The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated th...The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated through dealloying of annealed Fe_(76)Si_(9)B_(15)amorphous ribbons.The results of UV-vis spectra and FTIR indicated that AO II solution was degraded efficiently into unharmful molecules H_(2)O and CO_(2)on NPFe Si B electrode within 5 mins under the square-wave potential of±1.5 V.The degradation efficiency of the NP-Fe Si B electrode remains 98.9%even after 5-time recycling.The large amount of active surface area of the nanoporous Fe Si B electrode with lattice disorders and stacking faults,and alternate electrochemical redox reactions were mainly responsible for the excellent degradation performance of the NP-Fe Si B electrode.The electrochemical pulsed square-wave process accelerated the redox of Fe element in Fe-based nanoporous electrode and promoted the generation of hydroxyl radicals(·OH)with strong oxidizability as predominant oxidants for the degradation of azo dye molecules,which was not only beneficial to improving the catalytic degradation activity,but also beneficial to enhancing the reusability of the nanoporous electrode.This work provides a highly possibility to efficiently degrade azo dyes and broadens the application fields of nanoporous metals.展开更多
基金financially supported by Shi-changxu Innovation Center for Advanced Materials,Institute of Metal Research,Chinese Academy of Sciences,the National Natural Science Foundation of China(51790484,51671106)Chinese Academy of Sciences(ZDBSLY-JSC023)Fundamental Research Funds for the Central Universities(30919011404)。
文摘The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated through dealloying of annealed Fe_(76)Si_(9)B_(15)amorphous ribbons.The results of UV-vis spectra and FTIR indicated that AO II solution was degraded efficiently into unharmful molecules H_(2)O and CO_(2)on NPFe Si B electrode within 5 mins under the square-wave potential of±1.5 V.The degradation efficiency of the NP-Fe Si B electrode remains 98.9%even after 5-time recycling.The large amount of active surface area of the nanoporous Fe Si B electrode with lattice disorders and stacking faults,and alternate electrochemical redox reactions were mainly responsible for the excellent degradation performance of the NP-Fe Si B electrode.The electrochemical pulsed square-wave process accelerated the redox of Fe element in Fe-based nanoporous electrode and promoted the generation of hydroxyl radicals(·OH)with strong oxidizability as predominant oxidants for the degradation of azo dye molecules,which was not only beneficial to improving the catalytic degradation activity,but also beneficial to enhancing the reusability of the nanoporous electrode.This work provides a highly possibility to efficiently degrade azo dyes and broadens the application fields of nanoporous metals.