2 (1.23 VRHE) without a cocatalyst, which is higher than the photocurrent density reported to date for most BiVO4-based photoanodes. The onset potential decreases from 0.97 to 0.82 VRHE. According to the experimental and theoretical calculation results, the internal electric field formed at the heterojunction interface can induce a step-scheme charge transfer mechanism, which promotes the separation of photogenerated charge. Besides, the same direction between the internal electric field and the applied bias can reduce the applied bias voltage. Our results demonstrate that the construction of an S-scheme heterojunction is a preferable strategy that can be applied to design the photoanode for highly efficient PEC water splitting.
机译:ⅱ型异质结薄膜被广泛应用光电阳极光电化学(压电)水分裂。弱势群体通过降低氧化还原等缺点能力和排斥的发生photogenerated电荷转移。首先提出一个S-scheme异质结在压电陶瓷领域用作光电阳极。提出S-scheme BiVO4 / WO3光电阳极(S-BiVO4 / WO3)是典型的ⅱ型逆WO3 / BiVO4异质结光电阳极(IIWO3 /BiVO4),显示了更好的压电陶瓷表演3.22 mA cm-2 (1.23 VRHE)没有助催化剂,这是高于光电流密度对于大多数BiVO4-based迄今报告光电阳极。0.97到0.82 VRHE。和理论计算结果,内部电场形成异质结接口可以诱导step-scheme电荷转移机制,促进分离photogenerated电荷。内部电场和之间的方向应用偏差可以减少应用偏差电压。S-scheme异质结是一个建设更可取的策略可以应用到设计中高效的光电阳极压电陶瓷水分裂。

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