Template free mild hydrothermal synthesis of core-shell Cu2O(Cu)@CuO visible light photocatalysts for N-acetyl-para-aminophenol degradation

被引:46
|
作者
Karthikeyan, Sekar [1 ]
Chuaicham, Chitiphon [1 ]
Pawar, Radheshyam R. [1 ]
Sasaki, Keiko [1 ]
Li, Wei [2 ]
Lee, Adam F. [3 ]
Wilson, Karen [3 ]
机构
[1] Kyushu Univ, Fac Engn, Dept Earth Resources Engn, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[2] Aston Univ, Aston Inst Mat Res, European Bioenergy Res Inst, Birmingham B4 7ET, W Midlands, England
[3] RMIT Univ, Appl Chem & Environm Sci, Melbourne, Vic 3000, Australia
基金
日本学术振兴会;
关键词
CU2O NANOCRYSTALS; CHARGE SEPARATION; PARACETAMOL; HETEROJUNCTION; NANOPARTICLES; ARCHITECTURE; OXIDATION; PHARMACEUTICALS; NANOCOMPOSITES; PHOTOCATHODE;
D O I
10.1039/c9ta07009e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solar photocatalytic processes are a promising approach to environmental remediation, however their implementation requires improvements in visible light harvesting and conversion and a focus on low cost, Earth abundant materials. Semiconducting copper oxides are promising visible light photocatalysts for solar fuels and wastewater depollution. Here we report the mild, hydrothermal (template-free) synthesis of core-shell Cu2O(Cu)@CuO photocatalytic architectures for the visible light photocatalytic degradation of N-acetyl-para-aminophenol (APAP). Hollow and rattle-like core-shell nanosphere aggregates with diameters between 200 nm and 2.5 mm formed under different synthesis conditions; all comprised an inner Cu2O shell, formed of 10-50 nm nanoparticles, surrounded by a protective corona of CuO nanoparticles. High reductant and structure-directing agent concentrations promoted the formation of a yolk-like Cu2O/Cu core, associated with improved photophysical properties, notably a high oxidation potential and suppressed charge carrier recombination, that correlated with the highest apparent quantum efficiency (8%) and rate of APAP removal (7 mmol g(-1) min(-1)). Trapping experiments demonstrated hydroxyl radicals were the primary active species responsible for APAP oxidation to quinones and short chain carboxylic acids. Rattle-like core-shell Cu2O/Cu@CuO nanospheres exhibited excellent physiochemical stability and recyclability for APAP photocatalytic degradation.
引用
收藏
页码:20767 / 20777
页数:11
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