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具有丰富硫空位的镍掺杂黄铁矿/黄铁矿同质结的内电场诱导光生载流子分离用于高效还原Cr(VI)

Internal electric field induced photocarriers separation of nickel-doped pyrite/pyrite homojunction with rich sulfur vacancies for superior Cr(VI) reduction.

作者信息

Liu Chenrui, Xiao He, Liu Yun, Li Dejian, He Hao, Huang Xiaohan, Shen Wentao, Yan Zhiyan, Dang Zhi, Zhu Runliang

机构信息

Department of Environmental Science and Engineering, College of Environment and Resources, Xiangtan University, Xiangtan 411105, PR China.

Department of Environmental Science and Engineering, College of Environment and Resources, Xiangtan University, Xiangtan 411105, PR China.

出版信息

J Colloid Interface Sci. 2023 Jan;629(Pt B):847-858. doi: 10.1016/j.jcis.2022.09.129. Epub 2022 Sep 28.

Abstract

Improving the separation efficiency and transfer ability of photoinduced electrons/holes in pyrite (FeS)-based photocatalytic materials is significant for the photoreduction of hexavalent chromium (Cr(VI)) but still remains a challenge. Herein, a novel homojunction was prepared through in-situ growth of nickel (Ni) doped FeS nanoparticles on FeS nanobelts (denoted as Ni-FeS/FeS). Systematical characterizations revealed that Ni doped FeS nanoparticles have been successfully in situ grown along the lattice of FeS nanobelts. Photoreduction experiments demonstrated that the Ni-FeS/FeS homojunction with 2 mmol Ni doping contents (denoted as 2Ni-FeS/FeS) exhibited the optimum Cr(VI) reduction efficiency among the studied catalysts. Density Functional Theory (DFT) calculated results verified that Ni doping could not only be advantageous for the formation of sulfur vacancies but also modify the band gap and band structure of FeS nanoparticles. Moreover, several doping energy levels caused by Ni doping have also appeared near the Fermi level of FeS nanoparticles. The migration paths of electrons and the existence of internal electric field (IEF) in homojunction were further verified by the calculation of work function. To sum up, the doping energy levels and IEF that produced by homojunction played important roles in accelerating the separation efficiency of its photogenerated carriers.

摘要

提高基于黄铁矿(FeS)的光催化材料中光生电子/空穴的分离效率和转移能力对于六价铬(Cr(VI))的光还原具有重要意义,但仍然是一个挑战。在此,通过在FeS纳米带上原位生长镍(Ni)掺杂的FeS纳米颗粒制备了一种新型同质结(表示为Ni-FeS/FeS)。系统表征表明,Ni掺杂的FeS纳米颗粒已成功沿FeS纳米带的晶格原位生长。光还原实验表明,在研究的催化剂中,Ni掺杂量为2 mmol的Ni-FeS/FeS同质结(表示为2Ni-FeS/FeS)表现出最佳的Cr(VI)还原效率。密度泛函理论(DFT)计算结果证实,Ni掺杂不仅有利于硫空位的形成,还能改变FeS纳米颗粒的带隙和能带结构。此外,Ni掺杂引起的几个掺杂能级也出现在FeS纳米颗粒的费米能级附近。通过功函数的计算进一步验证了同质结中电子的迁移路径和内建电场(IEF)的存在。综上所述,同质结产生的掺杂能级和IEF在加速其光生载流子的分离效率方面发挥了重要作用。

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