Accumulation Of Atoms Research Articles

Controllable Microwave Heating for Energy-Efficient and Universal Synthesis of Atomically Dispersed Metals on Nitrogen-Doped Carbon Nanofibers.

Carbon-supported single-atom catalysts (SACs) have shown great potential in electrocatalysis, whereas traditional synthesis methods typically involve energy-intensive carbonization processes and unfavorable atomic migration and aggregation. Herein, an energy-efficient and universal strategy is developed to rapidly fabricate various SACs on nitrogen-doped hierarchically porous carbon nanofibers (M-TM/NPCNFs, TM = Fe, Co, Ni, FeCo, and FeNi) by electrospinning and controllable microwave heating technique. Such microwave heating technique enables an ultrafast heating rate (ramping to 900°C in 5 min) to greatly suppress the random migration and aggregation of metal species. Meanwhile, the energy consumption and time can be reduced to 2.5% and less than half an hour, respectively, compared to traditional pyrolysis methods. As a proof of concept, the synthesized M-Fe/NPCNFs with abundant Fe-N4 sites exhibit remarkable oxygen reduction reaction (ORR) activity with a high half-wave potential (E1/2 = 0.88 V) in alkaline media, excellent performance in Zn-air battery with a large discharge specific capacity (801 mAh g-1) and long-term cycle durability (over 1000 h), demonstrating the great potential of the microwave heating technique in efficient fabrication of SACs for energy related applications.

Achievements and Challenges in Surfactants-Assisted Synthesis of MOFs-Derived Transition Metal-Nitrogen-Carbon as a Highly Efficient Electrocatalyst for ORR, OER, and HER.

Metal-organic frameworks (MOFs) are excellent precursors for preparing transition metal and nitrogen co-doped carbon catalysts, which have been widely utilized in the field of electrocatalysis since their initial development. However, the original MOFs derived catalysts have been greatly limited in their development and application due to their disadvantages such as metal atom aggregation, structural collapse, and narrow pore channels. Recently, surfactants-assisted MOFs derived catalysts have attracted much attention from researchers due to their advantages such as hierarchical porous structure, increased specific surface area, and many exposed active sites. This review mainly focuses on the synthesis methods of surfactants-assisted MOFs derived catalysts and comprehensively introduces the action of surfactants in MOFs derived materials and the structure-activity relationship between the catalysts and the oxygen reduction reaction, oxygen evolution reaction, and hydrogen evolution reaction performance. Apparently, the aims of this review not only introduce the status of surfactants-assisted MOFs derived catalysts in the field of electrocatalysis but also contribute to the rational design and synthesis of MOFs derived catalysts for fuel cells, metal-air cells, and electrolysis of water toward hydrogen production.

Excellent radiation resistance via enforced local non-directional He diffusion in a WTaCrV multicomponent alloy containing coherent ordered nanoprecipitates

We design and investigate a W15Ta15Cr35V35 (at.%) multicomponent alloy (MCA) with exceptional radiation resistance. The sintered WTaCrV alloy exhibits a body-centered cubic (BCC) matrix with dispersed coherent ordered nanoprecipitates. After ∼3-hour irradiation under 400 keV He+ at room temperature (RT) and 450 °C with a fluence of 2 × 1017 ions/cm2, the irradiation hardening values of the MCA are about a quarter of those of pure tungsten counterparts irradiated at identical conditions. Besides, helium bubbles generated in the irradiated matrix of the MCA are much smaller, compared with those in the pure tungsten and other tungsten-rich alloys previously reported. The exceptional radiation resistance of the present WTaCrV alloy can be mainly attributed to two synergistic mechanisms. First, the high lattice distortion of the solid solution matrix promotes the local non-directional diffusion of irradiation defects, effectively suppressing the aggregation of irradiation defects and helium atoms along specific orientations. This facilitates more uniform nucleation of helium bubbles in the alloy matrix. Second, carbon was introduced during fast hot pressing sintering as interstitial solute to form carbon-rich coherent ordered nanoprecipitates. The carbon-vacancy complexes generated in the nanoprecipitates inhibit the nucleation and aggregation of helium atoms at the vacancies during He+ irradiation. The above two mechanisms synergistically enhance the resistance against He+ irradiation. This work thus demonstrates a design strategy for high radiation resistance alloys by introducing well-tuned ordered coherent nanoprecipitates in multicomponent alloy systems.

