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在FeO纳米棒上合理构建S掺杂的FeOOH以增强水氧化性能。

Rational construction of S-doped FeOOH onto FeO nanorods for enhanced water oxidation.

作者信息

Duc Quang Nguyen, Cao Van Phuoc, Majumder Sutripto, Jeong Jong-Ryul, Kim Dojin, Kim Chunjoong

机构信息

Department of Materials Science and Engineering, Chungnam National University, Daejeon 34134, Republic of Korea.

Department of Materials Science and Engineering, Chungnam National University, Daejeon 34134, Republic of Korea.

出版信息

J Colloid Interface Sci. 2022 Jun 15;616:749-758. doi: 10.1016/j.jcis.2022.02.117. Epub 2022 Feb 26.

Abstract

Hematite-based photoanode (α-FeO) is considered the promising candidate for photoelectrochemical (PEC) water splitting due to its relatively small optical bandgap. However, severe charge recombination in the bulk and poor surface water oxidation kinetics have limited the PEC performance of FeO photoelectrodes, which is far below the theoretical value. Herein, a new catalyst, S-doped FeOOH (S-FeOOH), has been immobilized onto the surface of the FeO nanorod (NR) array by a facile chemical bath deposition incorporated thermal sulfuration process. The grown S-FeOOH layer acts not only as an efficient catalyst layer to accelerate the water oxidation on the surface of photoelectrode but also constructs a heterojunction with the light absorption layer to facilitate the interface charge carrier separation and transfer. As expected, the modified S-FeOOH@FeO photoanode achieves a remarkable increase in PEC performance of 2.30 mA cm at 1.23 V versus the reversible hydrogen electrode (V) andan apparent negative shifted onset potential of 250 mV in comparison with pristine FeO (0.95 mA cm at 1.23 V). These results provide a simple and effective strategy to coupling oxygen evolution catalysts with photoanodes for practically high-performance PEC applications.

摘要

基于赤铁矿的光阳极(α-FeO)因其相对较小的光学带隙而被认为是光电化学(PEC)水分解的有前途的候选材料。然而,体相中的严重电荷复合和较差的表面水氧化动力学限制了FeO光电极的PEC性能,其远低于理论值。在此,一种新型催化剂S掺杂的FeOOH(S-FeOOH)通过简便的化学浴沉积结合热硫化工艺固定在FeO纳米棒(NR)阵列的表面。生长的S-FeOOH层不仅作为高效的催化剂层加速光电极表面的水氧化,还与光吸收层构建异质结以促进界面电荷载流子的分离和转移。正如预期的那样,与原始FeO(在1.23 V时为0.95 mA cm)相比,改性后的S-FeOOH@FeO光阳极在1.23 V相对于可逆氢电极(V)时的PEC性能显著提高至2.30 mA cm,并且起始电位明显负移250 mV。这些结果提供了一种简单有效的策略,用于将析氧催化剂与光阳极耦合以实现实际的高性能PEC应用。

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