Promoting the efficiency and selectivity of NO3--to-NH3 reduction on Cu-O-Ti active sites via preferential glycol oxidation with holes.

The combined reductive and oxidative reaction is the essence of a solar-driven photoredox system. Unfortunately, most of these efforts focus on the specific half-reactions, and the key roles of complete photoredox reactions have been overlooked. Taking the nitrate reduction reaction (NO3-RR) as a typical multiple-electrons involved process, the selective reduction of the NO3- into ammonia (NH3) synthesis with high efficiency is still a grand challenge. Herein, a rational oxidative half-reaction is tailored to achieve the selective conversion of NO3- to NH3 on Cu-O-Ti active sites. Through the coupled NO3-RR with glycol oxidation reaction system, a superior NH3 photosynthesis rate of 16.04 ± 0.40 mmol gcat-1 h-1 with NO3- conversion ratio of 100% and almost 100% of NH3 selectivity is reached on Cu-O-Ti bimetallic oxide cluster-anchored TiO2 nanosheets (CuOx@TNS) catalyst. A combination of comprehensive in situ characterizations and theoretical calculations reveals the molecular mechanism of the synergistic interaction between NO3-RR and glycol oxidation pair on CuOx@TNS. The introduction of glycol accelerates the h+ consumption for the formation of alkoxy (•R) radicals to avoid the production of •OH radicals. The construction of Cu-O-Ti sites facilitates the preferential oxidation of glycol with h+ and enhances the production of e- to participate in NO3-RR. The efficiency and selectivity of NO3--to-NH3 synthesis are thus highly promoted on Cu-O-Ti active sites with the accelerated glycol oxidative half-reaction. This work upgrades the conventional half photocatalysis into a complete photoredox system, demonstrating the tremendous potential for the precise regulation of reaction pathway and product selectivity.

Unraveling the Potential Dependence of Active Structures and Reaction Mechanism of Ni-based MOFs Electrocatalysts for Alkaline OER.

Nickel-based metal-organic frameworks (MOFs) with flexible structure units provide a broad platform for designing highly efficient electrocatalysts, especially for alkaline oxygen evolution reaction (OER). However, the stability of MOFs under harsh and dynamic reaction conditions poses significant challenges, resulting in ambiguous structure-activity relationships in MOFs-based OER research. Herein, Ni-benzenedicarboxylic acid-based MOF (NiBDC) is selected as prototypical catalyst to elucidate  its real active sites for OER and reaction pathway under different reaction states. Electrochemical measurements combined with X-ray absorption spectroscopy (XAS) and Raman spectroscopy reveal that the complete reconstruction of NiBDC to ß-NiOOH in the chronoamperometry activation process is responsible for significantly increased OER performance. In situ XAS and Raman results further demonstrate the electro-oxidation of ß-NiOOH into γ-NiOOH at high-potential state (above 1.6 V vs RHE). Furthermore, the collective evidences from key reaction intermediates and isotope-labeled products definitely unravel the potential dependence of OER mechanism: OER process at low-potential state proceeds mainly through the lattice oxygen-mediated mechanism, while adsorbate evolution mechanism emerges as the predominant pathway at high-potential state. Interestingly, the dynamically changing OER mechanism can not only reduce the required overpotential at the low-potential state but also improve the electrochemical stability of catalysts at high-potential state.

Recent Progress in Modular Electrochemical Synthesis of Hydrogen and High-Value-added Chemicals based on Solid Redox Mediator.

