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# Iron-Based Catalysts with Improved Oxygen Reduction Activity in Polymer Electrolyte Fuel Cells

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Science  03 Apr 2009:
Vol. 324, Issue 5923, pp. 71-74
DOI: 10.1126/science.1170051

## Abstract

Iron-based catalysts for the oxygen-reduction reaction in polymer electrolyte membrane fuel cells have been poorly competitive with platinum catalysts, in part because they have a comparatively low number of active sites per unit volume. We produced microporous carbon–supported iron-based catalysts with active sites believed to contain iron cations coordinated by pyridinic nitrogen functionalities in the interstices of graphitic sheets within the micropores. We found that the greatest increase in site density was obtained when a mixture of carbon support, phenanthroline, and ferrous acetate was ball-milled and then pyrolyzed twice, first in argon, then in ammonia. The current density of a cathode made with the best iron-based electrocatalyst reported here can equal that of a platinum-based cathode with a loading of 0.4 milligram of platinum per square centimeter at a cell voltage of ≥0.9 volt.

The desired high power density from polymer electrolyte membrane fuel cells (PEMFCs) can only be achieved by speeding up the otherwise slow reaction steps at their low operating temperatures (∼80°C) through catalysis. For the oxygen-reduction reaction (ORR), non–precious metal catalysts (NPMCs), which are potentially less expensive and more abundant, have been outperformed by Pt-based catalysts (1, 2), which exhibit high activity as the native metal. For metals such as Co and Fe, improved performance will require a robust method for increasing the reactivity of the metal ion through ligation.

Since 1964, when Jasinski observed that cobalt phthalocyanine catalyzed the ORR (3), a number of approaches have been explored to create practical NPMCs. Catalysts were first obtained by adsorbing Fe-N4 or Co-N4 macrocycles on a carbon support and pyrolyzing the resulting material in an inert atmosphere (4). A breakthrough was then achieved by Yeager when it was revealed that these often-expensive macrocycles could instead be substituted by individual N and Co precursors (5). This approach was followed by several groups, including ours (4, 616). Meanwhile, NPMC research using metal-N4 macrocycles has also progressed (1719).

Our previous approach in the synthesis of NPMCs for ORR has been to use NH3 as a nitrogen precursor. The catalysts were obtained by wet impregnation of carbon black with an iron precursor such as iron(II) acetate (FeAc), followed by a heat treatment in NH3; we refer to the products as Fe/N/C electrocatalysts. During pyrolysis at temperatures of ≥800°C, NH3 partly gasifies the carbon support, resulting in a mass loss that depends on the duration of the heat treatment (20). The disordered domains of the carbon support are preferentially gasified (2123). As a result, micropores are created in the carbon black particles. The mass loss at which maximum activity is reached [30 to 50 weight percent (wt %)] corresponds to the largest microporous surface area for the etched carbon, which suggests that these micropores (width ≤2 nm) host most of the catalytic sites (21).

The reaction of NH3 with the disordered carbon domains also produces the N-bearing functionalities needed to bind iron cations to the carbon support (24, 25). It has been proposed that most of the Fe/N/C catalytic sites consist of an iron cation coordinated by four pyridinic functionalities attached to the edges of two graphitic sheets, each belonging to adjacent crystallites on either side of a slit pore in the carbon support (21, 25). Thus, four factors have been identified as requirements for producing active Fe-based catalysts for ORR: (i) disordered carbon content in the catalyst precursor (20), (ii) iron, (iii) surface nitrogen, and (iv) micropores in the catalyst.

Our present approach, which introduces a new material (pore filler) and replaces impregnation with planetary ball-milling, has elevated the catalytic activity of an Fe-based NPMC by a factor of >35 relative to the previous best reported activity for Fe-based catalysts (11) (and within ∼10% of the best Pt-based catalysts). Furthermore, these NPMCs may also present opportunities for ORR in direct alcohol, formic acid, and alkaline fuel cells.

