Cao Shaowen, Jiang Jing, Zhu Bicheng, Yu Jiaguo
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, P. R. China.
Phys Chem Chem Phys. 2016 Jul 28;18(28):19457-63. doi: 10.1039/c6cp02832b. Epub 2016 Jul 5.
Cubic, octahedral and spherical platinum (Pt) nanoparticles (NPs) ex situ supported on a graphitic carbon nitride (g-C3N4) substrate are synthesized using a colloidal adsorption-deposition method for photocatalytic hydrogen evolution reactions. These Pt NPs of different shapes have similar sizes of around 10 nm but have different facets exposed. It is found that the visible-light-driven photocatalytic activities for the Pt/g-C3N4 hybrid photocatalysts follow the order as: cubic Pt/g-C3N4 < octahedral Pt/g-C3N4 < spherical Pt/g-C3N4, revealing the significant cocatalyst shape-sensitive photocatalytic activity in the Pt/g-C3N4 hybrids. This is mainly due to the different surface atomic structures of different exposed facets of Pt NPs, which lead to the disparity of active sites and adsorption energies in photocatalytic reactions.
采用胶体吸附沉积法合成了非原位负载在石墨相氮化碳(g-C3N4)基底上的立方、八面体和球形铂(Pt)纳米颗粒(NPs),用于光催化析氢反应。这些不同形状的Pt NPs尺寸相似,约为10 nm,但暴露的晶面不同。研究发现,Pt/g-C3N4复合光催化剂的可见光驱动光催化活性顺序为:立方Pt/g-C3N4 < 八面体Pt/g-C3N4 < 球形Pt/g-C3N4,这表明Pt/g-C3N4复合物中助催化剂形状对光催化活性有显著影响。这主要是由于Pt NPs不同暴露晶面的表面原子结构不同,导致光催化反应中活性位点和吸附能的差异。