Abstract
Transition metal single atom catalysts (SACs) with M1-Nx coordination configuration have shown outstanding activity and selectivity for hydrogenation of nitroarenes. Modulating the atomic coordination structure has emerged as a promising strategy to further improve the catalytic performance. Herein, we report an atomic Co1/NPC catalyst with unsymmetrical single Co1-N3P1 sites that displays unprecedentedly high activity and chemoselectivity for hydrogenation of functionalized nitroarenes. Compared to the most popular Co1-N4 coordination, the electron density of Co atom in Co1-N3P1 is increased, which is more favorable for H2 dissociation as verified by kinetic isotope effect and density functional theory calculation results. In nitrobenzene hydrogenation reaction, the as-synthesized Co1-N3P1 SAC exhibits a turnover frequency of 6560 h−1, which is 60-fold higher than that of Co1-N4 SAC and one order of magnitude higher than the state-of-the-art M1-Nx-C SACs in literatures. Furthermore, Co1-N3P1 SAC shows superior selectivity (>99%) toward many substituted nitroarenes with co-existence of other sensitive reducible groups. This work is an excellent example of relationship between catalytic performance and the coordination environment of SACs, and offers a potential practical catalyst for aromatic amine synthesis by hydrogenation of nitroarenes.
Similar content being viewed by others
Introduction
Chemoselective hydrogenation of nitroarenes is a key reaction in the fine chemical industry and has wide applications in the synthesis of pigments and pharmaceuticals1,2,3,4. Noble metal nanocatalysts (e.g., Pt, Au, and Pd) are usually used for this reaction5,6,7. However, noble metal catalysts are costly and their high activities usually come with unsatisfactory selectivity against many substituted nitroarenes8,9,10,11. Since Beller et al. reported highly selective traditional metal catalysts based on Co3O4@N/C and Fe3O4@N/C, it has sparked intensive research interest in this type of catalysts1,12. Among them, transition metal single-atom catalysts (SACs) with M1-Nx-C (M = Fe, Co, Ni, x = 2–6) coordination configuration exhibited much better activities than their counterpart nanoparticles while maintaining high selectivity, owing to their maximum atom efficiency and particular electronic structure13,14,15,16,17,18. Recently, Wang et al. found that the electron density of Ni single atoms increased with the decrease of Ni-N coordination numbers (CN), and the capability of Ni single sites to dissociate H2 was greatly enhanced, leading to higher catalytic activity in chemoselective hydrogenation of functionalized nitroarenes19. This result suggests that the catalytic activity of M1-Nx-C can also be enhanced by adjusting the coordination structure of transition metal SACs.
In most SACs, the central metal atoms were stabilized by coordination bonds with N, S, O, etc. atoms within support matrix20,21,22,23,24,25,26,27,28,29. The electronic and geometric structures of central metal atoms can be adjusted by tailoring the coordination environment, which would change the absorption energy of reactants on metal atoms and thus influence the catalytic process20,23,28,30. For SACs with M1-Nx-C sites, the symmetric electronic distribution may limit the activation of reactants, thereby leading to hampered catalytic kinetics and performances20,31. Recent studies have found that introducing heteroatom P for an unsymmetrical N/P mixed-coordination can further modulate the electronic properties of center metal atoms. The unsymmetrical geometric structure can evoke the distortion of electronic density and alter the d-band center20,23,28,31,32. For example, Yuan et al. prepared an N/P dual-coordinated Fe single-atom catalyst, which was more favorable for the adsorption of oxygen intermediates for ORR in fuel cell23. Li et al. reported that a Fe1-N3P1 single-atom nanozyme exhibited peroxidase-like catalytic activity, and the high activity was ascribed to the less positive charge on Fe atoms as P atoms are electron donors32. Thus, we anticipated that constructing the unsymmetrical N/P dual-coordinated transition metal SACs would improve the catalytic performance for the hydrogenation of nitroarenes.
In this work, we report an N/P dual-coordinated Co SAC (denoted as Co1/NPC) with Co1-N3P1 coordination structure and investigate its catalytic performance for chemoselective hydrogenation of nitroarenes. The single atomic feature and coordination structure of the Co1-N3P1 site are characterized through aberration-corrected high angle annular dark-field scanning transmission electron microscopy (AC HAADF-STEM), atomic-resolution electron energy-loss spectroscopy (EELS), X-ray photoelectron spectroscopy (XPS), and X-ray absorption spectrum (XAS). In nitrobenzene hydrogenation reaction, the Co1-N3P1 SAC exhibits a turnover frequency of 6560 h−1, which is 60 times higher than that of Co1-N4 SAC and 10 times higher than the state-of-the-art M1-Nx-C SACs in literatures. Furthermore, Co1-N3P1 SAC shows superior selectivity (>99%) toward many substituted nitroarenes with the co-existence of other sensitive reducible groups. The unprecedentedly high activity of Co1-N3P1 SAC can be ascribed to the upshift d-band center of Co single atoms, which is more favorable for H2 dissociation as verified by the kinetic isotope effect and density functional theory calculation results. This is an excellent example of such an unsymmetrical N/P dual-coordinated structure of metal SACs in hydrogenation.