Architecting double-shelled hollow carbon nanocages embedded bimetallic sites as bifunctional oxygen electrocatalyst for zinc-air batteries

Rational design of complex hollow nanostructures offers a great opportunity to construct various functional nanostructures. A novel in situ disassembly-polymerization-pyrolysis approach was developed to synthesize atomically dispersed Fe single atoms (Fe SAs) and tiny Co nanoparticles (Co NPs) binary sites embedded in double-shelled hollow carbon nanocages (Co NPs/Fe SAs DSCNs) without removing excess templates. The Co NPs/Fe SAs DSCNs displayed excellent bifunctional activity, boosting the realistic rechargeable zinc-air batteries with high efficiency, long-term durability, and reversibility, which is comparable to noble metal catalysts (Pt/C and RuO2). The enhanced catalytic activity should be attributed to as well as the strong interactions between Fe SAs and Co NPs with the nitrogen-doped carbon matrix, the exposure of more active sites, and the high-flux mass transportation. In addition, the confinement effect between the double C-N shells prevented the aggregation and corrosion of metal atoms, thus improving the durability of the Co NPs/Fe SAs DSCNs, further highlighting the structural advantages of carbon nanoreactor. This work provides guidance for further rational design and preparation of complex hollow structure materials with advanced bifunctional air cathodes.

Precipitation behavior and performance evolution of cold-rolled cu-Ti-Fe alloy during heat treatment

The CuTi alloy is extensively utilized for its high strength, excellent elasticity, and processability. Heat treatment processes are crucial for affecting the microstructure and properties. The effects of different aging processes on the microstructure and properties of cold-rolled Cu-Ti-Fe alloy were investigated, and the heat treatment parameters were optimized. The results show that the cold-rolled Cu-Ti-Fe alloy exhibits excellent comprehensive performance at 450 °C for 2 h, with the hardness of 342.2 HV, the electrical conductivity of 16.1 % IACS, and the tensile strength of 1051 MPa. The aggregation of solute atoms occurs in the early stages of aging. The uniformly distributed β'-Cu4Ti phase precipitates at peak aging, which has a coherent relationship with the matrix. The precipitation of Ti atoms enhances the electrical conductivity of the alloy, and the movement of dislocations is prevented by precipitates, increasing the strength. During the over-aging stage, the precipitates transform into β-Cu4Ti phases, losing complete coherency with the matrix. The coarsening of precipitates leads to the softening of the Cu-Ti-Fe alloy. Theoretical calculation results indicate that the thermal diffusion ability of solute atoms is the strongest and precipitates completely when the alloy aged at 450 °C. The precipitation strengthening mechanism plays a significant role in improving the strength.

The effect of ion implantation and annealing temperatures on the migration behavior of ruthenium in glassy carbon

Nuclear waste storage materials are inevitable in nuclear industry for preventing the release of radioactive waste products. Glassy carbon has been considered being beneficial to be used in the dry cask needed for nuclear waste storage. Thus, we studied the migration of ruthenium implanted in glassy carbon upon annealing. Our investigations show that ruthenium implantation caused defects in the glassy carbon structure, with more defects observed in the room temperature as-implanted samples compared to those implanted at 200 °C. Annealing the as-implanted samples from 500 to 800 °C showed no significant change in the ruthenium depth profiles, indicating the non-diffusivity of ruthenium in glassy carbon at these temperatures. However, annealing at higher temperatures (from 900 and 1300 °C) resulted in an increase in the maximum depth profile peaks, accompanied by a shift towards the surface, and a decrease in the full-width at half-maximum. These changes indicate the aggregation of ruthenium atoms in the near-surface region. Additionally, more ruthenium aggregation was observed in room temperature implanted samples compared to those implanted at 200 °C. This difference is attributed to the higher concentration of defects in room temperature implanted samples, which promotes ruthenium aggregation. Moreover, the migration and aggregation of ruthenium in the near-surface region contributed to an increase in the surface roughness of the glassy carbon.

Structural transitions in liquid semiconductor alloys: A molecular dynamics study with a neural network potential.

