Highly Efficient Electrocatalytic Upgrade of n-Valeraldehyde to Octane over Au SACs-NiMn2 O4 Spinel Synergetic Composites.

In this work, electrocatalytic upgrade of n-valeraldehyde to octane with higher activity and selectivity is achieved over Au single-atom catalysts (SACs)-NiMn2 O4 spinel synergetic composites. Experiments combined with density functional theory calculation collaboratively demonstrate that Au single-atoms occupy surface Ni2+ vacancies of NiMn2 O4 , which play a dominant role in n-valeraldehyde selective oxidation. A detailed investigation reveals that the initial n-valeraldehyde molecule preferentially adsorbs on the Mn tetrahedral site of NiMn2 O4 spinel synergetic structures, and the subsequent n-valeraldehyde molecule easily adsorbs on the Ni site. Specifically, Au single-atom surficial derivation over spinel lowers the adsorption energy (Eads ) of the initial n-valeraldehyde molecule, which will facilitate its adsorption on the Mn site of Au SACs-NiMn2 O4 . Furthermore, the single-atom Au surficial derivation not only alters the electronic structure of Au SACs-NiMn2 O4 but also lower the Eads of subsequent n-valeraldehyde molecule. Hence, the subsequent n-valeraldehyde molecules prefer adsorption on Au sites rather than Ni sites, and the process of two alkyl radicals originating from Mn-C4 H9 and Au-C4 H9 dimerization into an octane is accordingly accelerated. This work will provide an avenue for the rational design of SACs and supply a vital mechanism for understanding the electrocatalytic upgrade of n-valeraldehyde to octane.

An Adaptive Real-Time Detection Algorithm for Dim and Small Photoelectric GSO Debris.

Geosynchronous orbit (GSO) is the ideal orbit for communication, navigation, meteorology and other satellites, but the space of GSO is limited, and there are still a large number of space debris threatening the safety of spacecraft. Therefore, real-time detection of GSO debris is necessary to avoid collision accidents. Because radar is limited by transmitting power and operating distance, it is difficult to detect GSO debris, so photoelectric detection becomes the mainstream way to detect GSO debris. This paper presents an adaptive real-time detection algorithm for GSO debris in the charge coupled device (CCD) images. The main work is as follows: An image adaptive fast registration algorithm and an enhanced dilation difference algorithm are proposed. Combining with mathematical morphology, threshold segmentation and global nearest neighbor (GNN) multi-target tracking algorithm, the functions of image background suppression, registration, suspected target extraction and multi-target tracking are realized. The processing results of a large number of measured data show that the algorithm can detect dim geostationary earth orbit (GEO) and non-GEO debris in GSO belt stably and efficiently, and the processing speed meets the real-time requirements, with strong adaptive ability, and has high practical application value.

Heterostructured Co/Co3O4 anchored on N-doped carbon nanotubes as a highly efficient electrocatalyst for nitrate reduction to ammonia.

The electrochemical reduction of nitrate (NO3-) to ammonia (NH3) has emerged as an attractive approach for selectively reducing NO3- to highly value-added NH3 and removing NO3- pollutants simultaneously. In this work, a heterostructured Co/Co3O4 electrocatalyst anchored on N-doped carbon nanotubes was prepared and applied for the NO3- reduction towards NH3 under alkaline conditions. The catalyst achieves outstanding performance with up to 67% NH3 faradaic efficiency at -1.2 V vs. Hg/HgO and 8.319 mg h-1 mgcat-1 yield at -1.7 V vs. Hg/HgO. In addition, it also exhibits good long-term stability. 15N isotopic labelling experiments prove that the yielded NH3 is derived from NO3- species. In situ electrochemical Raman spectra revealed that the structure of the as-prepared catalyst showed outstanding stability and identified possible intermediates during the electrocatalytic NO3- reduction reaction (NO3RR).

Trash to treasure: electrocatalytic upcycling of polyethylene terephthalate (PET) microplastic to value-added products by Mn0.1Ni0.9Co2O4-δ RSFs spinel.