Results
Structural characterization
Supplementary Fig. 1 illustrates the synthesis procedures for preparing N/P dual-coordinated Co SAC (denoted as Co1/NPC) via a two-step process. First, tannic acid, (2-Aminoethyl)phosphonic acid (AePA), and cobalt ion precursors were co-adsorbed on the surface of graphitic carbon nitride (g-C3N4) nanosheets; then the resultant powder was subjected to pyrolysis under flowing Ar gas at 900 °C to obtain Co1/NPC, where the AePA was absent and the introduced-P species served as the donors for anchoring Co atoms (Supplementary Fig. 2). For comparison, N-coordinated Co SAC (denoted as Co1/NC) was also prepared via the same procedure without the addition of AePA. As exhibited in Raman spectra, the carbon matrices in both Co1/NPC and Co1/NC were disordered with a large number of defects (Supplementary Fig. 3). Only two broad peaks at ~24.3° and 42.6° could be observed from their X-ray diffraction (XRD) patterns (Supplementary Fig. 4), corresponding to (002) and (101) planes of carbon, suggesting highly dispersed states of Co species in both of two samples. Further increasing the pyrolysis temperature of Co1/NPC to 1000 °C led to the formation of Co2P nanoparticles (Supplementary Figs. 4, 5). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images show that both catalysts retain a two-dimensional layered structure and no obvious nanoparticles are observed (Supplementary Figs. 6, 7). Energy-dispersive spectroscopy (EDS) mappings reveal Co elements are distributed uniformly over the entire samples (Supplementary Figs. 8, 9). Additionally, Co single-atom feature in Co1/NPC and Co1/NC is directly observed by AC HAADF-STEM, as reflected by the highly dispersed bright dots due to the heavy Z-contrast (Fig. 1a and Supplementary Fig. 10). The Co loading in Co1/NPC was ~0.45 wt% as determined by the inductively coupled plasma mass spectroscopy (ICP-MS) analysis (Supplementary Table 1). The porosity features of Co1/NC and Co1/NPC were investigated using nitrogen physisorption measurements. Both catalysts displayed characteristics of IV-type N2 adsorption-desorption isotherms, suggesting the existence of mesopores, which would be beneficial for the exposure of active sites and mass transportation (Supplementary Fig. 11). The calculated BET-specific surface area of Co1/NC and Co1/NPC were 512 and 471 m2 g−1, respectively.
XPS was then applied to reveal the chemical structures of both Co SACs. In N 1s spectra, besides pyridinic N, pyrrolic N, graphitic N, and oxidized N species, a peak at 399.1 eV corresponding to Co-N can be distinguished33, indicating the existence of N coordination environment with Co single atoms in both catalysts (Fig. 1b and Supplementary Fig. 12). Note that from P 2p spectra in Fig. 1c, an obvious peak at ~129.3 eV corresponding to Co-P bond was presented in Co1/NPC23,31, which can also be observed in the comparison Co2P NPs/C (Supplementary Fig. 13); while it is absent in Co1/NC sample. These results suggest that the atomically dispersed Co atoms possess N/P dual-coordinated configuration in Co1/NPC, while only N-coordinated configuration in Co1/NC.
To further determine the coordination environment of Co single atoms, X-ray absorption fine structure (XAFS) measurements were conducted. Figure 1d shows the Co K-edge X-ray absorption near-edge structure (XANES) curves of Co1/NC and Co1/NPC, with Co foil, CoO, and cobalt phthalocyanine (CoPc) as reference samples. It can be seen that the absorption threshold positions for Co1/NC and Co1/NPC are located between Co foil and CoO, suggesting that the valence states of Co species are between 0 and +2 in both two catalysts. Moreover, the Co K-edge position and white line of Co1/NPC are lower than that of Co1/NC (inset of Fig. 1d), which indicates that Co atoms in Co1/NPC possess more negative charges than Co1/NC. Such difference could be attributed to the less electron transfer from Co to P because of the weaker electronegativity of P than N atoms20. The Fourier-transformed k3-weighted EXAFS (FT-EXAFS) spectra demonstrated that both Co1/NC and Co1/NPC only exhibited a prominent peak at 1.38 Å (without phase shift), no Co-Co peaks at 2.17 Å or larger bond distances were detected, confirming atomically dispersed Co species in Co1/NC and Co1/NPC (Supplementary Figs. 14, 15). The coordination configuration of Co moieties was further surveyed using quantitative least-squares EXAFS curve-fitting. The EXAFS spectrum of Co1/NPC was investigated by utilizing Co-N and Co-P backscattering pathways. The best-fitting analysis displays that the main peak at 1.38 Å could be satisfactorily interpreted as Co-N first-shell coordination with CN = 3.2 ± 0.1 and the shoulder peak at 1.77 Å originated from Co-P contribution with CN = 0.9 ± 0.1 (Fig. 1e and Supplementary Table 2), suggesting the possible Co1-N3P1 configuration in Co1/NPC. For comparison, fitting of Co1/NC resulted in an average of about four N atoms with a distance of 1.37 Å (Supplementary Fig. 14 and Supplementary Table 2). In order to better confirm the proposed configurations, the theoretical XANES spectrum were simulated based on the Co1-N3P1 model as well as Co1-N4, which presented a good agreement with the experimental data, indicating the rationality of the two structures (Fig. 1f and Supplementary Fig. 16).
