Covalent triazine frameworks, which are crosslinked porous polymers with two-dimensional molecular structures, are promising materials for heterogeneous catalysts. However, the application of the frameworks as electrocatalysts has not been achieved to date because of their poor electrical conductivity. Here we report that platinum-modified covalent triazine frameworks hybridized with conductive carbon nanoparticles are successfully synthesized by introducing carbon nanoparticles during the polymerization process of covalent triazine frameworks. The resulting materials exhibit clear electrocatalytic activity for oxygen reduction reactions in acidic solutions. More interestingly, the platinum-modified covalent triazine frameworks show almost no activity for methanol oxidation, in contrast to commercial carbon-supported platinum. Thus, platinum-modified covalent triazine frameworks hybridized with carbon nanoparticles exhibit selective activity for oxygen reduction reactions even in the presence of high concentrations of methanol, which indicates potential utility as a cathode catalyst in direct methanol fuel cells.
Covalent organic frameworks (COFs) have attracted a keen attention as novel catalyst platforms1,2,3,4,5,6 because of their unique physicochemical properties, including their nano-porous structure, mechanical robustness and high design flexibility. For example, Ding et al.7 reported that a palladium-modified imine-linked COF catalysed Suzuki–Miyaura coupling reactions with a high stability and an easy recyclability7. Chan-Thaw et al. deposited palladium nanoparticles on covalent triazine frameworks (CTFs) and demonstrated that this material was an effective catalyst for liquid-phase glycerol oxidation8. Another interesting example of a COF-based catalyst is platinum-modified CTF (Pt-CTF) developed by Palkovits et al.9,10, which has been known to function as a heterogeneous (solid) catalyst for partial oxidation of methane (CH4) to methylbisulfate (CH3OSO3H) in H2SO4 using oleum as an oxidant The Pt-CTF was developed by being inspired by Pt-bipyrimidine complex, known as a Periana catalyst, which could catalyse the same partial oxidation reaction11,12. Thus, the work carried out by Palkovits et al. is important in that they developed the concept of molecular complex catalysts to the robust heterogeneous Pt-CTF materials.
Pt-CTFs are attractive also as heterogeneous electrocatalysts, since molecular Pt complexes with a single metal centre is known to exhibit reaction selectivity in some homogeneous redox reactions, such as alkane oxidation13,14 and carbon dioxide reduction reactions15. Considering that molecular complex-based electrocatalysts are generally unstable, it is expected that Pt-CTFs can serve as electrocatalysts with both unique selectivity and high robustness. However, CTF-based materials have not previously been applied as electrocatalysts because of their poor electrical conductivity16. In the present work, we demonstrate a solution to this problem by synthesizing a hybrid material consisting of Pt-CTF and conductive carbon nanoparticles (CPs). The hybridized material (Pt-CTF/CP) exhibits electrocatalytic activity for oxygen reduction reaction (ORR) in acidic solution with a high methanol tolerance, which is a very attractive property for direct methanol fuel cells (DMFCs) as the methanol-crossover effect is one of the issues to be addressed17,18,19,20,21. To the best of our knowledge, this is the first demonstration of the potential for CTF-based materials to serve as electrocatalysts.
Morphological characterization of the Pt-CTF/CP
Pt-CTF/CP was synthesized by modifying the standard synthesis protocol of Pt-CTF9,10,22,23. Briefly, CTFs were obtained by in situ polymerization of 2,6-dicyanopyridinein-molten ZnCl2 containing CPs (the weight ratio of 2,6-dicyanopyridine to CP was 1: 1), after which the CTF/CP was impregnated with a platinum chloride salt to obtain Pt-CTF/CP. Scanning electron microscopic (SEM) inspection reveals that the particles of Pt-CTF/CP (20–200 nm, Fig. 1a) are much smaller than that of Pt-CTF polymerized without CPs (1–5 μm, Fig. 1b), suggesting that CTF is well mixed with CPs during the in situ polymerization. Then, we conducted high-resolution transmission electron microscopy (Fig. 1c) and the corresponding high-angle annular dark-field scanning transmission electron microscopy (Fig. 1d), the latter of which is a powerful tool for discerning individual heavy atoms24,25,26. It was confirmed that the bright spots corresponding to Pt atoms (the sizes <0.5 nm) were uniformly dispersed and almost no Pt nanoparticles (the sizes >1 nm) were observed (Fig. 1d). Such bright spots could not be observed on the CPs (without Pt-CTF) as shown in Supplementary Fig. 1. Figure 1e exhibits another high-resolution transmission electron microscopy image and the corresponding elemental maps (carbon, nitrogen and platinum) obtained by energy dispersive X-ray (EDX) technique. Notably, the EDX maps revealed that Pt and N atoms are localized at the edges of CPs, strongly suggesting that CPs (or the aggregates) are covered with Pt-CTF as schematically shown in Fig. 1f.
