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Direct electrosynthesis of 52% concentrated CO on silver’s twin boundary


The gaseous product concentration in direct electrochemical CO2 reduction is usually hurdled by the electrode’s Faradaic efficiency, current density, and inevitable mixing with the unreacted CO2. A concentrated gaseous product with high purity will greatly lower the barrier for large-scale CO2 fixation and follow-up industrial usage. Here, we developed a pneumatic trough setup to collect the CO2 reduction product from a precisely engineered nanotwinned electrocatalyst, without using ion-exchange membrane. The silver catalyst’s twin boundary density can be tuned from 0.3 to 1.5 × 104 cm−1. With the lengthy and winding twin boundaries, this catalyst exhibits a Faradaic efficiency up to 92% at −1.0 V and a turnover frequency of 127 s−1 in converting CO2 to CO. Through a tandem electrochemical-CVD system, we successfully produced CO with a volume percentage of up to 52%, and further transformed it into single layer graphene film.


Efficient catalyst design and complex product synthesis are two major challenges in electrochemical CO2 reduction reaction (CO2RR) toward industrial application. Defects engineering is one of the most effective strategies to promote catalyst’s performance, for defects have highly unsaturated coordinate-number and special electronic structure1,2,3. By introducing defects like doped atoms4,5, edges6, interphase boundaries7,8, grain boundaries9, and twin boundaries10 (TBs) in catalysts such as copper or silver, they tend to exhibit an outstanding activity with specific selectivity. Among those defects, TB, a mirror plane dividing the crystal lattice into two symmetric parts, shows many intriguing properties for its unique atomic arrangement11,12. Beneficial from the low interfacial energy, TB is one of the most stable defects in typical face-centered cubic (fcc) metals. Highly dense TBs have not only made copper highly conductive and mechanically stronger, but also more efficient to convert CO2 into CH410,11,12. Different from Cu, metal silver can selectively transform CO2 into CO, owing to its low adsorption energy of CO and high overpotential for hydrogen evolution reaction (HER)13,14. The fivefold twinned silver nanowires have been reported to be a prominent catalyst in CO2RR15, and recently study suggests that TB in this kind of silver nanowires shows two orders higher activity than (100) facet of silver nanocubes16. However, the exact catalytic contribution of Ag’s TB in nanocrystal has been mixed with other factors such as strain, size-effect, and capping agent. Therefore, it is still challenging to reveal the TB’s catalytic contribution under a well-defined condition.

Fabricating highly dense TBs on a plane electrode can eliminate the unwanted factors in nano-sized catalysts10. Nanotwinned Ag (Nt-Ag) can be obtained through sputtering Ag on special substrates like single-crystalline faceted silicon17, which requires premium instruments and high-quality substrates, limiting its industrial application. Pulsed electrodeposition has been widely applied to synthesize nanotwinned copper11,12, but its success on silver has not been achieved yet.

On the other hand, fixing carbon from CO2 and converting them into high value-added products such as medical molecules or electronic-grade graphene is one of the ultimate goals in CO2 reduction. It has been reported that graphene sheets with many defects can be produced from CO2 in molten salt18. In mild aqueous conditions, C5+ products have never been directly synthesized using CO2 as the only carbon source, due to the high thermodynamic stability of CO2. An alternative way for CO2 conversion is a “two-step” strategy, where CO2 firstly transforms into CO and CO subsequently evolves in the next chemical reaction into other products19,20. Although it has been regarded as one of the most promising ways for complex product synthesis, unfortunately, conventional H-type cells can produce CO with a volume fraction level of ~0.01–2%21,22,23,24,25,26,27,28,29,30. This is because the CO product is always mixed with the original stream of CO2 in this system. With introducing a three-phase interface, a gas-diffusion electrode (GDE) can largely enhance the CO yield and lift the CO concentration to several tens of percent21,22,23,31,32,33,34,35,36,37,38,39. However, with the sophisticated membrane system, the efficiency of GDE relies on meticulous parameter control such as the thickness and hydrophobicity of functional layers. The ion-change membrane also hinders the mass transfer between anolyte and catholyte and depletes the electrolyte like bicarbonate in some certain setup. In addition, high-efficient GDEs are mainly made of particle-like samples as their catalytic layer. As for plate electrodes like metal foils, which are more common in industrial electrosynthesis, it still cannot be fabricated into a GDE. Recently, pure carbonate (or bicarbonate) reduction was reported as an alternative way for CO2 utilization40,41,42. Assisted by a bipolar membrane, CO2 in situ released from carbonate (or bicarbonate) can be further reduced to CO. Without additional gaseous CO2 complementing, the product concentration is able to maintain a high level, but the Faradaic efficiency (FE) is also limited by the insufficient CO2 supplement.