Besides, we performed atomic-resolution electron energy-loss spectroscopy (EELS) analysis at a relatively low beam current to minimize electron-beam perturbations to provide strong evidence of Co1-N3P1 structure (Fig. 2a, b). The extracted Co L-edge EELS spectrum from Fig. 2d presents a clear Co signal (Fig. 2g), providing direct evidence for the presence of atomically dispersed Co species. More importantly, the existence of N, P dual-coordination vicinal to Co site is revealed by identifying the surrounding heteroatoms. From the N, P, and overlap maps (Fig. 2e, f, c), three N atoms (green) and one P atom (red) exist around the Co site. Atomic-scale N K-edge and P L-edge EELS spectra collected at the corresponding positions from Fig. 2e, f are further demonstrated by the N and P signals (Fig. 2h, i). This forcefully confirms the Co1-N3P1 configuration in Co1/NPC sample. Moreover, the formation energy of the Co1-N3P1 structure in the Co1/NPC sample was estimated to be about −0.864 eV by DFT calculation, indicating the high stability of the proposed configuration (Supplementary Fig. 17). These results revealed that the Co single sites in Co1/NPC were stabilized with N/P dual-coordinated structure, forming an unsymmetrical Co1-N3P1 geometric configuration (as depicted in Fig. 1f), which is different from the Co site in Co1/NC with traditional in-plane Co1-N4 configuration.
Catalytic performance
To evaluate the catalytic performances of the as-prepared Co SACs for the hydrogenation of nitroarenes, nitrobenzene is first chosen as a probe molecule. The reaction kinetics with Co1/NC and Co1/NPC were obtained at 110 °C with 3 MPa H2 in a Teflon-lined stainless steel autoclave. As shown in Fig. 3a, Co1/NPC exhibits significantly higher activity than that of Co1/NC. Nitrobenzene was completely converted with >99% amine selectivity in 210 min with Co1/NPC, while less than 20% conversion was observed with Co1/NC under the same reaction condition. In addition, no conversion was observed with NC and NPC supports, suggesting that atomic Co site was active species in both Co1/NC and Co1/NPC catalysts (Supplementary Fig. 18). The reaction rate (k) for hydrogenation of nitrobenzene over Co1/NPC could reach as high as 35.9 mol mol−1 min−1, which is ten times higher than that with Co1/NC (3.1 mol mol−1 min−1).
The turnover frequency value (TOF) (based on the substrate conversion at about 20%) of Co1/NPC is calculated to be 6560 h−1, which is over 60 times higher than that with Co1/NC (108 h−1) (Fig. 3b). Besides nitrobenzene, Co1/NPC also exhibited superior high activity and excellent selectivity (>99.7%) for hydrogenation of 3-nitrostyrene with TOF of 4499 h−1. The impressive activity of Co1/NPC is ten times higher than the state-of-the-art M1-Nx-C SACs in literature (Fig. 3c and Supplementary Table 3)34,35,36,37,38,39,40,41,42,43. Such excellent catalytic performance of Co1/NPC sample inspired us to carry out the reaction under milder conditions (e.g., 40 °C, 1 bar H2). A high nitrobenzene conversion of 97.2% was achieved within 5 h (Supplementary Fig. 19). To further compare the catalytic performance between Co1/NC and Co1/NPC, the apparent activation energies of these two catalysts were measured (Supplementary Fig. 20 and Supplementary Table 4). As shown in Fig. 3d, the calculated activation energy of Co1/NPC catalyst is about 21.8 kJ mol−1, which is much lower than that of Co1/NC (51.3 kJ mol−1).
In order to clarify the intrinsic higher activity of Co1-N3P1, the electronic properties of the central metal sites over Co1/NC and Co1/NPC are examined by electron-density isosurface and partial density of states from DFT calculations. Different charge distributions of the two models are observed (Fig. 3e). Compare to the Co1-N4 configuration, the symmetric electron structure is broken by introducing heteroatom P in Co1-N3P1. The Bader charge of the Co1-N3P1 site is estimated to be +0.81 e, while the Co1-N4 site is +0.97 e, indicating the Co atom in the Co1-N3P1 site carries more charge since the P element in the Co1/NPC transfers 2.308 e to support, which is consistent with the XAFS results. Moreover, the Co d-band center of Co1/NPC is up-shifted, much closer to the Fermi level (Fig. 3f). As a result, the antibonding state of Co atoms and adsorbed H2 species are more occupied, then such change enhances the capabilities of H2 dissociation6,44. Thus, Co1/NPC catalyst with Co1-N3P1 configuration exhibits much higher activity than that of Co1/NC with Co1-N4 configuration.
Catalytic hydrogenation mechanism
Such a large activity difference between Co1/NC and Co1/NPC implies that the hydrogenation activity is closely correlated with local coordination structure, which influences the electronic structure of Co single atoms. In order to elucidate the reaction mechanisms on both catalysts, we carried out a kinetic isotope effect (KIE) study to examine the H2 dissociation step. Using D2 for nitrobenzene hydrogenation, the reaction rate was slowed down by a factor of 3.25 for Co1/NC (Fig. 4a). For comparison, a larger KIE (kH/kD = 5.54) was observed on Co1/NPC catalyst (Fig. 4b). These results suggest that H2 dissociation undergoes heterolytic cleavage on both Co1/NC and Co1/NPC45,46,47.
