Scalable-doped Nanoporous 1T″ ReSe2 via a General Surface Co-Alloy Strategy.

Reliable and controllable doping of 2D transition metal dichalcogenides is an efficient approach to tailor their physicochemical properties and expand their functional applications. However, precise control over dopant distribution and scalability of the process remains a challenge. Here, we report a general method to achieve scalable in situ doping of centimeter-sized bicontinuous nanoporous ReSe2 films with transition metal atoms via surface coalloy growth. The distinct strains induced by the bending curvature of nanoporous structures and uniform dopants result in a local 1T' to 1T″ structure phase transition over nanoporous ReSe2 films. The as-prepared nanoporous Ru-ReSe2 with high 1T″ phase exhibits preferable electrochemical activity in hydrogen evolution reaction. The work demonstrates a unique and general approach to synthesize uniformly-doped transition metal dichalcogenides with 3D bicontinuous nanoporous structure, which can be scaled up to batch production for various applications.

Engineering the Morphology and Microenvironment of a Graphene-Supported Co-N-C Single-Atom Electrocatalyst for Enhanced Hydrogen Evolution.

Graphene-supported single-atom catalysts (SACs) are promising alternatives to precious metals for catalyzing the technologically important hydrogen evolution reaction (HER), but their performances are limited by the low intrinsic activity and insufficient mass transport. Herein, a highly HER-active graphene-supported Co-N-C SAC is reported with unique design features in the morphology of the substrate and the microenvironment of the single metal sites: i) the crumpled and scrolled morphology of the graphene substrate circumvents the issues encountered by stacked nanoplatelets, resulting in improved exposure of the electrode/electrolyte interfaces (≈10 times enhancement); ii) the in-plane holes in graphene preferentially orientate the Co atoms at the edge sites with low-coordinated Co-N3 configuration that exhibits enhanced intrinsic activity (≈2.6 times enhancement compared to the conventional Co-N4 moiety), as evidenced by detailed experiments and density functional theory calculations. As a result, this catalyst exhibits significantly improved HER activity with an overpotential (η) of merely 82 mV at 10 mA cm-2 , a small Tafel slope of 59.0 mV dec-1 and a turnover frequency of 0.81 s-1 at η = 100 mV, ranking it among the best Co-N-C SACs.

Hierarchical N-doping germanium/carbon nanofibers as anode for high-performance lithium-ion and sodium-ion batteries.

Germanium (Ge) has gained a great deal of attention as an anode material for sodium ion batteries (SIBs) and lithium ion batteries (LIBs) for its high theoretical capacity and ion diffusivity. Unfortunately, Ge particle pulverization triggered by huge volume expansion during the alloying and dealloying processes can cause rapid capacity fade. Herein we report a facile method for the preparation of ultrafine Ge nanoparticles embedded in hierarchical N-doped multichannel carbon fibers (denoted as Ge-NMCFs) by electrospinning. The hierarchical carbon matrix not only provides sufficient internal void space to accommodate the large volume expansion of Ge nanoparticles, but also provides numerous open channels for the easy access of electrolyte and Na/Li ions. As half-cell tests revealed, the composite provides discharge capacity of 303 mA h g-1 (1st cycle) and 160 mA h g-1 (700th cycle) for SIBs, 1146.7 mA h g-1 (1st cycle) and 600 mA h g-1 (500th cycle) for LIBs at a current density of 500 mA g-1 (all the presented capacity based on the total weight of Ge/C composites). Density functional theory calculation suggests that N-doped in carbon can enhance the Na/Li ion storage and improve the electrochemical performance. This demonstration is an important step towards the development of SIBs and LIBs with much higher specific energy capacity and longer cycle stability.

High-Energy-Density Rechargeable Mg Battery Enabled by a Displacement Reaction.

