Electrocatalytically Active Fe-(O-C2)4 Single-Atom Sites for Efficient Reduction of Nitrogen to Ammonia

Single-atom catalysts have demonstrated their superiority over other types of catalysts for various reactions. However, the reported nitrogen reduction reaction single-atom electrocatalysts for the nitrogen reduction reaction exclusively utilize metal–nitrogen or metal–carbon coordination configurations as catalytic active sites. Here, we report a Fe single-atom electrocatalyst supported on low-cost, nitrogen-free lignocellulose-derived carbon. The extended X-ray absorption fine structure spectra confirm that Fe atoms are anchored to the support via the Fe-(O-C₂)₄ coordination configuration. Density functional theory calculations identify Fe-(O-C₂)₄ as the active site for the nitrogen reduction reaction. An electrode consisting of the electrocatalyst loaded on carbon cloth can afford a NH₃ yield rate and faradaic efficiency of 32.1 μg h⁻¹ mg_cat.⁻¹ (5350 μg h⁻¹ mg_Fe⁻¹) and 29.3 %, respectively. An exceptional NH₃ yield rate of 307.7 μg h⁻¹ mg_cat.⁻¹ (51 283 μg h⁻¹ mg_Fe⁻¹) with a near record faradaic efficiency of 51.0 % can be achieved with the electrocatalyst immobilized on a glassy carbon electrode.     

Single‐Atom Catalysts for the Electrocatalytic Reduction of Nitrogen to Ammonia under Ambient Conditions

Powered by renewable electricity, the electrochemical reduction of nitrogen to ammonia is proposed as a promising alternative to the energy‐ and capital‐intensive Haber–Bosch process, and has thus attracted much attention from the scientific community. However, this process suffers from low NH₃ yields and Faradaic efficiency. The development of more effective electrocatalysts is of vital importance for the practical applications of this reaction. Of the reported catalysts, single‐atom catalysts (SACs) show the significant advantages of efficient atom utilization and unsaturated coordination configurations, which offer great scope for optimizing their catalytic performance. Herein, progress in state‐of‐the‐art SACs applied in the electrocatalytic N₂ reduction reaction (NRR) is discussed, and the main advantages and challenges for developing more efficient electrocatalysts are also highlighted.     

Single‐Atom Electrocatalysts

Recent years have witnessed a dramatic increase in the production of sustainable and renewable energy. However, the electrochemical performances of the various systems are limited, and there is an intensive search for highly efficient electrocatalysts by more rational control over the size, shape, composition, and structure. Of particular interest are the studies on single‐atom catalysts (SACs), which have sparked new interests in electrocatalysis because of their high catalytic activity, stability, selectivity, and 100 % atom utilization. In this Review, we introduce innovative syntheses and characterization techniques for SACs, with a focus on their electrochemical applications in the oxygen reduction/evolution reaction, hydrogen evolution reaction, and hydrocarbon conversion reactions for fuel cells (electrooxidation of methanol, ethanol, and formic acid). The electrocatalytic performance is further considered at an atomic level and the underlying mechanisms are discussed. The ultimate goal is the tailoring of single atoms for electrochemical applications.     

Highly Efficient CO2 Electroreduction on ZnN4‐based Single‐Atom Catalyst

The electrochemical reduction reaction of carbon dioxide (CO2RR) to carbon monoxide (CO) is the basis for the further synthesis of more complex carbon‐based fuels or attractive feedstock. Single‐atom catalysts have unique electronic and geometric structures with respect to their bulk counterparts, thus exhibiting unexpected catalytic activities. A nitrogen‐anchored Zn single‐atom catalyst is presented for CO formation from CO2RR with high catalytic activity (onset overpotential down to 24 mV), high selectivity (Faradaic efficiency for CO (FE_CO) up to 95 % at ?0.43 V), remarkable durability (>75 h without decay of FE_CO), and large turnover frequency (TOF, up to 9969 h^?1). Further experimental and DFT results indicate that the four‐nitrogen‐anchored Zn single atom (Zn‐N₄) is the main active site for CO2RR with low free energy barrier for the formation of *COOH as the rate‐limiting step.     