It is generally accepted that heterolytic cleavage of H2 on metal single atoms occurs to form metal-Hδ- and heteroatom-Hδ+ 45,48. Therefore, DFT calculations were further performed to understand the H2 heterolytic cleavage on Co1/NC and Co1/NPC, respectively. As shown in Supplementary Fig. 21, the H2 molecule is adsorbed on the Co atom of Co1/NPC with adsorption energy of −0.08 eV, and the bond length of H2 is 0.814 Å, which is much longer than free molecular H2 (0.752 Å) in the gas phase. While H2 molecule is adsorbed on Co atom of Co1/NC with adsorption energy of 0.033 eV, and the bond length of H2 is 0.783 Å. The much longer H-H bond length of adsorbed molecule H2 indicates that Co1/NPC has a higher activation ability for H2 dissociation than Co1/NC. Subsequently, one of the H atoms moves to a nearby heteroatom (N and P) to yield heteroatom-Hδ+, leaving another H atom on Co atom as Co-Hδ-. Direct dissociation of H2 on both Co1/NPC and Co1/NC in the absence of water, the transition state is almost the same (~1.21 eV), the only difference is that the dissociation of H2 on Co1/NPC is exothermic by 0.20 eV, while on Co1/NPC is endothermic by 1.11 eV, suggesting such dissociation manner on Co1-N4 site is thermodynamically unfavorable (Supplementary Fig. 22). The above difference in the DFT calculations confirms that Co1-N3P1 exhibits much higher catalytic activity for heterolytic cleavage of H2.
Ding et al.18. reported that the protic solvents play a dominant role in the case of Co-N-C-catalyzed hydrogenation of nitroarenes, where the solvent-mediated H-shuttling mechanism is crucial in the reaction pathway. Compared to the intrinsic hydrogen transfer, the protic solvent-mediated one usually possesses a lower activation barrier, leading to an enhancement of hydrogenation activity in the presence of water or alcohol49. Indeed, both Co1/NC and Co1/NPC show the best activities under ethanol/water solvent and significantly decreased activities in an aprotic solvent such as toluene, acetonitrile, THF, and n-hexane (Supplementary Fig. 23). Further DFT calculations suggest that the activation energy barriers with water-mediated H-shuttling mechanism for the heterolytic cleavage of H2 are lower by about 0.16 and 0.01 eV than that through direct dissociation on Co1-N3P1 and Co1-N4 sites, respectively (Fig. 4c, d). Both kinetic and thermodynamic results suggest that the dissociative activation of H2 with help of H2O is more favorable to Co1/NPC catalyst.
According to the previous reports, the hydrogenation reduction of nitrobenzene to aniline follows the Haber mechanism7, namely, PhNO2* → PhNOOH* → PhNO* → PhNOH* → PhNHOH* → PhNH* → PhNH2*. Based on the above results and reported mechanism in literature, the reaction pathway for hydrogenation of nitrobenzene over Co1-N3P1 catalyst is further proposed by virtue of DFT calculations, as shown in Fig. 5 and Supplementary Fig. 24. One H2 molecule first goes through heterolytic cleavage with the assistance of the H2O-mediated H-shuttling mechanism to form Co-Hδ- and P-Hδ+ at Co1-N3P1 sites, which can serve as the initial state for the hydrogenation process (Fig. 5a and Supplementary Fig. 25). Then, the target nitrobenzene molecule was adsorbed on the Co1-N3P1 site with a free energy of −0.78 eV (Fig. 5b, I). Subsequently, the activated H atom on Co-Hδ- and the O atom of PhNO2 are combined to produce PhNOOH intermediate, which is later reduced to PhNO intermediate by the H atom transfer from P-Hδ+ (II). Notably, the PhNO intermediate can be detected during the reaction process (Supplementary Fig. 26). After that, another H2 molecule is dissociated to form an activated H atom, which attacks the oxygen atom of PhNO and reduces it to PhNHOH (III, IV). It is worth noting that the adsorption energies of intermediates PhNO and PhNHOH on the Co1-N3P1 site are more favorable than Ph-NO2, ensuring the reaction progress of the targeted substrate (Supplementary Fig. 27). In the next step, the third H2 molecule participates in and the formed H atom interacts with PhNHOH to generate the final PhNH2 product (V, FS). It can be seen the whole process is highly endothermic, confirming the possibility of the proposed reaction path.
Substrate exploration and catalytic stability
A broad scope of substituted nitroarenes was tested to examine the chemoselectivity in nitroarene hydrogenation (Fig. 6). Co1/NPC shows impressive chemoselectivity toward the substituted nitroarenes in the presence of other sensitive reducible groups, such as alkenyl (99.7%, 2b), halogen (>98.9%, 2c–f), ketones (>99%, 2g, h), nitrile groups (>99%, 2i), etc. Notably, Co1/NPC also exhibits high activity and selectivity toward heterocyclic nitro-compounds (>99%, 2n–q). The superior high selectivity to corresponding anilines is ascribed to the unique character of metal SACs, where there is only one single metal atom for adsorption and activation of substrates.
Furthermore, Co1/NPC exhibited tolerable stability. As shown in Supplementary Fig. 28, a slight decrease of activity is observed after five cycles with Co1/NPC, which can be ascribed to the loss of some catalysts and active Co species during the recycling experiments (Supplementary Table 1). The AC HAADF-STEM image and Co K-edge EXAFS spectrum of spent Co1/NPC indicate that the atomically dispersed Co species is well preserved after five cycles (Supplementary Fig. 29). All these results demonstrate that the Co1/NPC catalyst with unsymmetrical Co1-N3P1 configuration possesses unprecedented high activity, high selectivity, and good stability to a wide scope of substrates for hydrogenation of nitroarenes.