Here, we developed a facile way to synthesize Nt-Ag with controllable TB density, which can serve as a high-performance CO2RR catalyst. With a new CO2 conversion system based on a pneumatic trough, ultrahigh-concentration CO was produced without using an ion-exchange membrane. By channeling the reduced CO stream into a chemical vapor deposition (CVD) system, we could finally convert the carbon atoms from CO2 into highly value-added single-layer graphene with extraordinary high quality.

Results and discussion

The pulsed electrochemical deposition was introduced to synthesize highly dense TBs. Under  a pulsed current density of 1 A cm−2, the nanotwinned catalyst with the most probable twin width of 10 nm (Nt-10) was prepared. Its TB structure was further characterized with high-resolution electronic transmission microscopy (HRTEM) and selected area electron diffraction (SAED). Under TEM observation (Fig. 1a), there are many highly dense lines, which were recognized as silver {111} facet, parallelly emerging on Ag crystal. The lattices at both sides of the line (Fig. 1b) symmetrically arranged, showing a typical TB structure. The SAED pattern (Fig. 1c) shows two sets of diffraction spots symmetrical about a common {111} plane, further confirming a representative TB structure.

Fig. 1: Silver catalysts with tunable TB density.

a TEM image of parallel TBs (scale bar: 10 nm). TB represents twin boundary. b The atomic arrangement of a representative TB in FFT-treated HR-TEM (scale bar: 1 nm). The two marked rhomboids represent the Burgers circuits. c The typical SAED pattern of silver’s TB. The white and yellow circles label diffraction spots of matrix and twin, respectively. df TEM images of Nt-10, Nt-18, and Nt-730, respectively (scale bar: 100 nm). The white dashed lines mark TBs. gi The twin width distribution of Nt-10, Nt-18, and Nt-730, respectively. j The statistical histogram of TB density.

In order to control the TB density, we annealed Nt-10 at 300 and 800 °C for 2 h to obtain Nt-18 and Nt-730, and then measured their TB width and TB density with statistic methods from randomly selected TEM images (Supplementary Fig. 1). As shown in Fig. 1d–f, after annealing, the TB density remarkably decreases. The twin widths of Nt-10 mainly concentrate on ~10 nm and its corresponding TB density was measured as ~1.48 × 105 cm−1 (Fig. 1g, j). In contrast to Nt-10, most TB widths in Nt-18 shift to ~18 nm (Fig. 1h), and the TB width distribution dispersion gets larger, giving rise to a lower TB density of 6.2 × 104 cm−1. After annealing at 800 °C, only ~2% TBs remain in Nt-730. The twin widths in Nt-730 grew up with a distribution from hundreds of nanometers to several microns and the most probable twin width expands to 730 nm (Fig. 1i).

In some cases, high-temperature annealing can change the catalyst surface morphology and facet orientation, which leads to unexpected variation in its catalytic performance. To investigate our samples’ surfaces change, we carried out scanning electron microscopy (SEM) observation and surface roughness factor measurement. After annealed at 300 and 800 °C, the macroscopical surface morphology barely changes (Supplementary Fig. 2). Annealing could rearrange the atoms of the surface at an atomic level, yet it is not enough to reshape the bulked Ag’s macroscopical morphology. The roughness factors measured by cyclic voltammetry (CV) of Nt-10, Nt-18, and Nt-730 are 8.8, 8.2, and 8.4, respectively (Supplementary Fig. 3 and Supplementary Table 1), further confirming that the surface morphology of all samples is similar. Facet orientation was evaluated with X-ray diffraction (XRD). For Nt-10, besides low-index (111) and (200) planes were detected at the 2θ of 38.4° and 44.5° (Supplementary Fig. 4), the high-index (220) and (311) which usually have higher catalytic activity were also found at 64.6° and 77.6°. To our surprise, even after annealing at 800 °C, the high-index facets still existed. The peak ratio of the high-index facet only changed slightly, although the results represent the bulk information, which can not be extrapolated to the surface facet change. In brief, by using pulsed electrodeposition and annealing methods, we obtained a series of bulked Ag samples with controllable TB density and similar surface circumstances, which were further used as a defect model to study CO2RR on TBs.