Because of its high theoretical volumetric capacity and dendrite-free stripping/plating of Mg, rechargeable magnesium batteries (RMBs) hold great promise for high energy density in consumer electronics. However, the lack of high-energy-density cathodes severely constrains their practical applications. Herein, for the first time, we report that a CuS cathode can fully reversibly work through a displacement reaction in CuS/Mg pouch cells at room temperature and provide a high capacity of ∼400 mA h/g in a MACC electrolyte, corresponding to the gravimetric and volumetric energy density of 608 W h/kg and1042 W h/L, respectively. Even after 80 cycles, CuS/Mg pouch cells can maintain a high capacity of 335 mA h/g. Detailed mechanistic studies reveal that CuS undergoes a displacement reaction route rather than a typical conversion mechanism. This work will provide a guide for more discovery of high-performance cathode candidates for RMBs.

Bacteria-Derived Biological Carbon Building Robust Li-S Batteries.

Lithium sulfur (Li-S) batteries are attracting increasing interest for high-density energy storage. However, the practical application is limited by the rapid capacity fading over repeated charge/discharge cycles which is largely attributed to the formation and shuttling of soluble polysulfide species. To address these issues, we develop a hierarchical structure composite with triple protection strategy via graphene, organic conductor PEDOT, and nitrogen and phosphorus codoped biological carbon to encapsulate sulfur species (GOC@NPBCS). This unique hierarchical structure can effectively immobilize the sulfur species while at the same time improve the electrical conductivity and ensure efficient lithium ion transport to enable excellent Li-S battery performance. In particular, the biological carbon derived from natural bacteria features inherent nitrogen and phosphorus codoping with a strong absorption to lithium polysulfides, which can greatly suppress the dissolution and shuttling of polysulfides that are responsible for rapid capacity fading. With these synergistic effects, the GOC@NPBCS cathode exhibits exceptionally stable cycling stability (an ultralow capacity fading rate of 0.045% per cycle during 1000 cycles at the current rate of 5 C), high specific capacity (1193.8 mAh g-1 at 0.5 C based on sulfur weight), and excellent rate capability.

Antimony Nanorod Encapsulated in Cross-Linked Carbon for High-Performance Sodium Ion Battery Anodes.

Antimony- (Sb) based materials have been considered as one of promising anodes for sodium ion batteries (SIBs) owing to their high theoretical capacities and appropriate sodium inserting potentials. So far, the reported energy density and cycling stability of the Sb-based anodes for SIBs are quite limited and need to be significantly improved. Here, we develop a novel Sb/C hybrid encapsulating the Sb nanorods into highly conductive N and S codoped carbon (Sb@(N, S-C)) frameworks. As an anode for SIBs, the Sb@(N, S-C) hybrid maintains high reversible capacities of 621.1 mAh g-1 at 100 mA g-1 after 150 cycles, and 390.8 mAh g-1 at 1 A g-1 after 1000 cycles. At higher current densities of 2, 5, and 10 A g-1, the Sb@(N, S-C) hybrid also can display high reversible capacities of 534.4, 430.8, and 374.7 mAh g-1, respectively. Such impressive sodium storage properties are mainly attributed to the unique cross-linked carbon networks providing highly conductive frameworks for fast transfer of ions and electrons, alleviating the volume expansion and preventing the agglomeration of Sb nanorods during the cycling.

Se-Doping Activates FeOOH for Cost-Effective and Efficient Electrochemical Water Oxidation.

Ni or Co is commonly required in efficient electrocatalysts for oxygen evolution reaction (OER). Although Fe is much more abundant and cheaper, full-Fe or Fe-rich catalysts suffer from insufficient activity. Herein, we discover that Se-doping can drastically promote OER on FeOOH and develop a facile on-site electrochemical activation strategy for achieving such a Se-doped FeOOH electrode via an FeSe precatalyst. Theoretical analysis and systematic experiments prove that Se-doping enables FeOOH as an efficient and low-cost OER electrocatalyst. By optimizing the electrode structure, an industrial-level OER current output of 500 mA cm-2 is secured at a low overpotential of 348 mV. The application of such an Fe-rich OER electrode in a practical solar-driven water splitting system demonstrates a high and stable solar-to-hydrogen efficiency of 18.55%, making the strategy promising for exploring new cost-effective and highly active electrocatalysts for clean hydrogen production.