Next, the nitrogen adsorption–desorption isotherms were obtained to analyse the pore structure of Pt-CTF/CP (Supplementary Fig. 2). Type IV isotherm and H2 hysteresis loop were observed, suggesting that porous structures existed in the synthesized Pt-CTF/CP27,28. The pore-size distribution calculated based on nonlocal density functional theory was shown in the inset of Supplementary Fig. 2. Although CP (Ketchenblack) is known to exhibit a peak at 3.6–3.7 nm (refs 29, 30), the synthesized Pt-CTF/CP exhibited peaks at 1.4 and 5.3 nm. The total pore volume and the BET surface area were estimated to be 0.79 cm3g−1 and 555 m2g−1, respectively.
Electrochemical characterizations of Pt-CTF/CP
Figure 2 shows current density (j) versus potential (U) curves for Pt-CTF/CP obtained in an oxygen-saturated 0.5 M H2SO4 solution. Although the ORR activity of Pt-CTF (without CP) was very low (blue curve), the ORR current increased significantly upon hybridization of Pt-CTF with CPs (red curve). This enhancement in ORR activity can be explained on the basis that both the electric conductivity and the electrochemically active surface area of the material were increased by the hybridization with CPs (Fig. 1a,b and Supplementary Table 1). In contrast, when the CTFs (without Pt) were hybridized with CPs (green curve), the ORR onset potential was much negative than that of Pt-CTF/CP, indicating that the Pt atoms in Pt-CTF/CP are an active centre for ORR. To the best of our knowledge, this is the first demonstration of the application of a CTF-based material as an electrocatalyst.
Next, to investigate the methanol tolerance of Pt-CTF/CP, we intentionally added methanol to a 0.5-M H2SO4 solution in the presence of oxygen. Cyclic voltammograms obtained in the presence of methanol are shown in Fig. 3. In case of a commercial 20 wt% Pt/C, the oxidation peak of methanol can be clearly observed at around +600 mV versus RHE (Fig. 3b). After the addition of 1 M methanol, the onset potential of the cathodic current shifted ~200 mV in the negative direction, reaching 580 mV versus RHE. In contrast, surprisingly, the overlap of the methanol oxidation current with that of the ORR was almost negligible for Pt-CTF/CP even in the presence of 1 M methanol. To directly compare the methanol oxidation activity of Pt-CTF/CP and 20 wt% Pt/C, we obtained cyclic voltammograms in H2SO4 solution containing methanol in the absence of dissolved oxygen (Fig. 4). The peak currents for methanol oxidation with Pt-CTF/CP (Fig. 4a) were ~1/40 compared with those with Pt/C (Fig. 4b). We confirmed that methanol oxidation is inactive even in 0.5 M HClO4 as shown in Supplementary Fig. 3, which excludes the possibility that the methanol tolerance originated from the suppression of methanol oxidation by strongly adsorbed sulfate/bisulfate31,32. Thus, the above results clearly showed that Pt-CTF/CP exhibits little activity with regard to methanol oxidation.
