TiO2 photocatalyst with single and dual noble metal co-catalysts for efficient water splitting and organic compound removal

被引:20
|
作者
Rozman, Nejc [1 ,6 ]
Nadrah, Peter [1 ]
Cornut, Renaud [2 ]
Jousselme, Bruno [2 ]
Bele, Marjan [3 ]
Drazic, Goran [3 ]
Gaberscek, Miran [3 ]
Kunej, Spela [4 ]
Skapin, Andrijana Sever [1 ,5 ]
机构
[1] Slovenian Natl Bldg & Civil Engn Inst, Dimiceva 12, Ljubljana 1000, Slovenia
[2] Univ Paris Saclay, CNRS, CEA, NIMBE,LICSEN, F-91191 Gif Sur Yvette, France
[3] Natl Inst Chem, Hajdrihova 19, Ljubljana 1000, Slovenia
[4] Jozef Stefan Inst, Jamova 39, Ljubljana 1000, Slovenia
[5] Fac Polymer Technol FTPO, Ozare 19, Slovenj Gradec 2380, Slovenia
[6] Mysteria Colorum Doo, Hajdrihova 19, Ljubljana 1000, Slovenia
关键词
Photocatalysis; Electrocatalysis; Water-splitting; Co-catalyst; HYDROGEN GENERATION; SOLAR-ENERGY; OXIDATION; CATALYSTS; TITANIA; ANATASE; RU; NANOMATERIALS; ATMOSPHERE; EVOLUTION;
D O I
10.1016/j.ijhydene.2021.07.129
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalysts can be used both for air cleaning and solar energy harvesting through water splitting. However, pure TiO2 photocatalysts are often inefficient and therefore co-catalysts are needed to improve the yield. To achieve this goal, we prepared TiO2 and deposited Pt, Ir and Ru co-catalysts on its surface. Two base TiO2 nanoparticles were used: P25 and rutile TiO2 synthesized via hydrothermal method. Co-catalysts were deposited by wet impregnation technique using single element and a combination of two elements (Pt and Ir or Pt and Ru), followed by annealing in either air or H-2/Ar. Annealing in reducing atmosphere increased the photocatalytic activity of oxidation of isopropanol compared to annealing in air. We demonstrated a clear influence of the co-catalysts on the photocatalytic degradation of isopropanol and on electrochemical water-splitting reaction. The platinum-containing samples showed the best HER activity. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:32871 / 32881
页数:11
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