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In situ growth of ultrathin Co-MOF nanosheets on α-Fe_2O_3 hematite nanorods for efficient photoelectrochemical water oxidation

机译:超薄Co-MOF纳米片在α-Fe_2O_3赤铁矿纳米棒上的原位生长,用于有效的光电化学水氧化

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Efficient charge transport is an important factor in photoelectrochemical (PEC) water splitting. The charge transfer at the semiconductor/electrolyte interface is of great importance, especially for the complex water oxidation reaction. In this study, we explored the feasibility of improving charge transfer efficiency at the interface of semiconductor/electrolyte by in situ growth of Co based Metal-Organic Frame work (Co-MOF) through a facile ion-exchanging method. Under optimized conditions, the Co-MOF nanosheet-modified hematite gave a photocurrent density of 2.0 mA cm(-2) (200% improvement) at 1.23 V-RHE with a cathodic shift of 180 mV in the photocurrent onset potential, in comparison to bare alpha-Fe2O3 (0.71 mA cm(-2)@1.23 VRHE). To elucidate the role of Co-MOF, X-ray photoelectron spectroscopy, electrochemical impedance spectroscopy and Mott-Schottky measurements were carried out. It was found that the atomically distributed Co2+ in Co-MOF possessed excellent hole storage capability and charge transfer efficiency, as evidenced by the high surface capacitance and extremely low surface charge transfer resistance.
机译:有效的电荷传输是光电化学(PEC)水分解的重要因素。半导体/电解质界面上的电荷转移非常重要,特别是对于复杂的水氧化反应而言。在这项研究中,我们探讨了通过简便的离子交换方法原位生长Co基金属有机框架(Co-MOF)来提高半导体/电解质界面电荷转移效率的可行性。在最佳条件下,Co-MOF纳米片修饰的赤铁矿在1.23 V-RHE上的光电流密度为2.0 mA cm(-2)(提高200%),而光电流起始电位的阴极位移为180 mV裸露的α-Fe2O3(0.71 mA cm(-2)@1.23 VRHE)。为了阐明Co-MOF的作用,进行了X射线光电子能谱,电化学阻抗谱和Mott-Schottky测量。结果发现,Co-MOF中原子分布的Co2 +具有极好的空穴存储能力和电荷转移效率,这由高表面电容和极低的表面电荷转移电阻证明。

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