Single-atom catalysts offering intriguing activity and selectivity are subject of intense investigation. Understanding the nature of single-atom active site and its dynamics under working state are crucial to improving their catalytic performances. Here, we identify at atomic level a general evolution of single atom into a near-free state under electrocatalytic hydrogen evolution condition, via operando synchrotron X-ray absorption spectroscopy. We uncover that the single Pt atom tends to dynamically release from the nitrogen-carbon substrate, with the geometric structure less coordinated to support and electronic property closer to zero valence, during the reaction. Theoretical simulations support that the Pt sites with weakened Pt–support interaction and more 5d density are the real active centers. The single-atom Pt catalyst exhibits very high hydrogen evolution activity with only 19 mV overpotential in 0.5 M H2SO4 and 46 mV in 1.0 M NaOH at 10 mA cm−2, and long-term durability in wide-pH electrolytes.
The advances in the rational design and controllable synthesis of catalysts at the atomic level have led to a booming development in the fundamental and applied researches of catalysis1,2,3,4,5. Recently, single-atom catalysts (SACs) that comprise isolated active metal centers have attracted considerable research interests, owing to its maximum atom efficiency and unique atomic structures and electronic properties6,7,8,9. For instance, downsizing the expensive Platinum (Pt) nanoparticle to single-atom dispersion provides an effective way to not only create cost-effective catalysts, but also improve its activity and selectivity toward several electrochemical reduction processes, such as hydrogen evolution reaction (HER), oxygen reduction reaction, nitrogen reduction reaction, and CO2 reduction reaction10,11,12,13, etc. Despite these progress, further exploration of novel SACs is still an important frontier in catalysis research, both from the aspects of materials synthesis and mechanistic understanding. To this end, an atomic-level identification of the nature of the single-atom active site is imperative so as to aid the targeted design of SACs.
For the SACs reported so far, the atomically dispersed metal atoms are usually anchored on specific substrates by chemical bonding with neighboring atoms, such as the metal-nitrogen-carbon (M-N-C) materials with the trace metal and nitrogen co-doped on the carbon support14,15. The catalytic activity and selectivity of SACs are highly dependent on the local coordination environment of the metal centers, in other words, the electronic and geometric interactions between the single atoms and support16. As such, the metal–support interaction by electron transfer between single metal atom and the nearest coordination atoms will affect the charge density and distribution of metal sites, which will further impact the overall catalytic properties of the SACs16,17. The strong interaction between the single metal atom and supported N/C atoms can lead to a large charge transfer from metal to N/C atoms. Consequently, the metal atom is positively charged, presenting cation-like high-valence states. Although these high-valence metal atoms are beneficial for some electro-oxidation reactions4,18,19, they might be unfavorable for electro-reduction reactions, owing to the less d electrons participating in the reaction. If the metal–support interaction becomes weak, the electronic structure of the center metal atom might resemble that of a free atom, making bonding with reactants more energetically preferred in electro-reduction reactions20. However, such free single atoms are rarely reported in the as-prepared SACs previously, mostly from the consideration of stability issue. Indeed, it has been reported that single-atom active site would undergo reconstruction in atomic configuration, accompanied by the variations in valence state, under the working conditions1,8,21. This means that the interaction between single metal atom and support would be self-adjusted in order to boost the catalytic reaction. Therefore, a deeper understanding of the working state of SACs may provide some new insights into the SACs.
Here, we report the discovery of a near-free single-atom Pt as a highly efficient active center under the electrochemical HER condition, by using operando X-ray absorption fine structure (XAFS) technique. The operando XAFS allows us to follow the structural evolutions of single-site metal centers, and unravels that the single-atom Pt becomes low-coordinated with its surrounding atoms, together with the close-to-zero valence state. As a result, the interaction between single metal atom and N-C support is weakened, leading to a near-free state of Pt, which energetically facilitates H2O adsorption in alkaline electrolyte, followed by a more optimized H adsorption. As such, single-atom Pt anchoring on the specific site of N-C framework, accessed via the atomic layer deposition (ALD) method, exhibits the superior HER performance with ultra-low overpotentials and long-term stability in wide-pH-range electrolytes.