Liquid-liquid phase transitions hold a unique and profound significance within condensed matter physics. These transitions, while conceptually intriguing, often pose formidable computational challenges. However, recent advances in neural network (NN) potentials offer a promising avenue to effectively address these challenges. In this paper, we delve into the structural transitions of liquid CdTe, CdS, and their alloy systems using molecular dynamics simulations, harnessing the power of an NN potential named LaspNN. Our investigations encompass both pressure and temperature effects. Through our simulations, we uncover three primary liquid structures around melting points that emerge as pressure increases: tetrahedral, rock salt, and close-packed structures, which greatly resemble those of solid states. In the high-temperature regime, we observe the formation of Te chains and S dimers, providing a deeper understanding of the liquid's atomic arrangements. When examining CdSxTe1-x alloys, our findings indicate that a small substitution of S by Te atoms for S-rich alloys (x > 0.5) exhibits a structural transition much different from CdS, while a large substitution of Te by S atoms for Te-rich alloys (x < 0.5) barely exhibits a structural transition similar to CdTe. We construct a schematic diagram for liquid alloys that considers both temperature and pressure, providing a comprehensive overview of the alloy system's behavior. The local aggregation of Te atoms demonstrates a linear relationship with alloy composition x, whereas that of S atoms exhibits a nonlinear one, shedding light on the composition-dependent structural changes.

Effect of Ta/Ni dual-interlayer on the microstructure and properties of high strength titanium alloy and steel composite plate

The combination of ultra-high-strength Ti-6Al-4V (TC4) titanium alloy and 30CrNiMoNb (6211) steel was achieved by adding Ta/Ni dual-interlayer and rolling at 950 °C through welding a symmetrical blank sleeve with a vacuum electron beam. In order to unveil the metallurgical bonding mechanism and the interfacial structure, SEM, XRD, and compression-shear performance tests were used. The results revealed the presence of thin-film brittle TiC, TiFe, and TiFe2 compounds at the TC4/6211 interface, resulting in an increased risk of interface mismatch and brittle fracture along the matrix phase interface, and the average interfacial bonding strength was tested at 323 MPa.In contrast, the TC4-Ta interface and the 6211-Ni interface in the TC4/Ta/Ni/6211 composite plate displayed good solid solution formation. The strengthening mechanism of the Ta/Ni dual-interlayer interfacial bonding was analyzed using selected area electron diffraction (SAED), revealing that the Ta-Ni diffusion region consisted of Ni3Ta and Ni2Ta. The addition of the Ta/Ni dual-interlayer prevented the aggregation of Ti and Fe atoms to form Ti-Fe compounds. The malleable intermetallic compounds of Ni3Ta and Ni2Ta effectively coordinated deformation, leading to an average interfacial bonding strength of 469 MPa, which was 45.2 % higher than the composite plate without Ta/Ni dual-interlayer.

First-principles study of Re in BCC-Mo: Diffusion behavior and interaction with point defects

Due to their some beneficial properties, molybdenum-based alloys, such as Mo-Re alloys, are recognized as potential structural materials for nuclear power reactors. Irradiation induced precipitation of rhenium (Re) atoms causes hardening and embrittlement of Mo-Re alloys, restricting their application. The interaction of rhenium (Re) atoms with point defects (PDs), as well as the diffusion behavior of Re atoms in BCC-Mo (Body Center Cubic-molybdenum), were investigated using first-principles methods. The results revealed that Re atoms exhibited high binding energies with both vacancy (Vac) and interstitial dumbbells. Furthermore, the binding energies increased with the number of Re atoms. The binding energies of Re with self-interstitial dumbbell (SIA, ie., Mo-Mo) and mixed interstitial dumbbell (Mo-Re) were quite close to. Due to the high exchange barrier between Vac and Re, the diffusion of rhenium through the vacancy-drag mechanism was difficult. Due to the low migration and rotation barrier of Mo-Re mixed interstitial dumbbell, the diffusion of Re atoms in Mo was dominated by the interstitial-mediated mechanism. From the perspective of diffusion dynamics, only interstitial dumbbells can promote the aggregation of Re atoms. By comparing the binding energy of interstitial dumbbell with interstitial dumbbell and interstitial dumbbell with Re atoms, pairs of Mo-Re interstitial dumbbell was suggested to be the nucleation sites to attract more interstitial dumbbells, thereby promoting the precipitation of Re clusters. It was because they had high binding energy and were difficult to decompose once combined.

