Electrodegradation of nitrogenous pollutants in sewage: from reaction fundamentals to energy valorization applications.

The excessive accumulation of nitrogen pollutants (mainly nitrate, nitrite, ammonia nitrogen, hydrazine, and urea) in water bodies seriously disrupts the natural nitrogen cycle and poses a significant threat to human life and health. Electrolysis is considered a promising method to degrade these nitrogenous pollutants in sewage, with the advantages of high efficiency, wide generality, easy operability, retrievability, and environmental friendliness. For particular energy devices, including metal-nitrate batteries, direct fuel cells, and hybrid water electrolyzers, the realization of energy valorization from sewage purification processes (, valuable chemical generation, electricity output, and hydrogen production) becomes feasible.

Vanadium-Doped Heterointerfaced NiN-MoO Nanosheets with Optimized H and HO Adsorption for Effective Alkaline Hydrogen Electrocatalysis.

Nickel (Ni)-based materials represent a compelling avenue as platinum alternatives in the realm of alkaline hydrogen electrocatalysis. However, conventional nickel nitrides (NiN) have long been hindered by sluggish hydrogen evolution kinetics in alkaline environments, owing to inadequate adsorption strengths of both hydrogen and water molecules. Herein, a novel approach is presented involving the design of vanadium (V)-doped NiN/MoO heterogeneous nanosheets (V-NiN@MoO), engineered to achieve optimized adsorption strengths for hydrogen evolution and oxidation reactions (HER/HOR).

Taking Advantage of Potential Coincidence Region: Insights into Gas Production Behavior in Advanced Self-Activated Hydrazine-Assisted Alkaline Seawater Electrolysis.

Water electrolysis assisted by hydrazine has emerged as a prospective energy conversion method for achieving efficient hydrogen generation. Due to the potential coincidence region (PCR) between the hydrogen evolution reaction (HER) and the electro-oxidation of hydrazine, the hydrazine oxidation reaction (HzOR) offers distinct advantages in terms of strategy amalgamation, device architecture, and the broadening of application horizons. Herein, we report a bifunctional electrocatalyst of interfacial heterogeneous FeP/CoP microspheres supported on Ni foam (FeCoP/NF).

Changes in α-Dicarbonyl Compound Contents during Storage of Various Fruits and Juices.

α-Dicarbonyl compounds (α-DCs) are commonly present in various foods. We conducted the investigation into concentration changes of α-DCs including 3-deoxyglucosone (3-DG), glyoxal (GO), and methylglyoxal (MGO) in fresh fruits and decapped commercial juices during storage at room temperature and 4 °C, as well as in homemade juices during storage at 4 °C. The studies indicate the presence of α-DCs in all samples.

Artificial Heterointerfaces with Regulated Charge Distribution of Ni Active Sites for Urea Oxidation Reaction.

In contrast to the thermodynamically unfavorable anodic oxygen evolution reaction, the electrocatalytic urea oxidation reaction (UOR) presents a more favorable thermodynamic potential. However, the practical application of UOR has been hindered by sluggish kinetics. In this study, hierarchical porous nanosheet arrays featuring abundant Ni-WO heterointerfaces on nickel foam (Ni-WO/NF) is introduced as a monolith electrode, demonstrating exceptional activity and stability toward UOR.

Enabling Internal Electric Field in Heterogeneous Nanosheets to Significantly Accelerate Alkaline Hydrogen Electrocatalysis.

Efficient bifunctional hydrogen electrocatalysis, encompassing both hydrogen evolution reaction (HER) and hydrogen oxidation reaction (HOR), is of paramount significance in advancing hydrogen-based societies. While non-precious-metal-based catalysts, particularly those based on nickel (Ni), are essential for alkaline HER/HOR, their intrinsic catalytic activity often falls short of expectations. Herein, an internal electric field (IEF) strategy is introduced for the engineering of heterogeneous nickel-vanadium oxide nanosheet arrays grown on porous nickel foam (Ni-VO/PNF) as bifunctional electrocatalysts for hydrogen electrocatalysis.

Heteroatom-Induced Accelerated Kinetics on Nickel Selenide for Highly Efficient Hydrazine-Assisted Water Splitting and Zn-Hydrazine Battery.

Hydrazine-assisted water electrolysis is a promising energy conversion technology for highly efficient hydrogen production. Rational design of bifunctional electrocatalysts, which can simultaneously accelerate hydrogen evolution reaction (HER)/hydrazine oxidation reaction (HzOR) kinetics, is the key step. Herein, we demonstrate the development of ultrathin P/Fe co-doped NiSe nanosheets supported on modified Ni foam (P/Fe-NiSe) synthesized through a facile electrodeposition process and subsequent heat treatment.

Taking Advantage of Potential Coincidence Region: Advanced Self-Activated/Propelled Hydrazine-Assisted Alkaline Seawater Electrolysis and Zn-Hydrazine Battery.

