Synthesis–structure–performance correlation for polyaniline–Me–C non-precious metal cathode catalysts for oxygen reduction in fuel cells
نویسندگان
چکیده
In this report, we present the systematic preparation of active and durable non-precious metal catalysts (NPMCs) for the oxygen reduction reaction in polymer electrolyte fuel cells (PEFCs) based on the heat treatment of polyaniline/metal/carbon precursors. Variation of the synthesis steps, heat-treatment temperature, metal loading, and the metal type in the synthesis leads to markedly different catalyst activity, speciation, and morphology. Microscopy studies demonstrate notable differences in the carbon structure as a function of these variables. Balancing the need to increase the catalyst’s degree of graphitization through heat treatment versus the excessive loss of surface area that occurs at higher temperatures is a key to preparing an active catalyst. XPS and XAFS spectra are consistent with the presence of Me–Nx structures in both the Co and Fe versions of the catalyst, which are often proposed to be active sites. The average speciation and coordination environment of nitrogen and metal, however, depends greatly on the choice of Co or Fe. Taken together, the data indicate that better control of the metal-catalyzed transformations of the polymer into new graphitized carbon forms in the heat-treatment step will allow for even further improvement of this class of catalysts.
منابع مشابه
Polyaniline-derived Non-Precious Catalyst for the Polymer Electrolyte Fuel Cell Cathode
This paper focuses on a new polyaniline-derived non-precious cathode catalyst with high oxygen-reduction activity, verified in electrochemical and fuel cell testing. The rotating disk (RDE) onset and half-wave potential (E1⁄2) of oxygen reduction were measured at 0.90 V and 0.77 V, respectively. Rotating ring-disk electrode (RRDE) study revealed very good selectivity in the fourelectron reducti...
متن کاملHigh-performance electrocatalysts for oxygen reduction derived from polyaniline, iron, and cobalt.
The prohibitive cost of platinum for catalyzing the cathodic oxygen reduction reaction (ORR) has hampered the widespread use of polymer electrolyte fuel cells. We describe a family of non-precious metal catalysts that approach the performance of platinum-based systems at a cost sustainable for high-power fuel cell applications, possibly including automotive power. The approach uses polyaniline ...
متن کاملPreparation of Nitrogen-Doped Graphene By Solvothermal Process as Supporting Material for Fuel Cell Catalysts
Development of efficient electrocatalysts for oxygen reduction reaction (ORR) is one of the most important issues for optimizing the performance of fuel cells and metal-air batteries. The introduction of nitrogen into carbon nanostructures has created new pathways for the development of non-precious electrocatalysts in fuel cells. In this work, nitrogen-doped graphene (NG) was synthesized by a ...
متن کاملOne –step synthesis of PdCo alloy nanoparticles decorated on reduced grahene oxide as an Electro-catalyst for Oxygen Reduction Reaction in Passive Direct Methanol Fuel Cells
We report a Pd-Co (3:1)/graphene oxide (Pd3Co /GO) catalyst through a one-step strategy. GO is synthesized from graphite electrodes using ionic liquid-assisted electrochemical exfoliation. Controllable GO-supported Pd3Co electrocatalystis then was reduced by ethylene glycol as a stabilizing agent to prepare highly dispersed PdCo nanoparticles on carbon graphene oxide to be used as oxygen reduct...
متن کاملSynthesis of nitrogen-doped onion-like carbon and its use in carbon-based CoFe binary non-precious-metal catalysts for oxygen-reduction
Nitrogen-doped onion-like carbon-rich materials were synthesized by heat treatment of a ‘‘hybrid’’ containing hexamethylene diamine complex in the presence of Co and Fe species while preparing non-precious metal electrocatalyst for oxygen-reduction. As demonstrated by electrochemical rotating disk electrode and fuel cell tests, the binary CoFe-based catalyst containing graphitized onion-like ca...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2011