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Enhancing the electro catalytic activity of manganese ferrite through cerium substitution for oxygen evolution in KOH solutions

机译:通过铈替代KOH溶液中的氧气释放增强锰铁氧体的电催化活性

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摘要

Alkaline water electrolysis (AWE) is the simplest way of producing hydrogen, an attractive fuel for the future. In view of their cost-effectiveness and durability, non-noble metal oxides are promising catalysts for AWE. Here, we studied the effect of Ce substitution on the OER activity of manganese ferrite. Ce substituted MnFe2O4 (0 <= x <= 0.8) was synthesized by a combustion method. Characterization techniques such as SEM, XRD, EDAX and XPS were used to analyse the surface morphology and the chemical composition of CexMnFe2-xO4. Substitution of Ce3+ in the cubic lattice of MnFe2O4 increases the conductivity of CexMnFe2-xO4, which results in the negative shift in the OER onset potential. Among all the Ce3+ substituted manganese ferrites, Ce0.2MnFe1.8O4 was found to be more active for OER in terms of current and stability. Notably, Ce0.2MnFe1.8O4 affords a current density of 10 mA cm(-2) at a small overpotential of similar to 310 mV and a Tafel slope value of 31 mV per decade, these values are comparable to the well-investigated non-noble metal oxides.
机译:碱性水电解(AWE)是生产氢的最简单方法,氢是未来的诱人燃料。考虑到它们的成本效益和耐久性,非贵金属氧化物是用于AWE的有前途的催化剂。在这里,我们研究了Ce替代对锰铁氧体OER活性的影响。通过燃烧法合成了Ce取代的MnFe 2 O 4(0≤x≤0.8)。 SEM,XRD,EDAX和XPS等表征技术用于分析CexMnFe2-xO4的表面形态和化学成分。 Ce3 +取代MnFe2O4的立方晶格会提高CexMnFe2-xO4的电导率,这会导致OER起始电势发生负向偏移。在所有Ce3 +取代的锰铁氧体中,就电流和稳定性而言,发现Ce0.2MnFe1.8O4对OER的活性更高。值得注意的是,Ce0.2MnFe1.8O4的电流密度为10mA cm(-2),在小的过电位下类似于310mV,Tafel斜率为每十年31mV,这些值可与经过充分研究的非贵金属氧化物。

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