An Efficient, Ecofriendly Bimetallic Fe-In MOF and its g-C3N4 Based Composites for Methanol Oxidation Reaction

被引:1
作者
Zaman, Neelam [1 ]
Iqbal, Naseem [1 ]
Noor, Tayyaba [2 ]
机构
[1] Natl Univ Sci & Technol NUST, US Pakistan Ctr Adv Studies Energy USPCAS E, Sect H 12, Islamabad 44000, Pakistan
[2] Natl Univ Sci & Technol NUST, Sch Chem & Mat Engn SCME, Islamabad 44000, Pakistan
关键词
Methanol oxidation reaction (MOR); Graphitic carbon nitride (g-C3N4); Electrocatalysis; Metal organic framework (MOF); GRAPHITIC CARBON NITRIDE; REDUCED GRAPHENE OXIDE; ELECTROCATALYTIC ACTIVITY; NANOPARTICLES; PERFORMANCE; NANOSHEETS; CATALYST; ELECTRODE; NANOCOMPOSITES; EVOLUTION;
D O I
10.1007/s10904-024-03280-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The absence of stable and highly active non-precious metal electrocatalysts as a substitute to precious metal i.e., Pt (state-of-the-art) for methanol oxidation reaction in the application of direct methanol fuel cell considerably impedes the commercialization of these energy devices. In this work the electrocatalytic investigation of Fe-In MOF and its g-C3N4-based composites (i.e., 5-8 wt% g-C3N4@ Fe-In MOF) for methanol oxidation is reported. All the catalysts were prepared via solvothermal method. XRD, SEM, EDX, and FTIR were used to characterize the Fe-In MOF and its 5-8wt% g-C3N4 composites. In comparison to other prepared g-C3N4 based Fe-In MOF composites, the 7wt% g-C3N4 @ Fe-In MOF catalyst showed much greater electrochemical activity (i.e., 95.54 mA/cm(2)) and stability of 72.45% in 1 M NaOH and 3 M CH3OH. Due to graphitic carbon nitride specified high catalytic activity, intercalation, ion exchange, and redox properties. Further, the availability of iron (Fe) and indium (In) may also show a significant role in enhancing the electrocatalytic performance of 7wt% g-C3N4 @ Fe-In MOF over Fe-In MOF. They could be viewed as stable and economical electrocatalysts due to their numerous advantageous characteristics in structure, content, and nitrogen doping level.
引用
收藏
页码:300 / 316
页数:17
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