Discussion
In summary, we produced an atomically dispersed Co1/NPC catalyst with an unsymmetrically Co1-N3P1 coordination structure. Due to the increased electron density and upshift d-band center of Co atoms in Co1-N3P1, H2 dissociation was proved to be more favorable, resulting in much enhanced catalytic activity. In nitrobenzene hydrogenation reaction, the as-prepared Co1-N3P1 SAC exhibited a 60-fold higher TOF value (6560 h−1) than that of Co1-N4 SAC and more than tenfold higher than the state-of-the-art M1-Nx-C SACs in literature. In addition, Co1-N3P1 SAC also displayed superior selectivity (>99%) towards the substituted nitroarenes with the co-existence of other sensitive reducible groups. This work provides new insight into rationally modulating the coordination structure of central metal atoms for boosting the catalytic performance of SACs in heterogeneous catalysis.
Methods
Synthesis of Co1/NPC and Co1/NC
In a typical procedure, Co(NO3)2·6H2O (6.5 mg), tannic acid (TA, 500 mg), and (2-Aminoethyl) phosphonic acid (AePA, 126 mg) were dissolved into 30 mL DI water at 100 °C (marked as solution A). g-C3N4 nanosheets (1 g) were dispersed well in 100 mL DI water with ultrasound (marked as solution B). Then, solution A was added dropwise into solution B with a strong stirring at 100 °C until the mixed system was forced to yield a slurry. Subsequently, the obtained powder after freeze-dried was pyrolyzed at 900 °C for 2 h under Ar atmosphere. Finally, the as-prepared material was directly used without further treatment, denoted as Co1/NPC.
The synthesis process for Co1/NC is the same as that of Co1/NPC except without the addition AePA.
Characterizations
The powder X-ray diffraction (XRD) patterns were recorded on a Rigaku D/max-2500n diffractometer with Cu Kα radiation (λ = 1.5418 Å) at 40 kV and 200 mA. The morphologies and microstructures of the samples were measured on the transmission electron microscopy (TEM) (JEM-2100F, JEOL, Japan) and the scanning electron microscopy (SEM) (HITACHI S-4800, Japan). Element mapping was characterized on TEM equipped with Oxford detection. X-ray photoelectron spectroscopy (XPS) measurements were performed on a VG Scientific ESCALab220i-XL electron spectrometer using 300 W Al kα radiation. Inductively coupled plasma atomic emission spectroscopy (ICP-AES) was conducted on a Shimadzu ICPE-9000 to confirm the loading content of metal on the catalysts. The AC HAADF-STEM images were carried out in a JEOL ARM300F at 300 kV, equipped with a probe spherical aberration corrector. Brunauer–Emmett–Teller (BET) surface areas were measured by N2 adsorption-desorption isotherms at 77 K with a Micromeritics ASAP 2460 instrument. The HAADF imaging and EELS mapping were both performed using a Nikon HERMES-100 aberration-corrected scanning transmission electron microscope under 60 kV accelerating voltage with a ~22 pA probe. The probe convergence semi-angle, HAADF collection semi-angle, and EELS collection semi-angle is 32 mrad, 75–210 mrad, and 0–75 mrad, respectively.
XAS measurements and analysis
The cobalt K-edges XAFS spectra of the standards and samples were collected at the beamline 1W1B of the Beijing Synchrotron Radiation Facility (BSRF). The typical energy of the storage ring was 2.5 GeV and the electron current was ~250 mA in the top-up mode. The white light was monochromatized by a Si (111) double-crystal monochromator and calibrated with a Co foil (K-edge at 7709 eV). Samples were pressed into thin slices and positioned at 45° to the incident beam in the sample holder. The XAFS spectra were recorded in fluorescence mode with a Lytle detector oriented at 90° to the incoming beam.
The XAFS data were analyzed using the software packages Demeter50. The spectra were normalized using Athena firstly, and then shell fittings were performed with Artemis. The χ(k) function was Fourier-transformed (FT) using k3 weighting, and all fittings were done in R-space. The coordination parameters of samples were obtained by fitting the experimental peaks with theoretical amplitude. The quantitative curve-fittings were conducted with a Fourier transform k-space range of 2.7–11.8 Å−1. The backscattering amplitude F(k) and phase shift Φ(k) were calculated by the FEFF7.0 code. While the curve-fitting, all the amplitude reduction factor S02 was set to the best-fit value of 0.87 determined from fitting the data of cobalt foil by fixing coordination numbers as the known crystallographic value. In order to fit the curves in the R-range of 1.0–2.0 Å, we considered Co-N and Co-P paths as the central-peripheral. For each path, the structural parameters, like coordination number (CN), interatomic distance (R), Debye–Waller factors (σ2), and inner potential correction (ΔE0) were opened to be varied.
