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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Active photocatalytic water splitting solar-to-hydrogen energy conversion: Chalcogenide photocatalyst Ba2ZnSe3 under visible irradiation
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Active photocatalytic water splitting solar-to-hydrogen energy conversion: Chalcogenide photocatalyst Ba2ZnSe3 under visible irradiation

机译:活性光催化水分解太阳能 - 氢气能转化:硫属化物光催化剂Ba2Znse3在可见辐照下

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摘要

The photocatalytic performance of Ba2ZnSe3 is investigated by means of density functional theory. The investigation confirms that Ba2ZnSe3 possesses large birefringence, considerable anisotropy in the optical response, and the absorption edge occurs in the visible region. The estimated optical band gap of Ba2ZnSe3 is about 2.70 eV, and the EPc and EPv are about -0.145 V(vs.NHE) and +2.605 V (vs.NHE), respectively. Thus, Ba2ZnSe3 possesses a high negative reduction potential of excited electrons due to its higher CB position, and hence, the location of the CBM and VBM accommodates the redox capacity. Thus, the Ba2ZnSe3 photocatalyst is expected to exhibit superior activity in visible-light-driven photocatalytic H-2 evolution. The electronic band structure shows high k-dispersion bands around the Fermi level, which implies low effective masses and, hence, the high mobility carriers enhance the charge transfer process. It was found that Ba2ZnSe3 possesses a great effective mass difference between electron (e(-)) and hole (h(+)), which can facilitate the e(-) and h(+) migration and separation, and finally improve the photocatalytic performance. The observed large mobility difference in Ba2ZnSe3 is useful to the separation of e(-) and h(+), reduction of the e(-) and h(+) recombination rate, and improvement of the photocatalytic activity. Thus, Ba2ZnSe3 could be a good photocatalyst due to rapid generation of e(-)-h(+) pairs with photoexcitation, and a high negative reduction potential of excited electrons due to its higher CB position. The excellent photocatalytic performance of Ba2ZnSe3 is due to hyperpolarizablity formed by ZnO4 tetrahedra and co-parallel BaSe7 polyhedra groups, and the layer structure favors the enhancement of the photocatalytic performance. The presence of the distorted (ZnO4)(4-) tetrahedral causes to increase the efficiency of the photocatalytic performance almost to double in comparison to other chalcogenide crystals. Based on these results, one can conclude that Ba2ZnSe3 satisfies all requirements to be an efficient photocatalyst. This will greatly improve the search efficiency and greatly help experiments to save resources in the exploration of new photocatalysts with good photocatalytic performance.
机译:通过密度泛函理论研究了Ba2ZnSe3的光催化性能。该研究证实,Ba2ZnSe3具有大的双折射,在光学响应中具有大量各向异性,并且在可见区域中发生吸收边缘。 BA2ZNSE3的估计光带隙是约2.70eV,EPC和EPV分别为-0.145V(Vs.nhe)和+ 2.605V(Vs.nhe)。因此,由于其越高的Cb位置,Ba2ZnSe3具有激发电子的高负降低电位,因此,CBM和VBM的位置适应氧化还原容量。因此,预期Ba2ZnSe3光催化剂预期在可见光驱动的光催化H-2进化中表现出优异的活性。电子频带结构在费米水平周围显示出高k色谱带,这意味着低有效质量,并且因此,高迁移率载波增强了电荷转移过程。发现Ba2ZnSe3具有电子(E( - ))和孔(H(+))之间的有效质量差异,这可以促进E( - )和H(+)迁移和分离,最终改善光催化剂表现。所观察到的Ba2ZnSe3的大型迁移率差异可用于分离E( - )和H(+),降低E( - )和H(+)重组率,以及改善光催化活性。因此,由于具有光透镜的快速产生E( - ) - H(+)对,并且由于其较高的Cb位置,因此Ba2ZnSe3可以是良好的光催化剂,以及激发电子的高负降低电位。 Ba2ZnSe3的优异光催化性能是由于ZnO4四面体和共同的基础7多面体组形成的超极化性,并且层结构有利于光催化性能的增强。与其他硫属化物晶体相比,扭曲(ZnO 4)(4-)四面向导致显着性能的效率几乎加倍。基于这些结果,可以得出结论,Ba2ZnSe3满足所有要求是有效的光催化剂。这将大大提高搜索效率,大大帮助实验,以节省新型光催化剂,以良好的光催化性能探索资源。

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