Platinum@Hexaniobate Nanopeapods: A Directed Photocatalytic Architecture for Dye-Sensitized Semiconductor H2 Production under Visible Irradiation

被引:4
作者
Chin, Clare Davis-Wheeler [1 ,2 ,3 ]
Fontenot, Patricia [4 ]
Rostamzadeh, Taha [1 ,2 ]
Treadwell, LaRico J. [3 ]
Schmehl, Russell H. [4 ]
Wiley, John B. [1 ,2 ]
机构
[1] Univ New Orleans, Dept Chem, New Orleans, LA 70148 USA
[2] Univ New Orleans, Adv Mat Res Inst, New Orleans, LA 70148 USA
[3] Sandia Natl Labs, Adv Mat Lab, Albuquerque, NM 87106 USA
[4] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
基金
美国国家科学基金会;
关键词
nanostructures; nanotubes; photocatalysis; water splitting; heterogeneous catalysis; charge carrier injection; LAYERED METAL-OXIDE; INDUCED ELECTRON-TRANSFER; NIOBATE NANOSHEETS; RUTHENIUM(II) COMPLEXES; PEROVSKITE NANOSHEETS; GOLD NANOPARTICLES; HYDROGEN EVOLUTION; LIGHT PHOTOLYSIS; BUILDING-BLOCKS; WATER;
D O I
10.1021/acsaem.2c01530
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
Platinum@hexaniobate nanopeapods (Pt@HNB NPPs) are a nanocomposite photocatalyst that was selectively engineered to increase the efficiency of hydrogen production from visible light photolysis. Pt@HNB NPPs consist of linear arrays of high surface area Pt nanocubes encapsulated within scrolled sheets of the semiconductor HxK4-xNb6O17 and were synthesized in high yield via a facile one-pot microwave heating method that is fast, reproducible, and more easily scalable than multi-step approaches required by many other state-of-the-art catalysts. The Pt@HNB NPPs' unique 3D architecture enables physical separation of the Pt catalysts from competing surface reactions, promoting electron efficient delivery to the isolated reduction environment along directed charge transport pathways that kinetically prohibit recombination reactions. Pt@HNB NPPs' catalytic activity was assessed in direct comparison to representative state-of-the-art Pt/semiconductor nanocomposites (extPt-HNB NScs) and unsupported Pt nanocubes. Photolysis under similar conditions exhibited superior H2 production by the Pt@HNB NPPs, which exceeded other catalyst H2 yields (mu mol) by a factor of 10. Turnover number and apparent quantum yield values showed similar dramatic increases over the other catalysts. Overall, the results clearly demonstrate that Pt@HNB NPPs represent a unique, intricate nanoarchitecture among state-of-the-art heterogeneous catalysts, offering obvious benefits as a new architectural pathway toward efficient, versatile, and scalable hydrogen energy production. Potential factors behind the Pt@HNB NPPs' superior performance are discussed below, as are the impacts of systematic variation of photolysis parameters and the use of a non-aqueous reductive quenching photosystem.
引用
收藏
页码:14687 / 14700
页数:14
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