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Photoelectrochemical water splitting using lithium doped bismuth vanadate photoanode with near-complete bulk charge separation

机译:掺锂钒酸铋光电阳极的光电化学水分解与近乎完全的电荷分离

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摘要

Photoelectrochemical performance of BiVO4 photoanode is limited by poor light absorption, charge separation and transfer efficiencies. For the first time in the literature, Li doped nano-porous BiVO4 photoanode showed complete bulk charge separation efficiency (similar to 100%) at 1.23 V vs RHE along with enhanced light absorption for water splitting. Li doping showed an increase (>20 times) in the photoelectrochemical water splitting compared to pristine BiVO4 photoanode. In particular, oxygen evolution catalyst was also employed for further improving the photoelectrochemical performance (4.2 +/- 0.18 mA cm(-2)) of Li:BiVO4 photoanodes. The density functional theory calculations showing the formation of inter-band with band gap reduction due to interstitial Li doping in BiVO4 structure support enhancement in photoelectrochemical performance. In addition, Li doping in the BiVO4 lattice void positions led to a record photocurrent density of 7.3 +/- 0.36 mA cm(-2) at 1.23 V vs RHE in the presence of hole scavenger under one sun illumination. Further, present study systematically demonstrates role of Li in BiVO4 host for water oxidation through a detailed characterization and study of optical and charge transport properties.
机译:BiVO4光电阳极的光电化学性能受到不良的光吸收,电荷分离和转移效率的限制。锂掺杂的纳米多孔BiVO4光电阳极在RHE的1.23 V电压下首次显示出完全的体电荷分离效率(接近100%),同时还增强了水分解的光吸收率。与原始BiVO4光电阳极相比,锂掺杂显示出光电化学水分解的增加(> 20倍)。特别是,还使用了析氧催化剂来进一步改善Li:BiVO4光阳极的光电化学性能(4.2 +/- 0.18 mA cm(-2))。密度泛函理论计算显示,由于BiVO4结构中的间隙Li掺杂导致带隙减少的带间形成,支持了光电化学性能的增强。此外,Li掺杂在BiVO4晶格空隙位置导致在1.23 V相对于RHE在一个阳光照射下存在空穴清除剂的情况下,记录的光电流密度为7.3 +/- 0.36 mA cm(-2)。此外,本研究通过详细表征和研究光学和电荷传输性质,系统地证明了Li在BiVO4主体中对水氧化的作用。

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