Surface engineering of hierarchical platinum-cobalt nanowires for efficient electrocatalysis

Abstract

Despite intense research in past decades, the lack of high-performance catalysts for fuel cell reactions remains a challenge in realizing fuel cell technologies for transportation applications. Here we report a facile strategy for synthesizing hierarchical platinum-cobalt nanowires with high-index, platinum-rich facets and ordered intermetallic structure. These structural features enable unprecedented performance for the oxygen reduction and alcohol oxidation reactions. The specific/mass activities of the platinum-cobalt nanowires for oxygen reduction reaction are 39.6/33.7 times higher than commercial Pt/C catalyst, respectively. Density functional theory simulations reveal that the active threefold hollow sites on the platinum-rich high-index facets provide an additional factor in enhancing oxygen reduction reaction activities. The nanowires are stable in the electrochemical conditions and also thermally stable. This work may represent a key step towards scalable production of high-performance platinum-based nanowires for applications in catalysis and energy conversion.

ARTICLE

Received 21 Dec 2015 | Accepted 5 May 2016 | Published 29 Jun 2016

Lingzheng Bu1, Shaojun Guo2,3, Xu Zhang4, Xuan Shen5, Dong Su5, Gang Lu4, Xing Zhu6, Jianlin Yao1, Jun Guo6

& Xiaoqing Huang1

Despite intense research in past decades, the lack of high-performance catalysts for fuel cell reactions remains a challenge in realizing fuel cell technologies for transportation applications. Here we report a facile strategy for synthesizing hierarchical platinum-cobalt nanowires with high-index, platinum-rich facets and ordered intermetallic structure. These structural features enable unprecedented performance for the oxygen reduction and alcohol oxidation reactions. The specic/mass activities of the platinum-cobalt nanowires for oxygen reduction reaction are 39.6/33.7 times higher than commercial Pt/C catalyst, respectively. Density functional theory simulations reveal that the active threefold hollow sites on the platinum-rich high-index facets provide an additional factor in enhancing oxygen reduction reaction activities. The nanowires are stable in the electrochemical conditions and also thermally stable. This work may represent a key step towards scalable production of high-performance platinum-based nanowires for applications in catalysis and energy conversion.

DOI: 10.1038/ncomms11850 OPEN

Surface engineering of hierarchical platinum-cobalt nanowires for efcient electrocatalysis

1 College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu 215123, China. 2 Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing 100871, China. 3 Department of Energy and Resources Engineering, College of Engineering, Peking University, Beijing 100871, China. 4 Department of Physics and Astronomy, California State University, Northridge 91330, California, USA. 5 Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, USA. 6 Testing and Analysis Center, Soochow University, Jiangsu 215123, China. Correspondence and requests for materials should be addressed to S.-J.G. (email: mailto:[email protected]

Web End [email protected] ) or X.-Q.H. (email: mailto:[email protected]

Web End [email protected] )

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Fuel cells are highly desired devices for advanced portable electronic devices and electrical vehicles as they are promising candidates for providing a sustainable, clean

and efcient energy supply15. The fuel cell catalyses the reactions between a fuel (methanol, ethanol and molecular hydrogen) at the anode and molecular oxygen at the cathode, converting chemical energy into electrical power via the electrochemical process68. Catalysts are the central components of fuel cell technologies and largely dictate their ultimate performance. To date, Pt-based nanomaterials are recognized as the most effective electrocatalysts for both the anodic oxidation reaction and the cathodic oxygen reduction reaction (ORR) in the fuel cells911. Currently, the state-of-the-art electrocatalysts are almost exclusively small platinum (Pt) nanoparticles (NPs) supported on carbon black (Pt/C). However, the practical large-scale commercialization of fuel cells is still a challenge because of the high cost, poor reaction kinetics, loss of electrochemical surface area and catalytic activity over long-term duration of commercial Pt catalysts1216.

Precise control over material structures at the nanoscale allows for command over both surface structure and composition, thereby imparting enhanced and new functionality1720. In the search for high-performance electrocatalysts910,2124, one-dimensional (1D) Pt alloy nanostructures represent a promising direction for advanced catalysis because they possess multiple advantages, such as inherent anisotropic morphology, high exibility, high surface area and high conductivity, compared with their 0D counterparts, making them work more effectively for ORR activity and durability enhancement than traditional Pt alloy NPs25,26. This is because during the catalysis process, individual nanowires (NWs) can have a higher surface area interacting with carbon support than NPs, which not only enhances electron transfer between oxygen and the Pt surface, but also facilitates bonding between the NWs and the carbon support, rendering high stability. These advantages have stimulated explorations of new synthetic routes to create various Pt-M (M iron (Fe)-, cobalt (Co)-, nickel (Ni))-based NWs, but

unfortunately usually leading to conventional large-diameter PtM-based NWs with smooth surfaces (lacking the strong electron effect), which are, however, not benecial for creating more active sites for maximizing electrocatalytic performance, and ultrathin Pt-M NWs with limited durability because of their relatively small diameters27,28. Therefore, the biggest issue in using Pt-M NWs for ORR is that there is always a trade-off between activity and durability, making them impractical for fuel cell devices. In this regard, the creation of a new class of PtM NWs with improved utilization of Pt atoms for simultaneous high catalytic activity and durability is highly desirable but remains a signicant challenge.

