Biomass-derived carbon quantum dot: "On-off-on" fluorescent sensor for rapid detection of multi-metal ions and green photocatalytic CO2 reduction in water

被引:10
作者
Raja, Sebastian [1 ,2 ]
da Silva, Gelson T. S. T. [1 ]
Anbu, Sellamuthu [3 ,4 ]
Ribeiro, Caue [1 ,2 ]
Mattoso, Luiz H. C. [1 ]
机构
[1] Embrapa Instrumentacao, Natl Nanotechnol Lab Agribusiness LNNA, BR-13560970 Sao Carlos, SP, Brazil
[2] Fed Univ Sao Carlos UFSCar, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil
[3] Univ Hull, Depts Chem & Biomed Sci, Cottingham Rd, Kingston Upon Hull HU6 7RX, England
[4] Univ East Anglia, Sch Chem, Norwich Res Pk, Norwich NR4 7TJ, England
基金
巴西圣保罗研究基金会;
关键词
Macauba; Carbon quantum dots; Metal ion detection; On-off-on; Visible-light; Photocatalytic CO2 reduction; ASCORBIC-ACID; SELECTIVE DETECTION; FE3+; NITROGEN; PROBE; CELL; FACILE; CU2+;
D O I
10.1007/s13399-023-04247-0
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
We have developed carbon quantum dots (CQDs) with excellent photoluminescence (PL) properties from macauba (Acrocomia aculeate) fibers; a widely available cellulosic biomass species of palm trees in South America. As-prepared CQDs showed quasi-spherical morphology with high aqueous solubility and strong excitation-dependent fluorescence behaviour. Interestingly, the CQDs display fluorescence 'turn-off' response with excellent sensitivity toward multi-metal ions including Fe3+, Cu2+ and Hg2+ with very low detection limits of 0.69 mu M, 0.99 mu M, 0.25 mu M, respectively. Notably, ascorbic acid (AA) induced a change in the (turn-off) fluorescence of Fe3+-CQDs, which caused an almost 70% revival of fluorescence (turn-on) by displacing Fe3+ ions. We have also harnessed CQDs as the visible-light-induced photocatalyst to reduce CO2 in water. Especially, the CQDs efficiently promote the photocatalytic reduction of CO2 into methane (CH4) with an evolution rate of 99.8 nmol/g at 436 nm in aqueous conditions. This indicates that the CQDs provide abundant active sites for CO2 adsorption and thus enhance the separation and migration of photo-induced charge carriers that efficiently reduce CO2 into CH4 without any co-catalyst in 100% water.
引用
收藏
页码:21925 / 21937
页数:13
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