Catalytic performance evaluation
For the liquid phase hydrogenation of nitrobenzene, substrates (2 mmol), catalyst (5 mg), and solvent (EtOH/H2O, v-v = 4:1, 40 mL) were added into a 100 mL high-pressure autoclave. Then the autoclave was flushed three times with H2 and charged to certain pressure (3 MPa H2). The reaction was performed at the desired temperature. The product was collected at the reserved time and immediately analyzed using gas chromatography in combination with mass spectrometry (Shimadzu GCMS-QP2010S). The TOF values were determined within the substrate conversion below 20%, and the calculation of TOF was based on the total Co amount in catalysts. To evaluate the reusability of catalyst, the samples from the last reaction were separated by centrifugation, washing with ethyl acetate to remove the substrate, and drying under the vacuum. For the kinetic isotope effect test, D2 and D2O are used instead of H2 and H2O.
DFT calculations
All the spin-polarized first-principles calculations have used the code VASP51,52,53. Valence electrons of O(2s, 2p), N(2s, 2p), H(1s), C(2s, 2p), P(3s, 3p), and Co(3d, 4 s) were treated on a basis of plane waves explicitly54, while the core electrons were described with the projector-augmented wave method55. Spin-polarized calculations were carried out at the level of the generalized gradient approximation (GGA) adopting the Perdew, Burke, and Ernzerhof (PBE) exchange-correlation functional56. A kinetic energy cutoff of 400 eV was used for all calculations. The truncation criteria for the electronic and ionic loops were 10−5 eV and 10−2 eV/Å, respectively. Long-range dispersion was included according to the D3 method introduced by Grimme54. The vacuum layer was set to 20 Å to avoid interaction from adjacent cells. All the transition states were determined by using the climbing image nudged elastic band (CINEB) method57,58 and transition states were characterized via frequency analysis to ensure a single imaginary frequency in the desired reaction direction. The pure graphene is modeled by a (7 × 7) supercell with 49 carbon atoms, and the Co-NxPy-Gr model is modeled by one cobalt atom adsorption at vacancy site which is composed by getting rid of two carbon atoms and the N and P atoms substitute for four carbon atoms around cobalt atom, respectively. Monkhorst–Pack (5 × 5 × 1) Γ-centered grid sampling for the Brillouin zone was used for geometry optimization, and dipole corrections were included in the z-direction for each model surface. To study the stability of Co binding on graphene with N, P dual-coordination, the formation energy, and adsorption energy were defined as follows:
In the equations, E(Co-NxPy-Gr) is the total energy of adsorbed systems, E(NxPy) is the energy of graphene with doped N and P, E(Co-bulk) is the energy of one atom in the most stable Co crystal, and E(Co) is the energy of cobalt in the gas phase.
Data availability
The data supporting the findings of this study are available within the article and its Supplementary Information. Source data are provided with this paper. Additional data are available from the corresponding authors on reasonable request.
References
Jagadeesh, R. V. et al. Nanoscale Fe2O3-based catalysts for selective hydrogenation of nitroarenes to anilines. Science 342, 1073–1076 (2013).
Zhang, L. L., Zhou, M. X., Wang, A. Q. & Zhang, T. Selective hydrogenation over supported metal catalysts: from nanoparticles to single atoms. Chem. Rev. 120, 683–733 (2020).
Lang, R. et al. Single-atom catalysts based on the metal-oxide interaction. Chem. Rev. 120, 11986–12043 (2020).
Yan, H. et al. Atomic engineering of high-density isolated Co atoms on graphene with proximal-atom controlled reaction selectivity. Nat. Commun. 9, 3197 (2018).
Wei, H. et al. FeOx-supported platinum single-atom and pseudo-single-atom catalysts for chemoselective hydrogenation of functionalized nitroarenes. Nat. Commun. 5, 6634 (2014).
Ye, T.-N. et al. Stable single platinum atoms trapped in sub-nanometer cavities in 12CaO•7Al2O3 for chemoselective hydrogenation of nitroarenes. Nat. Commun. 11, 1020 (2020).
Zhang, S. et al. High catalytic activity and chemoselectivity of sub-nanometric Pd clusters on porous nanorods of CeO2 for hydrogenation of nitroarenes. J. Am. Chem. Soc. 138, 2629–2637 (2016).
Boronat, M. et al. A molecular mechanism for the chemoselective hydrogenation of substituted nitroaromatics with nanoparticles of gold on TiO2 catalysts: a cooperative effect between gold and the support. J. Am. Chem. Soc. 129, 16230–16237 (2007).
Serna, P. & Corma, A. Transforming nano metal nonselective particulates into chemoselective catalysts for hydrogenation of substituted nitrobenzenes. ACS Catal. 5, 7114–7121 (2015).
Yang, X.-F. et al. Single-atom catalysts: a new frontier in heterogeneous catalysis. Acc. Chem. Res. 46, 1740–1748 (2013).
Fu, T. et al. Acid-resistant catalysis without use of noble metals: carbon nitride with underlying nickel. ACS Catal. 4, 2536–2543 (2014).
Westerhaus, F. A. et al. Heterogenized cobalt oxide catalysts for nitroarene reduction by pyrolysis of molecularly defined complexes. Nat. Chem. 5, 537–543 (2013).
Wang, Y. et al. Chemoselective hydrogenation of nitroaromatics at the nanoscale iron(III)-OH-platinum interface. Angew. Chem. Int. Ed. 59, 12736–12740 (2020).
Li, H. et al. Cobalt single atoms anchored on N-doped ultrathin carbon nanosheets for selective transfer hydrogenation of nitroarenes. Sci. China Mater. 62, 1306–1314 (2019).