Nonconjugated amylopectin-grafted copolymers with dual fluorescence/low-temperature phosphorescence emission and superior processability

Nonconjugated fluorescent polymers devoid of large π–π conjugated structures have received considerable attention due to their significant academic importance and broad application potentials in various fields. Herein, we report an effective strategy to fabricate multifunctional fluorescent amylopectin derivatives and reveal their unique aspects of aggregation-induced emission (AIE), cryogenic long-persistent phosphorescence (~6 s) and excellent processabilities characteristics, which are extremely different from traditional luminogens. These amylopectin-graft-poly(n-butyl acrylate-co-1-vinylimidazole) copolymers (Amylopectin-BVs) prepared by the grafting-from method employing RAFT and experienced subsequently with metal-ligand cross-linking. Specifically, clustering-triggered fluorescent emission or cryogenic long-persistent phosphorescence of amylopectin could be achieved by the aggregation of oxygen and nitrogen atoms along with conformation rigidification, which shows great promise in optoelectronic and biological applications.

Micromechanical response of graphene coating on nt-TiAl under nanoindentation

The nanoindentation response of graphene (Gr) coating on nanotwin titanium-aluminum (nt-TiAl) matrix composites was studied using molecular dynamics (MD) simulation. The indentation velocity, twin boundary spacing, and parallel and vertical Z-axes are studied. The results show that the bearing capacity and hardness of Gr coating is significantly higher than that after coating failure, and the load-displacement curve shows the same phenomenon. Damage to the substrate material at varying speeds is indicated by atomic aggregation near the Gr coating, with the center of aggregation showing a negative correlation with indentation velocity. The matrix's damaged area is larger when the twin layer is perpendicular to the Z-axis and deeper when parallel, showing that the twin structure limits material damage by hindering dislocation expansion. Moreover, the presence of Gr coating delayed the matrix's plastic deformation process. This delay effect significantly improves the mechanical properties of composites, which have potential applications in aerospace.

Single Co atoms incorporated on Fe-Ni-LDH with enriched oxygen vacancies for efficient peroxymonosulfate activation: Investigation of electron transfer mechanism

Although single atom catalysts (SACs) have been recognized as a prospective catalyst in advanced oxidation processes (AOPs) via persulfate activation, they still confronted with the issues of metal atoms aggregation and limit loading amounts. For addressing these issues, single Co atoms that incorporated on Fe-Ni layered double hydroxides (FeNi-LDHs) with oxygen vacancies is fabricated. Employing it as the support of Co atoms can not only minimize the aggregation of single metal atoms but also conductive to increase their loading amounts (up to 3.26 wt%), which is expected to display an unprecedented catalytic activity. 100 % of TC (20 mg/L) can be eliminated within 5 min in Co-FeNi-LDH/PMS system. Radical and nonradical pathway collectively contributed to the TC elimination in Co-FeNi-LDH/PMS system, in which the electron transfer process in nonradical pathway is confirmed as the dominate mechanism via electrochemical studies and quenching experiments. PMS was adsorbed by Co-FeNi-LDH to form a Co-FeNi-LDH/PMS* complex during the PMS activation. Subsequently, TC is decomposed by transferring electrons to the Co-FeNi-LDH/PMS* complex via “donor-acceptor complex” mechanism. Benefiting from this mechanism, the Co-FeNi-LDH/PMS system displays superior anti-interference capability against inorganic anions. This study provides a unique insight on the skillful design and application of SACs.

Asymmetric Ru-In atomic pairs promote highly active and stable acetylene hydrochlorination

Ru single-atom catalysts have great potential to replace toxic mercuric chloride in acetylene hydrochlorination. However, long-term catalytic stability remains a grand challenge due to the aggregation of Ru atoms caused by over-chlorination. Herein, we synthesize an asymmetric Ru-In atomic pair with vinyl chloride monomer yield (>99.5%) and stability (>600 h) at a gas hourly space velocity of 180 h−1, far surpassing those of the Ru single-atom counterparts. A combination of experimental and theoretical techniques reveals that there is a strong d-p orbital interaction between Ru and In atoms, which not only enables the selective adsorption of acetylene and hydrogen chloride at different atomic sites but also optimizes the electron configuration of Ru. As a result, the intrinsic energy barrier for vinyl chloride generation is lowered, and the thermodynamics of the chlorination process at the Ru site is switched from exothermal to endothermal due to the change of orbital couplings. This work provides a strategy to prevent the deactivation and depletion of active Ru centers during acetylene hydrochlorination.