An Enzyme‐Mimicking Single‐Atom Catalyst as an Efficient Multiple Reactive Oxygen and Nitrogen Species Scavenger for Sepsis Management

Sepsis, characterized by immoderate production of multiple reactive oxygen and nitrogen species (RONS), causes high morbidity and mortality. Despite progress made with nanozymes, efficient antioxidant therapy to eliminate these RONS remains challenging, owing largely to the specificity and low activity of exploited nanozymes. Herein, an enzyme‐mimicking single‐atom catalyst, Co/PMCS, features atomically dispersed coordinatively unsaturated active Co‐porphyrin centers, which can rapidly obliterate multiple RONS to alleviate sepsis. Co/PMCS can eliminate O₂^.? and H₂O₂ by mimicking superoxide dismutase, catalase, and glutathione peroxidase, while removing ^.OH via the oxidative‐reduction cycle, with markedly higher activity than nanozymes. It can also scavenge ^.NO through formation of a nitrosyl–metal complex. Eventually, it can reduce proinflammatory cytokine levels, protect organs from damage, and confer a distinct survival advantage to the infected sepsis mice.     

Single‐Atom Catalyst of Platinum Supported on Titanium Nitride for Selective Electrochemical Reactions

As a catalyst, single‐atom platinum may provide an ideal structure for platinum minimization. Herein, a single‐atom catalyst of platinum supported on titanium nitride nanoparticles were successfully prepared with the aid of chlorine ligands. Unlike platinum nanoparticles, the single‐atom active sites predominantly produced hydrogen peroxide in the electrochemical oxygen reduction with the highest mass activity reported so far. The electrocatalytic oxidation of small organic molecules, such as formic acid and methanol, also exhibited unique selectivity on the single‐atom platinum catalyst. A lack of platinum ensemble sites changed the reaction pathway for the oxygen‐reduction reaction toward a two‐electron pathway and formic acid oxidation toward direct dehydrogenation, and also induced no activity for the methanol oxidation. This work demonstrates that single‐atom platinum can be an efficient electrocatalyst with high mass activity and unique selectivity.     

Atomically Dispersed Nickel(I) on an Alloy‐Encapsulated Nitrogen‐Doped Carbon Nanotube Array for High‐Performance Electrochemical CO2 Reduction Reaction

Single‐atom catalysts (SACs) show great promise for electrochemical CO₂ reduction reaction (CRR), but the low density of active sites and the poor electrical conduction and mass transport of the single‐atom electrode greatly limit their performance. Herein, we prepared a nickel single‐atom electrode consisting of isolated, high‐density and low‐valent nickel(I) sites anchored on a self‐standing N‐doped carbon nanotube array with nickel–copper alloy encapsulation on a carbon‐fiber paper. The combination of single‐atom nickel(I) sites and self‐standing array structure gives rise to an excellent electrocatalytic CO₂ reduction performance. The introduction of copper tunes the d‐band electron configuration and enhances the adsorption of hydrogen, which impedes the hydrogen evolution reaction. The single‐nickel‐atom electrode exhibits a specific current density of ?32.87 mA cm^?2 and turnover frequency of 1962 h^?1 at a mild overpotential of 620 mV for CO formation with 97 % Faradic efficiency.     

Coordination Tunes Selectivity: Two‐Electron Oxygen Reduction on High‐Loading Molybdenum Single‐Atom Catalysts

Single‐atom catalysts (SACs) have great potential in electrocatalysis. Their performance can be rationally optimized by tailoring the metal atoms, adjacent coordinative dopants, and metal loading. However, doing so is still a great challenge because of the limited synthesis approach and insufficient understanding of the structure–property relationships. Herein, we report a new kind of Mo SAC with a unique O,S coordination and a high metal loading over 10 wt %. The isolation and local environment was identified by high‐angle annular dark‐field scanning transmission electron microscopy and extended X‐ray absorption fine structure. The SACs catalyze the oxygen reduction reaction (ORR) via a 2 e^? pathway with a high H₂O₂ selectivity of over 95 % in 0.10 m KOH. The critical role of the Mo single atoms and the coordination structure was revealed by both electrochemical tests and theoretical calculations.     