Microplastic pollution has emerged as a pressing environmental issue of global concern due to its detrimental effects on the environment and ecology. Restricted to their characters of complex composition, it is a great challenge to propose a more cost-effective approach to achieve highly selective conversion of microplastic into add-value products. Here we demonstrate an upcycling strategy for converting PET microplastics into added-value chemicals (formate, terephthalic acid and K2SO4). PET is initially hydrolyzed in KOH solution to produce terephthalic acid and ethylene glycol, which is subsequently used as an electrolyte to produce formate at the anode. Meanwhile, the cathode undergoes hydrogen evolution reaction to produce H2. Preliminary techno-economic analysis suggests that this strategy has certain economic feasibility and a novel Mn0.1Ni0.9Co2O4-δ rod-shaped fiber (RSFs) catalyst we synthesized can achieve high Faradaic efficiency (> 95%) at 1.42 V vs. RHE with optimistic formate productivity. The high catalytic performance can be attributed to the doping of Mn changing the electronic structure and reducing the metal-oxygen covalency of NiCo2O4, reducing the lattice oxygen oxidation in spinel oxide OER electrocatalysts. This work not only put forward an electrocatalytic strategy for PET microplastic upcycling but also guides the design of electrocatalysts with excellent performance.

Rod-Like Nanostructured Cu-Co Spinel with Rich Oxygen Vacancies for Efficient Electrocatalytic Dechlorination.

Dichloromethane (CH2Cl2) hydrodechlorination to methane (CH4) is a promising approach to remove the halogenated contaminants and generate clean energy. In this work, rod-like nanostructured CuCo2O4 spinels with rich oxygen vacancies are designed for highly efficient electrochemical reduction dechlorination of dichloromethane. Microscopy characterizations revealed that the special rod-like nanostructure and rich oxygen vacancies can efficiently enhance surface area, electronic/ionic transport, and expose more active sites. The experimental tests demonstrated that CuCo2O4-3 with rod-like nanostructures outperformed other morphology of CuCo2O4 spinel nanostructures in catalytic activity and product selectivity. The highest methane production of 148.84 µmol in 4 h with a Faradaic efficiency of 21.61% at -2.94 V (vs SCE) is shown. Furthermore, the density function theory proved oxygen vacancies significantly decreased the energy barrier to promote the catalyst in the reaction and Ov-Cu was the main active site in dichloromethane hydrodechlorination. This work explores a promising way to synthesize the highly efficient electrocatalysts, which may be an effective catalyst for dichloromethane hydrodechlorination to methane.

Facile Tailoring of the Electronic Structure and the d-Band Center of Copper-Doped Cobaltate for Efficient Nitrate Electrochemical Hydrogenation.

Electrocatalytic nitrate reduction is an effective strategy to eliminate nitrate's environmental impact and produce high-value-added ammonia products. However, most of the current reports focus on preparation strategies of catalysts, with poor exploration of the mechanism. In this work, we fabricated a binding-free Cu-doped Co3O4 electrode (Cu-Co3O4) to reveal the structure-activity relationship. Cu-Co3O4 exhibited a maximum Faradaic efficiency of ammonia of up to 86.5% at -0.6 V vs reversible hydrogen electrode in a neutral electrolyte, with the corresponding yield rate of 36.71 mmol h-1 g-1. In situ electrochemical Raman spectroscopy confirmed that the structure of Cu-Co3O4 exhibits excellent stability and durability. Theoretical analysis revealed that the interaction between Cu and Co induces the d-band center position of the mono-metal oxide to shift toward the center to optimize the nitrate reduction intermediate hydrodeoxygenation free-energy change, especially of *NOx (x = 1, 2, and 3). These results offer guidelines for the electrochemical reduction of nitrate with transition metal oxide electrocatalysts.

Soil heavy metal pollution and food safety in China: Effects, sources and removing technology.

Soil plays a fundamental role in food safety and the adverse effects of contaminants like heavy metal (loid)s on crop quality have threatened human health. Therefore, it is important to focus on the food safety and agricultural soil pollution by heavy metals, especially for China where the demand for food production is increasing. This review comprehensively introduced the current status of agricultural soil pollution by heavy metals in China, analyzed the main sources of contaminants, including the applications of pesticides and fertilizers, atmospheric deposition related to vehicle emissions and coal combustion, sewage irrigation and mining. Food safety and agricultural soil pollution by heavy metals, the removal technologies for soil remediation such as soil amendments, phytoremediation and foliar sprays were also introduced. The review can provide significant insights for policymakers, environmental engineers, and agro-technicians regarding soil contamination control and management strategies and technologies.