化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2014年
6期
2113-2119
,共7页
电化学%燃料电池%催化%氧还原%非贵金属催化剂
電化學%燃料電池%催化%氧還原%非貴金屬催化劑
전화학%연료전지%최화%양환원%비귀금속최화제
electrochemistry%fuel cell%catalysis%oxygen reduction reaction%non-noble metal catalyst
中心金属离子在非贵金属C-N复合物对氧还原反应(ORR)的电催化活性方面有重要作用。通过将含有多壁碳纳米管(MWCNTs)、聚苯胺与过渡金属Fe和Co的前驱体在N2气氛下于900℃下加热,得到了不同金属比例的C-N催化剂。采用SEM、XRD等对催化剂的结构进行了表征。利用电化学伏安技术,研究了催化剂对ORR的电催化活性及其稳定性。结果表明,当Fe与Co质量比为6:1时催化剂的催化活性最好,在酸性溶液中ORR起始电位达到0.52 V(vs SCE),电流密度为12.5 mA·mg-1@-0.3 V (vs SCE);在碱性溶液中ORR 起始电位为-0.09 V(vs SCE),电流密度为7.8 mA·mg-1@-0.8 V (vs SCE)。结果表明,催化剂中Fe与Co的质量比对催化剂的活性有很大影响。
中心金屬離子在非貴金屬C-N複閤物對氧還原反應(ORR)的電催化活性方麵有重要作用。通過將含有多壁碳納米管(MWCNTs)、聚苯胺與過渡金屬Fe和Co的前驅體在N2氣氛下于900℃下加熱,得到瞭不同金屬比例的C-N催化劑。採用SEM、XRD等對催化劑的結構進行瞭錶徵。利用電化學伏安技術,研究瞭催化劑對ORR的電催化活性及其穩定性。結果錶明,噹Fe與Co質量比為6:1時催化劑的催化活性最好,在痠性溶液中ORR起始電位達到0.52 V(vs SCE),電流密度為12.5 mA·mg-1@-0.3 V (vs SCE);在堿性溶液中ORR 起始電位為-0.09 V(vs SCE),電流密度為7.8 mA·mg-1@-0.8 V (vs SCE)。結果錶明,催化劑中Fe與Co的質量比對催化劑的活性有很大影響。
중심금속리자재비귀금속C-N복합물대양환원반응(ORR)적전최화활성방면유중요작용。통과장함유다벽탄납미관(MWCNTs)、취분알여과도금속Fe화Co적전구체재N2기분하우900℃하가열,득도료불동금속비례적C-N최화제。채용SEM、XRD등대최화제적결구진행료표정。이용전화학복안기술,연구료최화제대ORR적전최화활성급기은정성。결과표명,당Fe여Co질량비위6:1시최화제적최화활성최호,재산성용액중ORR기시전위체도0.52 V(vs SCE),전류밀도위12.5 mA·mg-1@-0.3 V (vs SCE);재감성용액중ORR 기시전위위-0.09 V(vs SCE),전류밀도위7.8 mA·mg-1@-0.8 V (vs SCE)。결과표명,최화제중Fe여Co적질량비대최화제적활성유흔대영향。
Transition metal has an important effect on the electrocatalytic activity of non-noble metal catalysts for oxygen reduction reaction (ORR). In this work, the precursor containing MWCNTs, polyaniline, Fe and Co was firstly synthesized, and then the precursor was heated at 900℃ under N2 to obtain the C-N catalysts with different Fe/Co mass ratios. The structure of the catalysts was investigated with SEM and X-ray diffraction. ORR activity of the catalysts in acidic and alkaline media was tested with voltammetry. The prepared catalyst with Fe/Co mass ratio of 6:1 presents the highest electrocatalytic activity for ORR. ORR current density at 2000 r·min-1 was 12.5 mA·mg-1@-0.3 V(vs SCE) in acidic solution and 7.8 mA·mg-1@-0.8 V(vs SCE) in alkaline solution, and onset potential of ORR was 0.52 V(vs SCE) in acidic solution and-0.09 V(vs SCE) in alkaline solution. Fe/Co mass ratio played a great role in the electrocatalytic activity of these non-noble metal catalysts for ORR.