过渡金属单原子电催化剂还原CO2制CO

电催化二氧化碳还原(ECR)技术是实现“碳中和”目标的一种理想途径,而过渡金属单原子催化剂具有电子结构可调、原子利用率高和活性位点均一等特点,在ECR研究中具有显著优势。本文首先介绍了单原子电催化剂在还原CO₂尤其是在选择性生成CO研究中的优势,然后综述了近年来Fe、Co、Ni及其他单原子电催化剂的反应位点调控策略与电催化选择性的调控机制,重点对质子耦合CO₂还原生成CO的中间过程调控进行了归纳总结,并简要展望了发展方向,以期为推动单原子催化剂在ECR中规模化应用提供指导和参考。     

From Metal–Organic Frameworks to Single‐Atom Fe Implanted N‐doped Porous Carbons: Efficient Oxygen Reduction in Both Alkaline and Acidic Media

It remains highly desired but a great challenge to achieve atomically dispersed metals in high loadings for efficient catalysis. Now porphyrinic metal–organic frameworks (MOFs) have been synthesized based on a novel mixed‐ligand strategy to afford high‐content (1.76 wt %) single‐atom (SA) iron‐implanted N‐doped porous carbon (Fe_SA‐N‐C) via pyrolysis. Thanks to the single‐atom Fe sites, hierarchical pores, oriented mesochannels and high conductivity, the optimized Fe_SA‐N‐C exhibits excellent oxygen reduction activity and stability, surpassing almost all non‐noble‐metal catalysts and state‐of‐the‐art Pt/C, in both alkaline and more challenging acidic media. More far‐reaching, this MOF‐based mixed‐ligand strategy opens a novel avenue to the precise fabrication of efficient single‐atom catalysts.     

Advanced Non-metallic Catalysts for Electrochemical Nitrogen Reduction under Ambient Conditions

The electrochemical reduction of nitrogen into ammonia under ambient conditions is a potential strategy for sustainable ammonia production. At present, one of the main research directions in the field of electrochemical nitrogen fixation is to improve the current efficiency and ammonia yield by developing efficient nitrogen reduction catalysts. To optimise the selectivity and catalytic activity of nitrogen reduction catalysts more efficiently, herein, we systematically summarise the progress of research on nitrogen reduction catalysts in recent years and present some general catalyst design strategies. Considering that it is difficult for metal-based catalysts to balance the competitive reactions of nitrogen activation and hydrogen evolution, we discuss in detail the advantages and application prospects of non-metallic catalysts in electrochemical nitrogen fixation. Moreover, both the design strategy of surface or interface defects, and how this atomic-level control of functionalisation helps to promote selectivity and catalytic activity are also discussed by theoretical and experimental electrochemistry. On this basis, we also discussed the future development direction, opportunities and challenges of nitrogen reduction electrocatalysts.     

Controlled Synthesis of a Vacancy‐Defect Single‐Atom Catalyst for Boosting CO2 Electroreduction

The reaction of precursors containing both nitrogen and oxygen atoms with Ni^II under 500 °C can generate a N/O mixing coordinated Ni‐N₃O single‐atom catalyst (SAC) in which the oxygen atom can be gradually removed under high temperature due to the weaker Ni?O interaction, resulting in a vacancy‐defect Ni‐N₃‐V SAC at Ni site under 800 °C. For the reaction of Ni^II with the precursor simply containing nitrogen atoms, only a no‐vacancy‐defect Ni‐N₄ SAC was obtained. Experimental and DFT calculations reveal that the presence of a vacancy‐defect in Ni‐N₃‐V SAC can dramatically boost the electrocatalytic activity for CO₂ reduction, with extremely high CO₂ reduction current density of 65 mA cm^?2 and high Faradaic efficiency over 90 % at ?0.9 V vs. RHE, as well as a record high turnover frequency of 1.35×10⁵ h^?1, much higher than those of Ni‐N₄ SAC, and being one of the best reported electrocatalysts for CO₂‐to‐CO conversion to date.     