Electrochemical synthesis of H2 and high-value-added chemicals is an efficient and cost-effective approach that can be powered using renewable electricity. Compared to a conventional electrochemical production system, the modular electrochemical production system (MEPS) based on a solid redox mediator (SRM) can separate the anodic and cathodic reactions in time and space. The MEPS can avoid the use of membranes and formation of useless products, as well as eliminate the mutual dependence of production rates at anode and cathode. The SRM can temporarily store or release electrons and ions to pair with cathodic and anodic reactions, respectively, in MEPS. Designing of SRMs with large charge capacity and good cyclability is of great significance for constructing a high-performance MEPS. This work summarizes the design principles, recent advances in MEPS based on SRM, and application in redox flow cells. Moreover, structure design strategies as well as in situ characterization techniques and theoretical calculations for SRM is also proposed. It is expected to promote the vigorous development of MEPS based on SRM. Finally, the challenges and perspectives of MEPS based on SRM are discussed.

Enhanced Electrochemical CO2 Reduction to Formate over Phosphate-Modified In: Water Activation and Active Site Tuning.

Electrochemical CO2 reduction reaction (CO2RR) offers a sustainable strategy for producing fuels and chemicals. However, it suffers from sluggish CO2 activation and slow water dissociation. In this work, we construct a (P-O)δ- modified In catalyst that exhibits high activity and selectivity in electrochemical CO2 reduction to formate. A combination of in situ characterizations and kinetic analyses indicate that (P-O)δ- has a strong interaction with K+(H2O)n, which effectively accelerates water dissociation to provide protons. In situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) measurements together with density functional theory (DFT) calculations disclose that (P-O)δ- modification leads to a higher valence state of In active site, thus promoting CO2 activation and HCOO* formation, while inhibiting competitive hydrogen evolution reaction (HER). As a result, the (P-O)δ- modified oxide-derived In catalyst exhibits excellent formate selectivity across a broad potential window with a formate Faradaic efficiency as high as 92.1 % at a partial current density of ~200 mA cm-2 and a cathodic potential of -1.2 V vs. RHE in an alkaline electrolyte.

Breaking the Scaling Relationship in C-N Coupling via the Doping Effects for Efficient Urea Electrosynthesis.

Electrochemical C-N coupling reaction based on carbon dioxide and nitrate have been emerged as a new "green synthetic strategy" for the synthesis of urea, but the catalytic efficiency is seriously restricted by the inherent scaling relations of adsorption energies of the active sites, the improvement of catalytic activity is frequently accompanied by the decrease in selectivity. Herein, a doping engineering strategy was proposed to break the scaling relationship of intermediate binding and minimize the kinetic barrier of C-N coupling. A thus designed SrCo0.39Ru0.61O3-δ catalyst achieves a urea yield rate of 1522 µg h-1 mgcat. -1 and faradic efficiency of 34.1 % at -0.7 V versus reversible hydrogen electrode. A series of characterizations revealed that Co doping not only induces lattice distortion but also creates rich oxygen vacancies (OV) in the SrRuO3. The oxygen vacancies weaken the adsorption of *CO and *NH2 intermediates on the Co and Ru sites respectively, and the strain effects over the Co-Ru dual sites promoting the occurrence of C-N coupling of the two monomers instead of selective hydrogenating to form by-products. This work presents an insight into molecular coupling reactions towards urea synthesis via the doping engineering on SrRuO3.

Carboxyl-Substituted Organic Molecule Assembled with MXene Nanosheets for Boosting Aqueous Na+ Storage.

Aqueous alkali-ion batteries have enormous promise as a kind of safe, reliable, and sustainable energy technologies for power supplies. Although organic molecules with tunable and diverse configurations are potential electroactive materials, their inadequate redox activity and electron affinity hinder the practical application for aqueous alkali-ion storage. Herein, a novel electron-withdrawing carboxyl-substituted dipyridophenazine (CDPPZ) organic molecule is designed and synthesized for aqueous Na+ storage. Significantly, the introduction of carboxyl functional groups not only serves as additional redox-active sites for reversible Na+ coordination, but also causes the rearrangement of intramolecular electron cloud density to reduce the energy level, thereby ensuring the high redox activity and superior electron affinity of the CDPPZ molecule. For portable electronics, a self-supporting, adhesive-free, and flexible CDPPZ@MXene electrode is further constructed by incorporating highly redox-active CDPPZ molecule with MXene nanosheets, which delivers a fast, stable, and unrivaled aqueous Na+ storage capability with a high reversible capacity of 172.6 mAh cm-3 and excellent redox stability over 4000 cycles. In situ dynamic analysis combined with theoretical calculations illustrates the Na+ storage mechanism and corresponding coordinated pathway. Finally, a high-performance flexible aqueous Na-ion battery is fabricated with exceptional energy/power density and remarkable cycling lifespan, further confirming its promising application prospect.