The catalytic performance of CO2RR on TBs was preliminarily investigated by linear scanning voltammetry (LSV) in CO2-saturated and N2-saturated solutions. As shown in Fig. 2a–c, on Nt-10, the current density (j) in CO2-saturated solution is larger than that in N2-saturated solution after −0.6 V, suggesting a preference of CO2RR over its competing reaction, namely the hydrogen evolution reaction. However, as TB density decreases, the j in the N2-saturated solution starts to rise and the counterpart in CO2-saturated solution gradually declines. Eventually, the j in N2-saturated solution on Nt-730 surpasses that in CO2-saturated solution, indicating the HER becomes dominated when TBs are deficient. A similar trend was also observed in their Nyquist plots (Supplementary Fig. 5 and Supplementary Table 2). For Nt-10, the charge-transfer resistance (Rct) in CO2-saturated solution (~2.0 kΩ cm2) is smaller than that in N2-saturated solution (~4.9 kΩ cm2). However, for Nt-730, this rank of value is inverse, proving that electrons on TBs could more easily transfer to CO2 rather than H+.

Fig. 2: The CO production on the silver’s TBs.

LSV curves obtained on a Nt-10, b Nt-18, and c Nt-730 in N2-saturated and CO2-saturated electrolyte. d The FECO under different applied cathode potentials in CO2-saturated electrolyte. e The correlation between \(j_{{\mathrm{CO}}}^{{\mathrm{EASA}}}\) and TB density at different potentials. f Nyquist plots of Nt-10, Nt-18, and Nt-730 at −0.7 V in CO2-saturated solution. All electrochemical measurements were carried out in a 0.5 M KHCO3 solution.

The precise gas and liquid products were further analyzed with gas chromatography (GC) and 1H nuclear magnetic resonance (NMR), respectively, (Supplementary Fig. 6). The GC spectrum shows that CO and H2 are the only gaseous products for all samples, while no any liquid products were detected. For Nt-10, the CO started to produce at a low potential of −0.8 V with a FECO of 74% in CO2-saturated 0.5 M KHCO3 solution and reached its maximum FECO of 92% at −1.0 V (Fig. 2d). With TB density declines, the FECO of Nt-18 and Nt-730 gradually decreased to 54 and 38% at −1.0 V, which manifests TB enhances the selectivity of CO production.

Our previous work reported a method to estimate the intrinsic activity of copper TB by correlating its activity with the corresponding density10. Using the same method, we separated intrinsic partial current densities of CO (jCO) on TB from that on plane atoms. In order to eliminate the effect brought by the difference of surface roughness, we used electrochemical active surface area (EASA) to normalize jCO (\(j_{{\mathrm{CO}}}^{{\mathrm{EASA}}}\)) to represent the activity of CO evolution. As shown in Fig. 2e, \(j_{{\mathrm{CO}}}^{{\mathrm{EASA}}}\) displays a linear relation with TB density from −0.8 to −1.0 V. The values of slope and intercept represent the intrinsic jCO on TB and plane, respectively. The calculated results are summarized in Supplementary Fig. 7. Notably, at −1.0 V, the intrinsic jCO on TB is ~33 mA cm−2, corresponding to the turnover frequency (TOF) of 127 s−1, which is believed to be the highest value in electrochemical CO evolution from CO2 (Supplementary Fig. 8 and Supplementary Table 3). By contrast, the jCO on a plane is only ~0.1 mA cm−2 at the same condition, corresponding to the TOF of 0.39 s−1, ~0.3% of the activity on TB atoms. At more negative potentials, such linear relation was not observed, for the mass-transfer process becomes dominated on TB-rich samples.

The pulsed electrochemical deposition allows us to fabricate TBs on diverse substrates such as inert metals and carbon materials (Supplementary Fig. 9). The Nt-Ag deposited on different substrates remains similarly high catalytic performance (Supplementary Fig. 10), which endows Nt-Ag with universal application in future. As TB is one of the most stable defects in fcc metals, the Nt-10 can endure long-time reaction with nearly no performance decline in 32 h (Supplementary Fig. 11). The SEM images and XRD patterns before and after reaction did not show a significant change in Nt-10’s morphology and facet orientation (Supplementary Fig. 12 and Supplementary Fig. 13). More detailed structural information was given by TEM observation (Supplementary Fig. 14). After a 12-h reaction, TB still maintained its density with a negligible change in twin width. For other active centers, we observed that dislocations changed both in position and atomic arrangement and the facets were slightly contaminated, further displaying the prominent stability of TBs over other defects.

