Alba Garzón
Manjón
*a,
Tobias
Löffler
b,
Michael
Meischein
c,
Hajo
Meyer
c,
Joohyun
Lim‡
a,
Valerie
Strotkötter
c,
Wolfgang
Schuhmann
*b,
Alfred
Ludwig
*c and
Christina
Scheu
*a
aMax-Planck-Institut für Eisenforschung GmbH, Max-Planck-Straße 1, 40237 Düsseldorf, Germany. E-mail: a.garzon@mpie.de; c.scheu@mpie.de
bAnalytical Chemistry—Center for Electrochemical Sciences (CES), Faculty of Chemistry and Biochemistry, Ruhr University Bochum, Universitätsstr. 150, D-44780 Bochum, Germany. E-mail: wolfgang.schuhmann@rub.de
cMaterials Discovery and Interfaces, Institute for Materials, Faculty of Mechanical Engineering, Ruhr University Bochum, Universitätsstr. 150, D-44780 Bochum, Germany. E-mail: alfred.ludwig@rub.de
First published on 12th November 2020
Complex solid solution electrocatalysts (often called high-entropy alloys) present a new catalyst class with highly promising features due to the interplay of multi-element active sites. One hurdle is the limited knowledge about structure–activity correlations needed for targeted catalyst design. We prepared Cr–Mn–Fe–Co–Ni nanoparticles by magnetron sputtering a high entropy Cantor alloy target simultaneously into an ionic liquid library. The synthesized nanoparticles have a narrow size distribution but different sizes (from 1.3 ± 0.1 nm up to 2.6 ± 0.3 nm), different crystallinity (amorphous, face-centered cubic or body-centered cubic) and composition (i.e. high Mn versus low Mn content). The Cr–Mn–Fe–Co–Ni complex solid solution nanoparticles possess an unprecedented intrinsic electrocatalytic activity for the oxygen reduction reaction in alkaline media, some of them even surpassing that of Pt. The highest intrinsic activity was obtained for body-centered cubic nanoparticles with a low Mn and Fe content which were synthesized using the ionic liquid 1-etyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide [Emimi][(Tf)2N].
Traditional wet synthesis routes are suitable for the synthesis of single-element or binary alloys.16,17 The synthesis of single-phase CSSNPs demands a technique with great control over the nucleation process down to the atomic scale, which can be achieved by combinational co-sputtering into ionic liquids (ILs),18,19 which offers an almost unlimited flexibility for the used pure elements. ILs are excellent dispersion media to control size, structure and composition of CSSNPs.20,21 Additionally, ILs act as a media for growth and as stabilizer for highly stable colloidal solutions,22 devoid of any other chemical stabilizers which could affect the CSSNPs catalytic properties.
CSSNPs compositions can be defined by co-sputtering of several elements simultaneously from individual targets or by using alloy targets.18,21 In addition, the desired phase, crystallinity and size of the CSSNPs can be modulated by means of post-annealing treatment.21 Co-sputtering is a high-throughput deposition technique, which allows for screening, but also upscaling of the production of CSSNPs seems feasible.23
In an earlier work1 we used 1-butyl-3-methylimidazolium bis (trifluoromethylsulfonyl)imide [Bmim][(Tf)2N] as IL to synthesize binary, quaternary and one type of quinary CSSNPs. The quinary NPs were in the as-grown state amorphous and had an average composition of Cr39Mn2Fe12Co24Ni2321 and they showed similarly high electrocatalytic ORR activity as Pt-NPs prepared by sputtering into the same IL.1 However, other ILs were not used for the synthesis of quinary NPs until now. We used before the concept of sputtering into a library of ILs with different anions and cations for the formation of pure Ag NPs.20 An influence of the IL's molecular structure on the NPs size and morphology was found.
These results motivated us to synthesize Cr–Mn–Fe–Co–Ni NPs by sputtering into a library of eight different ILs. Identical process parameters as ensured by simultaneous preparation as well as cleaning steps allow to compare the effect of different ILs on the CSSNPs formation and their behavior during the ORR. Aberration-corrected (scanning) transmission electron microscopy ((S)TEM) complemented with energy-dispersive X-ray spectroscopy (EDS) are used to characterize the CSSNPs. The results show that the CSSNPs size, crystal structure, and composition depend on the used IL, and accordingly variations in the electrocatalytic ORR activities are observed. Using this approach, we identify several CSSNPs with a high intrinsic activity even higher than Pt.