Hydrazine-assisted water electrolysis presents a promising energy conversion technology for highly efficient hydrogen production. Owing to the potential coincidence region between hydrogen evolution reaction (HER) and hydrazine electro-oxidation, hydrazine oxidation reaction (HzOR) exhibits specific advantages on strategy combination, device construction, and application expansion. Herein, we report a bifunctional electrocatalyst of porous Ni foam-supported interfacial heterogeneous NiP/CoP microspheres (denoted NiCoP/NF), which takes full advantage of this potential coincidence region.

Rational Synthesis of Core-Shell-Structured Nickel Sulfide-Based Nanostructures for Efficient Seawater Electrolysis.

Versatile electrocatalysis at higher current densities for natural seawater splitting to produce hydrogen demands active and robust catalysts to overcome the severe chloride corrosion, competing chlorine evolution, and catalyst poisoning. Hereto, the core-shell-structured heterostructures composed of amorphous NiFe hydroxide layer capped Ni S nanopyramids which are directly grown on nickel foam skeleton (NiS@LDH/NF) are rationally prepared to regulate cooperatively electronic structure and mass transport for boosting oxygen evolution reaction (OER) performance at larger current densities. The prepared NiS@LDH/NF delivers the anodic current density of 1000 mA cm at the overpotential of 341 mV in 1.

Interface Metal Oxides Regulating Electronic State around Nickel Species for Efficient Alkaline Hydrogen Electrocatalysis.

Heterogeneous electrocatalysis typically depends on the surface electronic states of active sites. Modulating the surface charge state of an electrocatalysts can be employed to improve performance. Among all the investigated materials, nickel (Ni)-based catalysts are the only non-noble-metal-based alternatives for both hydrogen oxidation and evolution reactions (HOR and HER) in alkaline electrolyte, while their activities should be further improved because of the unfavorable hydrogen adsorption behavior.

Defect-rich cobalt pyrophosphate hybrids decorated CdZnS for efficient photocatalytic hydrogen evolution: Defect and interface engineering.

Photocatalysts with highly efficient charge separation are of critical significance for improving photocatalytic hydrogen production performance. Herein, a cost-effective and high-performance composite photocatalyst, cobalt-phosphonate-derived defect-rich cobalt pyrophosphate hybrids (CoPPi-M) modified CdZnS is rationally devised via defect and interface engineering, in which the co-catalyst CoPPi-M delivers a strong interaction with host photocatalyst CdZnS, rendering CdZnS/CoPPi-M with a remarkably improved efficiency of charge separation and migration. Besides, CdZnS/CoPPi-M exhibits a hydrophilic surface with ample access to electrons and a strong reduction ability of electrons.

Spatially isolated cobalt oxide sites derived from MOFs for direct propane dehydrogenation.

The "active site isolation" strategy has been proved to be efficient for enhancing the catalytic performance in propane dehydrogenation (PDH). Herein, spatially isolated cobalt oxide sites within nitrogen-doped carbon (NC) layers supported on silicalite-1 zeolite (CoO@NC/S-1) were synthesized by a two-step process consisting of the pyrolysis of bimetallic Zn/Co zeolitic imidazole frameworks loaded on silicalite-1 (ZnCo-ZIF/S-1) under N and the subsequent calcination in air atmosphere. This catalyst possesses exceptional catalytic performance for PDH with the propane conversion of 40% and the propene selectivity of >97%, and no apparent deactivation is observed after 10 h PDH reaction at 600 °C.

Aqueous Rechargeable Zn-N Battery Assembled by Bifunctional Cobalt Phosphate Nanocrystals-Loaded Carbon Nanosheets for Simultaneous NH Production and Power Generation.

Developing cost-effective and controllable technologies beyond traditional overall N electrocatalysis is critical for the large-scale production of NH through electrochemical N reduction reaction (NRR) under ambient conditions. Herein, the aqueous rechargeable Zn-N battery, assembled by coupling the bifunctional cobalt phosphate nanocrystals-loaded heteroatoms-doped carbon nanosheets (CoPi/NPCS) as cathode electrocatalyst and the commercial Zn plate as anode with KOH electrolyte, was fabricated for the sustainable reduction of N to NH and power generation during discharge process. Benefiting from the desirable active components of cobalt phosphate nanocrystals and the synergistic effect between nanocrystals and carbon substrates, the CoPi/NPCS catalyst exhibits the enhanced NRR and oxygen evolution reaction (OER) performance in alkaline electrolyte.

Mesoporous CdZnS with abundant surface defects for efficient photocatalytic hydrogen production.

The practical application of photocatalytic water splitting for hydrogen evolution hinges on the development of high-efficient and low-cost photocatalysts. Defects engineering has emerged as a promising strategy to enhance photocatalytic activity effectively. Herein, a facile and versatile co-precipitation method is proposed to fabricate mesoporous Cd-Zn-S solid solutions (E-CdZnS) with abundant surface defects by the inorganic salts formed in the reaction system as self-template.

Transition Metal Phosphide-Based Materials for Efficient Electrochemical Hydrogen Evolution: A Critical Review.