Phase Control on Surface for the Stabilization of High Energy Cathode Materials of Lithium Ion Batteries.

The development of high energy electrode materials for lithium ion batteries is challenged by their inherent instabilities, which become more aggravated as the energy densities continue to climb, accordingly causing increasing concerns on battery safety and reliability. Here, taking the high voltage cathode of LiNi0.5Mn1.5O4 as an example, we demonstrate a protocol to stabilize this cathode through a systematic phase modulating on its particle surface. We are able to transfer the spinel surface into a 30 nm shell composed of two functional phases including a rock-salt one and a layered one. The former is electrochemically inert for surface stabilization while the latter is designated to provide necessary electrochemical activity. The precise synthesis control enables us to tune the ratio of these two phases, and achieve an optimized balance between improved stability against structural degradation without sacrificing its capacity. This study highlights the critical importance of well-tailored surface phase property for the cathode stabilization of high energy lithium ion batteries.

Hollow Carbon Nanobelts Codoped with Nitrogen and Sulfur via a Self-Templated Method for a High-Performance Sodium-Ion Capacitor.

Sodium-ion capacitors (SICs) have attracted enormous attention due to their high energy density and high power density. In this work, N and S codoped hollow carbon nanobelts (N/S-HCNs) are synthesized by a self-templated method. The as-synthesized carbon nanobelts exhibit excellent performance in pseudocapacitance and electric double layer anions adsorption. After pairing the N/S-HCNs cathode with a tin foil anode in a carbonate electrolyte, the obtained SIC achieves a high specific capacity of 400 mAh g-1 at 1 A g-1 (based on the mass of cathode material) and energy density of 250.35 Wh kg-1 at 676 W kg-1 (based on the total mass of cathode and anode materials). Besides, the presented SIC also demonstrates high cycling stability with almost 100% capacity retention after 10 000 cycles, which is among the best results of the reported SICs, suggesting the potential for high-performance energy storage applications.

Zn-Doped Cu(100) facet with efficient catalytic ability for the CO2 electroreduction to ethylene.

Electrochemically converting CO2 into fuels and chemicals is an appealing strategy to create energy rich products. The highly demanded product ethylene has been preferably produced on Cu-based catalysts with abundant exposed Cu(100) facets. However, the performance is still limited by the large energy barrier for the C-C dimerization. Here, to lower the energy barrier, we tailor the electronic structure of Cu(100) by doping a series of transition metals using the density functional theory (DFT) method. The zinc-doped Cu(100) surface has shown a superior catalytic performance. Mechanistic study further reveals that doping with Zn alters the electronic structure around Cu, adjusts the atomic arrangement in the active sites and makes the catalyst surface electronegative, which is conducive to the activation of acidic molecular CO2 and the reduction of the energy barrier for C-C dimerization. This work reveals that the doping of Cu with transition metals has great potential in promoting the electrochemical CO2-to-C2H4 conversion. This work also provides deep insights into the formation mechanisms of C2H4, thus guiding the design of Cu-based bimetallic catalysts for its effective production.

Nitrogen, Fluorine, and Boron Ternary Doped Carbon Fibers as Cathode Electrocatalysts for Zinc-Air Batteries.

Zinc-air batteries with high-density energy are promising energy storage devices for the next generation of energy storage technologies. However, the battery performance is highly dependent on the efficiency of oxygen electrocatalyst in the air electrode. Herein, the N, F, and B ternary doped carbon fibers (TD-CFs) are prepared and exhibited higher catalytic properties via the efficient 4e- transfer mechanism for oxygen reduction in comparison with the single nitrogen doped CFs. More importantly, the primary and rechargeable Zn-air batteries using TD-CFs as air-cathode catalysts are constructed. When compared to batteries with Pt/C + RuO2 and Vulcan XC-72 carbon black catalysts, the TD-CFs catalyzed batteries exhibit remarkable battery reversibility and stability over long charging/discharging cycles.