Structural characterization of Pt1/N-C single-atomic site catalyst
We synthesized atomically dispersed Pt on a metal-organic framework (MOF) derived N-C framework (sample designated as Pt1/N-C) using ALD. It is noted that each carbon ring of Uio-66-NH2 anchors one -NH2 group, and the -NH2-derived uncoordinated N site may act as the anchoring site for Pt atom during the ALD process (Supplementary Fig. 1). The combination of well-defined MOF structure and ALD technique helps atomic-level precise deposition of single-atom Pt on the specific N-C site with nearly uniform local coordination environments. The atomic-resolution scanning transmission electron microscopy (STEM) performed in high-angle annular dark field (HAADF) mode show that most Pt species are isolated and uniformly dispersed on the N-C substrate (bright spots corresponding to single-atom Pt) (Fig. 1a). The STEM-coupled energy-dispersive spectroscopy (EDS) element mapping further corroborates the presence of C, N, and Pt elements, and the homogeneous distribution of Pt throughout the octahedral-shaped sample (Fig. 1b). The single-Pt-atom site was further supported by CO-absorbed diffuse reflectance infrared Fourier transform spectroscopy (CO-DRIFTS). As shown in Supplementary Fig. 2a, the narrow and quasi-symmetrical band at ∼ 2084 cm−1, which remain unchanged during CO desorption, can be ascribed to linearly adsorbed CO on single-atom Pt. For comparison, we synthesized Pt nanoparticles (Pt-NPs) by treating the Pt1/N-C in a 20% H2/Ar flow at 300 °C (Supplementary Fig. 3). The CO-DRIFTS spectra of Pt-NPs exhibit a redshift of the IR peak from 2058 to 2052 cm−1 (Supplementary Fig. 2b) during CO desorption, which correlate with changes in dipole–dipole coupling between CO on the surface of Pt crystal22,23,24,25. Pt content in Pt1/N-C is ∼ 2.5 wt% as determined by the coupled plasma optical emission spectrometry (ICP–OES) analysis. Note that when using the Uio-66 derived C framework as the substrate, small Pt clusters are formed (Supplementary Fig. 4) under the same ALD process, confirming that the uncoordinated N atoms in the N-C framework provide essential sites for immobilizing single-atom Pt3,26,27. Furthermore, Pt-N coordination can be confirmed by N K-edge X-ray absorption spectroscopy and N1s X-ray photoelectron spectroscopy results (Fig. 1c and Supplementary Fig. 5). The N K-edge absorption spectrum of pure N-C framework without Pt can be characterized by four nitrogen features: pyridinic (peak a, 398.5 eV), pyrrolic (peak b, 399.4 eV), graphitic (peak c, 401.6 eV), and C-N-C or C-N σ* bond (peak d, 407.3 eV), respectively28,29,30. After Pt deposition, the pyrrolic peak b remains constant, whereas the pyridinic peak a is damped and split into two peaks (a1 and a2), where a2 is derived from a portion of pyridinic N bonded to Pt atoms, in accordance with the previous reports31,32.
Operando X-ray absorption spectroscopy study
To reveal the nature of the single-Pt-atom site under electro-reduction working conditions, the operando XAFS measurements using a purpose-built cell were performed on Pt1/N-C catalyst during HER. Carbon cloth was used as the working electrode for loading catalyst, together with Ag/AgCl reference electrode and carbon rod counter electrode in an electrochemical cell (Supplementary Fig. 6). As shown in Supplementary Fig. 7, the catalysts were homogeneously adhered in the gap of the carbon fibers without obvious aggregation, meaning that the catalysts may be fully exposed to the electrolyte so that subtle variations of the Pt active sites can be discerned.
Figure 1d shows the evolutions of normalized Pt L3-edge X-ray absorption near-edge structure (XANES) spectra with applied potential. The XANES spectrum of catalyst is characterized by the strong white-line peak, which corresponds to transition from the occupied Pt 2p3/2 core–electron to empty 5d states, and thus is indicative of 5d-band occupancy33,34. It can be obviously discerned that the overall white-line intensity (HA) decreases as applying negative potential during the reaction (Fig. 1d). Specifically, the white-line intensities of the catalyst under ex situ, open circuit and +0.5 V (vs. RHE, all voltages mentioned hereafter are normalized to RHE scale) conditions remain unchanged (Fig. 1e), suggesting that the single-atom Pt site is structurally stable without chemical adsorption of reactant species in the electrolyte. This is reasonable as +0.5 V is commonly considered as located in the double layer region where only capacitive charging process occurs on the electrode surface without any redox reaction35,36. When the applied potential negatively shifts to +0.15 V and to −0.07 V, the white-line intensity gradually decreases, indicating a higher 5d occupancy of Pt. Here, the unoccupied 5d states mainly arise from the hybridization between Pt and nearby C/N atoms from support. Hence, higher 5d occupancy implies the less charge transfer from the single-atom Pt to the nearby C/N atoms at +0.15 V and −0.07 V.
