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Induced dipole in vanadium-doped zinc oxide nanosheets and its effects on photoelectrochemical water splitting

机译:含钒掺杂氧化锌纳米液中的偶极子及其对光电化学水分裂的影响

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Appropriate control of energy band bending at the interface between semiconductors and electrolytes are closely related to performance of photoelectrochemical (PEC) water splitting. Dipoles formed near the surface of semiconductors induces energy band bending at the interface. Energy band bending control has been demonstrated by employing charged molecules and piezoelectric materials. However, chemical and piezoelectric approaches have demerit of chemical instability and inducement of instantaneous dipole, respectively. To overcome these problems, we adopted the ferroelectric material for PEC water splitting, where spontaneous dipoles in the material can be oriented by applying external electric field. In this work, we hydrothermally synthesized vanadium (V)-doped ferroelectric ZnO nanosheets and employed to systematically investigate the dipole effect on performance of V-doped ZnO PEC for water oxidation. Consequently, positively polarized V-doped ZnO photoanode exhibits 125% enhanced water splitting efficiency compared to negatively polarized ones due to favorable band bending for carrier transport from semiconductor to water.
机译:适当控制半导体和电解质之间界面处的能带弯曲与光电化学(PEC)水分裂的性能密切相关。在半导体表面附近形成的偶极诱导在界面处弯曲能带弯曲。通过采用带电分子和压电材料来证明能带弯曲控制。然而,化学和压电方法分别具有化学不稳定性和瞬时偶极子的诱导。为了克服这些问题,我们采用了PEC水分裂的铁电材料,其中材料中的自发偶极可以通过施加外部电场定向。在这项工作中,我们热量合成钒(V) - 掺杂铁电ZnO纳米蛋白酶,并用于系统地研究偶极效应对水氧化的V掺杂ZnO PEC的性能。因此,与带负极化的带有良好的带弯曲,用于从半导体到水的载体传输,相比,正极化的V掺杂ZnO光电码表现出125%增强的水分裂效率。

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