Interfacial Interactions in Monolayer and Few-Layer SnS/CH3 NH3 PbI3 Perovskite van der Waals Heterostructures and Their Effects on Electronic and Optical Properties.

A high light-absorption coefficient and long-range hot-carrier transport of hybrid organic-inorganic perovskites give huge potential to their composites in solar energy conversion and environmental protection. Understanding interfacial interactions and their effects are paramount for designing perovskite-based heterostructures with desirable properties. Herein, we systematically investigated the interfacial interactions in monolayer and few-layer SnS/CH3 NH3 PbI3 heterostructures and their effects on the electronic and optical properties of these structures by density functional theory. It was found that the interfacial interactions in SnS/CH3 NH3 PbI3 heterostructures were van der Waals (vdW) interactions, and they were found to be insensitive to the layer number of 2D SnS sheets. Interestingly, although their band gap decreased upon increasing the layer number of SnS, the near-gap electronic states and optical absorption spectra of these heterostructures were found to be strikingly similar. This feature was determined to be critical for the design of 2D layered SnS-based heterostructures. Strong absorption in the ultraviolet and visible-light regions, type II staggered band alignment at the interface, and few-layer SnS as an active co-catalyst make 2D SnS/CH3 NH3 PbI3 heterostructures promising candidates for photocatalysis, photodetectors, and solar energy harvesting and conversion. These results provide first insight into the nature of interfacial interactions and are useful for designing hybrid organic-inorganic perovskite-based devices with novel properties.

Chevrel Phase Mo6 T8 (T = S, Se) as Electrodes for Advanced Energy Storage.

With the large-scale applications of electric vehicles in recent years, future batteries are required to be higher in power and possess higher energy densities, be more environmental friendly, and have longer cycling life, lower cost, and greater safety than current batteries. Therefore, to develop alternative electrode materials for advanced batteries is an important research direction. Recently, the Chevrel phase Mo6 T8 (T = S, Se) has attracted increasing attention as electrode candidate for advanced batteries, including monovalent (e.g., lithium and sodium) and multivalent (e.g., magnesium, zinc and aluminum) ion batteries. Benefiting from its unique open crystal structure, the Chevrel phase Mo6 T8 cannot only ensure rapid ion transport, but also retain the structure stability during electrochemical reactions. Although the history of the research on Mo6 T8 as electrodes for advanced batteries is short, there has been significant progress on the design and fabrication of Mo6 T8 for various advanced batteries as above mentioned. An overview of the recent progress on Mo6 T8 electrodes applied in advanced batteries is provided, including synthesis methods and diverse structures for Mo6 T8 , and electrochemical mechanism and performance of Mo6 T8 . Additionally, a briefly conclusion on the significant progress, obvious drawbacks, emerging challenges and some perspectives on the research of Mo6 T8 for advanced batteries in the near future is provided.

WS2 Moiré Superlattices Supporting Au Nanoclusters and Isolated Ru to Boost Hydrogen Production.

Maximizing the catalytic activity of single-atom and nanocluster catalysts through the modulation of the interaction between these components and the corresponding supports is crucial but challenging. Herein, guided by theoretical calculations, a nanoporous bilayer WS2 Moiré superlattices (MSLs) supported Au nanoclusters (NCs) adjacent to Ru single atoms (SAs) (Ru1/Aun-2LWS2) is developed for alkaline hydrogen evolution reaction (HER) for the first time. Theoretical analysis suggests that the induced robust electronic metal-support interaction effect in Ru1/Aun-2LWS2 is prone to promote the charge redistribution among Ru SAs, Au NCs, and WS2 MSLs support, which is beneficial to reduce the energy barrier for water adsorption and thus promoting the subsequent H2 formation. As feedback, the well-designed Ru1/Aun-2LWS2 electrocatalyst exhibits outstanding HER performance with high activity (η10 = 19 mV), low Tafel slope (35 mV dec-1), and excellent long-term stability. Further, in situ, experimental studies reveal that the reconstruction of Ru SAs/NCs with S vacancies in Ru1/Aun-2LWS2 structure acts as the main catalytically active center, while high-valence Au NCs are responsible for activating and stabilizing Ru sites to prevent the dissolution and deactivation of active sites. This work offers guidelines for the rational design of high-performance atomic-scale electrocatalysts.