To obtain the quantitative information of electronic structural evolutions, we examine the valence state and formal d-band holes count of Pt. The above-described variations can be described more clearly from the differential XANES (∆XANES) spectra by subtracting the spectra collected at different potentials from that of Pt foil reference (Supplementary Fig. 8). The valence states and formal d-band hole counts of Pt can be determined quantitatively by integrating the area of the white-line peak in the ∆XANES spectra. It can be found that the mean valence state of Pt decreases from 1.89 to 1.17 and 1.12 for the catalyst at the potentials from +0.5 V to +0.15 V and −0.07 V (Fig. 2b), respectively, implying that the Pt site is reduced close-to-zero valence toward the metallic state. The formal d-band hole count was estimated using a slope of 1.174 unit area per d-band hole obtained from Pt0 foil (5d96s1) and PtIVO2 (5d66s0) standards. The absolute number of d-band holes for the ex situ Pt1/N-C is 2.420, which is reduced to 1.877 and 1.838 for the Pt1/N-C under +0.15 V and −0.07 V (Fig. 2a), suggesting the increased d-band electrons of Pt, verifying the weaker interaction between the Pt and the N-C substrate under working states.
The evolution of coordination configuration of single-atom Pt was further identified by extended X-ray absorption fine structure (EXAFS) (Supplementary Fig. 9 and 10). The Fourier-transformed (FT) k2-weighted EXAFS spectra for Pt1/N-C at the corresponding applied potentials all present a single dominant peak at ca. 1.6 Å that can be assigned to the coordination between Pt atom and C/N/O light atoms. However, the intensity of FT peak damps by ∼13 and 35% when the applied potentials negatively shift from +0.5 V to +0.15 V and to −0.07 V (Fig. 2c), respectively, suggesting the distinct variations of the local geometric structure of Pt site under working conditions. The geometric variations can also be reflected by the increased structural disorder, as revealed from the features in the XANES post-edge plateau corresponding to the interference of photoelectrons with local atoms. As shown in Fig. 1e inset, the intensity of the oscillation hump (HP) decreases with the increased potential, confirming dynamically disordered structures around the Pt atom33. Note that the above evolutions of the atomic and electronic structures are reversible as demonstrated in Supplementary Fig. 11 and 12.
Then, we would like to reveal the detail evolutions of geometric configuration of single-Pt site. To first confirm the geometric structure of the ex situ state, we performed EXAFS curve fitting considering two backscattering paths of Pt–C and Pt–N from N-C framework, for the Pt1/N-C under ex situ, open-circuit, and +0.5 V conditions (Fig. 2c and Supplementary Fig. 13). The best fitting analyses give four coordination number of Pt-C/N (Supplementary Table 1). Considering the limit of XAFS in differentiating Pt-C and Pt-N coordination because of the close scattering amplitude of C and N, we resort to the density functional theory (DFT) calculations considering several configurations, including Pt1-C3N1, Pt1-C2N2, and Pt1-C1N3 (Supplementary Fig. 14). Quantitatively, the Pt atom donates 0.47, 0.59 and 0.64 e to the support in Pt1-C3N1 Pt1-C2N2, and Pt1-C1N3, respectively (where e is the elementary charge) (Supplementary Table 2). The corresponding oxidation states of Pt estimated by normalizing Bader charges (see Supplementary Note 2) are 1.96 to 2.48 and 2.70 for Pt1-C3N1, Pt1-C2N2, and Pt1-C1N3, respectively (Fig. 2b and Supplementary Note 2). Hence, the calculated Pt valence state of Pt1-C3N1 (1.96) is more close to that (1.89) derived from XANES analyses. Based on these considerations, the best EXAFS fitting gives three Pt-C bonds (R = 2.04 Å) and one Pt-N bond (R = 2.09 Å) (Supplementary Table 1). Moreover, structures containing more than one Pt-N coordination, i.e., Pt1-C2N2, and Pt1-C1N3 can be reasonably excluded since it is unlikely for one Pt bridging two N atoms with N-N distance of ca. 10 Å between two adjacent N atoms in Uio-66-NH2.
