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在分级多孔 TiO 上共催化 Pt/PtO 相结纳米点以实现高效光催化制氢。

Cocatalyzing Pt/PtO Phase-Junction Nanodots on Hierarchically Porous TiO for Highly Enhanced Photocatalytic Hydrogen Production.

机构信息

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology , 122 Luoshi Road, Wuhan 430070, Hubei, China.

EMAT (Electron Microscopy for Materials Science), University of Antwerp , 171 Groenenborgerlaan, B-2020 Antwerp, Belgium.

出版信息

ACS Appl Mater Interfaces. 2017 Sep 6;9(35):29687-29698. doi: 10.1021/acsami.7b07226. Epub 2017 Aug 24.

DOI:10.1021/acsami.7b07226
PMID:28812876
Abstract

Phase-junctions between a cocatalyst and its semiconductor host are quite effective to enhance the photocatalytic activity and are widely studied, while reports on the phase-juncted cocatalyst are still rare. In this work, we report the deposition of the Pt/PtO phase-juncted nanodots as cocatalyst via NaOH modification of an interconnected meso-macroporous TiO network with high surface area and inner-particle mesopores to enhance the performance of photocatalytic H production. Our results show that NaOH modification can largely influence Pt/PtO phase-juncted nanodot formation and dispersity. Compared to the TiO nanoparticles, the hierarchically meso-macroporous TiO network containing 0.18 wt % Pt/PtO phase-juncted cocatalyst demonstrates a highest photocatalytic H rate of 13 mmol g h under simulated solar light, and possesses a stable cycling activity without obvious decrease after five cycles. Such high H production performance can be attributed to both the phase-juncted Pt/PtO providing more active sites while PtO suppresses the undesirable hydrogen back reaction, and the special hierarchically porous TiO network with inner-particle mesopores presenting short diffusion path lengths for photogenerated electrons and enhanced light harvesting efficiency. This work suggests that Pt/PtO phase-juncted cocatalyst on hierarchically porous TiO nanostructures is a promising strategy for advanced photocatalytic H production.

摘要

在增强光催化活性方面,助催化剂与其半导体主体之间的相界非常有效,并且得到了广泛的研究,而关于相界助催化剂的报道仍然很少。在这项工作中,我们通过具有高表面积和内孔介孔的互连介孔-大孔 TiO 网络的 NaOH 改性,报告了沉积 Pt/PtO 相界纳米点作为助催化剂,以提高光催化析氢性能。我们的结果表明,NaOH 改性可以极大地影响 Pt/PtO 相界纳米点的形成和分散性。与 TiO2 纳米颗粒相比,含有 0.18wt%Pt/PtO 相界助催化剂的分级介孔-大孔 TiO 网络在模拟太阳光下表现出最高的光催化 H2 生成速率为 13mmol g h-1,并且具有稳定的循环活性,在五次循环后没有明显下降。如此高的 H2 生成性能归因于相界 Pt/PtO 提供了更多的活性位点,同时 PtO 抑制了不希望的氢逆反应,以及具有内孔介孔的特殊分级多孔 TiO 网络,其具有用于光生电子的短扩散路径长度和增强的光捕获效率。这项工作表明,在分级多孔 TiO2 纳米结构上的 Pt/PtO 相界助催化剂是一种用于先进光催化析氢的有前途的策略。

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