Herein, we report the synthesis of a class of hierarchical Pt-Co NWs enclosed with high-density high-index facts through a robust large-scalable wet-chemical approach as electrocatalysts for fuel cell reactions. Unlike conventional Pt-M NWs, these hierarchical Pt-Co NWs with highly uneven surfaces are tailored to have an ordered intermetallic structure, high-index facets and a Pt-rich surface, which can meet several critical design criteria for efcient nanoelectrocatalysts29. They are fully functional for both high-performance anodic and cathodic fuel cell reactions, such as methanol oxidation reaction (MOR), ethanol oxidation reaction (EOR) and ORR that largely outperform those based on the commercial Pt/C catalyst. In particular, they deliver unprecedented ORR performance with the promising specic and mass activities of 7.12 mA cm 2 and 3.71 A mg 1Pt at0.9 V versus reversible hydrogen electrode (RHE), which are39.6 and 33.7 times higher than those of the state-of-the-art Pt/C catalyst (Johnson Matthey, 20 wt% Pt, 0.18 mA cm 2 and0.11 A mg 1Pt), making the hierarchical Pt-Co NWs the most

active electrocatalyst among the Pt-Co-based nanomaterials for ORR reported to date, to the best of our knowledge30. Moreover, the hierarchical Pt-Co NWs show superior cycling stability in the ORR condition with negligible activity decay over the course of 20,000 cycles and are also thermally stable with no morphology change after annealing up to 500 C. Their high thermal stability may provide a catalytic platform for high-temperature catalytic reactions, which is not easily achieved by particulate nanostructures because of their deformation or aggregation during the annealing treatment31,32. These hierarchical Pt-Co NWs enclosed with high-index facets enabled by our colloidal chemistry technique reported herein are promising catalyst candidates with unprecedented catalytic activity and stability for practical proton exchange membrane fuel cells.

ResultsSynthesis and characterization of hierarchical Pt-Co NWs. The wet-chemical approach to produce the hierarchical Pt-Co NWs involves the use of platinum(II) acetylacetonate (Pt(acac)2) and cobalt(III) acetylacetonate (Co(acac)3) as the metal precursors, oleylamine as solvent and surfactant, cetyltrimethylammonium chloride (CTAC) as the structure-directing agent, and glucose as a reducing agent. Briey, Pt(acac)2, Co(acac)3, oleylamine, glucose and CTAC in the controlled molar ratios were added into a 35-ml glass vial. After the glass vial had been capped, the mixture was fully ultrasonicated for around 1.5 h, heated from room temperature to 160 C in 0.5 h, then kept at 160 C for 8 h in an oil bath, and nally naturally cooled to room temperature (see the Methods section for details). The resulting black colloidal products were subjected to centrifugation and washed three times with ethanol/cyclohexane (v:v, 9:1) mixture. A variety of synthetic parameters, such as precursor, reducing agent and surfactant, were carried out for studying the optimal conditions for synthesizing well-dened Pt-Co NWs. The results show that the successful preparation of hierarchical Pt-Co NWs is highly controlled by the amount of CTAC, the select of Co(acac)3 and the use of glucose (Supplementary Figs 14).

Transmission electron microscopy (TEM) and high-angle annular dark-eld scanning TEM (HAADF-STEM) were used to characterize the morphology of the as-prepared hierarchical Pt-Co NWs. The TEM and STEM images show that the product consists of abundant nanostructure with 1D contour at the rst glance (Fig. 1 and Supplementary Fig. 5). The NWs were the dominant product with the typical yield over 90%. The length of the NWs is in the range of several micrometres and the average aspect ratio is B50. Strikingly, high-magnication HAADF-

STEM (inset in Fig. 1a) and TEM images (Fig. 1b) reveal that each NW has a highly uneven diameter along their entire length, exhibiting highly uneven and the crenel-like hierarchical nanostructure. The overall Pt/Co composition is quantitatively determined to be 74.8/25.2 (Pt3Co), measured by inductively coupled plasma atomic emission spectroscopy (ICP-AES) and TEM energy-dispersive X-ray spectroscopy (TEM-EDS; Fig. 1c). The surface molar ratio of Pt to Co obtained from X-ray photoelectron spectroscopy (XPS) is 95.2/4.8, much higher than that of overall Pt/Co composition, revealing the Pt-rich surface structure (Supplementary Fig. 6). The powder X-ray diffraction (PXRD) pattern of the hierarchical Pt-Co NWs (Fig. 1d) displays the distinct facet-centred cubic structure associated with the alloyed Pt3Co (Pt3Co, JCPDS No. 29-0499). The alloyed structure was also conrmed by the STEM-EDS elemental mapping analysis, where the distributions of Pt and Co are even through the whole NW, despite the hierarchical Pt3Co NWs having very uneven surfaces (Fig. 1e and Supplementary Fig. 7).

