Operando Laboratory X-ray Absorption Spectroscopy and UV-Vis Study of Pt/TiO2 Photocatalysts during Photodeposition and Hydrogen Evolution Reactions

被引:8
|
作者
Kozyr, Elizaveta G. [1 ,2 ]
Njoroge, Peter N. [1 ]
Chapek, Sergei V. [1 ]
Shapovalov, Viktor V. [1 ]
Skorynina, Alina A. [1 ]
Pnevskaya, Anna Yu. [1 ]
Bulgakov, Alexey N. [1 ]
Soldatov, Alexander V. [1 ]
Pellegrino, Francesco [2 ]
Groppo, Elena [2 ]
Bordiga, Silvia [2 ]
Mino, Lorenzo [2 ]
Bugaev, Aram L. [1 ,3 ]
机构
[1] Southern Fed Univ, Smart Mat Res Inst, Sladkova 178-24, Rostov Na Donu 344090, Russia
[2] Univ Turin, Dept Chem, Via Giuria 7, I-10125 Turin, Italy
[3] Paul Scherrer Inst, Forschungsstr 111, CH-5232 Villigen, Switzerland
关键词
operando spectroscopy; XANES; photocatalysis; platinum catalyst; UV-Vis; HER; photodeposition; ACTIVE-SITE; NANOPARTICLES; OXIDATION; XAFS; CELL;
D O I
10.3390/catal13020414
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
Photocatalytic hydrogen (H-2) production is a promising route for alternative energetics. Understanding structure-activity relationships is a crucial step towards the rational design of photocatalysts, which requires the application of operando spectroscopy under relevant working conditions. We performed an operando investigation on a catalytic system during the photodeposition of Pt on TiO2 and photostimulated H-2 production, using simultaneous laboratory X-ray absorption spectroscopy (XAS), UV-Vis spectroscopy, and mass spectrometry. XAS showed a progressive increase in Pt fluorescence for Pt deposited on TiO2 for over an hour, which is correlated with the signal of the produced H-2. The final Pt/TiO2 catalyst contained Pt(0) particles. The electronic features corresponding to the Pt4+ species in the UV-Vis spectrum of the solution disappear as soon as UV radiation is applied in the presence of formic acid, which acts as a hole scavenger, resulting in the presence of Pt(0) particles in solution.
引用
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页数:10
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