X-ray characterizations of Pt-CTF/CP
Characterizations of Pt-CTF/CP were conducted using various X-ray techniques to obtain information on the molecular mechanism of the methanol tolerance. The surface concentration of each element was determined by an X-ray photoelectron spectroscopy (XPS), and the results are summarized in Table 1. Peaks assignable to Pt and N were confirmed, and the Pt/N elemental ratio did not show a clear dependence on the amount of CP (the right column of Table 1), implying that the structures of Pt-CTFs are essentially identical even by hybridizing with CPs. In addition, the surface concentration of C, which was calculated with XPS, became higher with the increasing ratio of CP. Taking into account that the CP aggregates are uniformly covered by Pt-CTFs (Fig. 1), these results indicated that the thickness of Pt-CTFs is less than the escape depth of photoelectrons (ca. ~3 nm) as schematically shown in Fig. 1f, which enabled the Pt-CTF to possess electronic conduction with the CPs.
The details of the electronic structures of Pt-CTFs were investigated by taking XPS and X-ray absorption near-edge structures (XANES; Supplementary Figs 4–7). The Pt-4f7/2 peaks were located at 72.5 eV for Pt-CTF/CP and 72.2 eV for Pt-CTF (Supplementary Fig. 4). These binding energies were over 1 eV higher than those for metal Pt (70.9 eV), revealing that the valence state of Pt was Pt(II)33,34. In addition, XANES of Pt L3 edge shown in Supplementary Fig. 5 exhibited that the white-line intensities at 11,562 eV for Pt-CTF (1.45) and Pt-CTF/CP (1.46) are higher than those for metal Pt (1.24), indicating that Pt atoms existed as oxidized forms in both Pt-CTF and Pt-CTF/CP35. Thus, the Pt-4f XPS and the XANES results also show that there was no formation of Pt aggregates (metal Pt) on Pt-CTFs. Next, we focused on the N-1s XPS spectrum (Supplementary Fig. 6 and Supplementary Table 2). The N-1s peak at 399.2 eV observed for the 2,6-dicyanopyridine (that is, the catalyst monomer, Supplementary Fig. 7) was not observed for the Pt-CTF/CP, indicating that the cyclical trimerization of cyano reaction groups efficiently proceeded. The N-1s peak of Pt-CTF/CP could be deconvoluted into C2NH (398–399 eV) and C3N (400–401 eV)4. The peak assigned to C2NH was shifted to the higher-energy side upon Pt loading on both CTF and CTF/CP, indicating that the electron density of the N atoms became lower in the presence of Pt atoms. The decrease in the electron density of the N atoms can be explained by considering the formation of Pt-N coordination bonds (this point will be argued later). All the features described above were confirmed even for Pt-CTF (that is, without CPs), indicating that the hybridization with CPs did not influence on the electronic properties of N atoms in Pt-CTFs.
Next, we conducted extended X-ray absorption fine structure (EXAFS) analyses of Pt L3 edge to obtain information on the molecular structure of Pt-CTF/CP. Fourier transformations of k3-weighted EXAFS oscillations for Pt-CTF/CPs, Pt-CTFs, commercial Pt(bpy)Cl2 (bpy: 2,2'-bipyridine), PtO2, K2PtCl4 and Pt metal are shown in Fig. 5. The peak corresponding to a Pt–Pt bond at 2.6 Å was not observed at all for Pt-CTF/CPs. Instead, two peaks at R=1.5 and 1.9 Å assignable to Pt–N and Pt–Cl bonds, respectively, were clearly observed, indicating that Pt exists in the form of a single atom as illustrated in Fig. 1f. The ratio of the Pt–N peak to the Pt–Cl peak for Pt-CTFs corresponded to that for Pt(bpy)Cl2 (model PtN2Cl2 complex), implying that Pt atoms mainly existed as PtN2Cl2. It should be noted here that there was no clear difference in the EXAFS spectra between Pt-CTF/CP and Pt-CTF, indicating that the molecular structure of Pt-CTF is maintained upon the hybridization with CPs.