For NPMCs, it is meaningful to speak in terms of volumetric activity for ORR (1) because its product with electrode thickness predicts the kinetic current density (A cm–2) of the cathode. Because of mass-transport limitations related to electrode thickness, NPMC cathodes must attain the same kinetic current density as Pt-based cathodes without exceeding a thickness of ∼100 μm (1). This criterion defines a target for volumetric activity (A cm–3) for NPMCs. [The activity is originally measured in amperes per gram of NPMC; conversion from A $Math$ to A $Math$ is described in (26).] For NPMCs, the U.S. Department of Energy (DOE) has set a 2010 target of 130 A cm–3 as measured in a fuel cell at 0.8 V iR-free cell voltage (i.e., after correction for ohmic loss R), at 80°C, and at O2 and H2 absolute pressures of 1 bar (27). All volumetric activity values reported in this work correspond to these reference conditions. For the best catalysts synthesized by our group to date by impregnation of FeAc on carbon black followed by heat treatment in NH3 at 950°C, a volumetric activity of 0.8 to 1.5 A cm–3 was obtained (28, 29). This value is comparable to the value of 2.7 A cm–3 (recalculated for O2 and H2 pressures of 1 bar) obtained by Wood et al. for a Fe/N/C catalyst (11). All of these activities are still well below the DOE 2010 target of 130 A cm–3.

The volumetric activity is the product of the catalytic site density and the activity of a single site. The latter varies with voltage and is an intrinsic property of the catalytic site. If the catalytic activity of the site is left unchanged, increased volumetric activity can only be achieved by increasing the site density. The volumetric catalytic activity may be improved by increasing the Fe content. However, doing so increases the activity proportionally only up to ∼ 0.2 nominal wt % Fe, beyond which the activity levels off and eventually decreases (29). Furthermore, when catalysts were prepared using he impregnation method on nonmicroporous carbon black and pyrolyzed in pure NH3, the micropore surface area of the resulting catalysts was shown to govern the catalytic activity; the nitrogen and iron content were usually nonlimiting (21).

In a recent study, we impregnated FeAc onto highly microporous carbon supports followed by pyrolysis in NH3 (30). An example of a highly microporous carbon black is Black Pearls 2000 with a Brunauer-Emmett-Teller (BET) surface area of 1379 m2 g–1 and a micropore area of 934 m2 g–1. By contrast, a typical carbon support of lower porosity such as Vulcan XC-72R has a BET surface area of 213 m2 g–1 and a micropore area of 114 m2 g–1. Surprisingly, the use of highly microporous carbon supports did not improve the activity relative to catalysts made with nonmicroporous carbon supports. We concluded that only the micropores created during heat treatment in NH3 may host catalytic sites. The micropores in the as-received microporous carbon blacks do not bear the surface nitrogen necessary to form catalytic sites. Because these carbon blacks have little disordered carbon content, surface nitrogen is difficult to add during pyrolysis in NH3.

In the present work, to capitalize on the high micropore content of microporous carbon blacks and to overcome the limitations resulting from their lack of disordered carbon, we filled these micropores with a mixture of pore filler (PF) and iron precursor (Fig. 1). Doing so created a catalyst precursor that complies with the factors required for producing active NPMCs, as described above. To overcome the limitation of solubility and/or adsorbability associated with the impregnation method, we used planetary ball-milling to fill the pores of the microporous carbon support with PF and iron precursor. Planetary ball-milling uses both friction and impact effects to force the filler materials (PF and iron precursor) into the pores of the carbon support while leaving its microstructure relatively unaffected.

For all catalysts in the present work, we used Black Pearls 2000 (Cabot; micropore surface area 934 m2 g–1) as the microporous carbon black and FeAc as the iron precursor. Micropores are defined as pores having a width of ≤20 Å. We chose two pore fillers: perylene-tetracarboxylic dianhydride (PTCDA), which is nitrogen-free, and 1,10-phenanthroline (phen), which is N-bearing. For catalysts made using PTCDA, the N atoms necessary to form catalytic sites arise from its reaction with NH3 during pyrolysis. For catalysts made with phen, the pyrolysis may be performed either in Ar or NH3 because phen already contains nitrogen. Note that phen forms a complex with Fe2+.