Interestingly, for the catalyst under +0.15 V, the Pt–C/N coordination number reduced to 2, together with the appearance of one additional Pt–O coordination (R = 2.06 Å) (Fig. 2d and Supplementary Fig. 15), which is possibly arisen from the adsorption of the oxygen-related group from H2O or OH–. Considering that OH– adsorption should occur in a more positive potential region of 0.65 ∼ 0.85 V35, and in alkaline HER, the catalytic cycle is initiated by adsorption of H2O onto the active site. Hence, we can conclude that the Pt–O coordination can be ascribed to adsorption of H2O molecules. This is also consistent with the rate limitation step of dissociation of the absorbed H2O at this stage. The reduced coordination number of Pt with support indicate that Pt atoms are released from support, this effect we consider is beneficial for the adsorption of H2O molecules. Furthermore, only twofold Pt–C/N coordination was obtained for the catalyst at −0.07 V, where the water is dissociated into OH– and adsorbed H*, followed by the attack of another proton to generate H2. However, Pt–H coordination can hardly be discerned, owing to the small scattering amplitude of H37. Hence, only twofold Pt–C/N coordination is considered in the EXAFS fitting (Fig. 2d and Supplementary Fig. 16). These coordinative evolutions of Pt can be further confirmed by the wavelet transform analysis, as shown in Supplementary Fig. 17.
We want to note that these findings of near-free Pt state during electro-reduction reaction hold true in wide-pH environments. As shown in Supplementary Fig. 18, the operando XAFS measurements were also carried out in 0.1 m HClO4 (pH = 1) and 1.0 m NaOH (pH = 14) under the applied potential of +0.15 V. The variation trends of XANES and EXAFS spectra in pH1 and pH14 are analogous to those in pH 13, showing the significantly reduced intensities of white-line peak and FT peak. Through the quantitative analyses, we demonstrate that the single-atom Pt resemble the free atom during HER, with low coordination to the support and the valence state close to zero. We reckon that such evolutions of the single-Pt sites might directly boost the HER in wide-pH electrolytes.
Theoretical investigations based on DFT calculations were carried out to unravel the influences of the evolved configurations on the electronic structure. According to the above EXAFS fitting models, two possible and stable two-coordinate configurations, i.e., Pt1-C2 and Pt1-C1N1, were constructed for simulating the varied Pt local structure under realistic reaction, as shown in Fig. 3a. On the basis of Bader charge analysis, the charge transfer from the Pt atom to support is only ca. 0.1 ∼ 0.2 e for the Pt1-C2 and Pt1-C1N1, much smaller than 0.47 e for Pt1-C3N1 (Supplementary Table 2). As such, the Pt–support interactions of the two-coordinate models are much weaker than that of the ex situ Pt1-C3N1 model.
Based on the models in Fig. 3a, we then explore the potential HER activity of less-coordinate Pt1-C2 and Pt1-C1N1 sites. The overall HER pathway can be described by a three-state diagram comprising the initial catalyst-water state, to the catalyst-H intermediate state, and the final catalyst+H2 state. The Gibbs free-energy of atomic hydrogen adsorption, |ΔGH*|, has been considered as a reasonable descriptor of the HER activity. As is known, Pt shows the optimal level for H adsorption step with a near-zero ΔGH* (ca. 0.09 eV), owing to its suitable d-band position38,39. As shown in Fig. 3b, the ΔGH* of the two Pt1-C2 sites (0.17 and 0.06 eV) are closer to 0 eV, compared to that of ex situ Pt1-C3N1 site (0.40 eV). Moreover, both Pt1-C1N1 sites exhibit significantly larger |ΔGH*|, meaning that hydrogen adsorption on Pt1-C1N1 sites are too strong to desorb. The DFT analyses, in combination with the above XANES, indicate that the Pt in Pt1-C2 sites have more 5d densities close to free-atom Pt, leading to a more favorable H* adsorption, thus facilitating the HER in acid condition. For the HER in an alkaline media, the water dissociation kinetics from the Volmer step may determine the overall reaction rate. The DFT calculations show that the water adsorption on the two-coordinate sites is more favorable than that on the Pt1-C3N1 site, as the H2O adsorption energy decrease from 0.45 eV to 0.3 ∼ 0.35 eV (Fig. 3b).
