Graphene Bridge for Photocatalytic Hydrogen Evolution with Gold Nanocluster Co-Catalysts

被引:4
|
作者
Mousavi, Hanieh [1 ]
Small, Thomas D. [1 ]
Sharma, Shailendra K. [2 ]
Golovko, Vladimir B. [2 ]
Shearer, Cameron J. [1 ]
Metha, Gregory F. [1 ]
机构
[1] Univ Adelaide, Dept Chem, Adelaide, SA 5005, Australia
[2] Univ Canterbury, Sch Phys & Chem Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Christchurch 8140, New Zealand
基金
澳大利亚研究理事会;
关键词
gold nanocluster; reduced graphene oxide; SrTiO3; photocatalysis; hydrogen evolution reaction; AEROBIC OXIDATION; CLUSTERS; OXIDE; TIO2; EFFICIENT;
D O I
10.3390/nano12203638
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, the UV light photocatalytic activity of an Au101NC-AlSrTiO3-rGO nanocomposite comprising 1 wt% rGO, 0.05 wt% Au-101(PPh3)(21)Cl-5 (Au101NC), and AlSrTiO3 evaluated for H-2 production. The synthesis of Au101NC-AlSrTiO3-rGO nanocomposite followed two distinct routes: (1) Au101NC was first mixed with AlSrTiO3 followed by the addition of rGO (Au101NC-AlSrTiO3:rGO) and (2) Au101NC was first mixed with rGO followed by the addition of AlSrTiO3 (Au101NC-rGO:AlSrTiO3). Both prepared samples were annealed in air at 210 degrees C for 15 min. Inductively coupled plasma mass spectrometry and high-resolution scanning transmission electron microscopy showed that the Au101NC adhered almost exclusively to the rGO in the nanocomposite and maintained a size less than 2 nm. Under UV light irradiation, the Au101NC-AlSrTiO3:rGO nanocomposite produced H-2 at a rate 12 times greater than Au101NC-AlSrTiO3 and 64 times greater than AlSrTiO3. The enhanced photocatalytic activity is attributed to the small particle size and high loading of Au101NC, which is achieved by non-covalent binding to rGO. These results show that significant improvements can be made to AlSrTiO3-based photocatalysts that use cluster co-catalysts by the addition of rGO as an electron mediator to achieve high cluster loading and limited agglomeration of the clusters.
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页数:13
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