The hierarchical Pt3Co NWs are single crystalline, revealed by both selected-area electron diffraction and atomic resolution

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Figure 1 | Morphology and structure characterization of hierarchical Pt-Co nanowires. Representative (a) STEM image, (b) TEM image, (c) TEM-EDS, (d) PXRD pattern and (e) STEM-ADF image and EDS elemental mappings of the hierarchical Pt3Co NWs. Inset in a is an enlarged STEM image.

The composition is Pt/Co 74.8/25.2, as revealed by ICP-AES. The scale bars in a, inset of a, b and e are 200, 20, 10 and 10 nm, respectively.

HAADF-STEM measurements (Fig. 2a,b and Supplementary Fig. 7). To identify the unconventional NWs, a number of techniques was utilized to further analyse the structure of hierarchical Pt3Co NWs. Figure 2c is an atomic-resolution

HAADF-STEM image along the [001] zone axis. The local ordering is observed, corresponding to the L12-ordered inter-metallic structure of Pt3Co. The projected L12 unit cell is composed of a periodic square array of pure Co columns surrounded by Pt columns at the face centres and corners of each unit cell (Fig. 2g). As the contrast of HAADF-STEM image is proportional to the average atomic numbers of the columns (Z-contrast),33 the Pt columns have higher brightness than that of the Co columns in Fig. 2df. This is different from the homogeneous alloyed phase, which has all columns with equal intensity and without the super periodicity. From the structural perspective, the ordered phases with denite composition and structure can provide the predictable control over structural, geometric and electronic effects for catalysis optimization, which cannot be afforded by the widely created conventional alloys.30 In order to identify the crystal indices of the at planes in the

hierarchical Pt3Co NWs, we applied a HAADF-STEM electron tomography technique to visualize the three-dimensional (3D) structure of the hierarchical Pt3Co NWs. The HAADF-STEM images were acquired from 65o to 65o with the intervals of 1o.

Figure 2hj and the inset show the 3D reconstructed tomograms of an individual hierarchical Pt3Co NW at 60o, 0o and 60o and

corresponding HAADF-STEM images. Combined the results from electron tomography with those from the atomic resolution HAADF-STEM image shown in Fig. 2k, we found the [001] plane of the NWs aligns very close to the grid plane. Furthermore, by analysis of the cross-sectional structure along o1014 direction of Pt3Co NWs, we could deduce the indexes of the at planes as [310] and [110] (Fig. 2l). As the hierarchical Pt3Co

NWs contain many uneven surfaces, high-density [310], high-index facets will be introduced onto individual NWs, which is the key to achieve high electrocatalyic activity.

Growth mechanism. The ability to make hierarchical Pt3Co NWs with unconventional surface structures is the most striking

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Figure 2 | Structure analysis of hierarchical Pt-Co nanowires. (a) TEM image of an individual hierarchical Pt3Co NW. The inset shows the corresponding selected-area electron diffraction pattern. (b,c) Atomic-resolution HAADF-STEM images of Pt3Co NWs along [001] zone axis. The inset in (c) shows the corresponding Fast Fourier Transform (FFT) pattern. (d,e)The enlarged HAADF-STEM images from the region with L12-ordered intermetallic structure.

(f) FFT-ltered HAADF-STEM image from the same area of e. (g) Schematic diagram of the L12-ordered intermetallic structure of Pt3Co. (hj) A series of reconstructed 3D tomograms at viewing angles of 60o (h), 0o (i) and 60o (j), the as-acquired HAADF-STEM images are shown in the insets. (k) An

atomic resolution HAADF-STEM image at the viewing angles of 0o, and (l) indexes of the at planes of the Pt3Co NWs. The scale bars in ac, hk are 100, 2, 1, 10, 10, 10 and 2 nm, respectively.

feature of our approach. 1D Pt-M nanostructures with such features have not been achieved previously, to the best of our knowledge. To understand their growth mechanism, the intermediates collected at different growth durations were carefully investigated (Fig. 3ah). The TEM results show that ultrathin NWs were already formed at the early stage of the synthesis (30 min, Fig. 3a). These ultrathin NWs are of essentially pure Pt nanomaterials, as revealed by the PXRD and energy dispersive X-ray spectroscopy analyses (Fig. 3e,f). The diameter of ultrathin NWs is measured to be around 2 nm. As the reaction time was prolonged to 1 h, the surface of the NWs became more uneven (Fig. 3b), along with the average diameter increased from 2 to 5 nm. 8.9% Co was detected in the NWs of 5 nm (Fig. 3f). Together with the increase of the diameter in the NWs, further increase in the Co content and the presence of obvious humps in the intermediates were observed after 3.0 h (Fig. 3c,f). When the reaction time was 5.0 h, typical hierarchical PtCo NWs were obtained (Fig. 3d) with the Pt/Co ratio of about 3/1 (Fig. 3f). When the reaction time was increased to 8 h, there was no

signicant change in the diameter and morphology of NWs (Fig. 3g,h). These time-dependent structure and composition changes reveal that the formation of such hierarchical Pt3Co NWs relies upon the initial formation of ultrathin Pt NWs, the reduction of Co species onto the preformed NWs, and hereafter the inter-diffusion to form alloyed Pt3Co NWs (Fig. 3e,f). As time goes on, the diffraction peaks shift towards higher 2y values with the increase of Co content (Fig. 3e). During the reaction time from 1.0 to 3.0 h, both the peak positions in the PXRD patterns and the structure of the NWs in unevenness change obviously. High-resolution TEM (HRTEM) and elemental mappings of the hierarchical Pt-Co NW intermediates at different growth times were also carried out. As shown in the HRTEM images (Supplementary Fig. 8), as the reaction proceeds, the humps on the surface of the preformed Pt NWs gradually evolve. As revealed by the HAADF-STEM elemental mappings, the Pt and Co distributions of each hierarchical Pt-Co NW intermediates are even throughout the whole growth process, despite the contents of Co increase as the reaction time prolonged

