It is essential to screen novel luminophores and co-reactants for the development of electrochemiluminescence(ECL)systems.In this work,a series of 1,8-naphthalimide-modified graphitic carbon nitride(CN/1,8-NDI_(x))ECL...It is essential to screen novel luminophores and co-reactants for the development of electrochemiluminescence(ECL)systems.In this work,a series of 1,8-naphthalimide-modified graphitic carbon nitride(CN/1,8-NDI_(x))ECL luminophores were successfully developed for the quantitative determination of Cu^(2+)with K_(2)S_(2)O_(8)as a co-reactant.When CN/1,8-NDI_(x)was immobilized on the surface of the glassy carbon electrode(GCE),a strong ECL signal could be produced(at a potential of-1.3 V vs.Ag/AgCl),which was threefold stronger than that of unmodified g-C_(3)N_(4).The intensity of ECL could be linearly quenched by Cu^(2+)over a concentration range from 5×10^(-9)to 1×10^(-4)mol/L,and with a low limit of detection(LOD)of0.86 nmol/L.Our results may provide a new perspective on the novel ECL platforms development.展开更多
A novel Ni doped carbon quantum dots(Ni-CQDs)fluorescence probe was synthesized by facile electrolysis of monoatomic Ni dispersed porous carbon(Ni–N–C).The obtained Ni-CQDs showed a high quantum yield of 6.3%with th...A novel Ni doped carbon quantum dots(Ni-CQDs)fluorescence probe was synthesized by facile electrolysis of monoatomic Ni dispersed porous carbon(Ni–N–C).The obtained Ni-CQDs showed a high quantum yield of 6.3%with the strongest excitation and emission peaks of 360 nm and 460 nm,and maintained over 90%of the maximum fluorescence intensity in a wide p H range of 3–12.The metal ions detectability of Ni-CQDs was enhanced by Ni doping and functional groups modification,and the rapid and selective detection of Fe^(3+)and Cu^(2+)ions was achieved with Ni-CQDs through dynamic and static quenching mechanism,respectively.On one hand,the energy band gap of Ni-CQDs was regulated by Ni doping,so that excited electrons in Ni-CQDs were able to transfer to Fe^(3+)easily.On the other hand,the abundant functional groups promoted the generation of static quenching complexation between Cu^(2+)and Ni-CQDs.In metal ions detection,the linear quantitation range of Fe^(3+)and Cu^(2+)were 100–1000μM(R^(2)=0.9955)and 300–900μM(R^(2)=0.9978),respectively.The limits of detection(LOD)were calculated as 10.17 and 7.88μM,respectively.Moreover,the fluorescence quenched by Cu^(2+)could be recovered by EDTA2-due to the destruction of the static quenching complexation.In this way,NiCQDs showed the ability to identify the two metal ions to a certain degree under the condition of Fe^(3+)and Cu^(2+)coexistent.This work paves the way of facile multiple metal ion detection with high sensitivity.展开更多
基金financially supported by the National Natural Science Foundation of China(22172011,22078049)
文摘It is essential to screen novel luminophores and co-reactants for the development of electrochemiluminescence(ECL)systems.In this work,a series of 1,8-naphthalimide-modified graphitic carbon nitride(CN/1,8-NDI_(x))ECL luminophores were successfully developed for the quantitative determination of Cu^(2+)with K_(2)S_(2)O_(8)as a co-reactant.When CN/1,8-NDI_(x)was immobilized on the surface of the glassy carbon electrode(GCE),a strong ECL signal could be produced(at a potential of-1.3 V vs.Ag/AgCl),which was threefold stronger than that of unmodified g-C_(3)N_(4).The intensity of ECL could be linearly quenched by Cu^(2+)over a concentration range from 5×10^(-9)to 1×10^(-4)mol/L,and with a low limit of detection(LOD)of0.86 nmol/L.Our results may provide a new perspective on the novel ECL platforms development.
基金the National Natural Science Foundation of China(Nos.21776302 and 21776308)the Science Foundation of China University of Petroleum,Beijing(No.2462020YXZZ033)。
文摘A novel Ni doped carbon quantum dots(Ni-CQDs)fluorescence probe was synthesized by facile electrolysis of monoatomic Ni dispersed porous carbon(Ni–N–C).The obtained Ni-CQDs showed a high quantum yield of 6.3%with the strongest excitation and emission peaks of 360 nm and 460 nm,and maintained over 90%of the maximum fluorescence intensity in a wide p H range of 3–12.The metal ions detectability of Ni-CQDs was enhanced by Ni doping and functional groups modification,and the rapid and selective detection of Fe^(3+)and Cu^(2+)ions was achieved with Ni-CQDs through dynamic and static quenching mechanism,respectively.On one hand,the energy band gap of Ni-CQDs was regulated by Ni doping,so that excited electrons in Ni-CQDs were able to transfer to Fe^(3+)easily.On the other hand,the abundant functional groups promoted the generation of static quenching complexation between Cu^(2+)and Ni-CQDs.In metal ions detection,the linear quantitation range of Fe^(3+)and Cu^(2+)were 100–1000μM(R^(2)=0.9955)and 300–900μM(R^(2)=0.9978),respectively.The limits of detection(LOD)were calculated as 10.17 and 7.88μM,respectively.Moreover,the fluorescence quenched by Cu^(2+)could be recovered by EDTA2-due to the destruction of the static quenching complexation.In this way,NiCQDs showed the ability to identify the two metal ions to a certain degree under the condition of Fe^(3+)and Cu^(2+)coexistent.This work paves the way of facile multiple metal ion detection with high sensitivity.