We choose these 8 different ILs as we want to study systematically the effect on the molecular chain, lengths and structure. In addition, they have a high purity and stability and low water content. The different properties of the ILs are expected to lead to differences in NP properties.
We investigated the intrinsic electrocatalytic activity of the individual CSSNPs after NP immobilization at etched carbon nanoelectrodes from IL as demonstrated and established in an earlier work.1 The voltammetric activity curves are summarized in Fig. 2 and indeed, a strong effect of IL-dependent NP properties on activity can be observed. The group of IL 1, IL 6, IL 7, and IL 8 presents the highest catalytic performance (with the order IL 6 > IL 7 > IL 8 > IL 1) followed by the group of IL 3, IL 4 and IL 5. CSSNPs synthesized with IL 2 have an intrinsic activity which lies between the two groups and is similar to the benchmark Pt NPs. Please note that all curves including Pt seem to be shifted towards higher overpotentials due to the low mass loading of the isolated NPs. As described in more detail in the ESI of ref. 24, a mass loading reduced by two orders of magnitude and constant background noise level provided by the carbon electrode and a Tafel slope of 80 mV dec−1 would imply a visible Pt current exceeding the background current at 160 mV higher overpotential. This finding is in accordance with ref. 1, where we also used IL 2 to produce one amorphous quinary NP system (Cr39Mn2Fe12Co24Ni23), which outperformed binary and quaternary CSSNPs (an in situ phase transformation video showing the transition from the amorphous to the crystalline state is added in the ESI†). In the present work, the most active CSSNPs show considerably higher intrinsic activity than the benchmark Pt NPs, showcasing the high potential of NP property optimization to exploit the paradigm changing concept of CSS catalysts.
Fig. 2 Comparison of intrinsic ORR activity in alkaline media of CSSNPs immobilized on etched carbon nanoelectrodes from ILs 1 to 8 in comparison to Pt NPs. |
Note that a completely stable “blank” electrode signal cannot be maintained, implying that a slight overcorrection is performed by subtracting the electrode polarization curve prior to NP immobilization.25 This effect causes an “oxidative bump” at about 700 mV vs. reversible hydrogen electrode (RHE) where usually the current increase of the blank electrode becomes visible. For the active samples (CSSNPs in IL 1, IL 2, IL 6, IL 7 and IL 8) this effect does not play a role since they reach the maximum current already at lower overpotentials. For the less active samples (CSSNPs in IL 3, IL 4 and IL 5), however, a deviation at low currents is obtained, which is counteracted once the kinetic CSSNP current starts to dominate at higher overpotentials and the influence of the carbon instability becomes insignificant. Such a bump is also observed when subtracting two consecutive blank electrode cycles without any NPs attached and, therefore, it is not attributed to any NP property. All polarization curves were normalized by the plateau current of the first current wave, which provides a mass loading independent information about the position of the most favorable adsorption peak and thus, the potential in intrinsic activity for this catalyst.24
In order to clarify the origin of the differences in the CSSNPs activities, aberration-corrected high resolution (HR)TEM and EDS data acquisition in STEM were required to analyze the size, structure and composition of the CSSNPs at the atomic scale.
The average size of the CSSNPs ranges from 1.3 ± 0.1 nm to 2.6 ± 0.3 nm for the different ILs (Fig. 3). Histograms for the size distribution were obtained for the different CSSNPs by analyzing up to 20 HRTEM images. The data are presented in the ESI Fig. S1.†
The crystal structure of the CSSNPs could not be determined by selected area diffraction experiments due to the high contribution from the amorphous signal of the carbon-coated TEM grid. Thus, crystal structures were analyzed by fast Fourier transformation (FFT) and the results are shown as insets in Fig. 3. As the CSSNPs were too small to be tilted into a specific zone axis HRTEM images were taken with random orientation of the CSSNPs. The FFT analysis revealed that by choosing the appropriate IL, the CSSNPs can be synthesized in either amorphous, face centered cubic (fcc) or body centered cubic (bcc) state (Fig. 3). We showed earlier that by ex situ annealing of the initially amorphous NP prepared by DC sputtering, or by high-power impulse magnetron sputtering crystalline NPs can be produced using IL 2.21 Here we demonstrate that depending on the IL used we can synthesize CCSNPS with different crystal structures. It should be noted that the different crystal structures are not due to crystallization caused by the electron beam as they were all acquired with similar electron dose rates and at the same 300 keV energy of the incident electron beam.