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Figure 3 | Growth mechanism and structural tuning. Typical TEM images of hierarchical Pt3Co NWs intermediates collected from (a) 0.5, (b) 1, (c) 3 and (d) 5 h. (e) PXRD patterns of hierarchical Pt3Co NWs intermediates collected from the reactions at different reaction times. (f) The composition ratio changes of Co to Pt for the hierarchical Pt3Co NWs intermediates, as determined by ICP-AES measurements. Typical TEM images and HAADF-STEM images of (gh) hierarchical Pt3Co NWs, (i,j) hierarchical Pt7Co NWs and (k,l) hierarchical Pt10Co NWs collected from 8 h reactions. The scale bars in ad, g, i and k are 20 nm. The scale bars in h,j and l are 100 nm.

(Supplementary Fig. 9). As the presence of very clear humps is coincident with the large increase of Co content in the Pt3Co

NWs, we infer that the different reduction potentials and diffusions of Pt and Co should be the major driving force for the creation of such hierarchical NWs in the present condition, being consistent with the synthesis of the unconventional silicon NWs with periodic shell, where the diffusion of silicon adatoms is believed to be the most signicant kinetic factor in controlling the growth of periodic shell.34

These TEM and composition studies as a function of reaction time indicate that the amount of Co(acac)3 introduced can signicantly affect the growth of the hierarchical Pt-Co NWs. As shown in Supplementary Fig. 4a,b, the conventional NWs rather than hierarchical ones were obtained when the synthesis was carried out in the absence of Co(acac)3, whereas the introduction of Co(acac)3 could greatly impact the growth of NWs (Fig. 3il). If the amount of Co(acac)3 was reduced from 9.0 to 3.0 and1.5 mg, the diameter of the obtained hierarchical Pt-Co NWs changed from 12 to 18 and 21 nm, associated with the reduced density of bumps (Fig. 3il and Supplementary Figs 1016). When the amount of Co(acac)3 was increased to 12.0 mg, the diameter and structure of hierarchical Pt-Co NWs were almost unchanged (Supplementary Fig. 4c,d). The hierarchical Pt-Co

NWs were yielded once Co(acac)3 was fed, although the hierarchical feature was highly depended on the amount of Co(acac)3 introduced. These results might be caused by the amount of Co(acac)3, which could dictate the reduction/diffusion behaviour of Co during the growth, and thus control the hierarchical degree of the Pt-Co NWs.34

MOR and EOR performance. The hierarchical Pt-Co NWs were loaded on a commercial carbon (C, Vulcan) support by simply sonicating the Pt-Co NWs and C in cyclohexane, then washed with an ethanol/cyclohexane mixture and an ethanol/acetic acid mixture. Through such treatments, the hierarchical Pt-Co NWs were uniformly deposited onto carbon support with slightly composition changes from Pt74.8Co25.2 to Pt75.5Co24.5,

while retaining their original nanostructures (Fig. 4a and Supplementary Figs 17 and 18). The limited loss of the Co was mainly caused by the formation of Pt-rich surface after this treatment, as conrmed by XPS characterization (Supplementary Fig. 19). Once the Pt-rich surface is present as a thin shell in a core/shell structure, both its activity and durability can be greatly enhanced as a result of the simultaneous downshift of its d-band centre and surface strain induced in the Pt surface25,27.

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Figure 4 | Alcohol electro-oxidation performance comparison. (a) Representative TEM image and (b) CVs of different catalysts in 0.1 M HClO4 solution. (c) CVs and (d) histogram of mass and specic activities of different catalysts for MOR in 0.1 M HClO4 0.2 M methanol solution. (e) CVs and

(f) histogram of mass and specic activities of different catalysts for EOR in 0.1 M HClO4 0.2 M ethanol solution. The scale bar in a is 20 nm.