Less-Coordinated Atomic Copper-Dimer Boosted Carbon-Carbon Coupling During Electrochemical CO2 Reduction.

This work reports a metal-organic framework (MOF) with less-coordinated copper dimers, which displays excellent electrochemical CO2 reduction (eCO2 RR) performance with an advantageous current density of 0.9 A cm-2 and a high Faradaic efficiency of 71% to C2 products. In comparison with MOF with Cu monomers that are present as Cu1 O4 with a coordination number of 3.8 ± 0.2, Cu dimers exist as O3 Cu1 ···Cu2 O2 with a coordination number of 2.8 ± 0.1. In situ characterizations together with theoretical calculations reveal that two *CO intermediates are stably adsorbed on each site of less-coordinated Cu dimers, which favors later dimerization via a key intermediate of *CH2 CHO. The highly unsaturated dual-atomic Cu provides large-quantity and high-quality actives sites for carbon-carbon coupling, achieving the optimal trade-off between activity and selectivity of eCO2 RR to C2 products.

Interfacial Electron Transfer in Chemical and Biological Transformation of Pollutants in Environmental Catalysis.

Interfacial electron transfer (IET) is essential for chemical and biological transformation of pollutants, operative across diverse lengths and time scales. This Perspective presents an array of multiscale molecular simulation methodologies, supplemented by in situ monitoring and imaging techniques, serving as robust tools to decode IET enhancement mechanisms such as interface molecular modification, catalyst coordination mode, and atomic composition regulation. In addition, three IET-based pollutant transformation systems, an electrocatalytic oxidation system, a bioelectrochemical spatial coupling system, and an enzyme-inspired electrocatalytic system, were developed, demonstrating a high effect in transforming and degrading pollutants. To improve the effectiveness and scalability of IET-based strategies, the refinement of these systems is necessitated through rigorous research and theoretical exploration, particularly in the context of practical wastewater treatment scenarios. Future endeavors aim to elucidate the synergy between biological and chemical modules, edit the environmental functional microorganisms, and harness machine learning for designing advanced environmental catalysts to boost efficiency. This Perspective highlights the powerful potential of IET-focused environmental remediation strategies, emphasizing the critical role of interdisciplinary research in addressing the urgent global challenge of water pollution.

A Spectroscopic Study on Nitrogen Electrooxidation to Nitrate.

As a potential substitute technique for conventional nitrate production, electrocatalytic nitrogen oxidation reaction (NOR) is gaining more and more attention. But, the pathway of this reaction is still unknown owing to the lack of understanding on key reaction intermediates. Herein, electrochemical in situ attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and isotope-labeled online differential electrochemical mass spectrometry (DEMS) are employed to study the NOR mechanism over a Rh catalyst. Based on the detected asymmetric NO2 - bending, NO3 - vibration, N=O stretching, and N-N stretching as well as isotope-labeled mass signals of N2 O and NO, it can be deduced that the NOR undergoes an associative mechanism (distal approach) and the strong N≡N bond in N2 prefers to break concurrently with the hydroxyl addition in distal N.

New Opportunity for in Situ Exsolution of Metallic Nanoparticles on Perovskite Parent.