The superior catalytic performance of Nt-10 is attributed to that TBs lower the barrier of the charge-transfer process from the electrode to CO2 and dynamically weaken the activity of competing HER. In CO2-saturated electrolyte, Nt-730 has a high Rct of ~6.3 kΩ cm2 (Fig. 2f and Supplementary Table 2), while highly dense TBs in Nt-10 remarkably reduce Rct to ~2.0 kΩ cm2, fastening the CO evolution on silver. In contrast, the competing HER on TB was largely suppressed. At all potentials, both FEH2 and \(j_{{\mathrm{H2}}}^{{\mathrm{EASA}}}\) show a conspicuous decrease with TB density rising (Supplementary Fig. 15). Further chemically dynamic research using Tafel plots and Nyquist plots in N2-saturated electrolyte were carried out to investigate about the competition with HER. The Tafel slopes on Nt-10 and Nt-730 were measured as 301 and 276 mV dec−1 (Supplementary Fig. 16), suggesting that TB dynamically deactivates the HER on silver. The corresponding Nyquist plots (Supplementary Fig. 17) also show a smaller Rct on Nt-730 than Nt-10’s, which confirms HER has a higher dynamic barrier of electron-transfer from TB.

With the superior catalytic performance on Nt-10, we designed a tandem system based on a pneumatic trough to collect CO product and further transform it into graphene film (Fig. 3a). In conventional H-type cells or GDE, CO2 and gas products share the same outlet, and the products are therefore diluted by CO2. In our system, the product is separated from the inlet of CO2 with a pneumatic trough (Supplementary Fig. 18). When CO2 was bubbled into the electrolyte, the dissolved CO2 can diffuse to the surface of the electrode while undissolved gas was expelled outside the pneumatic trough. Therefore, the CO product is isolated by the pneumatic trough from CO2 feedstock and the anodic products without using premium ion-exchange membranes. Compared with the GDE structure, this system is suitable for more types of solid materials, including metal plates and particles on appropriate supports. Moreover, the absence of an ion-exchange membrane simplifies the cell structure and facilitates the mass exchange between anolyte and catholyte. We performed the chronopotentiometry at a constant current of 30 mA in pneumatic-trough-based cell and commercial H-type cell with/without Nafion 117 membrane for 24 h (Fig. 3b). The initial cell voltage of our system is ~3.3 V, slightly lower than that of the commercial H-type cell, which is mainly attributed to the lower ohmic resistance originated from different electrolyzers’ shapes (Supplementary Fig. 19). We observed that both the pneumatic-trough-based cell and the H-type cell without using Nafion 117 membrane maintained stable cell voltages, while in a Nafion 117 membrane system, the cell voltage continuously climbing after 8 h. In a detailed pH and conductivity study (Supplementary Fig. 20), the possible mechanism can be attributed to inefficient ion exchange, marked with a continuous depletion of KHCO3 in the anolyte, and a continuous accumulation of KHCO3 in the catholyte. By choosing different electrolytes at both sides, such as using H2SO4 as the anolyte and KHCO3 as the catholyte, the cell voltage can keep stable for a longer time, despite that a small amount of CO2 may form at the interface between Nafion membrane and KHCO3 catholyte (Supplementary Fig. 21). Overall, the low ohmic resistance and higher cell voltage stability of pneumatic-trough-based cell lifts the energy conversion efficiency and benefits an energy conversion efficiency of up to ~53% on Nt-10 (Supplementary Fig. 22).

Fig. 3: Tandem system for graphene synthesis.

a The schematic diagram of “two-step” synthesis of graphene from CO2. b Cell voltages at a constant current density of 30 mA cm−2 in pneumatic-trough-based cell and H-type cell with/without Nafion 117 membrane. The area of the electrode is ~1 cm2. The “overflow” represents the applied voltage reaches the maximum of our electrochemical workstation (20 V). The κa represents the electric conductivity of anolyte. c The literature summary of FECO and initial CO concentration21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,40,41. The red, green, gray, and blue spots represent the results of this work, carbonate reduction systems, GDE systems, and H-type cell systems, respectively. d The TEM image of graphene film edge (scale bar: 10 nm) The e raw and f FFT-treated HRTEM images of graphene film lattice (scale bar: 2 nm). g The SAED pattern of graphene film and the intensity profile of diffraction spots along (2\(\overline 1 \overline 1\)0), (1\(\overline 1\)00), (0\(\overline 1\)10), and (\(\overline 1 \overline 1\)20) facet. h Raman spectrum of graphene film.