The resulting hierarchical Pt-Co NWs catalysts (Pt-Co NWs/C) were initially evaluated as anodic oxidation electrocatalysts for both MOR and EOR. To this end, three hierarchical PtCo NWs/C with distinct compositions, namely Pt3Co NWs/C (Supplementary

Figs 57 and 17), Pt7Co NWs/C (Supplementary Figs 1113 and17) and Pt10Co NWs/C (Supplementary Figs 1416 and 17), were selected, and benchmarked against commercial Pt/C from JM (Pt/C, 20 wt% Pt on Vulcan XC72R carbon, Pt particle size: 25 nm, Supplementary Fig. 20). The catalysts were dispersed in a mixture of isopropanol/water/Naon, and then drop onto glassy carbon electrode. The loading amount of Pt was kept to be 1.25 mg for all the catalysts. The cyclic voltammograms (CVs) of different electrocatalysts in N2-purged 0.1 M perchloric acid solution at a sweep rate of 50 mV s 1 are shown in Fig. 4b. The current responses from hydrogen adsorption/desorption processes appear in the potential range of 0.050.35 V. The electrochemically active

surface areas (ECSAs) of Pt3Co NWs/C, Pt7Co NWs/C, Pt10Co NWs/C, Pt3Co NPs/C and Pt/C catalysts were calculated to be52.1, 42.3, 25.8, 38.7 and 58.8 m2 g 1, respectively. Among all the Pt-Co NWs/C catalysts, the Pt3Co NWs/C catalysts display the highest ECSA of 52.1 m2 g 1 because of the most high-density dendritic structure, comparable to that of the commercial Pt/C(58.8 m2 g 1) catalyst.

The MOR measurements were carried out in 0.1 M

HClO4 0.1 M CH3OH solutions at a sweep rate of 50 mV s 1.

Figure 4c compares the CVs of three different Pt-Co NWs/C and commercial Pt/C for methanol electrooxidation. The mass and specic activities of all the catalysts are presented in Fig. 4d, in which the Pt3Co NWs/C shows the highest mass activity and specic activity. The peak current densities in the forward (positive) potential scan were 1.95, 1.53, 0.90 and 0.44 mA cm 2 on the Pt3Co NWs/C, Pt7Co NWs/C, Pt10Co NWs/C and Pt/C

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catalyst, respectively. The maximum mass activity of Pt3Co

NWs/C is measured to be 1.02 A mg 1Pt, which is 1.59, 4.43 and4.08 times higher than those of the Pt7Co NWs/C, Pt10Co NWs/C and Pt/C catalysts, respectively (Fig. 4d). We also evaluated the electrocatalytic activities of the Pt-Co NWs/C catalysts for EOR. As expected, all the Pt-Co NWs/C catalysts exhibit excellent electrocatalytic activity towards EOR (Fig. 4e), in which Pt3Co

NWs/C has the highest activities by displaying excellent specic activity of 1.55 mA cm 2 and high mass activity of 0.81 A mg 1

Pt, which are 3.78 and 3.37 times higher than those of commercial Pt/C, respectively (Fig. 4f), and higher than those of a home-made Pt3Co NPs/C (Supplementary Figs 21 and 22 and Supplementary

Tables 1 and 2).

ORR performance. With their unique structural features, the Pt-Co NWs/C catalysts were further evaluated as cathodic electrocatalysts for ORR. Figure 5a shows the ORR polarization curves of the different catalysts recorded at room temperature in an O2-saturated 0.1 M HClO4 solution. The kinetic currents at0.9 V versus RHE were normalized to ECSA and the mass loading of Pt to obtain the specic and mass activities, respectively. Among three kinds of Pt-Co NWs/C investigated, Pt3Co NWs/C has the highest specic activity of 7.12 mA cm 2 at 0.9 V versus

RHE (Fig. 5b) with an impressive improvement factor of 39.6 over commercial Pt/C catalyst. Its mass activity reaches to3.71 A mg 1Pt, 33.7-fold higher than that of commercial Pt/C catalyst. Although the Pt3Co NPs/C catalyst has the same composition with the Pt3Co NWs/C catalyst, the ORR activities of the Pt3Co NPs/C catalyst are much lower than the Pt3Co NWs/C catalyst (Fig. 5 and Supplementary Fig. 22), further displaying the super-high performance for ORR of the Pt3Co NWs/C catalyst (Supplementary Table 3). Those results make the Pt3Co NWs/C the most efcient catalyst ever achieved in the Pt-Co-based ORR catalysts to date to the best of our knowledge30, whose specic and mass activities are higher than those of the recent Pt-based nanocatalysts.3538

The hierarchical Pt-Co NWs/C catalyst also shows superior electrochemical stability, accessed by using an accelerated durability test between 0.6 and 1.1 V (versus RHE) in 0.1 M HClO4 at a scan rate of 100 mV s 1. Figure 5c,d shows the ORR polarization curves of the hierarchical Pt3Co NWs/C catalyst before and after 10,000, 15,000 and 20,000 potential cycles. After 20,000 potential cycles, the activity of the hierarchical Pt3Co

NWs/C catalyst is still as high as 3.41 A mg 1Pt (91.9% of the initial value), which is 31-fold higher than that of the commercial

Pt/C catalyst. The morphology and composition of hierarchical Pt3Co NWs/C catalyst after 20,000 electrochemical cycles was thoroughly studied (Fig. 5g,h and Supplementary Figs 23 and 24), showing there is no morphology (Fig. 5g and Supplementary Figs 23 and 24), alloyed structure (Fig. 5h and Supplementary Fig. 24) and composition changes (Supplementary Fig. 23) on the hierarchical Pt-Co NWs after 20,000 potential cycles. For a comparison, only B60% of initial activity could be retained (Fig. 5e,f), and serious NP aggregation was observed for the commercial Pt/C catalyst after the identical durability tests (Supplementary Fig. 20c,d). All these data indicate that hierarchical Pt-Co NWs are stable for ORR in strong acid solution.