To analyze the crystal structure of the different CSSNPs, we used the second reflection due to the following reason. For the fcc structure, the first reflection is {111} and the corresponding lattice spacing is d1 = 0.208 nm and the second is {022} with d2 = 0.180 nm. For bcc, the first reflection is {011} corresponding to d1 = 0.205 nm and the second {002} with d2 = 0.145 nm. Thus, while the difference in the lattice plane spacing {111} for fcc and {011} for bcc is too small, they can be distinguished by the lattice planes with the higher Miller indices.
CSSNPs synthesized in IL 2, IL 3 and IL 7 do not show a long-range order and are thus considered amorphous. A fcc structure of the CSSNPs was found when using IL 1 and IL 4, while those synthesized with IL 5, IL 6 and IL 8 possess bcc structure. In general, the CSSNPs in the ILs showed a high stability over time and no agglomerates in the colloidal solution were formed after more than one month.
The chemical composition of individual CSSNPs was analyzed by EDS in STEM mode. EDS quantification was achieved using the non-matrix factorization, three main components were identified which were related to the individual CSSNPs, the surrounding IL and the noise/background stemming from the TEM carbon grid. Only the component representative for the individual NPs was quantitatively analyzed of the EDS data by applying principal component analysis.26 In order to get compositional values with high accuracy, we determined k-factors from the Cr18Mn20Fe20Co21Ni21 target. The chemical composition was calculated and averaged for ∼20 CSSNPs. The quantitative analysis revealed that the chemical composition of the individual CSSNPs depends on the IL used in the synthesis. The data together with the observed crystal structure are summarized in Table 1. Fig. 4 shows exemplary the EDS elemental mapping from the CSSNPs synthesized using IL 8. For these NPs as well as for the ones prepared using the other ILs a homogenous distribution of the five elements was observed.
Fig. 4 STEM high angle annular dark field image and corresponding EDS elemental mapping from the CSSNPs synthesized in IL 8. All elements are homogenously distributed. |
Elements | CSSNPs in IL 1 (at%) | CSSNPs in IL 2 (at%) | CSSNPs in IL 3 (at%) | CSSNPs in IL 4 (at%) | CSSNPs in IL 5 (at%) | CSSNPs in IL 6 (at%) | CSSNPs in IL 7 (at%) | CSSNPs in IL 8 (at%) |
---|---|---|---|---|---|---|---|---|
Cr | 37 ± 1 | 39 ± 3 | 25 ± 2 | 32 ± 2 | 25 ± 1 | 40 ± 2 | 37 ± 1 | 24 ± 1 |
Mn | 11 ± 2 | 2 ± 1 | 19 ± 1 | 2 ± 1 | 5 ± 1 | 6 ± 1 | 5 ± 1 | 10 ± 1 |
Fe | 14 ± 2 | 12 ± 2 | 29 ± 3 | 17 ± 1 | 16 ± 2 | 8 ± 1 | 15 ± 2 | 19 ± 1 |
Co | 19 ± 2 | 24 ± 2 | 24 ± 1 | 9 ± 2 | 25 ± 2 | 27 ± 2 | 24 ± 2 | 23 ± 1 |
Ni | 19 ± 3 | 23 ± 3 | 3 ± 1 | 40 ± 2 | 29 ± 2 | 19 ± 2 | 19 ± 3 | 24 ± 1 |
Crystal structure | fcc | Amorphous | Amorphous | fcc | bcc | bcc | Amorphous | bcc |
The results on the use of different ILs shows the important finding that the molecular structure of the IL influences the size, the composition and the crystal structure as discussed in more detail below. It also demonstrates the capabilities of the synthesis protocol where we kept all parameters identical except for the IL involved which allows to draw the conclusion that the NP properties can be tailored by the choice of the IL.