Pd-Sn Alloy Catalysts for Direct Synthesis of Hydrogen Peroxide from H2 and O2 in a Microchannel Reactor.

Direct synthesis of hydrogen peroxide (DSHP) from H2 and O2 offers a promising alternative to the present commercial anthraquinone method, but it still faces the challenges of low H2O2 productivity, low stability of catalysts, and high risk of explosion. Herein, by loading in a microchannel reactor, the as-synthesized Pd-Sn alloy materials exhibit high catalytic activity for H2O2 production, presenting a H2O2 productivity of 3124 g kgPd-1 h-1. The doped Sn atoms on the surface of Pd not only facilitate the release of H2O2 but also effectively slow down the deactivation of catalysts. Theoretical calculations demonstrate that the Pd-Sn alloy surface has the property of antihydrogen poisoning, showing higher activity and stability than pure Pd catalysts. The deactivation mechanism of the catalyst was elucidated, and the online reactivation method was developed. In addition, we show that the long-life Pd-Sn alloy catalyst can be achieved by supplying an intermittent flow of hydrogen gas. This work provides guidance on how to prepare high performance and stable Pd-Sn alloy catalysts for the continuous and direct synthesis of H2O2.

Efficient electrosynthesis of formamide from carbon monoxide and nitrite on a Ru-dispersed Cu nanocluster catalyst.

Conversion into high-value-added organic nitrogen compounds through electrochemical C-N coupling reactions under ambient conditions is regarded as a sustainable development strategy to achieve carbon neutrality and high-value utilization of harmful substances. Herein, we report an electrochemical process for selective synthesis of high-valued formamide from carbon monoxide and nitrite with a Ru1Cu single-atom alloy under ambient conditions, which achieves a high formamide selectivity with Faradaic efficiency of 45.65 ± 0.76% at -0.5 V vs. RHE. In situ X-ray absorption spectroscopy, coupled with in situ Raman spectroscopy and density functional theory calculations results reveal that the adjacent Ru-Cu dual active sites can spontaneously couple *CO and *NH2 intermediates to realize a critical C-N coupling reaction, enabling high-performance electrosynthesis of formamide. This work offers insight into the high-value formamide electrocatalysis through coupling CO and NO2- under ambient conditions, paving the way for the synthesis of more-sustainable and high-value chemical products.

Sb2S3-templated synthesis of sulfur-doped Sb-N-C with hierarchical architecture and high metal loading for H2O2 electrosynthesis.

Selective two-electron (2e-) oxygen reduction reaction (ORR) offers great opportunities for hydrogen peroxide (H2O2) electrosynthesis and its widespread employment depends on identifying cost-effective catalysts with high activity and selectivity. Main-group metal and nitrogen coordinated carbons (M-N-Cs) are promising but remain largely underexplored due to the low metal-atom density and the lack of understanding in the structure-property correlation. Here, we report using a nanoarchitectured Sb2S3 template to synthesize high-density (10.32 wt%) antimony (Sb) single atoms on nitrogen- and sulfur-codoped carbon nanofibers (Sb-NSCF), which exhibits both high selectivity (97.2%) and mass activity (114.9 A g-1 at 0.65 V) toward the 2e- ORR in alkaline electrolyte. Further, when evaluated with a practical flow cell, Sb-NSCF shows a high production rate of 7.46 mol gcatalyst-1 h-1 with negligible loss in activity and selectivity in a 75-h continuous electrolysis. Density functional theory calculations demonstrate that the coordination configuration and the S dopants synergistically contribute to the enhanced 2e- ORR activity and selectivity of the Sb-N4 moieties.