Theoretical investigation. To shed light on the high-ORR performance on the hierarchical PtCo NWs, we performed density functional theory (DFT) calculations for the oxygen adsorption energy (EO) on the same high-index NW facets as observed in the HAADF-STEM measurements. EO is widely used as a descriptor for ORR activities, and there exists an optimal value of Eo, for which the ORR activity reaches the

maximum39,40. For convenience, this optimal EO was shift to 0 eV, thus DEO represented the difference of a given EO value relative to this optimal reference. It is known that the surface Co atoms in the PtCo NWs could dissolve under the electrochemical conditions, and be etched away, leading to core/shell-like structures with pure Pt as the shell. For such core/shell structures, in general, both surface strain and ligand effect could inuence their catalytic activities, which are the subject of our rst-principles simulations. Two typical adsorption sites, a bridge site at the edge of the NW and a hollow site on the facet of the NW, were examined on three surfaces, including [110], [310] and (2 1) missing-row reconstructed (MRR)-[310]. To examine

the ligand effect on each of the three surfaces, we compared the pure Pt surface and the Pt3Co alloy surface with the top-layer Co atoms completely etched away (Pt3Co/Pt). To examine the strain effect, we calculated DEO as a function of a compressive strain, ranging from 0 to 3%. The results of DEO are shown in Fig. 6a,b and Supplementary Fig. 25. Moreover, we also calculated DEO on

the [111] facet of Pt NPs with the particle diameter ranging from 3 to 8 nm using a combined quantum mechanics-molecular mechanics method,41,42 and the results are shown in Fig. 6c. First, we found that the threefold hollow sites on both [110] and MRR-[310] surfaces were highly active for ORR. Their DEO values were much closer to zero than that of Pt NPs, suggesting that the threefold hollow sites on the NWs could offer superior ORR activities to the Pt NPs. This similar enhancement in ORR activities has also been observed on the threefold hollow sites of high-index [211] surfaces calculated by Norskov et al.43 Hence, the additionally enhanced ORR activities in our Pt3Co NWs can be attributed to the threefold hollow sites on the high-index facets. Second, DEO was found to increase linearly as a function of the compressive strain on both [110] and MRR-[310] surfaces, as shown in Fig. 6a,b. The compressive strain could relieve the over-binding of oxygen to the surfaces, thus enhance the ORR activities. In contrast, the ligand effect was negligible as the DEO values on the pure Pt and the Pt3Co/Pt surfaces were almost the same. Therefore, the further improved ORR activities on the high-index faceted PtCo NWs stem from: (i) the active threefold hollow sites and (ii) the compressive strain on the Pt surface owing to the smaller atomic size of Co.

Anti-aggregation properties. Another signicant feature of the hierarchical Pt-Co NWs is that they can exhibit excellent anti-aggregation properties upon the high-temperature annealing treatment. As shown in Supplementary Fig. 26, the hierarchical Pt3Co NWs can be thermally stable up to 500 C, as the 1D hierarchical structure was largely maintained after they were annealed at 500 C for 1 h in N2 atmosphere. The high thermal stability of the hierarchical Pt3Co NWs is benecial for the design of catalytic systems for high-temperature reactions or chemical processes, which is not easily achieved by the particulate Pt nanocrystals because of their poor anti-deformation ability.

DiscussionTo summarize, we demonstrate a large-scalable, wet-chemical approach to synthesize a class of Pt-Co NWs consisting of large-density high-index facets and Pt-rich surfaces. These features enable them to exhibit impressive activity and durability towards both the alcohol oxidations and ORR, to satisfy requirements for efcient electrocatalytic applications. They show high specic and mass activities for both MOR and EOR, largely outperforming those based on the commercial Pt/C catalyst. For the cathodic ORR, they can deliver unprecedented activities that are higher than the best Pt-Co-based catalysts for ORR, representing the highest activities ever achieved in the

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a

b

Pt/C (JM)

Pt7Co/C

Pt10Co/C

Pt3Co/C

10

12

0.3

0.2

0.1

0.0

Pt/C (JM)

Pt7Co/C

5 4 3 2 1 0

Pt10Co/C

Pt3Co/C

J(mA cm2 )

J(mA cm2 )

J(mA cm2 )

0 1 2 3 4 5 6

8 6 4 2 0

J(mA cm2 )

J(mA cm2 )

J(mA cm2 )

Mass activity Specific activity

0.4 0.6 0.8 1.0

Potential (V; RHE)

J(A mg1 ) Pt

J(A mg1 ) Pt

J(A mg1 ) Pt

c d

Pt3Co/C

0 1 2 3 4 5 6

0 1 2 3 4 5 6

Pt3Co/C Initial

After 15 k cycles

InitialAfter 15 k cycles

After 10 k cycles After 20 k cycles

6

4

After 10 k cycles After 20 k cycles

InitialAfter 15 k cycles

9

6

3

0

2

0.4 0.6 0.8 1.0

Potential (V; RHE)

0 Mass activity Specific activity

e

f

0.2

0.1

0.0

Pt/C (JM)

Pt/C (JM)

0.4 0.6 0.8 1.0

Potential (V; RHE)

InitialAfter 15 k cycles

After 10 k cycles After 20 k cycles

After 10 k cycles

After 20 k cycles

Mass activity Specific activity

g h

Pt Pt

+

Co

Co

Figure 5 | ORR performance comparison. (a) ORR polarization curves and (b) ORR-specic activities and mass activities of different catalysts.