Regulating the Coordination Environment of MOF‐Templated Single‐Atom Nickel Electrocatalysts for Boosting CO2 Reduction

The general synthesis and control of the coordination environment of single‐atom catalysts (SACs) remains a great challenge. Herein, a general host–guest cooperative protection strategy has been developed to construct SACs by introducing polypyrrole (PPy) into a bimetallic metal–organic framework. As an example, the introduction of Mg²⁺ in MgNi‐MOF‐74 extends the distance between adjacent Ni atoms; the PPy guests serve as N source to stabilize the isolated Ni atoms during pyrolysis. As a result, a series of single‐atom Ni catalysts (named Ni_SA‐N_x‐C) with different N coordination numbers have been fabricated by controlling the pyrolysis temperature. Significantly, the Ni_SA‐N₂‐C catalyst, with the lowest N coordination number, achieves high CO Faradaic efficiency (98 %) and turnover frequency (1622 h^?1), far superior to those of Ni_SA‐N₃‐C and Ni_SA‐N₄‐C, in electrocatalytic CO₂ reduction. Theoretical calculations reveal that the low N coordination number of single‐atom Ni sites in Ni_SA‐N₂‐C is favorable to the formation of COOH* intermediate and thus accounts for its superior activity.     

Direct Observation of Dynamic Bond Evolution in Single‐Atom Pt/C3N4 Catalysts

Single‐atom catalysts are promising platforms for heterogeneous catalysis, especially for clean energy conversion, storage, and utilization. Although great efforts have been made to examine the bonding and oxidation state of single‐atom catalysts before and/or after catalytic reactions, when information about dynamic evolution is not sufficient, the underlying mechanisms are often overlooked. Herein, we report the direct observation of the charge transfer and bond evolution of a single‐atom Pt/C₃N₄ catalyst in photocatalytic water splitting by synchronous illumination X‐ray photoelectron spectroscopy. Specifically, under light excitation, we observed Pt?N bond cleavage to form a Pt⁰ species and the corresponding C=N bond reconstruction; these features could not be detected on the metallic platinum‐decorated C₃N₄ catalyst. As expected, H₂ production activity (14.7 mmol h^?1 g^?1) was enhanced significantly with the single‐atom Pt/C₃N₄ catalyst as compared to metallic Pt‐C₃N₄ (0.74 mmol h^?1 g^?1).     

Dual Metal Active Sites in an Ir1/FeOx Single‐Atom Catalyst: A Redox Mechanism for the Water‐Gas Shift Reaction

Herein, we report a theoretical and experimental study of the water‐gas shift (WGS) reaction on Ir₁/FeO_x single‐atom catalysts. Water dissociates to OH* on the Ir₁ single atom and H* on the first‐neighbour O atom bonded with a Fe site. The adsorbed CO on Ir₁ reacts with another adjacent O atom to produce CO₂, yielding an oxygen vacancy (O_vac). Then, the formation of H₂ becomes feasible due to migration of H from adsorbed OH* toward Ir₁ and its subsequent reaction with another H*. The interaction of Ir₁ and the second‐neighbouring Fe species demonstrates a new WGS pathway featured by electron transfer at the active site from Fe³⁺?O???Ir²⁺?O_vac to Fe²⁺?O_vac???Ir³⁺?O with the involvement of O_vac. The redox mechanism for WGS reaction through a dual metal active site (DMAS) is different from the conventional associative mechanism with the formation of formate or carboxyl intermediates. The proposed new reaction mechanism is corroborated by the experimental results with Ir₁/FeO_x for sequential production of CO₂ and H₂.     