Let us consider here about the molecular mechanism of the methanol-tolerant ORR electrocatalytic activity of Pt-CTF/CP. First, we consider about the ORR on a single Pt site. An oxygen molecule is known to adsorb on a single Pt atom through either the Griffiths model (side-on adsorption) or the Pauling model (end-on adsorption)36. After the adsorption, π donation from the oxygen 2π orbitals to the unoccupied Pt 5d orbitals, and the π back donation from occupied Pt 5d orbitals to the oxygen 2π* orbitals could simultaneously occur, resulting in the O–O bond activation36,37. In fact, Nakamura et al.38 revealed using 18O isotopic infrared study that a single Pt atom and an oxygen molecule exchanged electrons, forming Pt–O2 adduct through the side-on adsorption. Li et al.39 also demonstrated by using first-principles calculations that the O–O bond was activated on single Pt site via the π back donation through the end-on adsorption, resulting in the weakening of the O–O bond. These reported lines of work suggested that electrocatalytic ORR could proceed even on a single Pt atom.
On the contrary, a number of researchers have suggested that at least two Pt atoms are needed to oxidize methanol40,41,42,43,44,45,46. It is well known that methanol can be oxidized via a dual-path mechanism on Pt, that is, the carbon monoxide (CO) pathway and the non-CO pathway44,45,47. Cuesta45,48 revealed by using cyanide-modified Pt electrode that dehydrogenation reaction of methanol to CO, a critical step of the CO pathway, required at least three contiguous Pt sites. As for the non-CO pathway, Osawa and colleagues44 proposed a molecular mechanism based on the results obtained from in situ infrared (IR) absorption spectroscopy. They suggested that adsorbed oxygenated species (that is, Oad or OHad) on the Pt site next to the methanol absorption site are needed for first dehydrogenation of the O–H bond in methanol. This molecular mechanism was further supported by Kuzume et al.49 again by in situ IR absorption spectroscopy. The previous lines of work have thus revealed that at least two adjacent Pt sites are required for methanol oxidation regardless of whether the reaction proceeds via the CO or the non-CO pathways. Actually, to the best of our knowledge, there have been no reports of methanol oxidation on a single Pt-atom site. Considering these literatures, the methanol tolerance of Pt/CTF is reasonably explained because the EXAFS results demonstrated that the Pt atoms in Pt/CTF were isolated.
In conclusion, we successfully synthesized Pt-CTF hybridized with CP, preserving its electronic and molecular structure, which exhibited ORR activity in acidic solutions with a high methanol tolerance. The methanol tolerance of the Pt-CTF/CP indicates that the methanol-crossover effect can be ignored. This property allows a considerable increase in the concentration of methanol in DMFC; consequently, the energy density of DMFC is expected to increase because of the use of Pt-CTF/CP. Another interesting aspect of this work is that it is the first demonstration of electrocatalytic function in CTF-based materials. This was achieved by hybridizing non-conductive CTFs with conductive CPs. We anticipate that this methodology could be applied generally to other CTFs with unique catalytic properties.
Synthesis procedure of Pt-CTF/CP
CTF/CP was synthesized by polymerization of 2,6-dicyanopyridine in a molten salt of zinc chloride (ZnCl2). Specifically, 1.363 g ZnCl2 (Wako), 0.129 g 2,6-dicyanopyridine (Sigma) and 0.129 g KetchenBlack EC600JD were mixed in a globe box. The mixture was placed in a Pyrex glass tube and the tube was sealed, evacuated, heated and kept at a terminal temperature of 400 °C for 21 h. The resulting powder was washed with 0.1 M HCl, water, tetrahydrofolate and acetonitrile, and dried in vacuo. Pt atoms were modified by impregnation in 160 mM K2[PtCl4] (Wako) aqueous solution at 60 °C for 4 h before being washed with water and acetone.
Electrochemical activity for ORR was evaluated using a rotating disk electrode. Working electrodes were first prepared by dispersing 5 mg of powder samples in 175 μl ethanol and 47.5 μl Nafion solution (5 wt% solution in a mixture of lower aliphatic alcohols and water, Aldrich). A 7-μl aliquot of ink was dropped on a glassy carbon electrode (0.196 cm−2). The catalyst loading was controlled at 0.8 mg cm−2. A Pt wire and Ag/AgCl (saturated KCl) were used as the counter and reference electrodes, respectively. Commercial 20 wt% Pt/C and Pt-Vulcan XC-72 were purchased from Tanaka Kikinzoku and Fuel Cell Earth, respectively. The electrical conductivity of the catalysts was measured with a resistivity meter (Mitsubishi Chemical, Loresta GP). The working electrode was rotated with a rotation speed of 1,500 r.p.m.