One of the main challenges for advanced metallic nanoparticles (NPs) supported functional perovskite catalysts is the simultaneous achievement of a high population of NPs with uniform distribution as well as long-lasting high performance. These are also the essential requirements for optimal electrode catalysts used in solid oxide fuel cells and electrolysis cells (SOFCs and SOECs). Herein, we report a facile operando manufacture way that the crystal reconstruction of double perovskite under reducing atmosphere can spontaneously lead to the formation of ordered layered oxygen deficiency and yield segregation of massively and finely dispersed NPs. The real-time observation of this emergent process was performed via an environmental transmission electron microscope. Density functional theory calculations prove that the crystal reconstruction induces the loss of coordinated oxygen surrounding B-site cations, serving as the driving force for steering fast NP growth. The prepared material shows promising capability as an active and stable electrode for SOFCs in various fuels and SOECs for CO2 reduction. The conception exemplified here could conceivably be extended to fabricate a series of supported NPs perovskite catalysts with diverse functionalities.

"Bowling Collision Effect" of CoMo6 Polyoxometalate Units Enables Wide Temperature Range from -20 to 60 °C and Dendrite Mitigation Li-S Batteries.

To improve the performance of Lithium-Sulfur (Li-S) batteries, the reaction catalysts of lithium polysulfides (LiPSs) reactions should have the characteristics of large surface area, efficient atomic utilization, high conductivity, small size, good stability, and strong adjustability. Herein, Anderson-type polyoxometalate ([TMMo6O24]n-, TM = Co, Ni, Fe, represented by TMMo6 POMs) are used as the modified materials for Li-S battery separator. By customizing the central metal atoms, this work gains insights into the layer-by-layer electron transfer mechanism between TMMo6 units and LiPSs, similar to the collision effect of a bowling ball. Theoretical analysis and in situ experimental characterization show that the changes of CoMo6 units with moderate binding energy and lowest Gibbs free energy result in the formation of robust polar bonds and prolonged S─S bonds after adsorption. Hence, the representative Li-S battery with CoMo6 and graphene composite modified separator has a high initial capacity of 1588.6 mA h g-1 at 0.2 C, excellent cycle performance of more than 3000 cycles at 5 C, and uniform Li+ transport over 1900 h. More importantly, this work has revealed the inherent contradiction between the kinetics and thermodynamics, achieving a stable cycle in the temperature range of -20 to 60 °C.

Structure-Activity Relationships in Oxygen Electrocatalysis.

Oxygen electrocatalysis, as the pivotal circle of many green energy technologies, sets off a worldwide research boom in full swing, while its large kinetic obstacles require remarkable catalysts to break through. Here, based on summarizing reaction mechanisms and in situ characterizations, the structure-activity relationships of oxygen electrocatalysts are emphatically overviewed, including the influence of geometric morphology and chemical structures on the electrocatalytic performances. Subsequently, experimental/theoretical research is combined with device applications to comprehensively summarize the cutting-edge oxygen electrocatalysts according to various material categories. Finally, future challenges are forecasted from the perspective of catalyst development and device applications, favoring researchers to promote the industrialization of oxygen electrocatalysis at an early date.

Freestanding Ammonium Vanadate Composite Cathodes with Lattice Self-Regulation and Ion Exchange for Long-Lasting Ca-Ion Batteries.

Calcium-ion batteries (CIBs) have emerged as a promising alternative for electrochemical energy storage. The lack of high-performance cathode materials severely limits the development of CIBs. Vanadium oxides are particularly attractive as cathode materials for CIBs, and preinsertion chemistry is often used to improve their calcium storage performance. However, the room temperature cycling lifespan of vanadium oxides in organic electrolytes still falls short of 1000 cycles. Here, based on preinsertion chemistry, the cycling life of vanadium oxides is further improved by integrated electrode and electrolyte engineering. Utilizing a tailored Ca electrolyte, the constructed freestanding (NH4)2V6O16·1.35H2O@graphene oxide@carbon nanotube (NHVO-H@GO@CNT) composite cathode achieves a 305 mAh g-1 high capacity and 10 000 cycles record-long life. Additionally, for the first time, a Ca-ion hybrid capacitor full cell is assembled and delivers a capacity of 62.8 mAh g-1. The calcium storage mechanism of NHVO-H@GO@CNT based on a two-phase reaction and the exchange of NH4 + and Ca2+ during cycling are revealed. The lattice self-regulation of V─O layers is observed and the layered vanadium oxides with Ca2+ pillars formed by ion exchange exhibit higher capacity. This work provides novel strategies to enhance the calcium storage performance of vanadium oxides via integrated structural design of electrodes and electrolyte modification.