Coupling Glucose-Assisted Cu(I)/Cu(II) Redox with Electrochemical Hydrogen Production.

Water electrolysis is a sustainable technology for hydrogen production since this process can utilize the intermittent electricity generated by renewable energy such as solar, wind, and hydro. However, the large-scale application of this process is restricted by the high electricity consumption due to the large potential gap (>1.23 V) between the anodic oxygen evolution reaction and the cathodic hydrogen evolution reaction (HER). Herein, a novel and efficient hydrogen production system is developed for coupling glucose-assisted Cu(I)/Cu(II) redox with HER. The onset potential of the electrooxidation of Cu(I) to Cu(II) is as low as 0.7 VRHE (vs reversible hydrogen electrode). In situ Raman spectroscopy, ex situ X-ray photoelectron spectroscopy, and density functional theory calculation demonstrates that glucose in the electrolyte can reduce the Cu(II) into Cu(I) instantaneously via a thermocatalysis process, thus completing the cycle of Cu(I)/Cu(II) redox. The assembled electrolyzer only requires a voltage input of 0.92 V to achieve a current density of 100 mA cm-2 . Consequently, the electricity consumption for per cubic H2 produced in the system is 2.2 kWh, only half of the value for conventional water electrolysis (4.5 kWh). This work provides a promising strategy for the low-cost, efficient production of high-purity H2 .

Electrochemical nitrogen fixation via bimetallic Sn-Ti sites on defective titanium oxide catalysts.

The efficient adsorption and activation of inert N2 molecules on a heterogeneous electrocatalyst surface are critical toward electrochemical N2 fixation. Inspired by the bimetallic sites in nitrogenase, herein, we developed a bi-metallic tin-titanium (Sn-Ti) structure in Sn-doped anatase TiO2 via an oxygen vacancy induced engineering approach. Density functional theory (DFT) calculations indicated that Sn atoms were introduced in the oxygen vacancy sites in anatase TiO2 (101) to form Sn-Ti bonds. These Sn-Ti bonds provided both strong σ-electron accepting and strong π-electron donating capabilities, thus serving as both N2 adsorption and catalytic N2 reduction sites. In 0.1 M KOH aqueous solution, the Sn-TiO2 electrocatalyst achieved a NH3 production rate of 10.5 µgh-1cm-2 and a corresponding Faradaic efficiency (FENH3) of 8.36% at -0.45 V vs. reversible hydrogen electrode (RHE). Our work suggests the potential of atomic-scale designing and constructing bimetallic active sites for efficient electrocatalytic N2 fixation.

Precise tuning of heteroatom positions in polycyclic aromatic hydrocarbons for electrocatalytic nitrogen fixation.

The electrochemical dinitrogen reduction represents an attractive approach of converting N2 and water into ammonia, while the rational design of catalytic active centers remains challenging. Investigating model molecular catalysts with well-tuned catalytic sites should help to develop a clear structure-activity relationship for electrochemical N2 reduction. Herein, we designed several polycyclic aromatic hydrocarbon (PAH) molecules with well-defined positions of boron and nitrogen atoms. Theoretical calculations revealed that the boron atoms possess high local positive charge densities as Lewis acid sites, which are beneficial for N2 adsorption and activation, thus serving as major catalytic active sites for N2 electrochemical reduction. Furthermore, the close vicinity of two boron atoms can further enhance the local positive density and subsequent catalytic activity. Using the PAH molecule with two boron atoms separated by two carbon atoms (B-2C-B), a high NH3 production rate of 34.58 µg·h-1·cm-2 and a corresponding Faradaic efficiency (5.86%) were achieved at -0.7 V versus reversible hydrogen electrode, substantially exceeding the other PAHs with single boron or nitrogen-containing molecular structures.