The ORR polarization curves were recorded at room temperature in an O2-saturated 0.1 M HClO4 aqueous solution at a sweep rate of 10 mVs 1 and a rotation rate of 1,600 r.p.m. (c) ORR polarization curves of the hierarchical Pt3Co NWs/C catalyst before and after 10,000, 15,000 and 20,000 potential cycles between 0.6 and 1.1 V versus RHE. (d) The changes on specic activities and mass activities of the hierarchical Pt3Co NWs/C catalyst before and after 10,000, 15,000 and 20,000 potential cycles. (e) ORR polarization curves of the commercial Pt/C catalyst before and after 10,000, 15,000 and 20,000 potential cycles between 0.6 and 1.1 V versus RHE. (f) The changes on specic activities and mass activities of the commercial Pt/C catalyst before and after 10,000, 15,000 and 20,000 potential cycles. The durability tests were carried out at room temperature in 0.1 M HClO4 at a scan rate of100 mVs 1. (g) HAADF-STEM image and (h) elemental mappings of the hierarchical Pt3Co NWs/C after 20,000 cycles. The scale bars in g and h are 50 and 10 nm, respectively. The elemental mapping in h comes from the red-dotted line-marked area in g.

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NATURE COMMUNICATIONS | DOI: 10.1038/ncomms11850 ARTICLE

Top view Side view

310

a

111

Pt Co O

Pt PtCo

b

E o(eV)

0.20.0 0.2 0.40.20.0 0.2 0.4

0 1 2 3

Strain (%)

c

+ +

+

+

+

+

E o(eV)

0.20.0 0.2 0.4

3 5 7

+++ +++

Pt PtCo

d (nm)

Figure 6 | DFT calculations of oxygen adsorption energy. (a) Atomistic model of [110] surface and DEO as a function of compressive strain. (b) Atomistic model of the MRR-[310] surface and DEO as a function of compressive strain. Blue cross represents the missing atomic row on the top layer of [310]

surface. The black and red curves correspond to DEO values on the pure Pt and Pt3Co/Pt surface. (c) DEO on [111] facet of the Pt NPs as a function of the particle size. The NP was modelled by an icosahedron with 20 [111] facets. The horizontal dashed line indicates the optimal DEO value.

Pt-Co-based ORR catalysts, to the best of our knowledge. DFT studies indicate that the high ORR activities on the PtCo NWs mainly originate from the hollow sites on the [110] and [310] high-index facets of NWs. Most signicantly, without sacricing the ORR activities, they show good stability for ORR over the long-term course of 20,000 cycles. Therefore, our nding may open up opportunities for the rational design of practically relevant catalysts with excellent activity and superior durability, which could impact broad areas such as ne chemical productions, fuel cells, batteries and beyond.

Methods

Preparation of hierarchical Pt3Co NWs. In a typical preparation of hierarchical Pt3Co NWs, platinum(II) acetylacetonate (Pt(acac)2, 10 mg), cobalt (III) acetylacetonate (Co(acac)3, 9.0 mg), CTAC (32.0 mg), glucose (60.0 mg) and 5 ml oleylamine were added into a vial (volume: 35 ml). After the vial had been capped, the mixture was ultrasonicated for 90 min. The resulting homogeneous dark green mixture was then heated from room temperature to 160 C in30 min and maintained at 160 C for 8 h in an oil bath, before it was cooled to room temperature. The resulting colloidal products were collected by centrifugation and washed three times with an ethanol/cyclohexane mixture. The synthesis conditions for hierarchical Pt7Co and Pt10Co NWs were similar to that of hierarchical Pt3Co NWs except changing the amount of Co(acac)3 to 3.0 and1.5 mg, respectively.

Characterization. PXRD patterns were collected using an XPert-Pro X-ray powder diffractometer equipped with a Cu radiation source (l 0.15406 nm). The

morphology and size of the NWs were determined by TEM (Hitachi, HT7700) at 120 kV. Selected-area electron diffraction, HRTEM, HAADF-STEM and the 3D visualization of tomographic reconstruction tests were conducted on a JEOL-2100F transmission electron microscope at an acceleration voltage of 200 kV. High-resolution STEM imaging and elemental mapping analysis were carried out on a Hitachi HD2700C (200 kV) STEM with a probe aberration corrector, at the Center for Functional Nanomaterials, Brookhaven National Lab. Low-resolution energy dispersive X-ray spectroscopy was performed on a scanning electron microscope (Hitachi, S-4700). All the XPS spectra of the hierarchical Pt-Co NWs were collected by XPS (Thermo Scientic, ESCALAB 250 XI). The concentration of all the catalysts was determined by the ICP-AES (710-ES, Varian). The catalysts after the stability tests were collected and scratched off the electrode with the aid of sonication in ethanol for further TEM characterization.