Above analysis on adsorption energy demonstrates that hydrogen adsorption on Pt1-C2 sites is significantly improved comparing with that on Pt1-C3N1 site. To investigate the underlying reason, we carried out partial density of state (PDOS) analysis (Supplementary Fig. 19 and Fig. 3c). The dominant d band features (−1 ∼ −3.5 eV) of the three surfaces are nearly degenerate, compared to the broad d band of bulk Pt (Supplementary Fig. 19). The d band positions of both Pt1-C2 are lower than that of Pt1-C3N1, indicating weaker Pt–support interaction. Besides, an obvious peak appears near the Fermi level (0 eV) for the Pt1-C3N1 surface (Supplementary Fig. 19, pointed by arrows), suggesting relatively strong hybridization between Pt and C/N orbitals and reflecting strong bindings between Pt atoms and substrates. In contrast, the Pt sites of both two Pt1-C2 structures provide much smaller DOS at the Fermi level, further verifying the weakened Pt–support interaction, meaning that Pt atoms become freer from the supports under reaction conditions. We consider that such near-free Pt with more 5d density and low-valence state is favorable for the adsorption of H2O and H reactants. This can be confirmed by the DOS of the Pt1-C3N1 and Pt1-C2 surfaces (Supplementary Fig. 20). Compared with Pt1-C3N1, the prominent peaks of Pt1-C2 surfaces at the Fermi level imply higher localized electron density on Pt site, which may benefit the activation of H2O molecules and thus boosts HER activity.
Moreover, we consider the cases of a hydrogen atom adsorbed on the Pt1-C3N1 and two Pt1-C2 surfaces, and calculate the corresponding DOS projected onto the H 1 s states and Pt d bands (Fig. 3c, the middle and right panels). In the H 1 s PDOS, the dominant features are the H 1s-Pt 5d bonding resonances below the Fermi level, distinct in energy position and intensity for three different surfaces. In particular, the antibonding states are all above the Fermi level but in different energy position (noted by the arrows), by which the occupancy of antibonding states can be discerned. For instance, the antibonding states of Pt1-C3N1 is close to Fermi level, meaning a relative high occupancy. Although both Pt1-C2-1 and Pt1-C2-2 show higher energy position of antibonding, indicating lower antibonding occupancy and less repulsive interaction between H 1 s and Pt 5d orbitals, leading to the stronger Pt-H interaction. Note that the antibonding position of Pt1-C2-2 is lower than that of Pt1-C2-1, but the bonding state intensity of Pt1-C2-2 is much higher than that of Pt1-C2-1, resulting in a stronger hydrogen adsorption on Pt1-C2-2, consistent with the ΔGH* values.
Figure 3d shows schematic illustration of the interaction between Pt 5d and H 1 s orbitals. When the hydrogen adsorbate hybridizes with the d band of Pt, the adsorbate state split into localized bonding and antibonding states. The higher position of the antibonding, the stronger Pt-H interaction. Based on the above analysis, we reckon that with the evolution of Pt site from four-coordinate to two-coordinate, the antibonding states upshift to higher energy position, leading to lower occupancy and consequent stronger hydrogen adsorption. Hence, the theoretical insights emphasize the importance of the evolution of electronic and atomic structures of Pt into a near-free state under the electro-reduction potentials for the high HER activity.
