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由 FeO 纳米棒阵列和底层 SbSe 薄层组成的直接 Z scheme 结构光阳极系统,可提高光电化学水分解性能。

Direct Z scheme-fashioned photoanode systems consisting of FeO nanorod arrays and underlying thin SbSe layers toward enhanced photoelectrochemical water splitting performance.

机构信息

Eco-Materials and Renewable Energy Research Center (ERERC), Jiangsu Key Laboratory for Nano Technology, Nanjing University, Nanjing 210093, China.

出版信息

Nanoscale. 2018 Dec 20;11(1):109-114. doi: 10.1039/c8nr08292h.

Abstract

An elegant Z-scheme-fashioned photoanode consisting of Fe2O3 nanorod arrays and underlying thin Sb2Se3 layers was rationally constructed. The photocurrent density of the Sb2Se3-Fe2O3 Z-scheme photoanode reached 3.07 mA cm-2 at 1.23 V vs. RHE, three times higher than that of pristine Fe2O3 at 1.03 mA cm-2. An obvious cathodic shift of the photocurrent onset potential of about 200 mV was also observed. The transient photovoltage response demonstrates that the suitable band edges (ECB ∼ -0.4 eV and EVB ∼ 0.8 eV) of Sb2Se3, match well with Fe2O3 (ECB ∼ 0.29 eV and EVB ∼ 2.65 eV), permitting the photoexcited electrons on the conduction band of the Fe2O3 to transfer to the valence band of Sb2Se3, and recombine with the holes therein, thus allowing a high concentration of holes to collect in the Fe2O3 for water oxidation. The transient absorption spectra further corroborate that the built-in electric field in the p-n heterojunction leads to a more effective separation and a longer lifetime of the charge carriers.

摘要

合理构建了由 Fe2O3 纳米棒阵列和底层 Sb2Se3 薄层组成的优雅 Z 型结构光阳极。Sb2Se3-Fe2O3 Z 型光阳极的光电流密度在 1.23 V 时达到 3.07 mA cm-2,比原始 Fe2O3 的 1.03 mA cm-2 高 3 倍。还观察到光电流起始电位明显的阴极偏移约 200 mV。瞬态光电压响应表明,Sb2Se3 的合适能带边缘(ECB∼-0.4 eV 和 EVB∼0.8 eV)与 Fe2O3(ECB∼0.29 eV 和 EVB∼2.65 eV)匹配良好,允许 Fe2O3 导带中的光激发电子转移到 Sb2Se3 的价带,并与其中的空穴复合,从而允许在 Fe2O3 中收集高浓度的空穴进行水氧化。瞬态吸收光谱进一步证实,p-n 异质结中的内置电场导致载流子的更有效分离和更长寿命。

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