Electrochemical conversion of CO2 into fuel has been regarded as a promising approach to achieve the global carbon cycle.Herein,we report an efficient cobalt catalyst with a unique flower-like morphology synthesized b...Electrochemical conversion of CO2 into fuel has been regarded as a promising approach to achieve the global carbon cycle.Herein,we report an efficient cobalt catalyst with a unique flower-like morphology synthesized by a green and facile hydrothermal method,in which n-butylamine is used as the capping agent.The resultant catalyst shows superior electrocatalytic activity toward CO2 electroreduction,which is highly selective for generating formate with a Faraday efficiency of 63.4%.Electrochemical analysis reveals that the oxide on the surface is essential for the electrocatalysis of the CO2 reduction reaction.Cyclic voltammograms further suggest that this catalyst is highly active for the oxidation of reduced product,and can thus be seen as a bifunctional catalyst.展开更多
Aniline,pyrrole and phenanthroline,which have different nitrogen compositions,are used as carbon precursors to synthesize nitrogen-doped ordered mesoporous carbons（NOMCs） by the nanocasting method.The effect of the ...Aniline,pyrrole and phenanthroline,which have different nitrogen compositions,are used as carbon precursors to synthesize nitrogen-doped ordered mesoporous carbons（NOMCs） by the nanocasting method.The effect of the precursor on the resultant NOMC is extensively investigated by nitrogen adsorption-desorption measurements,scanning electron microscopy,X-ray photoelectron spectroscopy（XPS）,cyclic voltammetry and rotating ring-disk electrode measurements.Salient findings are as follows.First,the precursor has a significant influence on the specific surface area and textural properties.The NOMC materials derived from pyrrole（C-PY-900：765 m^2/） and phenanthroline（C-Phen-900：746 m^2/） exhibit higher specific surface areas than the aniline analog（C-PA-900：569 m^2/）.Second,the XPS results indicate that the total nitrogen content（ca.3.1–3.3 at%） is similar for the three carbon sources,except for a slight difference in the nitrogen configuration.Furthermore,the content of the nitrogen-activated carbon atoms is found to closely depend on the precursor,which is the highest for the phenanthroline-derived carbon.Third,the electrochemical results reveal that the electrocatalytic activity follows in the order C-PA-900 C-PY-900 C-Phen-900,confirming that the nitrogen-activated carbon atoms are the active sites for the oxygen reduction reaction（ORR）.In summary,the precursor has considerable influence on the composition and textural properties of the NOMC materials,of which the ORR electrocatalytic activity can be enhanced through optimization of the NOMCs.展开更多
A robust oxygen‐related electrocatalyst,composed of spinel iron‐cobalt oxide and nitrogen‐dopedordered mesoporous carbon(NOMC),was developed for rechargeable metal‐air batteries.Electrochemicaltests revealed that ...A robust oxygen‐related electrocatalyst,composed of spinel iron‐cobalt oxide and nitrogen‐dopedordered mesoporous carbon(NOMC),was developed for rechargeable metal‐air batteries.Electrochemicaltests revealed that the optimal catalyst Fe_(0.5)Co/NOMC exhibits superior activity with ahalf‐wave potential of 0.89 V(vs.reversible hydrogen electrode)for the oxygen reduction reactionand an overpotential of 0.31 V at 10 mA cm^(−2)for the oxygen evolution reaction.For demonstration,the catalyst was used in the assembly of a rechargeable zinc‐air battery,which exhibited an exceptionallyhigh energy density of 820 Wh kg−1 at 100 mA cm^(−2),a high power density of 153 mW cm^(−2)at1.0 V,and superior cycling stability up to 432 cycles(144 h)under ambient air.展开更多
The development of efficient and cost‐effective metal‐free electrocatalysts for oxygen reduction reaction(ORR)has become crucial for electrochemical energy systems.However,reasonably validating and precisely regulat...The development of efficient and cost‐effective metal‐free electrocatalysts for oxygen reduction reaction(ORR)has become crucial for electrochemical energy systems.However,reasonably validating and precisely regulating the active sites for designing optimized materials are still challenging.Herein,we report a precise and controllable tandem strategy to boost the ORR activity based on metal‐free covalent organic frameworks(MFCOFs)comprising imine‐N,thiophene‐S,or triazine‐N.Among these MFCOFs,post‐tandem BTT‐TAT‐COF structure displayed a more positive catalytic capability and excellent electrochemical stability,indicating that the synergistic catalysis of multiple active sites induced the ORR catalytic activity through the conjugated skeleton of the structure.Density‐functional theory calculations suggest that the series‐connected backbone contained highly effective electrocatalytic active centers and provided synergistic catalysis.More importantly,this strategy highlights new opportunities for the advancement of efficient COF‐based metal‐free ORR catalysts.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
文摘Electrochemical conversion of CO2 into fuel has been regarded as a promising approach to achieve the global carbon cycle.Herein,we report an efficient cobalt catalyst with a unique flower-like morphology synthesized by a green and facile hydrothermal method,in which n-butylamine is used as the capping agent.The resultant catalyst shows superior electrocatalytic activity toward CO2 electroreduction,which is highly selective for generating formate with a Faraday efficiency of 63.4%.Electrochemical analysis reveals that the oxide on the surface is essential for the electrocatalysis of the CO2 reduction reaction.Cyclic voltammograms further suggest that this catalyst is highly active for the oxidation of reduced product,and can thus be seen as a bifunctional catalyst.