Maximizing the Number of Interfacial Sites in Single‐Atom Catalysts for the Highly Selective,Solvent‐Free Oxidation of Primary Alcohols

The solvent‐free selective oxidation of alcohols to aldehydes with molecular oxygen is highly attractive yet challenging. Interfacial sites between a metal and an oxide support are crucial in determining the activity and selectivity of such heterogeneous catalysts. Herein, we demonstrate that the use of supported single‐atom catalysts (SACs) leads to high activity and selectivity in this reaction. The significantly increased number of interfacial sites, resulting from the presence of individually dispersed metal atoms on the support, renders SACs one or two orders of magnitude more active than the corresponding nanoparticle (NP) catalysts. Lattice oxygen atoms activated at interfacial sites were found to be more selective than O₂ activated on metal NPs in oxidizing the alcohol substrate. This work demonstrates for the first time that the number of interfacial sites is maximized in SACs, providing a new avenue for improving catalytic performance by developing appropriate SACs for alcohol oxidation and other reactions occurring at metal–support interfacial sites.     

Single Mn Atom Anchored on Nitrogen-Doped Graphene as a Highly Efficient Electrocatalyst for Oxygen Reduction Reaction

Single Mn atom on nitrogen-doped graphene (MnN₄-G) has exhibited good structural stability and high activity for the adsorption and dissociation of an O₂ molecule, becoming a promising single-atom catalyst (SAC) candidate for oxygen reduction reaction (ORR). However, the catalytic activity of MnN₄-G for the ORR and the optimal reaction pathway remain obscure. In this work, density-functional theory calculations were employed to comprehensively investigate all the possible pathways and intermediate reactions of the ORR on MnN₄-G. The feasible active sites and the most stable adsorption configurations of the intermediates and transition states during the ORR were identified. Screened from all the possibilities, three optimal four-electron O₂ hydrogenation pathways with an ultralow energy barrier of 0.13 eV were discovered that are energetically more favorable than direct O₂ dissociation pathways. Analysis of the free energy diagram further verified the thermodynamical feasibility of the three pathways. Thus, MnN₄-G possesses superior ORR activity. This study provides a fundamental understanding of the design of highly efficient SACs for the ORR.     

Atomically Dispersed Nickel(I) on an Alloy-Encapsulated Nitrogen-Doped Carbon Nanotube Array for High-Performance Electrochemical CO2 Reduction Reaction

Single-atom catalysts (SACs) show great promise for electrochemical CO₂ reduction reaction (CRR), but the low density of active sites and the poor electrical conduction and mass transport of the single-atom electrode greatly limit their performance. Herein, we prepared a nickel single-atom electrode consisting of isolated, high-density and low-valent nickel(I) sites anchored on a self-standing N-doped carbon nanotube array with nickel–copper alloy encapsulation on a carbon-fiber paper. The combination of single-atom nickel(I) sites and self-standing array structure gives rise to an excellent electrocatalytic CO₂ reduction performance. The introduction of copper tunes the d-band electron configuration and enhances the adsorption of hydrogen, which impedes the hydrogen evolution reaction. The single-nickel-atom electrode exhibits a specific current density of −32.87 mA cm⁻² and turnover frequency of 1962 h⁻¹ at a mild overpotential of 620 mV for CO formation with 97 % Faradic efficiency.     

General π‐Electron‐Assisted Strategy for Ir,Pt, Ru,Pd, Fe,Ni Single‐Atom Electrocatalysts with Bifunctional Active Sites for Highly Efficient Water Splitting

Both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) are crucial to water splitting, but require alternative active sites. Now, a general π‐electron‐assisted strategy to anchor single‐atom sites (M=Ir, Pt, Ru, Pd, Fe, Ni) on a heterogeneous support is reported. The M atoms can simultaneously anchor on two distinct domains of the hybrid support, four‐fold N/C atoms (M@NC), and centers of Co octahedra (M@Co), which are expected to serve as bifunctional electrocatalysts towards the HER and the OER. The Ir catalyst exhibits the best water‐splitting performance, showing a low applied potential of 1.603 V to achieve 10 mA cm^?2 in 1.0 m KOH solution with cycling over 5 h. DFT calculations indicate that the Ir@Co (Ir) sites can accelerate the OER, while the Ir@NC₃ sites are responsible for the enhanced HER, clarifying the unprecedented performance of this bifunctional catalyst towards full water splitting.