We first investigated the effect of the wt % of PTCDA in the catalyst precursor. Four different wt % PTCDA values (0, 25, 50, 75) were used with a constant nominal Fe loading of 0.2 wt %. Optimal volumetric activities of 1.8, 8.5, 22, and 27 A cm–3 were obtained, respectively. The experimental conditions and corresponding fuel cell polarization curves are given in fig. S3 (26). Next, a PF loading of 50 wt % (PTCDA or phen) was chosen to investigate the effect of nominal Fe loading in the catalyst precursor. Catalyst precursors made with PTCDA were pyrolyzed in NH3 and those made with phen in Ar, both at 1050°C. Although better volumetric activities were obtained with the PTCDA series (Table 1), we investigated the effect of a subsequent 5-min pyrolysis in NH3 for the phen series. This subsequent pyrolysis amplified the volumetric activity of the Ar-pyrolyzed phen series by a factor of ≤20. These amplified activities surpassed those of the PTCDA series. Given the notable improvement in activity of the phen-based catalysts after a second pyrolysis in NH3, we prepared phen-based catalysts (with 1 wt % nominal Fe content) using a single pyrolysis in NH3 at 1050°C. The volumetric activities of the latter catalysts (16 to 29 A cm–3) were lower than those achieved using a two-step pyrolysis, first in Ar at 1050°C, then in NH3 at 950°C.

Table 1.

Catalytic activity for optimized catalysts. Volumetric activities are at 0.8 V iR-free cell voltage at reference conditions of 80°C and 1 bar O2 and H2. Black Pearls 2000 was used as the carbon support. The mass ratio of pore filler to carbon support was 1:1. Catalyst loading for all tests was ∼1 mg cm–2. The Nafion-to-catalyst ratio (NCR) was 2 unless otherwise noted.

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Two factors were further optimized on the most active catalyst corresponding to 1 wt % nominal Fe content (64 A cm–3, Table 1): (i) the mass loss during pyrolysis in NH3, and (ii) the Nafion-to-catalyst ratio (NCR) in the cathode (Nafion is a proton-conducting perfluoro polyethylene sulfonic acid polymer made by DuPont). The optimal mass loss and NCR were found to be ∼30% and ∼1.5, respectively, leading to an increase in volumetric activity from 64 to 99 A cm–3, which is much closer to the 2010 DOE performance target of 130 A cm–3 for ORR on NPMCs. (See table S2 for additional details on mass activity, mass loss during pyrolysis, micropore surface area, and nitrogen content.)

Polarization curves (both as-measured and corrected to the DOE fuel cell test reference conditions) in terms of volumetric current density for our best NPMC and for the presumed best NPMC reported to date by Wood et al. (11) are shown in Fig. 2. The DOE volumetric activity target for ORR on NPMCs is specified for 0.8 V iR-free cell voltage and under reference conditions. The kinetic activity (free of ohmic and mass transport losses) of the NPMCs at 0.8 V iR-free cell voltage cannot be directly read from the corrected polarization curves, but must instead be estimated by extrapolating the kinetically controlled Tafel slope observed at higher cell voltage. Our best NPMC shows a factor of >35 activity enhancement relative to the presumed previous best NPMC.

The results of 100-hour durability tests in fuel cells using hydrogen/oxygen and hydrogen/air as anode/cathode gases are shown in fig. S4. Relative to the stable current densities obtained by Bashyam and Zelenay (32) for tests performed under the same conditions (0.2 A cm–2 with H2/O2 at 0.5 V; 0.13 to 0.14 A cm–2 with H2/air at 0.4 V), the initial current densities produced by the catalyst in this work (0.75 A cm–2 with H2/O2 at 0.5 V; 0.58 A cm–2 with H2/air at 0.4 V) were much higher and remained higher throughout the 100-hour period, with final values of 0.33 A cm–2 with H2/O2 at 0.5 V and 0.36 A cm–2 with H2/air at 0.4 V.

The best NPMC in this work has a much higher initial activity, but less stability, than those prepared by Bashyam and Zelenay according to a nonpyrolytic method based on a cobalt salt and polypyrrole deposited on carbon black (32). Continued research must now focus on improving the stability of these NPMCs and optimizing their cathode mass-transport properties.

Supporting Online Material

Materials and Methods

SOM Text

Figs. S1 to S4

Tables S1 and S2

References

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