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