More importantly, the CO product in our system would not be directly diluted by the CO2 feedstock. The theoretical ceiling of CO concentration in this system equals to catalyst’s FECO. However, under real electrochemical circumstances, the CO2 will escape from the CO2-saturated electrolyte. The escape rate can be influenced by the temperature, electrolyzer shape, and roughness of the electrode43. Under our most optimal condition, the initial concentration of CO can reach up to 52% (Supplementary Fig. 23), higher than the CO concentration in most GDE systems (Fig. 3c and Supplementary Table 4). The high concentration of CO makes it possible to be applied in industrial processes. With simple gas purification, we pumped CO product into tube furnace for graphene growth. The detailed growth conditions were described in the Supplementary Information and Supplementary Fig. 24.

Graphene is a valuable carbon material with fascinating performance in electronic devices44. Many efforts have been devoted to converting CO2 to graphene, yet high-quality graphene film has not been achieved45,46. The major obstacle is the two oxygen atoms in CO2. Although it has been reported a moderate amount of oxygen is beneficial to high-quality graphene growth47,48, surplus oxygen in the CO2 molecules, however, can etch graphene49. With partially deoxidize CO2 into CO, CO can transform into a continuous graphene film (Supplementary Fig. 25). The TEM image of the film’s edge indicates most area of the film is single layer (Fig. 3d), and its lattice structure under HRTEM observation is perfect with few defects (Fig. 3e, f). Its corresponding SAED spots also exhibit a typical single-layer graphene pattern (Fig. 3g). Particularly, the diffraction intensities of (2\(\overline 1 \overline 1\)0), (1\(\overline 1\)00), (0\(\overline 1\)10), and (\(\overline 1 \overline 1\)20) are about the same, consistent with the feature of single-layer graphene50. Further Raman spectrum analysis (Fig. 3h) shows an IG/I2D of 0.45 and a full width at half maximum (FWHM) of 25 cm−1 for 2D peak, corresponding to single-layer structure51,52. The low ID suggests the film is with few defects.

By contrast, we pumped pure CO2 into our system under similar conditions, but no graphene film formed. Instead, CO2 transforms into snow-flake-like graphene fragments with an average size of ~16 μm (Supplementary Fig. 26). The discontinuity of graphene fragments is mainly due to the etching of CO2. Its TEM observation (Supplementary Fig. 27) indicates the layer number of most graphene is more than 7. Raman spectrum (Supplementary Fig. 28) also shows that IG/I2D at the most regions is higher than 2.75 with a very large FWHM of the 2D peak of ~60 cm−1, manifesting a much thicker graphene layer.

In conclusion, we developed a method to synthesize TBs on Ag, with a TB density of 1.5 × 105 cm−1. Powered by these TBs, the electrocatalyst can easily transfer electron to CO2 and surpass the competing HER. With a tandem two-step system, the direct CO product from CO2RR can reach an industrial concentration without using ion-exchange membrane, and successfully transformed into high quality single-layer graphene. This work further fulfills our understanding of CO2RR with controllable TB defects and boosts the development of electrochemical CO2RR toward industrial production.


Silver catalyst preparation

The Nt-10 was deposited on a piece of graphite paper or other substrates using current-pulse mode in a two-electrode system, with an anode of silver foil. The electrolyte is a 1 M AgNO3 solution. The on-time and off-time of the pulsed current were set as 20 and 2000 ms, respectively, with the peak current density of 1 A cm−2. After deposition, the as-prepared Ag was stripped from the graphite paper.

The Nt-18 and Nt-730 were synthesized by annealing the Nt-10 at 300 and 800 °C, respectively, in the H2 atmosphere for 2 h.

Graphene growth

Graphene film was synthesized with the CVD method on copper foil. First, a piece of copper foil with a thickness of 30 μm was electrochemically polished in 85wt.% H3PO4 solution for ~1 min. The counter electrode is also copper foil with twenty times larger area. The applied voltage is 5 V. The as-prepared copper foil was then put in tube furnace for graphene growth. The tandem graphene growth system is composed of three functional parts (Supplementary Fig. 22)—gas purification part, CO activation part and graphene growth part. The gas purification part contains three purification tubes filled with NaOH/asbestos, dried silica gel and MnO, respectively, in order to remove unfavored CO2, water and O2. The CO activation part is 6 g of commercial Ni/Al2O3 catalyst (Sichuan Shutai Co. Ltd.), which can transform CO into hydrocarbon intermediates. The graphene growth part is a conventional CVD tube furnace. Before graphene growth, the copper foil was annealing in air atmosphere (25 mttor) at 1060 °C for 10 s, then H2 (50 sccm, ~8000 Pa) as the reductant was flowed into quartz tube. Subsequently, 300 mL of CO product was pumped into the tandem system. With adjusting the flow rate of CO product, the total pressure was controlled at ~8400 Pa for at least 5 min. Graphene fragment using pure CO2 was synthesized in the similar way, but NaOH/asbestos and MnO was removed for they can adsorb CO2.