Combining operando XAFS characterization and DFT calculation, we reveal for the first time that the single-atom Pt tend to evolve into a more freestanding state, which can substantially boost HER in both preferred water adsorption and moderate hydrogen adsorption. Thus, the electrocatalytic HER activities of Pt1/N-C was examined in wide-pH electrolytes, including 1.0 m KOH and 0.5 m H2SO4 solutions. For comparison, the HER performance of the pristine N-C substrate and commercial 20% Pt/C were also measured under the same test conditions. As shown in Fig. 4a, at the current density of 10 mA cm−2, the Pt1/N-C delivers a very small overpotential of 46 and 19 mV in alkaline and acid solution, respectively, superior to those of Pt/C (57 and 25 mV). In contrast, the pristine N-C substrate exhibits negligible HER activity in both acid and alkaline, as the current densities of N-C are close to zero, confirming that the high HER activity of Pt1/N-C is contributed by the single-atom Pt sites. Notably, the Tafel slope of Pt1/N-C in 1.0 m KOH is 36.8 mV dec−1, lower than that of Pt/C (39.8 mV dec−1), indicating the Volmer–Heyrovsky mechanism as the HER pathway39. The Tafel slope of Pt1/N-C (14.2 mV dec−1) in 0.5 m H2SO4 is also comparable to that of Pt/C (18.6 mV dec−1) (Fig. 4b). The result of HER catalyzing stability test is present in Fig. 4c, which shows negligible loss of current density in both acid and alkaline electrolytes in 20 hours, demonstrating excellent long-time durability of the Pt1/N-C catalysts. Also, the single-atom structure and dispersion are preserved, as can be confirmed by the electron microscopic and XAFS measurements for the Pt1/N-C catalyst after the long-time HER test (Supplementary Fig. 21). Moreover, the turnover frequencies (TOFs) of Pt1/N-C are 22.07 and 1.89 H2 s−1 in acid and alkaline, 10 and 12 times higher than those of Pt/C, respectively (Fig. 4d). To the best of our knowledge, the HER performances in the wide-pH electrolytes of our Pt1/N-C catalyst are almost the best among the SACs reported recently, as summarized in Supplementary Table 3. These results confirm that the Pt1/N-C possesses the best intrinsic HER activity that is mainly contributed by the reconstructed single-Pt sites.
On the basis of the operando XAFS, we identify the atomic and electronic structural evolutions of the single-atom Pt site under electrochemical HER. We uncover that the Pt atom tends to be a near-free state resembling a free metallic atom, that is, the interaction and charge transfer between Pt and N-C support is weakened. Theoretical simulations support that the near-free single-atom Pt possesses the favorable bonding energies with the reactants, responsible for the superior HER activity. Our study highlights the importance of creating more free single metal atoms while remaining stable for boosting the electrochemical reduction reactions. These findings also suggest a new insight into tailoring the coordination environment of single-atom active sites for developing high-performance single-atom electrocatalyst.
Synthesis of Uio-66-NH2 derived N-C framework
At first, a mixture of ZrCl4 (37.76 mg, 0.162 mmol) and H2BDC-NH2 (29.34 mg, 0.162 mmol) was dissolved in 36 mL DMF plus 4.0 mL HAc in a 60 mL glass vial, then sonicated for 1 h. The vial was sealed and heated at 120 °C for 24 h in an oven. The product was then centrifuged, washed with a mixture of methanol and DMF (volume ratio = 1:4), and then dried under vacuum at 90 °C. Then, powder of Uio-66-NH2 was placed in a tube furnace and heated to 700 °C in a heating procedure of 2 °C/min and preserved for 3 h, under a flowing argon atmosphere. After cooling to room temperature, the black powder was collected and dispersed in 30 mL H2O containing 0.2 mol HF for 8 h, and then centrifuged, washed with methanol and H2O (volume ratio = 1:4) and dried under vacuum at 100 °C.
ALD preparation of Pt1/N-C
Pt ALD was carried out on a viscous flow reactor (GEMSTAR-6 Benchtop ALD, Arradiance) by alternatively exposing to MeCpPtMe3 precursor and O2 (99.999%) at 150 °C. Ultrahigh purity N2 (99.999%) was used as the carrier gas at a flow rate of 200 mL/min. The Pt precursor was heated to 65 °C to get a sufficient vapor pressure. The reactor inlets were held at 110 °C to avoid any precursor condensation. The timing sequence was 80, 120, 60, and 120 s for the MeCpPtMe3 exposure, N2 purge, O2 exposure, and N2 purge, respectively.