Single-Atom Catalysts through Pressure-Controlled Metal Diffusion.

Single-atom catalysts (SACs) open up new possibilities for advanced technologies. However, a major complication in preparing high-density single-atom sites is the aggregation of single atoms into clusters. This complication stems from the delicate balance between the diffusion and stabilization of metal atoms during pyrolysis. Here, we present pressure-controlled metal diffusion as a new concept for fabricating ultra-high-density SACs. Reducing the pressure inhibits aggregation substantially, resulting in almost three times higher single-atom loadings than those obtained at ambient pressure. Molecular dynamics and computational fluid dynamics simulations reveal the role of a metal hopping mechanism, maximizing the metal atom distribution through an increased probability of metal-ligand binding. The investigation of the active site density by electrocatalytic oxygen reduction validates the robustness of our approach. The first realization of Ullmann-type carbon-oxygen couplings catalyzed on single Cu sites demonstrates further options for efficient heterogeneous catalysis.

Effects of the Substitution of B and C for P on Magnetic Properties of FePCB Amorphous Alloys

In the present study, first-principles molecular dynamics simulations were employed to study the effects of small amounts of B and C substituted for P on the structure and magnetic properties of Fe80P13C7, Fe80P10C7B3, and Fe80P8C9B3 amorphous alloys. A small amount of B and C replacing P atoms increases the icosahedral structure of the amorphous alloys, especially the increase in the regular icosahedral structure. The saturation magnetization of the three kinds of amorphous alloys gradually increases with the addition of B and C atoms, and the results of experimental and simulated calculations show consistent trends. The substitution of P atoms by B and C atoms leads to the aggregation of Fe atoms, which increases the magnetic moment of the iron atoms. In addition, the improvement of local structural symmetry may be one of the reasons for the increase in saturation magnetization of amorphous alloys. The substitution of a small number of B and C atoms plays an important role in improving the saturation magnetization of the amorphous alloy, which has a certain guiding significance for the development of amorphous alloys with excellent soft magnetic properties.

Continuous‐Flow Solution Plasma for the Atom‐Economic Synthesis of Single/Dual‐Atom Catalysts

AbstractSingle‐atom catalysts (SACs) manifest unique advantages in various aspects of catalysis but face challenges in atom‐economic synthesis. Solution reduction holds the promise of fast, continuous, and low‐cost synthesis of SACs, however, almost no chemical, electrochemical, or photochemical reduction can avoid the aggregation of metal atoms in solution. The issue becomes even tougher to composite dual‐atom metals together. Herein, a continuous‐flow solution plasma (CSP) method is developed, which utilizes high‐flux hydrated electrons, hydrogen radicals, and enhanced metal–support interaction, to achieve over 97% capture efficiency of metal precursors to fabricate CeO2‐based single‐atom Au, Rh, Pd, Ru, and Pt in only 0.03‐s residence time. Further, a programmed CSP synthesis of Au1Rh1/CeO2 and Au1Pd1/CeO2 dual‐atom catalysts is demonstrated. Under Xe lamp irradiation, Au1Rh1/CeO2 breaks room temperature constraints in CO conversion for the water–gas shift reaction with a T50 (the temperature at which 50% CO conversion occurs) of 298 K. The innovative CSP technology provides an atom‐economic approach to the continuous production of SACs using clean electricity without any additional reducing agent, paving the way for the programmed and green synthesis of SACs for industrial catalysis, energy conversion, and environment remedy applications.

Rational design of Fe, N co-doped porous carbon derived from conjugated microporous polymer as an electrocatalytic platform for oxygen reduction reaction