X-ray photoelectron spectra (Axis Ultra, Kratos Analytical Co.) were taken with monochromated Al Kα X-rays at hν=1,486.6 eV. For detailed chemical analysis, backgrounds of core-level spectra were subtracted using the Shirley method. N-1s spectra were fitted with Voigt (70% Gaussian and 30% Lorentzian) functions. Hard X-ray absorption measurements (XAFS) were performed at the hard X-ray beam line BL01B01 at SPring-8, Japan and by using R-XAS Looper (Rigaku). Transmission-yield spectra were acquired using a double-crystal Si (111) monochromator. The morphological structures were characterized using TEM with an EDX detector (ARM-200F, JEOL) and SEM (SU-8000, Hitachi). The nitrogen adsorption–desorption isotherm at 77 K was obtained by a BET (NOVA-4200e, Quantachrome).
How to cite this article: Kamiya, K. et al. Platinum-modified covalent triazine frameworks hybridized with carbon nanoparticles as methanol-tolerant oxygen reduction electrocatalysts. Nat. Commun. 5:5040 doi: 10.1038/ncomms6040 (2014).
Cote, A. P. et al. Porous, crystalline, covalent organic frameworks. Science 310, 1166–1170 (2005).
Chan-Thaw, C. E., Villa, A., Prati, L. & Thomas, A. Triazine-based polymers as nanostructured supports for the liquid-phase oxidation of alcohols. Chem. Eur. J. 17, 1052–1057 (2011).
Ding, S.-Y. & Wang, W. Covalent organic frameworks (COFs): from design to applications. Chem. Soc. Rev. 42, 548–568 (2013).
Chan-Thaw, C. E. et al. Influence of periodic nitrogen functionality on the selective oxidation of alcohols. Chem. Asian J. 7, 387–393 (2012).
Feng, X., Ding, X. & Jiang, D. Covalent organic frameworks. Chem. Soc. Rev. 41, 6010–6022 (2012).
Pachfule, P., Kandambeth, S., Diaz, D. D. & Banerjee, R. Highly stable covalent organic framework-Au nanoparticles hybrids for enhanced activity for nitrophenol reduction. Chem. Commun. 50, 3169–3172 (2014).
Ding, S.-Y. et al. Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki-Miyaura coupling reaction. J. Am. Chem. Soc. 133, 19816–19822 (2011).
Chan-Thaw, C. E. et al. Covalent triazine framework as catalytic support for liquid phase reaction. Nano Lett. 10, 537–541 (2010).
Palkovits, R., Antonietti, M., Kuhn, P., Thomas, A. & Schueth, F. Solid catalysts for the selective low-temperature oxidation of methane to methanol. Angew. Chem. Int. Ed. 48, 6909–6912 (2009).
Palkovits, R. et al. Development of molecular and solid catalysts for the direct low-temperature oxidation of methane to methanol. ChemSusChem 3, 277–282 (2010).
Periana, R. A. et al. Platinum catalysts for the high-yield oxidation of methane to a methanol derivative. Science 280, 560–564 (1998).
Kua, J., Xu, X., Periana, R. A. & Goddard, W. A. Stability and thermodynamics of the PtCl2 type catalyst for activating methane to methanol: a computational study. Organometallics 21, 511–525 (2002).
Shilov, A. E. & Shul'pin, G. B. Activation of C-H bonds by metal complexes. Chem. Rev. 97, 2879–2932 (1997).
Stahl, S. S., Labinger, J. A. & Bercaw, J. E. Homogeneous oxidation of alkanes by electrophilic late transition metals. Angew. Chem. Int. Ed. 37, 2181–2192 (1998).
Mitton, S. J. & Turculet, L. Mild reduction of carbon dioxide to methane with tertiary silanes catalyzed by platinum and palladium silyl pincer complexes. Chem. Eur. J. 18, 15258–15262 (2012).