Electrochemical measurements. The catalysts were redispersed in a mixture solvent containing isopropanol and Naon (5%; v-v 1:0.005) to form a

homogeneous catalyst ink by sonicating for 30 min. The concentration of Pt was xed to be 0.25 mg ml 1 based on ICP-AES measurement. Five microlitres of the dispersion was transferred onto the GC electrode. The Pt/C catalyst (20 wt%,

25 nm Pt NPs on Vulcan XC-72 carbon support, JM), was prepared by sonicating its ink in an aqueous dispersion (1.25 mg ml 1). Five microlitres of the dispersion was transferred onto the GC electrode with the loading amount of metal at 1.25 mg.

A CHI660E electrochemical analyzer (CHI Instruments) was used for testing the MOR and EOR of different catalysts. The MOR and EOR measurements were carried out in 0.1 M HClO4 0.2 M methanol and 0.1 M HClO4 0.2 M ethanol at

room temperature, respectively. The CV technique and conventional three-electrode system were applied to evaluate the electrochemical properties of various catalysts. A leak-free saturated calomel electrode was used as the reference electrode and a Pt wire was used as the counter electrode. The ECSA was determined by integrating the hydrogen adsorption charge on the CVs at the rate of 50 mV s 1 at room temperature in N2-saturated 0.1 M HClO4 solution. In the

CV measurements for MOR and EOR, the electrode potential was scanned at a rate of 50 mV s 1. All the catalyst electrodes were cleaned before data collection with a steady-state CV. The current was normalized to Pt amount and ECSA to get mass and specic activities, respectively.

The electrochemical measurements for ORR were performed using a glassy-carbon Rotating Disk Electrode (Pine Research Instrumentation, diameter: 5 mm, area: 0.196 cm2) connected to an installation of rotating electrode speed control (Pine Research Instrumentation, model: AFMSRCE). A leak-free saturated calomel electrode was used as the reference electrode and a Pt wire was used as the counter electrode. The electrolyte was 0.1 M HClO4. The loading amount of Pt for the hierarchical Pt10Co NWs/C, Pt7Co NWs/C, Pt3Co NWs/C, Pt3Co NPs/C and the commercial Pt/C (JM) catalysts was all kept at 6.4 mg cm 2. ORR measurements were conducted in 0.1 M HClO4 solutions purged with the saturated O2 during the measurements. The scan and rotation rates for ORR measurements were10 mV s 1 and 1,600 r.p.m., respectively. In the ORR polarization curves, the current densities were normalized in reference to the geometric area of the glassy carbon electrode (0.196 cm2). For each catalyst, the kinetic current was normalized to the loading amount of Pt and ECSA in order to generate mass and specic activities, respectively. The accelerated durability tests were performed at room temperature in 0.1 M HClO4 solutions by applying the cyclic potential sweeps between 0.6 and 1.1 V versus RHE at a sweep rate of 100 mV s 1 for 20,000 cycles.

DFT calculations. The oxygen adsorption energy EO was dened as

EO E[surf O] E[surf] E[O2]/2, where E[surf O] and E[surf] are the total

energies of the [110] or [310] surface with and without the O adsorbate, respectively. E[O2] is the total energy of an oxygen molecule. A four-layer slab was used in the calculations. The atoms in the top two layers were fully relaxed while the rest of the atoms were xed in their equilibrium positions. The DFT calculations were carried out using the VASP package44,45 with the projector augmented wave pseudopotentials46 and PerdewBurkeErnzerh of generalized gradient approximation.47 An energy cutoff of 400 eV was used for the plane-wave basis set. The Brillouin zone was sampled on the basis of the MonkhorstPack scheme48 with a 7 5 1 k-point mesh. The force convergence criterion for atomic

relaxation was 0.02 eV 1.

Data availability. All relevant data are available from the authors on request.

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Acknowledgements

This work was nancially supported by the start-up supports from the Soochow

University and Peking University, Young Thousand Talented Program, the National

Natural Science Foundation of China (21571135), the National Basic Research Program

of China (Battery) and the Priority Academic Program Development of Jiangsu Higher

Education Institutions (PAPD). The work at California State University Northridge was

supported by the US Army Research Ofce via the MURI grant W911NF-11-1-0353.

TEM work carried out in part at the Center for Functional Nanomaterials, Brookhaven

National Laboratory, which is supported by the US Department of Energy, Ofce of Basic

Energy Sciences, under Contract No. DE-SC0012704.

Author contributions

X.H. and S.G. conceived and supervised the research. X.H., S.G. and L.B. designed the

experiments. X.H., S.G., L.B., X.S., D.S., X.Z. and J.G. performed most of the experiments

and data analysis. X.H., S.G., L.B., X.Z., D.S., J.Y. and J.G. participated in various aspects

of the experiments and discussions. X.Z. and G.L. performed the DFT simulations. X.H.,

S.G. and L.B. wrote the paper. All authors discussed the results and commented on the

manuscript.

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