Porous iron–nitrogen-doped carbons (FeNC) offer a great platform for construction of cathodic oxygen reduction reaction (ORR) catalysts in fuel cells. However, challenges still remain regarding with the collapse of carbon-skeleton during pyrolysis, uneven distribution of active sites and aggregation of metal atoms. In this work, we synthesized Fe, N co-doped conjugated microporous polymer (FeN-CMP) through a facile bottom-up strategy using 1,3,5-triethynylbenzene and iron-chelated 3,8-dibromo-1,10-phenanthroline as monomers, ensuring the uniform coordination of N with Fe element in network. Then, the resulting FeN-CMP was treated by pyrolysis without structural collapse to obtain porous FeNC electrocatalyst for ORR. The most active catalyst was fabricated under 900 °C, which exhibits remarkable ORR activity in alkaline medium with half-wave potential of 0.796 V (18 mV and 105 mV positive deviation from the commercial Pt/C catalyst and post-doping catalyst), high selectivity with nearly 4e- transfer process and excellent methanol tolerance. Our study first developed porous FeNC electrocatalysts derived from Fe, N-anchoring CMPs based on pre-functionalization of monomers, which exhibits great potential as an alternative to commercial Pt/C catalyst for ORR, and provides a feasible strategy of developing multi-atoms doping catalysts for energy storage and conversion as well as heterogeneous catalysis.

Rapid Joule-heating synthesis of metal/carbon-based electrocatalysts for efficient carbon dioxide reduction

Carbon-loaded metal nanoparticles (NPs) are widely employed as functional materials for electrocatalysis. In this study, a rapid thermal shock method was developed to load various metal nanoparticles onto carbon supports. Compared to conventional pyrolysis processes, Joule heating enables rapid heating to elevated temperatures within a short period, effectively preventing the migration and aggregation of metal atoms. Simultaneously, the anchoring effect of defective carbon carriers ensures the uniform distribution of NPs on the carbon supports. Additionally, nitrogen doping can significantly enhance the electronic conductivity of the carbon matrix and strengthen the metal-carbon interactions, thereby synergistically improving catalyst performance. When used as electrocatalysts for electrocatalytic CO2 reduction, bismuth-, indium-, and tin/carbon-carrier-based catalysts exhibit excellent Faraday efficiencies of 92.8%, 86.4%, and 73.3%, respectively, for formate generation in flow cells. The influence of different metals and calcination temperatures on catalytic performance was examined to provide valuable insights into the rational design of carbon-based electrocatalysts with enhanced electrocatalytic activity.

Surface-Enriched Room-Temperature Liquid Bismuth for Catalytic CO2 Reduction.

Bismuth-based electrocatalysts are effective for carbon dioxide (CO2) reduction to formate. However, at room temperature, these materials are only available in solid state, which inevitably suffers from surface deactivation, declining current densities, and Faradaic efficiencies. Here, the formation of a liquid bismuth catalyst on the liquid gallium surface at ambient conditions is shown as its exceptional performance in the electrochemical reduction of CO2 (i.e., CO2RR). By doping a trace amount of bismuth (740ppm atomic) in gallium liquid metal, a surface enrichment of bismuth by over 400 times (30 at%) in liquid state is obtained without atomic aggregation, achieving 98% Faradic efficiency for CO2 conversion to formate over 80 h. Ab initio molecular simulations and density functional theory calculations reveal that bismuth atoms in the liquid state are the most energetically favorable sites for the CO2RR intermediates, superior to solid Bi-sites, as well as joint GaBi-sites. This study opens an avenue for fabricating high-performing liquid-state metallic catalysts that cannot be reached by elementary metals under electrocatalytic conditions.

Effect of the nitrogen/carbon ratio in the organic ligand of a nickel single-atom catalyst on its electrochemical activity in CO2 reduction

Simple, large-scale synthesis of metal single-atom catalysts (SACs) is limited by the aggregation of metal atoms on the support material surface. The N atoms in small organic ligands (SOLs) can anchor single metal atoms, affording abundant surface-active sites. In this study, we investigated the effect of the nitrogen/carbon ratio (N/C) in SOLs on the properties of the resultant Ni single-atom confined nitrogen-doped carbon black (Ni-NCB). The N/C ratio affected the thermal stability of Ni-NCB_N/Cs during carbonization, and the optimal Ni-NCB (Ni-NCB_0.5) was synthesized with the SOL 2-methylimidazole. Ni-NCB_0.5 achieved a CO partial current density of > 500 mA cm–2 and high CO Faradaic efficiency (96.4 %) in the CO2 reduction reaction. The 3- and 4-cell stack systems with Ni-NCB_0.5 (25 cm2 area per unit cell) exhibited an overall current of 10 A, high CO selectivity (> 96.0 %), and long-term stability (50 h). This synthetic strategy for SACs can be commercialized and even extended to other industrial electrocatalysts.