Efficient purification of a nitrate and chlorate mixture in water via photoredox activated intermediate coupling-decoupling pathway.

Nitrate (NO3-) is a widespread contaminant that threatens human health and ecological safety. Meanwhile, the disinfection byproducts chlorate (ClO3-) is generated inevitably in conventional wastewater treatment. Therefore, the contaminants mixture of NO3- and ClO3- are universal in common emission units. Photocatalysis technology is a feasible approach for the synergistic abatement of contaminant mixture, where matching suitable oxidation reactions is a potential strategy to improve the photocatalytic reduction reactions. Herein, formate (HCOOH) oxidation is introduced to facilitate the photocatalytic reduction of the NO3- and ClO3- mixture. As a result, high purification efficiency of NO3- and ClO3- mixture are achieved, evidenced by 84.6% e--dependent removal of the mixture at a reaction time of 30 min, with 94.5% N2 selectivity and 100% Cl- selectivity, respectively. Specifically, by the close combination of in-situ characterizations and theoretical calculations, the detailed reaction mechanism is revealed, in which the intermediate coupling-decoupling route from NO3- reduction and HCOOH oxidation is established by the chlorate-induced photoredox activation, leading to the significantly enhanced efficiency for the wastewater mixture purification. The practical application of this pathway is established for simulated wastewater to show its wide applicability. This work provides new insights into photoredox catalysis technology for its environmental application.

Aromatic Organic Small-Molecule Material with (020) Crystal Plane Activation for Wide-Temperature and 68000 Cycle Aqueous Calcium-Ion Batteries.

Calcium-ion batteries are an emerging energy storage device owing to the low redox potential of Ca2+/Ca and the naturally abundant reserves of the Ca element. However, the high charge density and large radius of Ca2+ lead to a low calcium storage capacity or unsatisfactory cycling performance for most electrode materials. Herein, we report the organic crystal 3,4,9,10-perylenetetracarboxylic diimide (PTCDI) as an anode material for aqueous calcium-ion batteries (ACIBs) in a water-in-salt electrolyte. PTCDI delivers a high discharge capacity of 131.8 mAh g-1, excellent rate performance (86.2 mAh g-1@10000 mA g-1), and an ultralong life of 68000 cycles (over 470 days) with a high capacity retention of 72.7%. The calcium storage mechanism of PTCDI is shown to be an enolization reaction by in situ attenuated total reflectance Fourier-transform infrared and ex situ X-ray photoelectron spectroscopy. The activation mechanism of PTCDI microribbon splitting along the (020) crystal plane is studied by in situ X-ray diffraction, 3D tomography reconstruction technologies, and ex situ transmission electron microscopy. In addition, the Ca2+ storage sites and diffusion pathways of PTCDI are studied by density functional theory calculations. Finally, by matching a high-voltage Prussian blue analogue cathode, the assembled aqueous calcium-ion full cells exhibit excellent wide-temperature operating capability (-20 to +50 °C) and an ultralong life of 30000 cycles. Further, an aqueous calcium-ion pouch cell is constructed and exhibits a long lifetime of over 500 cycles.

Emerging Applications of Synchrotron Radiation X-Ray Techniques in Single Atomic Catalysts.