The morphologies of the samples were examined by scanning electron microscopy and TEM on FEI-30 ESEM and JEOL-2100F systems at an accelerating voltage of 200 kV. EDS elemental mapping were obtained on a 26FEI Talos F200X device at 200 kV. HAADF–STEM, high-resolution TEM results were obtained on a JEM-ARM 200 F instrument at 200 kV. The concentration of Pt atoms was directly measured by ICP–OES (Optima 7300 DV, PerkinElmer). XPS measurements were carried out on an ESCALAB MKII instrument equipped with an Mg Kα source (hν = 1253.6 eV). The binding energy scale of all measurements was calibrated by referencing C 1 s to 284.5 eV. N K-edge XANES measurements were performed at the photoemission endstation at BL10B and BL12B beamlines of the National Synchrotron Radiation Laboratory (NSRL), China.
DRIFTS CO chemisorption measurements were performed on a Bruker IFS 66 v/s FTIR spectrometer equipped with a liquid nitrogen cooled HgCdTe (MCT) detector and a low-temperature reaction cell (Praying Mantis Harrick). The sample was loaded into the reaction cell and a background spectrum was collected. Next, the sample was exposed to 20% CO in Ar at a flow rate of 30 mL/min for 30 min to reach the CO saturation coverage. Then we purged the sample with Ar to remove the gas phase CO from the cell, and a series of DRIFT spectra were collected during both the CO-adsorption and the Ar-purgation process (256 scans, 4 cm−1).
All electrochemical measurements were carried out in a typical three-electrode electrochemical cell using graphite rod as the counter electrode and saturated Ag/AgCl as the reference electrode. The catalyst ink (5 mg catalyst + 765 μL water + 200 μL ethanol) was sonicated for 2 h to make the catalyst homogeneously dispersed, then 35 μL Nafion solution (5 wt%) was added to the ink and sonicated for 30 min. The as-prepared ink (10 μL) was loaded onto the glass carbon electrode to form the working electrode. Commercial 20% Pt/C catalyst was from Shanghai River Sen Electric Co. The sample loading was determined to be ∼0.25 mg cm−2. The HER activity measurement was carried out in high purity H2-saturated 0.5 m H2SO4 (pH 0.1) and 1.0 m KOH (pH 13.8), using linear sweep voltammetry with a scan rate of 5 mV s−1. The HER stability was evaluated by measuring amperometric i–t curve under the overpotential (J = 10 mA cm−2). The potentials were calibrated to RHE using Pt mesh as working electrode (Supplementary Fig. 22):
Operando XAFS measurements
The Pt L3-edge (11,564 eV) XAFS spectra were measured at the 1W1B beamline of Beijing Synchrotron Radiation Facility (BSRF), China. The storage ring of BSRF was operated at 2.5 GeV with a maximum electron current of 250 mA. The hard X-ray was monochromatized with a Si (111) doublecrystal monochromator and detuned by 30% to remove harmonics. Operando XAFS measurements were performed in the fluorescence mode. Position of the absorption edge (E0) was calibrated using Pt foil.
XAFS data analysis
The acquired EXAFS data were processed according to standard procedures using the ATHENA module implemented in the IFEFFIT software packages40. The k2-weighted χ (k) data in the k-space ranging from 3.0 to 11.0 Å−1 were Fourier-transformed to real (R) space using hanning windows (dk = 1.0 Å−1) to separate the EXAFS contributions from different coordination shells. To obtain the detailed structural parameters around the Pt atom in the as-prepared samples, quantitative curve fittings were carried out for the Fourier-transformed k2χ(k) in R-space using the ARTEMIS module of IFEFFIT. Effective backscattering amplitudes F(k) and phase shifts Φ(k) of all fitting paths were calculated with the ab initio code FEFF8.0. For the Pt1/N-C samples, a k-range of 3.0 ∼ 11.0 Å−1 was used and curve fittings were carried out in R-space within an R range of (1.0, 2.1) Å for k2-weighted χ(k) functions. The number of independent points is given by
As for the sample under various conditions, the Fourier-transformed curves all showed a single prominent coordination peak at ∼1.6 Å assigned to the Pt-C/N coordination. For the ex situ Pt1/N-C sample, two separate Pt-C and Pt-N scattering paths were included for fitting. The combination of oxidation state and EXAFS fittings demonstrate that four-coordinate Pt with three Pt-C bonds and one Pt-N bond, is most reasonable for ex situ sample, as well as the open circuit and +0.5 V sample. The FT peak intensity of the sample under +0.15 V declines by 13%, which may arise from the Pt-C/N bonds breaking, together with an additional Pt-O coordination from H2O adsorption. Thus, the scattering paths of Pt-C/N and Pt-O were considered. Although under −0.07 V, the FT peak intensity further declines by 35%, which is ascribed to the dissociation of the adsorbed H2O followed by H adsorption on Pt, leading to only Pt-C/N path considered for EXAFS fitting. It should be mentioned that under operating conditions, the structures derived from EXAFS fitting may correspond to the species that are most present in the rate-limiting step. Hence, under +0.15 V, the water absorbed on Pt1-C2 or Pt1-C1N1 structures (H2O-Pt1-C2, H2O-Pt1-C1N1) are considered because the reaction is limited by dissociation of the absorbed H2O. Although under −0.07 V, the rate-limiting step is Heyrovsky step determined by the Tafel slope, leading to high-coverage absorbed H keep intact on Pt from desorption, and thus H-Pt1-C2 and H-Pt1-C1N1 structures are considered.
