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Cobalt and Iron Oxides Co-supported on Carbon Nanotubes as an Efficient Bifunctional Catalyst for Enhanced Electrocatalytic Activity in Oxygen Reduction and Oxygen Evolution Reactions

机译:在碳纳米管上共支撑的钴和氧化铁作为有效的双功能催化剂,以增强氧气还原和氧气进化反应的电催化活性

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Developing efficient non-precious metal electrocatalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in energy conversion and storage devices is highly desirable but challenging. This report describes a general approach for preparing cobalt and iron oxide nanoparticles cosupported on nitrogen-doped carbon materials as an efficient oxygen electrode catalyst with an improved catalytic activity toward OER and ORR; these nanoparticles were obtained through pyrolysis of Co- and Fe-based metal-organic frameworks grown directly on the surface of polyvinylimidazolefunctionalized carbon nanotubes (CNTs). The Fe/Co-CNTs-800 catalyst pyrolyzed at 800 ℃ exhibited high electrocatalytic activity for ORR, with only ~50 mV lesser activity than that of Pt/C at the half-wave potential, and for OER, with only ~70 mV lesser activity than that of RuO2 at a current density of 10 mA;;cm~(-2) in a 0.1 M KOH solution. The potential difference between OER and ORR for Fe/Co-CNTs-800 (ΔE_(OER-ORR)) was 0.905 V, which was significantly lower than that for noble-metal catalysts (20 wt% Pt/C (1.137 V) and RuO2 (1.341 V)). The preparation temperature and value of Fe/Co in the catalyst composite are crucial for achieving high electrocatalytic activity for both ORR and OER.
机译:在能量转化和存储装置中,开发有效的非纯粹金属电催化剂,用于氧气进化反应(OER)和氧还原反应(ORR)是非常可取的,但具有挑战性。该报告描述了一种在氮掺杂的碳材料上固定的钴和氧化铁纳米颗粒的一般方法,作为有效的氧电极催化剂,对OER和ORR具有改善的催化活性;这些纳米颗粒是通过直接在聚乙烯基咪唑功能的碳纳米管(CNT)表面生长的共生长的co和fe的金属有机框架来获得的。 Fe/Co-CNTS-800催化剂在800℃处的催化剂对ORR表现出高的电催化活性,仅在半波电位下的PT/C的活性低约50 mV,而OER的活性仅为PT/C,仅降低了约70 mV在0.1 M KOH溶液中,在10 mA的电流密度下的活性比RUO2的活性。 Fe/Co-CNTS-800(ΔE_(OER-orr))OER和ORR之间的电位差为0.905 V,显着低于Noble-Metal催化剂(20 wt%PT/C(1.137 V)和RUO2(1.341 V))。 Fe/Co在催化剂复合材料中的制备温度和值对于在ORR和OER中都能达到高电催化活性至关重要。

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