Developing low-cost and high-efficient noble-metal-free cocatalysts has been a challenge to achieve economic hydrogen production.In this work,molybdenum oxides(MoO3-x)were in situ loaded on polymer carbon nitride(PCN)...Developing low-cost and high-efficient noble-metal-free cocatalysts has been a challenge to achieve economic hydrogen production.In this work,molybdenum oxides(MoO3-x)were in situ loaded on polymer carbon nitride(PCN)via a simple one-pot impregnation-calcination approach.Different from post-impregnation method,intimate coupling interface between high-dispersed ultra-small MoO3-xnanocrystal and PCN was successfully formed during the in situ growth process.The MoO3-x-PCN-X(X=1,2,3,4)photocatalyst without noble platinum(Pt)finally exhibited enhanced photocatalytic hydrogen performance under visible light irradiation(λ>420 nm),with the highest hydrogen evolution rate of 15.6μmol/h,which was more than 3 times that of bulk PCN.Detailed structure-performance revealed that such improvement in visible-light hydrogen production activity originated from the intimate interfacial interaction between high-dispersed ultra-small MoO3-xnanocrystal and polymer carbon nitride as well as efficient charge carriers transfer brought by Schottky junction formed.展开更多
Molecular doping has been proven to be an effective approach to adjusting the electronic structure of polymeric carbon nitride(PCN)and thus improving its optical properties and photocatalytic activity.Herein,theobromi...Molecular doping has been proven to be an effective approach to adjusting the electronic structure of polymeric carbon nitride(PCN)and thus improving its optical properties and photocatalytic activity.Herein,theobromine,a compound composed of an imidazole ring and a pyrimidine ring,was first copolymerized with urea to prepared doped PCN.Experimental investigations and theoretical calculations indicate that,a narrowing in band gap and a positive shift in valence band positon happened to the theobromine doped PCN,owing to the synergistic effect between the pyrimidine ring and the imidazole ring in the theobromine molecule.Moreover,it is shown that the doping with theobromine at a suitable mass fraction makes the obtained sample exhibit decreased photoluminescent emission,enhanced photocurrent density,and reduced charge-transport resistance.Consequently,an enhancement in the photocatalytic activity for water oxidation is found for the sample,which oxygen evolution rate is 4.43 times higher than that of the undoped PCN.This work sheds light on the choice of the molecular dopants for PCN to improve its photocatalytic performance.展开更多
基金the National Natural Science Foundation of China(No.21872093)the National Key Research and Development Program of China(No.2018YFB1502001)the Center of Hydrogen Science of Shanghai Jiao Tong University。
文摘Developing low-cost and high-efficient noble-metal-free cocatalysts has been a challenge to achieve economic hydrogen production.In this work,molybdenum oxides(MoO3-x)were in situ loaded on polymer carbon nitride(PCN)via a simple one-pot impregnation-calcination approach.Different from post-impregnation method,intimate coupling interface between high-dispersed ultra-small MoO3-xnanocrystal and PCN was successfully formed during the in situ growth process.The MoO3-x-PCN-X(X=1,2,3,4)photocatalyst without noble platinum(Pt)finally exhibited enhanced photocatalytic hydrogen performance under visible light irradiation(λ>420 nm),with the highest hydrogen evolution rate of 15.6μmol/h,which was more than 3 times that of bulk PCN.Detailed structure-performance revealed that such improvement in visible-light hydrogen production activity originated from the intimate interfacial interaction between high-dispersed ultra-small MoO3-xnanocrystal and polymer carbon nitride as well as efficient charge carriers transfer brought by Schottky junction formed.
基金supported by the National Natural Science Foundation of China(21276088,U1507201)Natural Science Foundation of Guangdong Province(2014A030312009)China Postdoctoral Science Foundation(2018M640784)~~
文摘Molecular doping has been proven to be an effective approach to adjusting the electronic structure of polymeric carbon nitride(PCN)and thus improving its optical properties and photocatalytic activity.Herein,theobromine,a compound composed of an imidazole ring and a pyrimidine ring,was first copolymerized with urea to prepared doped PCN.Experimental investigations and theoretical calculations indicate that,a narrowing in band gap and a positive shift in valence band positon happened to the theobromine doped PCN,owing to the synergistic effect between the pyrimidine ring and the imidazole ring in the theobromine molecule.Moreover,it is shown that the doping with theobromine at a suitable mass fraction makes the obtained sample exhibit decreased photoluminescent emission,enhanced photocurrent density,and reduced charge-transport resistance.Consequently,an enhancement in the photocatalytic activity for water oxidation is found for the sample,which oxygen evolution rate is 4.43 times higher than that of the undoped PCN.This work sheds light on the choice of the molecular dopants for PCN to improve its photocatalytic performance.
