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光电催化降解表面活性剂污染物并同时生成绿色氢气

Photoelectrocatalytic Surfactant Pollutant Degradation and Simultaneous Green Hydrogen Generation.

作者信息

Davies Katherine Rebecca, Allan Michael G, Nagarajan Sanjay, Townsend Rachel, Asokan Vijayshankar, Watson Trystan, Godfrey A Ruth, Maroto-Valer M Mercedes, Kuehnel Moritz F, Pitchaimuthu Sudhagar

机构信息

SPECIFIC, Faculty of Science and Engineering, Swansea University, Swansea SA2 8PP, Wales.

Department of Chemistry, Faculty of Science and Engineering, Swansea University, Singleton Park, SA2 8PP Swansea, Wales.

出版信息

Ind Eng Chem Res. 2023 Jun 2;62(45):19084-19094. doi: 10.1021/acs.iecr.3c00840. eCollection 2023 Nov 15.

Abstract

For the first time, we demonstrate a photoelectrocatalysis technique for simultaneous surfactant pollutant degradation and green hydrogen generation using mesoporous WO/BiVO photoanode under simulated sunlight irradiation. The materials properties such as morphology, crystallite structure, chemical environment, optical absorbance, and bandgap energy of the WO/BiVO films are examined and discussed. We have tested the anionic type (sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants (benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants. A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min, respectively, by applying 1.75 V applied potential vs RHE to the circuit, under 1 sun was achieved. An interesting competitive phenomenon for photohole utilization was observed between surfactants and adsorbed water. This led to the formation of HO from water alongside surfactant degradation (anode) and hydrogen evolution (cathode). No byproducts were observed after the direct photohole mediated degradation of surfactants, implying its advantage over other AOPs and biological processes. In the cathode compartment, 82.51 μmol/cm and 71.81 μmol/cm of hydrogen gas were generated during the BAC-C12 and S2NS surfactant degradation process, respectively, at 1.75 V RHE applied potential.

摘要

首次,我们展示了一种光电催化技术,即在模拟太阳光照射下,使用介孔WO/BiVO光阳极同时降解表面活性剂污染物并生成绿色氢气。研究并讨论了WO/BiVO薄膜的材料特性,如形态、微晶结构、化学环境、光吸收率和带隙能量。我们测试了阴离子型(2-萘磺酸钠(S2NS))和阳离子型表面活性剂(苄基烷基二甲基氯化铵化合物(BAC-C12))作为模型污染物。在1个太阳光照强度下,通过向电路施加相对于可逆氢电极(RHE)为1.75 V的外加电势,分别在60分钟和90分钟时实现了S2NS和BAC-C12表面活性剂的完全去除。在表面活性剂和吸附水之间观察到了光空穴利用的有趣竞争现象。这导致了在表面活性剂降解(阳极)和析氢(阴极)的同时,由水形成羟基自由基(HO)。表面活性剂直接通过光空穴介导降解后未观察到副产物,这意味着其相对于其他高级氧化过程和生物过程具有优势。在阴极室中,在施加1.75 V RHE电势的情况下,分别在BAC-C12和S2NS表面活性剂降解过程中产生了82.51 μmol/cm²和71.81 μmol/cm²的氢气。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5185/10655085/9ce6340135fc/ie3c00840_0001.jpg

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