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用于增强光电化学水分解的三氧化钨/钼酸铋/磷酸钴三维核壳异质结构

Three-dimensional core-shell heterostructure of tungsten trioxide/bismuth molybdate/cobalt phosphate for enhanced photoelectrochemical water splitting.

作者信息

Sayed Mostafa Saad, Mohapatra Debananda, Baynosa Marjorie Lara, Shim Jae-Jin

机构信息

School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Republic of Korea; Analysis and Evaluation Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Republic of Korea.

出版信息

J Colloid Interface Sci. 2021 Sep 15;598:348-357. doi: 10.1016/j.jcis.2021.03.105. Epub 2021 Mar 22.

Abstract

Hydrogen has attracted increasing attention as clean energy for fuel cells over the past decade. Photoelectrochemical (PEC) water splitting is considered the most feasible production method but its practical efficiency depends significantly on the photogeneration rate of electron (e) and hole (h) on a semiconductor photoanode and the rapid separation of these charge carriers. A proper match of small and large bandgap positions is also necessary. This paper presents a three-dimensional core-shell heterostructured tungsten trioxide/bismuth molybdate/cobalt phosphate (WO/BiMoO/Co-Pi) photocatalyst synthesized using simultaneous hydrothermal and electrodeposition techniques. Uniform BiMoO nanoflakes formed on WO nanoplates as evidenced by various micro-spectroscopic techniques. The as-prepared WO/BiMoO/Co-Pi hetero-photocatalyst exhibited significantly high photoelectrochemical activity, where its photocurrent efficiency was 4.6 times greater than that of the constituent WO Such drastic improvement in the PEC properties can be corroborated by the appropriate bandgap alignment among WO, BiMoO, and Co-Pi, resulting in a sufficient charge carrier density with efficient, fast charge-transport complementing their structural-morphological synergy. Furthermore, a heterojunction charge-transfer mechanism was proposed to verify the role of the co-catalyst, Co-Pi, in enhancing the photocurrent at the WO/BiMoO photoanode under the same applied bias.

摘要

在过去十年中,氢气作为燃料电池的清洁能源受到了越来越多的关注。光电化学(PEC)水分解被认为是最可行的生产方法,但其实际效率在很大程度上取决于半导体光阳极上电子(e)和空穴(h)的光生速率以及这些电荷载流子的快速分离。小带隙和大带隙位置的适当匹配也是必要的。本文介绍了一种采用水热和电沉积同步技术合成的三维核壳异质结构三氧化钨/钼酸铋/磷酸钴(WO₃/Bi₂MoO₆/Co-Pi)光催化剂。各种微观光谱技术证明,在WO₃纳米板上形成了均匀的Bi₂MoO₆纳米片。所制备的WO₃/Bi₂MoO₆/Co-Pi异质光催化剂表现出显著的高光电化学活性,其光电流效率比组成成分WO₃高4.6倍。PEC性能的如此大幅提高可以通过WO₃、Bi₂MoO₆和Co-Pi之间适当的带隙排列得到证实,从而产生足够的电荷载流子密度,并具有高效、快速的电荷传输,补充了它们的结构形态协同作用。此外,还提出了一种异质结电荷转移机制,以验证助催化剂Co-Pi在相同外加偏压下增强WO₃/Bi₂MoO₆光阳极光电流方面的作用。

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