The chemical composition for the individual CSSNPs, as shown in Table 1, reveals that the sputtered atoms are not interacting equally with the different ILs. If an atom has a sufficient high energy for diffusion inside the IL, it can cluster together with other atoms forming nuclei, which need to overcome a critical nucleus radius to start the growth of CSSNPs. Thus, the composition of individual CSSNPs should be also related locally to the chemical environment and, hence, to the elements of the ILs surrounding the individual nuclei during earlier stages of the nucleation process.27
Furthermore, there are three main observations. First, we only observed up to 11 at% of Mn in the CSSNPs expect for IL 3. From this we can speculated that all the others ILs can act as a chemical barrier for Mn diffusion from the surface at the IL droplet/volume filling into the cavity interior. For the IL 3 the higher content of Mn can be due to the absence of fluorine groups.28 Second, Ni shows for IL 3 a composition of only 3 at% inside of the CSSNPs. This phenomenon can be due to the specific morphology and charge distribution of the IL 3, which is not favorable for Ni diffusion. Third, Fe has a low concentration <10 at% in IL 6. The main difference between IL 6 and IL 7 is in their ethyl group form base cation. Thus, it seems that a larger group is needed to allow Fe to enter inside the IL matrix.
The size and the crystal structure are affected by the type of the IL used. The sputtered atoms can diminish the hydrogen bonding network of the IL and lead to a difference in the electrostatic and van der Waals interaction. Furthermore, the Coulomb forces of ILs and the different interactions can lead to various growth mechanisms yielding different crystal structures and sizes, which could be related to the functional group of the IL.28
The comparison of ORR activity at a required overpotential to reach −0.5 a.u. on the normalized current scale is summarized in Table 2 and is correlated to composition, particle size and crystallinity. On a first glance it looks like that the group of the most active CSSNPs were obtained irrespective of their crystallinity as they possess a bcc, amorphous or fcc state. However, when comparing the ones with similar sizes (those synthesized with IL 6, IL7 and IL 4) we observe that the one with bcc structure (IL6) has a higher activity then the one in an amorphous state (IL7) and the one with a fcc structure. Thus, our results indicate that the crystalline structure does play, at least, a minor role. The NP size is known to affect the activity due to higher surface areas of smaller particles and different ratios of edge/corner active sites compared to regular lattice plane active sites.29 Due to normalizing the current, differences in surface area are already taken into account and the effect on activity would directly displayed by activity trends However, there is no pronounced trend visible, indicating a minor effect compared to the other NP properties.
Four samples show very high activity, namely CSSNPs prepared with IL 1, IL 6, IL 7, and IL 8 (Fig. 3). CSSNPs in IL 2 is following with a small, but clear shift of 120 mV and finally, three samples show a very low activity (CSSNPs in IL 3, IL 4 and IL 5). The different activities can be predominantly related to the different CSSNPs compositions which are determined by the used ILs. Three out of four samples with low activity contain one element with a content of only 1–2 at% (see Table 2), which might be below the threshold of still preserving a CSS phase. In the literature the minimum content in a CSS phase for all elements should be at least 5 at%.25 For the four active samples, each element is at least present with 5 at% and the NPs are assumed to possess a CSS structure.30 Thus, the fluorocarbon from the ILs can play an important role in generating more even content NPs since it was present in all ILs stabilizing the active class of NPs (IL 1, IL 2, IL 6 and IL 8). Comparing the different samples, the composition appears to be most important. This is in line with the current understanding that the presence of a complex solid solution and its constitution at the surface are responsible for the activity. To reach high activities, increased content of Cr and Co are required. The high activity differences showcase the importance of composition optimization for CSS catalysts.
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/d0nr07632e |
‡ Current address: Department of Chemistry, Kangwon National University, Chuncheon 24341, Republic of Korea. |
This journal is © The Royal Society of Chemistry 2020 |