During curve fittings, the Debye–Waller factors (σ2) and bond length (R) were treated adjustably for all samples in all paths. For the ex situ sample, N and R were treated as adjustable parameters for both Pt-N and Pt-C shells, whereas their σ2 and ΔE0 were set equal in order to reduce the number of fitting parameters. Thus, the number of the adjustable parameters for the ex situ sample is Npara = 6 ≤ Nipt. For the +0.50 V sample, ΔE0 of the Pt-C/N path was set equal to that of the ex situ sample, other parameters were treated adjustably. Npara = 6. For the +0.15 V and −0.07 V sample, ΔE0 of the Pt-C/N path were set equal to that of the ex situ sample. In addition, the fitting strategy of the 0.15 V-pH1 sample was identical to −0.07 V sample; while the fitting strategy of +0.15 V-pH14 sample was identical to that of the +0.15 V sample. Using these strategies, all generated R factors are smaller than 0.01, indicating excellent quality.
All theoretical calculations were performed using Vienna ab initio simulation packages41. The exchange–correlation interaction was described by the generalized gradient approximation with the Perdew–Burke–Ernzerhof functional42. A two-dimensional carbon/nitrogen matrix supercell was built on a 8 × 8 unit cell for the four-coordinate Pt1-C3N1 system, to simulate the two-coordinate Pt intermediate, we modulated the pristine graphene surface with 16 (Pt1-C2-1, Pt1-C1N1-1) and 15 (Pt1-C2-2, Pt1-C1N1-2) carbon/nitrogen atoms removed. The effects of the varying hydrogenation degrees of the dangling carbon atoms around the defects have been investigated (Supplementary Fig. 23). Considering that these dangling carbon atoms would undergo hydrogenation during electrochemical reduction, thus they were saturated with H atoms in the main text. The plane wave cutoff was set to 500 eV, with the convergence of energy and force set to 1 × 10−5 and 0.01 eV Å−1, respectively. To avoid the interaction between two adjacent layers the vacuum thickness was set to 15 Å. The Brillouin zone was sampled by a 5 × 5 × 1 k-point grid with the Monkhorst–Pack scheme for structural optimization and a 10 × 10 × 1 k-point grid for electronic structure calculations for all systems. The solvent effects were considered by using the Poisson–Boltzmann implicit solvent model with the dielectric constant set to be 78.4 for solvent water43.
The data supporting the findings of this study are available from the corresponding author upon reasonable request.
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This research was supported by China Ministry of Science and Technology under Contract of 2017YFA0208300 and 2017YFA0402800, the National Natural Science Foundation of China (grants no. 21471143, 21533007, 11621063) and the Fundamental Research Funds for the Central Universities (KY2310000020, WK2340000076, WK2060030029), and Youth Innovation Promotion Association CAS (CX2310000091). We thank NSRL, BSRF, and SSRF for the synchrotron beam time.
The authors declare no competing interests.
Peer review information Nature Communications thanks Bin Liu and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Fang, S., Zhu, X., Liu, X. et al. Uncovering near-free platinum single-atom dynamics during electrochemical hydrogen evolution reaction. Nat Commun 11, 1029 (2020). https://doi.org/10.1038/s41467-020-14848-2
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