Guo, J. et al. Conjugated organic framework with three-dimensionally ordered stable structure and delocalized π clouds. Nat. Commun. 4, 2736 (2013).
Krewer, U., Vidakovic-Koch, T. & Rihko-Struckmann, L. Electrochemical oxidation of carbon-containing fuels and their dynamics in low-temperature fuel cells. Chemphyschem 12, 2518–2544 (2011).
Argyropoulos, P., Scott, K. & Taama, W. M. The effect of operating conditions on the dynamic response of the direct methanol fuel cell. Electrochim. Acta 45, 1983–1998 (2000).
Daems, N., Sheng, X., Vankelecom, I. F. J. & Pescarmona, P. P. Metal-free doped carbon materials as electrocatalysts for the oxygen reduction reaction. J. Mater. Chem. A 2, 4085–4110 (2014).
Gewirth, A. A. & Thorum, M. S. Electroreduction of dioxygen for fuel-cell applications: materials and challenges. Inorg. Chem. 49, 3557–3566 (2010).
Brownson, D. A. C., Kampouris, D. K. & Banks, C. E. An overview of graphene in energy production and storage applications. J. Power Sources 196, 4873–4885 (2011).
Kuhn, P., Thomas, A. & Antonietti, M. Toward tailorable porous organic polymer networks: a high-temperature dynamic polymerization scheme based on aromatic nitriles. Macromolecules 42, 319–326 (2009).
Kuhn, P., Antonietti, M. & Thomas, A. Porous, covalent triazine-based frameworks prepared by ionothermal synthesis. Angew. Chem. Int. Ed. 47, 3450–3453 (2008).
Herzing, A. A., Kiely, C. J., Carley, A. F., Landon, P. & Hutchings, G. J. Identification of active gold nanoclusters on iron oxide supports for CO oxidation. Science 321, 1331–1335 (2008).
Sun, S. et al. Single-atom catalysis using Pt/graphene achieved through atomic layer deposition. Sci. Rep. 3, 1775 (2013).
Qiao, B. et al. Single-atom catalysis of CO oxidation using Pt1/FeOx . Nat. Chem. 3, 634–641 (2011).
Kuhn, P., Forget, A., Su, D., Thomas, A. & Antonietti, M. From microporous regular frameworks to mesoporous naterials with ultrahigh surface area: dynamic reorganization of porous polymer networks. J. Am. Chem. Soc. 130, 13333–13337 (2008).
Kuhn, P., Forget, A., Hartmann, J., Thomas, A. & Antonietti, M. Template-free tuning of nanopores in carbonaceous polymers through ionothermal synthesis. Adv. Mater. 21, 897–901 (2009).
Wang, G. et al. Improving the DMFC performance with Ketien Black EC 300J as the additive in the cathode catalyst layer. J. Power Sources 180, 176–180 (2008).
Tashima, D., Yoshitama, H., Otsubo, M., Maeno, S. & Nagasawa, Y. Evaluation of electric double layer capacitor using Ketjenblack as conductive nanofiller. Electrochim. Acta 56, 8941–8946 (2011).
Cohen, J. L., Volpe, D. J. & Abruna, H. D. Electrochemical determination of activation energies for methanol oxidation on polycrystalline platinum in acidic and alkaline electrolytes. Phys. Chem. Chem. Phys. 9, 49–77 (2007).
Kolics, A. & Wieckowski, A. Adsorption of bisulfate and sulfate anions on a Pt(111) electrode. J. Phys. Chem. B 105, 2588–2595 (2001).
Hidai, S. et al. Platinum oxidation responsible for degradation of platinum-cobalt alloy cathode catalysts for polymer electrolyte fuel cells. J. Power Sources 215, 233–239 (2012).
Wang, H. et al. Influence of size-induced oxidation state of platinum nanoparticles on selectivity and activity in catalytic methanol oxidation in the gas phase. Nano Lett. 13, 2976–2979 (2013).
Russell, A. E. & Rose, A. X-ray absorption spectroscopy of low temperature fuel cell catalysts. Chem. Rev. 104, 4613–4635 (2004).