基金supported by the National Natural Science Foundation of China(21476087,21576101)the Innovation Project of Guangdong Department of Education(2014KTSCX016)+1 种基金the Science&Technology Research Project of Guangdong Province(2013B010405005,2014A010105041)the Fundamental Research Funds for the Central Universities~~
文摘Aniline,pyrrole and phenanthroline,which have different nitrogen compositions,are used as carbon precursors to synthesize nitrogen-doped ordered mesoporous carbons（NOMCs） by the nanocasting method.The effect of the precursor on the resultant NOMC is extensively investigated by nitrogen adsorption-desorption measurements,scanning electron microscopy,X-ray photoelectron spectroscopy（XPS）,cyclic voltammetry and rotating ring-disk electrode measurements.Salient findings are as follows.First,the precursor has a significant influence on the specific surface area and textural properties.The NOMC materials derived from pyrrole（C-PY-900：765 m^2/） and phenanthroline（C-Phen-900：746 m^2/） exhibit higher specific surface areas than the aniline analog（C-PA-900：569 m^2/）.Second,the XPS results indicate that the total nitrogen content（ca.3.1–3.3 at%） is similar for the three carbon sources,except for a slight difference in the nitrogen configuration.Furthermore,the content of the nitrogen-activated carbon atoms is found to closely depend on the precursor,which is the highest for the phenanthroline-derived carbon.Third,the electrochemical results reveal that the electrocatalytic activity follows in the order C-PA-900 C-PY-900 C-Phen-900,confirming that the nitrogen-activated carbon atoms are the active sites for the oxygen reduction reaction（ORR）.In summary,the precursor has considerable influence on the composition and textural properties of the NOMC materials,of which the ORR electrocatalytic activity can be enhanced through optimization of the NOMCs.
文摘A robust oxygen‐related electrocatalyst,composed of spinel iron‐cobalt oxide and nitrogen‐dopedordered mesoporous carbon(NOMC),was developed for rechargeable metal‐air batteries.Electrochemicaltests revealed that the optimal catalyst Fe_(0.5)Co/NOMC exhibits superior activity with ahalf‐wave potential of 0.89 V(vs.reversible hydrogen electrode)for the oxygen reduction reactionand an overpotential of 0.31 V at 10 mA cm^(−2)for the oxygen evolution reaction.For demonstration,the catalyst was used in the assembly of a rechargeable zinc‐air battery,which exhibited an exceptionallyhigh energy density of 820 Wh kg−1 at 100 mA cm^(−2),a high power density of 153 mW cm^(−2)at1.0 V,and superior cycling stability up to 432 cycles(144 h)under ambient air.
文摘The development of efficient and cost‐effective metal‐free electrocatalysts for oxygen reduction reaction(ORR)has become crucial for electrochemical energy systems.However,reasonably validating and precisely regulating the active sites for designing optimized materials are still challenging.Herein,we report a precise and controllable tandem strategy to boost the ORR activity based on metal‐free covalent organic frameworks(MFCOFs)comprising imine‐N,thiophene‐S,or triazine‐N.Among these MFCOFs,post‐tandem BTT‐TAT‐COF structure displayed a more positive catalytic capability and excellent electrochemical stability,indicating that the synergistic catalysis of multiple active sites induced the ORR catalytic activity through the conjugated skeleton of the structure.Density‐functional theory calculations suggest that the series‐connected backbone contained highly effective electrocatalytic active centers and provided synergistic catalysis.More importantly,this strategy highlights new opportunities for the advancement of efficient COF‐based metal‐free ORR catalysts.
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.