Zhang, L. et al. Atomically dispersed Co catalyst for efficient hydrodeoxygenation of lignin-derived species and hydrogenation of nitroaromatics. ACS Catal. 10, 8672–8682 (2020).
Zhou, P. et al. High performance of a cobalt-nitrogen complex for the reduction and reductive coupling of nitro compounds into amines and their derivatives. Sci. Adv. 3, NO. e1601945 (2017).
Liu, W. et al. Single-atom dispersed Co-N-C catalyst: structure identification and performance for hydrogenative coupling of nitroarenes. Chem. Sci. 7, 5758–5764 (2016).
Li, M. et al. Origin of the activity of Co-N-C catalysts for chemoselective hydrogenation of nitroarenes. ACS Catal. 11, 3026–3039 (2021).
Zhou, D. et al. Tuning the coordination environment of single-atom catalyst M-N-C towards selective hydrogenation of functionalized nitroarenes. Nano Res. 11, 1–9 (2021).
Wan, J. et al. In situ phosphatizing of triphenylphosphine encapsulated within metal-organic frameworks to design atomic Co1-P1N3 interfacial structure for promoting catalytic performance. J. Am. Chem. Soc. 142, 8431–8439 (2020).
Wei, X. et al. Cross-linked polyphosphazene hollow nanosphere-derived N/P-doped porous carbon with single nonprecious metal atoms for the oxygen reduction reaction. Angew. Chem. Int. Ed. 59, 14639–14646 (2020).
Long, X. et al. Graphitic phosphorus coordinated single Fe atoms for hydrogenative transformations. Nat. Commun. 11, 4074 (2020).
Yuan, K. et al. Boosting oxygen reduction of single iron active sites via geometric and electronic engineering: nitrogen and phosphorus dual coordination. J. Am. Chem. Soc. 142, 2404–2412 (2020).
Ren, Y. et al. Unraveling the coordination structure-performance relationship in Pt1/Fe2O3 single-atom catalyst. Nat. Commun. 10, 4500 (2019).
Liu, J. et al. Direct observation of metal oxide nanoparticles being transformed into metal single atoms with oxygen-coordinated structure and high-loadings. Angew. Chem. Int. Ed. 60, 15248–15253 (2021).
Wang, L. et al. A sulfur-tethering synthesis strategy toward high-loading atomically dispersed noble metal catalysts. Sci. Adv. 5, eaax6322 (2019).
Zhang, J. et al. Tuning the coordination environment in single-atom catalysts to achieve highly efficient oxygen reduction reactions. J. Am. Chem. Soc. 141, 20118–20126 (2019).
Shang, H. et al. Engineering unsymmetrically coordinated Cu-S1N3 single atom sites with enhanced oxygen reduction activity. Nat. Commun. 11, 3049 (2020).
Hai, X. et al. Engineering local and global structures of single Co atoms for a superior oxygen reduction reaction. ACS Catal. 10, 5862–5870 (2020).
Chen, C. et al. Zero-valent palladium single-atoms catalysts confined in black phosphorus for efficient semi-hydrogenation. Adv. Mater. 33, 2008471 (2021).
Chen, Y. et al. Atomic-level modulation of electronic density at cobalt single-atom sites derived from metal-organic frameworks: enhanced oxygen reduction performance. Angew. Chem. Int. Ed. 60, 3212–3221 (2021).
Ji, S. et al. Matching the kinetics of natural enzymes with a single-atom iron nanozyme. Nat. Catal. 4, 407–417 (2021).
Zhang, Y., Jiao, L., Yang, W., Xie, C. & Jiang, H.-L. Rational fabrication of low-coordinate single-atom Ni electrocatalysts by MOFs for highly selective CO2 reduction. Angew. Chem. Int. Ed. 60, 7607–7611 (2021).
Zhang, F. et al. In situ mosaic strategy generated Co-based N-doped mesoporous carbon for highly selective hydrogenation of nitroaromatics. J. Catal. 348, 212–222 (2017).
Qu, Y., Yang, H., Wang, S., Chen, T. & Wang, G. Hydrogenation of nitrobenzene to aniline catalyzed by C-60-stabilized Ni. Catal. Commun. 97, 83–87 (2017).
He, J. et al. Strategic defect engineering of metal-organic frameworks for optimizing the fabrication of single-atom catalysts. Adv. Funct. Mater. 31, 2103597 (2021).
Wang, H. et al. Highly efficient hydrogenation of nitroarenes by N-doped carbon-supported cobalt single-atom catalyst in ethanol/water mixed solvent. ACS Appl. Mater. Interfaces 12, 34021–34031 (2020).
Cai, Q. et al. Boosted catalytic hydrogenation performance using isolated Co sites anchored on nitrogen-incorporated hollow porous carbon. J. Phys. Chem. C. 125, 5088–5098 (2021).
Sun, X. et al. Single cobalt sites in mesoporous N-doped carbon matrix for selective catalytic hydrogenation of nitroarenes. J. Catal. 357, 20–28 (2018).
Sun, X. et al. Metal-organic framework mediated cobalt/nitrogen-doped carbon hybrids as efficient and chemoselective catalysts for the hydrogenation of nitroarenes. ChemCatChem 9, 1854–1862 (2017).
Tian, S. et al. Single-atom Fe with Fe1N3 structure showing superior performances for both hydrogenation and transfer hydrogenation of nitrobenzene. Sci. China Mater. 64, 642–650 (2021).