As hydrogen has been increasingly considered as promising sustainable energy supply, electrochemical overall water splitting driven by highly efficient non-noble metal electrocatalysts has aroused extensive attention. Transition metal phosphides (TMPs) have demonstrated remarkable electrocatalytic performance, including high activity and robust durability towards hydrogen evolution reaction (HER) in acidic and alkaline as well as neutral electrolytes. In this Review, up-to-date progress of TMP-based HER electrocatalysts is summarized.

Iron-Salt Thermally Emitted Strategy to Prepare Graphene-like Carbon Nanosheets with Trapped Fe Species for an Efficient Electrocatalytic Oxygen Reduction Reaction in the All-pH Range.

Earth-abundant, highly active, and durable electrocatalysts toward oxygen reduction reaction (ORR) in the all-pH range are highly required for practical application of electrochemical energy conversion technologies. Here, non-noble-metal graphene-like carbon nanosheets with trapped Fe species (Fe-N/GPC) are developed by an iron-salt thermally emitted strategy, which integrates the modulation of the electronic structure for boosted intrinsic activity with the engineering of hierarchical porosity for enriched active sites. The ORR electrocatalytic performance of Fe-N/GPC-800 achieves the half-wave potentials of 0.

Engineering the Core-Shell-Structured NCNTs-NiSi@Porous Si Composite with Robust Ni-Si Interfacial Bonding for High-Performance Li-Ion Batteries.

A new strategy has been innovatively proposed for wrapping the Ni-incorporated and N-doped carbon nanotube arrays (Ni-NCNTs) on porous Si with robust Ni-Si interfacial bonding to form the core-shell-structured NCNTs-NiSi@Si. The hierarchical porous silicon core was first fabricated via a novel self-templating synthesis route based on two crucial strategies: in situ thermal evaporation of crystal water from the perlite for producing porous SiO and subsequent magnesiothermic reduction of porous SiO into porous Si. Ni-NCNTs were subsequently constructed based on the Ni-catalyzed tip-growth mechanism and were further engineered to fully wrap the porous Si microparticles by forming the NiSi alloy at the heterojunction interface.

Well-Defined MoC Nanoparticles Embedded in Porous N-Doped Carbon Matrix for Highly Efficient Electrocatalytic Hydrogen Evolution.

On the design of efficient and affordable electrocatalysts for water reduction half reaction, this paper fabricates molybdenum carbide nanoparticles uniformly loaded in highly porous N-doped carbon matrix derived from polyaniline-molybdate monolith with the use of graphitic carbon nitride (g-CN) as template. The obtained molybdenum carbide-carbon hybrid catalysts (MoC@NCS) exhibit extraordinarily electrochemical hydrogen evolution activity with a small overpotential of 89 and 81 mV to deliver a current density of 10 mA cm in alkaline (1.0 M KOH) and acidic (0.

Uniquely integrated Fe-doped Ni(OH) nanosheets for highly efficient oxygen and hydrogen evolution reactions.

Developing high-efficiency electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is vital for the production of hydrogen on a large scale by electrocatalytic splitting of water. Herein, Fe-doped Ni(OH) nanosheets directly grown on commercial Ni foam (FeNiOH/NF) were fabricated through a facile hydrothermal method in (NH)SO aqueous solution containing iron salts. The integrated architecture with hierarchical pores is beneficial for exposing sufficient catalytically active sites and providing evaluated structural and electrical properties.

[Microwave ablation of the canine prostate: an experimental study].

Objective: To investigate the effect of transrectal ultrasound-guided microwave ablation of canine prostate tissue.

Methods: Guided by transrectal ultrasound, we conducted microwave ablation on each side of the prostate in 12 male dogs, 6 at 40 W/ 120 s (group A) and the other 6 at 40 W/160 s (group B), and observed the changes in the thermal lesions using grayscale ultrasound. After thermal ablation, we measured the volume of the thermal lesions by contrast-enhanced ultrasound (CEUS).

[Effect of vascular endothelial growth factor on bone marrow-derived mesenchymal stem cell proliferation and the signaling mechanism].

Objective: To observe the effect of vascular endothelial growth factor (VEGF) on bone marrow-derived mesenchymal stem cell (MSC) proliferation and explore the signaling mechanism involved.

Methods: MSC culture was performed following the classical whole bone marrow adhering method. The characteristics of MSC were identified by induction of multi-lineage differentiation and flow cytometry for surface marker analysis (CD34, CD45, CD29, and CD90).

[Ultrasound-guided transrectal microwave ablation of the prostate in dogs].

Objective: To investigate the feasibility and safety of ultrasound-guided transrectal microwave ablation in reducing the prostate volume.

Methods: Ultrasound-guided transrectal microwave ablation of both sides of the prostate was conducted on experimental dogs with the output volume of 30W for 120 seconds. The dogs were sacrificed on the very day of the ablation, and the prostate and its surrounding tissues were excised for observation of the thermal lesions and pathological examination.

[The study of follow up of percutaneous microwave ablation for uterine fibroids treatment].

Objective: To study the prognosis of fibroid after ultrasound-guidance percutaneous microwave ablation (PMAUF).

Methods: From Mar. 2007 to Jul.