Facile aqueous synthesis of β-AgI nanoplates as efficient visible-light-responsive photocatalyst

被引:64
作者
Jiang, Wen [1 ]
An, Changhua [1 ,2 ]
Liu, Junxue [2 ]
Wang, Shutao [2 ]
Zhao, Lianming [2 ]
Guo, Wenyue [1 ,2 ]
Liu, Jinxiang [3 ]
机构
[1] China Univ Petr, Coll Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] China Univ Petr, Coll Sci, Dept Mat Phys & Chem, Qingdao 266580, Peoples R China
[3] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTRONIC-STRUCTURE; ROOM-TEMPERATURE; NANOCRYSTALS; NANOPARTICLES; CONDUCTIVITY; CONVERSION; PHASE; FACET; MOS2;
D O I
10.1039/c3dt52028e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Owing to far-ranging industrial applications and theoretical researches, tailored synthesis of well-defined nanocrystals has attracted substantial research interest. Herein, beta-AgI nanoplates have been synthesized through a facile polyvinylpyrrolidone (PVP)-assisted-aqueous-solution (PAAS) method under mild conditions. The parametric studies on the effect of ratio of reactants, solvents and surfactants were performed, revealing that a molar ratio of I- to Ag+ of 1.2 in deionized water and the presence of appropriate PVP as stabilizing agent can stimulate the preferred orientation growth of AgI nanoplates. The as-synthesized AgI nanoplates exhibit excellent photocatalytic activity and enhanced durability towards the degradation of organics, i.e., rhodamine B (RhB), under visible light illumination in comparison with corresponding bulk nanoparticles. A possible photocatalytic reaction mechanism was discussed, revealing O-2(center dot-) and h(+) are main reactive species and free (OH)-O-center dot radicals in solution also contribute to the degradation reaction. The superior photocatalytic performance renders the as-achieved AgI nanoplates promising candidates for applications in the fields of environmental purification or water disinfection. The present work opens an avenue to the synthesis of other shaped silver halide nanophotocatalysts.
引用
收藏
页码:300 / 305
页数:6
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