Characterization of structure

The structure characterization condition is similar to our previous work10. XRD was carried out with a Bruker AXS D8 Advance X-ray Powder Diffractometer operated at 1600 W power (40 kV, 40 mA) using Cu Kα radiation. Transmission electron microscopy (TEM) were performed on an HT7700 Exalens operated at 120 kV. High-resolution TEM observation was carried out with a Tecnai G2 F20 S-Twin microscopy operated at 200 kV. Scanning electron microscopy (SEM) was carried out on a Phenom Prox operated at 15 kV. Raman spectrum was performed with a Jobin Yvon Lab RAM HR800 equipped with a 514 nm laser.

EASA measurement

A CV from −0.1 to 0.1 V (vs. RHE, except as otherwise noted), was carried out with the different scan rates of 40, 60, 80, 100, and 120 mV s−1 in a CO2-saturated 0.5 M KHCO3 solution at room temperature. We correlated the charging current density at 0.0 V with its corresponding scan rate. The double-layer capacitance (Cdl) is the slope of the fitted line.

LSV measurement

The LSV measurement was carried out in N2-saturated or CO2-saturated 0.5 M KHCO3 solution from 0 to −1.2 V at a scan rate of 50 mV s−1.

EIS measurement

The EIS measurement was carried out at −0.7 V with a frequency from 0.1 Hz to 100 kHz, and an amplitude of 5 mV. The measured impedances were normalized by multiplying the EASA.

Catalytic evaluation of CO2 reduction

CO2 reduction was carried out in 0.5 M KHCO3 solution. The counter electrode and reference electrode are a 3 × 4 cm2 of IrO2 mesh electrode and the Ag/AgCl (3 M KCl solution), respectively. The potential vs. RHE was converted from the potential vs. Ag/AgCl by the following equation:

$$E_{{\mathrm{RHE}}} = E_{{\mathrm{Ag/AgCl}}}+ {\mathrm{ 0}}{\mathrm{.197 + 0}}{\mathrm{.059pH}}$$

CO2 was bubbled into electrolyte before the electrochemical measurement to reach a saturated concentration. After reaction at a set potential, we recorded the total amount of electrical charge (Q) and collected the cathodic gas in a certain volume (Vg) with a home-built electrochemical cell (Supplementary Fig. 18). The Faradaic efficiency of the gas products (FEg) was analyzed with the GC equipped with a thermal conductivity detector (TCD) and a hydrogen flame ionization detector (FID). The collected gas products were injected into GC to obtain their concentration (Cg). The FEg was calculated as the following equation:

$${\mathrm{FE}}_g = \frac{{{{zPF}} \times V_g \times C_g}}{{{\mathrm{RTQ}}}}$$

where R, F, z, P, and T represent gas constant, Faradaic constant, the number of transferred charges, environment pressure, and temperature, respectively.

The liquid products were detected with 1H NMR recorded by a Bruker Avance III HD (500 MHz). We added electrolyte into the cathodic part of an H-type cell, which is separated by a Nafion-117 ion-exchange membrane. After the reaction finished, the electrolyte was mixed up with D2O and DMSO and the liquid products were further detected by 1H NMR.

Data availability

The authors declare that the data supporting the findings of this study are available within the article and the corresponding Supporting Information file. All other relevant source data are available from the corresponding author upon reasonable request.


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The authors are grateful for the financial support from the National Natural Science Foundation of China (21771040 and 62074043), the National Key Research and Development Program of China (2017YFA0207303 and 2016YFA0203900).

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C.T. and Z.S. conceived the project, analyzed the data, and wrote the paper. C.T. synthesized the catalysts. C.T. and T.X. performed the evaluation of the liquid product and analyzed the gas products. C.T. and P.G. contributed to the graphene growth and physical characterizations of material. Z.S. supervised all research phases and revised the paper. All authors read and commented on the paper.

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Correspondence to Zhengzong Sun.

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Tang, C., Gong, P., Xiao, T. et al. Direct electrosynthesis of 52% concentrated CO on silver’s twin boundary. Nat Commun 12, 2139 (2021).

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