Yang, F. et al. Atomically dispersed Ni as the active site towards selective hydrogenation of nitroarenes. Green. Chem. 21, 704–711 (2019).
Wang, X. & Li, Y. Chemoselective hydrogenation of functionalized nitroarenes using MOF-derived Co-based catalysts. J. Mol. Catal. A: Chem. 420, 56–65 (2016).
Kuai, L. et al. Titania supported synergistic palladium single atoms and nanoparticles for room temperature ketone and aldehydes hydrogenation. Nat. Commun. 11, 48 (2020).
Liu, P. et al. Photochemical route for synthesizing atomically dispersed palladium catalysts. Science 352, 797–801 (2016).
Bai, L. et al. Explaining the size dependence in platinum-nanoparticle-catalyzed hydrogenation reactions. Angew. Chem. Int. Ed. 55, 15656–15661 (2016).
Qin, R. et al. Alkali ions secure hydrides for catalytic hydrogenation. Nat. Catal. 3, 703–709 (2020).
Liu, W. et al. A durable nickel single-atom catalyst for hydrogenation reactions and cellulose valorization under harsh conditions. Angew. Chem. Int. Ed. 57, 7071–7075 (2018).
Merte, L. R. et al. Water-mediated proton hopping on an iron oxide surface. Science 336, 889–893 (2012).
Ravel, B. & Newville, M. ATHENA, ARTEMIS, HEPHAESTUS: data analysis for X-ray absorption spectroscopy using IFEFFIT. J. Synchrotron Radiat. 12, 537–541 (2005).
Kresse, G. & Joubert, D. From ultrasoft pseudopotentials to the projector augmented-wave method. Phys. Rev. B 59, 1758–1775 (1999).
Kresse, G. & Furthmuller, J. Efficiency of ab-initio total energy calculations for metals and semiconductors using a plane-wave basis set. Comp. Mater. Sci. 6, 15–50 (1996).
Kresse, G. & Furthmuller, J. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. Phys. Rev. B 54, 11169–11186 (1996).
Grimme, S., Antony, J., Ehrlich, S. & Krieg, H. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. J. Chem. Phys. 132, 154104 (2010).
Blochl, P. E. Projector augmented-wave method. Phys. Rev. B 50, 17953–17979 (1994).
Perdew, J. P., Burke, K. & Ernzerhof, M. Generalized gradient approximation made simple. Phys. Rev. Lett. 77, 3865–3868 (1996).
Henkelman, G., Uberuaga, B. P. & Jonsson, H. A climbing image nudged elastic band method for finding saddle points and minimum energy paths. J. Chem. Phys. 113, 9901–9904 (2000).
Henkelman, G. & Jonsson, H. Improved tangent estimate in the nudged elastic band method for finding minimum energy paths and saddle points. J. Chem. Phys. 113, 9978–9985 (2000).
Acknowledgements
We thank the National Key R&D Program of China (Grant No. 2018YFA0703503 and 2018YFA0208504, C.C. and W.S.), the National Natural Science Foundation of China (NSFC 21932006, W.S.), the Youth Innovation Promotion Association of CAS (2017049, C.C.), Beijing Outstanding Young Scientist Program (BJJWZYJH01201914430039, W.Z.) and National Science Basic Research Program of Shaanxi (No. S2020-JC-WT-0001, X.Y.) for financial support. We thank the beamline 1W1B station in Beijing Synchrotron Radiation Facility (BSRF) and Dr. Lirong Zheng for help in XAFS characterization.
Author information
Authors and Affiliations
Contributions
H.J., C.C., and W.S. were responsible for most of the investigations, methodology development, data collection/analysis, and writing the original manuscript. P.L. assisted with the experiments analysis. X.Y. conducted the DFT calculations. P.C. helped to analyze the XAFS results. J.S. and W.Z. helped to conduct the atomic-resolution EELS. C.C. and W.S. were responsible for the funding and resources acquisition, supervising the project, revising, and editing the manuscript.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Communications thanks Chun Zhang, Jianglan Shui and the other, anonymous, reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jin, H., Li, P., Cui, P. et al. Unprecedentedly high activity and selectivity for hydrogenation of nitroarenes with single atomic Co1-N3P1 sites. Nat Commun 13, 723 (2022). https://doi.org/10.1038/s41467-022-28367-9
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-022-28367-9
- Springer Nature Limited
This article is cited by
-
Multifunctional Film Assembled from N-Doped Carbon Nanofiber with Co–N4–O Single Atoms for Highly Efficient Electromagnetic Energy Attenuation
Nano-Micro Letters (2024)
-
Fabrication of 3d-4f Hetero-metallic Catalyst of Co/CN-CeO2 Incorporating Nitrogen-doped Carbon for High Performance Hydrogenation of Nitroarenes
Journal of Inorganic and Organometallic Polymers and Materials (2024)
-
Preparation of magnetic biochar functionalized by polyvinyl imidazole and palladium nanoparticles for the catalysis of nitroarenes hydrogenation and Sonogashira reaction
Scientific Reports (2023)
-
Supramolecular tuning of supported metal phthalocyanine catalysts for hydrogen peroxide electrosynthesis
Nature Catalysis (2023)
-
Developing a class of dual atom materials for multifunctional catalytic reactions
Nature Communications (2023)