Toda, T., Igarashi, H., Uchida, H. & Watanabe, M. Enhancement of the electroreduction of oxygen on Pt alloys with Fe, Ni, and Co. J. Electrochem. Soc. 146, 3750–3756 (1999).
Lim, D.-H. & Wilcox, J. DFT-based study on oxygen adsorption on defective graphene-supported Pt nanoparticles. J. Phys. Chem. C 115, 22742–22747 (2011).
Nakamura, A., Tatsuno, Y., Yamamoto, M. & Otsuka, S. Oxygen-18 isotopic infrared study of dioxygen-transition metal complexes. J. Am. Chem. Soc. 93, 6052–6058 (1971).
Li, T. & Balbuena, P. B. Computational studies of the interactions of oxygen with platinum clusters. J. Phys. Chem. B 105, 9943–9952 (2001).
Gasteiger, H. A., Markovic, N., Ross, P. N. & Cairns, E. J. Electro-oxidation of small organic molecules on well-characterized Pt-Ru alloys. Electrochim. Acta 39, 1825–1832 (1994).
Hernandez-Fernandez, P. et al. Relevance of the nature of bimetallic PtAu nanoparticles as electrocatalysts for the oxygen reduction reaction in the presence of methanol. J. Power Sources 177, 9–16 (2008).
Kim, Y. T. et al. Fine size control of platinum on carbon nanotubes: From single atoms to clusters. Angew. Chem. Int. Ed. 45, 407–411 (2006).
Nishanth, K. G., Sridhar, P., Pitchumani, S. & Shukla, A. K. A DMFC with methanol-tolerant-carbon-supported-Pt-Pd-alloy cathode. J. Electrochem. Soc. 158, B871–B876 (2011).
Chen, Y. X., Miki, A., Ye, S., Sakai, H. & Osawa, M. Formate, an active intermediate for direct oxidation of methanol on Pt electrode. J. Am. Chem. Soc. 125, 3680–3681 (2003).
Cuesta, A. At least three contiguous atoms are necessary for CO formation during methanol electrooxidation on platinum. J. Am. Chem. Soc. 128, 13332–13333 (2006).
McNicol, B. D. Electrocatalytic problems associated with the development of direct methanol-air fuel cells. J. Electroanal. Chem. 118, 71–87 (1981).
Lai, S. C. S., Lebedeva, N. P., Housmans, T. H. M. & Koper, M. T. M. Mechanisms of carbon monoxide and methanol oxidation at single-crystal electrodes. Top Catal. 46, 320–333 (2007).
Cuesta, A. Atomic ensemble effects in electrocatalysis: the site-knockout strategy. Chemphyschem 12, 2375–2385 (2011).
Kuzume, A., Mochiduki, Y., Tsuchida, T. & Ito, M. Methanol oxidation on a Pt(111)-OH/O surface. Phys. Chem. Chem. Phys. 10, 2175–2179 (2008).
Synchrotron radiation experiments were performed at the BL01B1 beam line of SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI; Proposal nos 2013B1123 and 2013A1598). We thank Dr T. Ina for his technical support during XAFS measurements at SPring-8.
The authors declare no competing financial interests.
About this article
Cite this article
Kamiya, K., Kamai, R., Hashimoto, K. et al. Platinum-modified covalent triazine frameworks hybridized with carbon nanoparticles as methanol-tolerant oxygen reduction electrocatalysts. Nat Commun 5, 5040 (2014). https://doi.org/10.1038/ncomms6040
This article is cited by
Recent advances in regulating the local environment of M-N4 structure for tailored chemical reactions
Nano Research (2023)
Regulating electronic structure of CoN4 with axial Co—S for promoting oxygen reduction and Zn-air battery performance
Nano Research (2023)
Nature Catalysis (2022)
Pyrenetetraone-based covalent organic framework as an effective electrocatalyst for oxygen reduction reaction
Nano Research (2022)
Metal organic frameworks as emergent oxygen-reducing cathode catalysts for microbial fuel cells: a review
International Journal of Environmental Science and Technology (2022)