Single atom catalysts (SACs) can achieve a maximum atom utilization efficiency of 100%, which provides significantly increased active sites compared with traditional catalysts during catalytic reactions. Synchrotron radiation technology is an important characterization method for identifying single-atom catalysts. Several types of internal information, such as the coordination number, bond length and electronic structure of metals, can all be analyzed. This review will focus on the introduction of synchrotron radiation techniques and their applications in SACs. First, the fundamentals of synchrotron radiation and the corresponding techniques applied in characterization of SACs will be briefly introduced, such as X-ray absorption near edge spectroscopy and extended X-ray absorption fine structure spectroscopy and in situ techniques. The detailed information obtained from synchrotron radiation X-ray characterization is described through four routes: 1) the local environment of a specific atom; 2) the oxidation state of SACs; 3) electronic structures at different orbitals; and 4) the in situ structure modification during catalytic reaction. In addition, a systematic summary of synchrotron radiation X-ray characterization on different types of SACs (noble metals and transition metals) will be discussed.

Synergic Reaction Kinetics over Adjacent Ruthenium Sites for Superb Hydrogen Generation in Alkaline Media.

Ruthenium (Ru)-based electrocatalysts as platinum (Pt) alternatives in catalyzing hydrogen evolution reaction (HER) are promising. However, achieving efficient reaction processes on Ru catalysts is still a challenge, especially in alkaline media. Here, the well-dispersed Ru nanoparticles with adjacent Ru single atoms on carbon substrate (Ru1,n -NC) is demonstrated to be a superb electrocatalyst for alkaline HER. The obtained Ru1,n -NC exhibits ultralow overpotential (14.8 mV) and high turnover frequency (1.25 H2  s-1 at -0.025 V vs reversible hydrogen electrode), much better than the commercial 40 wt.% Pt/C. The analyses reveal that Ru nanoparticles and single sites can promote each other to deliver electrons to the carbon substrate. Eventually, the electronic regulations bring accelerated water dissociation and reduced energy barriers of hydroxide/hydrogen desorption on adjacent Ru sites, then an optimized reaction kinetics for Ru1,n -NC is obtained to achieve superb hydrogen generation in alkaline media. This work provides a new insight into the catalyst design in simultaneous optimizations of the elementary steps to obtain ideal HER performance in alkaline media.

Microstructural development during heat treatment of a commercially available dental-grade lithium disilicate glass-ceramic.

OBJECTIVE: To elucidate the microstructural evolution of a commercial dental-grade lithium disilicate glass-ceramic using a wide battery of in-situ and ex-situ characterization techniques. METHODS: In-situ X-ray thermo-diffractometry experiments were conducted on a commercially available dental-grade lithium disilicate glass-ceramic under both non-isothermal and isothermal heat treatments in air. These analyses were complemented by experiments of ex-situ X-ray diffractometry, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, differential scanning calorimetry, and field-emission scanning electron thermo-microscopy. RESULTS: It was found that the non-fired blue block consists of ∼40 vol % crystals embedded in a glass matrix. The crystals are mainly lithium metasilicate (Li2SiO3) along with small amounts of lithium orthophosphate (Li3PO4) and lithium disilicate (Li2Si2O5). Upon heating, the glassy matrix in the as-received block first crystallizes partially as SiO2 (i.e., cristobalite) at ∼660 °C. Then, the SiO2 crystals react with the original Li2SiO3 crystals at ∼735 °C, forming the desired Li2Si2O5 crystals by a solid-state reaction in equimolar concentration (SiO2 + Li2SiO3 → Li2Si2O5). Precipitation of added colourant Ce ions in the form of CeO2 appears at ∼775 °C. These events result in a glass-ceramic material with the aesthetic quality and mechanical integrity required for dental restorations. It also has a microstructure consisting essentially of elongated Li2Si2O5 grains in a glassy matrix plus small cubic CeO2 grains at the outermost part of the surface. SIGNIFICANCE: It was found that by judiciously controlling the heat treatment parameters, it is possible to tailor the microstructure of the resulting glass-ceramics and thus optimizing their performance and lifespan as dental restorations.