Computational screening of defective BC3-supported single-atom catalysts for electrochemical CO2 reduction.

The electrochemical CO2 reduction reaction (eCO2RR) driven by renewable electricity offers a green and sustainable technology for synthesizing chemicals and managing global carbon balance. However, developing electrocatalysts with high activity and selectivity for producing C1 products (CO, HCOOH, CH3OH, and CH4) remains a daunting task. In this study, we conducted comprehensive first-principles calculations to investigate the eCO2RR mechanism using B-defective BC3-supported transition metal single-atom catalysts (TM@BC3 SACs). Initially, we evaluated the thermodynamic and electrochemical stability of the designed 26 TM@BC3 SACs by calculating the binding energy and dissolution potential of the anchored TM atoms. Subsequently, the selectivity of the eCO2RR and hydrogen evolution reaction (HER) on stable SACs was determined by comparing the free energy change (ΔG) for the first protonation of CO2 with the ΔG of *H formation. The stability and selectivity screening processes enabled us to narrow down the pool of SACs to the 14 promising ones. Finally, volcano plots for the eCO2RR towards different C1 products were established by using the adsorption energy descriptors of key intermediates, and three SACs were predicted to exhibit high activity and selectivity. The limiting potentials (UL) for HCOOH production on Pd@BC3 and Ag@BC3 are -0.11 V and -0.14 V. CH4 is a preferred product on Re@BC3 with UL of -0.22 V. Elaborate electronic structure calculations elucidate that the activity and selectivity originate from the sufficient activation of the C-O bond and the strong orbital hybridization between crucial intermediates and metal atoms. The proposed catalyst screening criteria, constructed volcano plots and predicted SACs may provide a theoretical foundation for the development of computationally guided catalyst designs for electrochemical CO2 conversion to C1 products.

g-C3N4 as ballistic electron transport "Tunnel" in CsPbBr3-based ternary photocatalyst for gas phase CO2 reduction.

Perovskite CsPbBr3 quantum dot shows great potential in artificial photosynthesis, attributed to its outstanding optoelectronic properties. Nevertheless, its photocatalytic activity is hindered by insufficient catalytic active sites and severe charge recombination. In this work, a CsPbBr3@Ag-C3N4 ternary heterojunction photocatalyst is designed and synthesized for high-efficiency CO2 reduction. The CsPbBr3 quantum dots and Ag nanoparticles are chemically anchored on the surface of g-C3N4 sheets, forming an electron transfer tunnel from CsPbBr3 quantum dots to Ag nanoparticles via g-C3N4 sheets. The resulting CsPbBr3@Ag-C3N4 ternary photocatalyst, with spatial separation of photogenerated carriers, achieves a remarkable conversion rate of 19.49 µmol·g-1·h-1 with almost 100 % CO selectivity, a 3.13-fold enhancement in photocatalytic activity as compared to CsPbBr3 quantum dots. Density functional theory calculations reveal the rapid CO2 adsorption/activation and the decreased free energy (0.66 eV) of *COOH formation at the interface of Ag nanoparticles and g-C3N4 in contrast to the g-C3N4, leading to the excellent photocatalytic activity, while the thermodynamically favored CO desorption contributes to the high CO selectivity. This work presents an innovative strategy of constructing perovskite-based photocatalyst by modulating catalyst structure and offers profound insights for efficient CO2 conversion.

Design of Inner Matching Three-Stage High-Power Doherty Power Amplifier Based on GaN HEMT Model.

This paper introduces the structure and characteristics of an internal-matching high-power Doherty power amplifier based on GaN HEMT devices with 0.25 µm process platforms from the Nanjing Electronic Devices Institute. Through parameter extraction and load-pull testing of the model transistor, an EE_HEMT model for the 1.2 mm gate-width GaN HEMT device was established. This model serves as the foundation for designing a high-power three-stage Doherty power amplifier. The amplifier achieved a saturated power gain exceeding 9 dB in continuous wave mode, with a saturated power output of 49.7 dBm. The drain efficiency was greater than 65% at 2.6 GHz. At 9 dB power back-off point, corresponding to an output power of 40.5 dBm, the drain efficiency remained above 55%. The performance of the amplifier remains consistent within the 2.55-2.62 GHz frequency range. The measured power, efficiency, and gain of the designed Doherty power amplifier align closely with the simulation results based on the EE_HEMT model, validating the accuracy of the established model. Furthermore, the in-band matching design reduces the size and weight of the amplifier. The amplifier maintains normal operation even after high and low-temperature testing, demonstrating its reliability. In conjunction with DPD (digital pre-distortion) for the modulated signal test, the amplifier exhibits extremely high linearity (ACLR < -50.93 dBc). This Doherty power amplifier holds potential applications in modern wireless communication scenarios.

Identification of Potential Abnormal Methylation-Modified Genes in Coronary Artery Ectasia.

Background: Coronary artery ectasia (CAE) is an easily recognized abnormality of coronary artery anatomy and morphology. However, its pathogenesis remains unclear. Objectives: This study aimed to identify abnormal methylation-modified genes in patients with CAE, which could provide a research basis for CAE. Methods: Peripheral venous blood samples from patients with CAE were collected for RNA sequencing to identify differentially expressed genes (DEGs), followed by functional enrichment. Then, the DNA methylation profile of CAE was downloaded from GSE87016 (HumanMethylation450 BeadChip data, involving 11 cases and 12 normal controls) to identify differentially methylated genes (DMGs). Finally, after taking interaction genes between DEGs and DMGs, abnormal methylation-modified genes were identified, followed by protein-protein interaction analysis and expression validation using reverse transcriptase polymerase chain reaction. Results: A total of 152 DEGs and 4318 DMGs were obtained from RNA sequencing and the GSE87016 dataset, respectively. After taking interaction genes, 9 down-regulated DEGs due to hypermethylation and 11 up-regulated DEGs due to hypomethylation were identified in CAE. A total of 10 core abnormal methylation-modified genes were identified, including six down-regulated DEGs due to hypermethylation (netrin G1, ADAM metallopeptidase domain 12, immunoglobulin superfamily member 10, sarcoglycan dela, Dickkopf WNT signaling pathway inhibitor 3, and GATA binding protein 6), and four up-regulated DEGs due to hypomethylation (adrenomedullin, ubiquitin specific peptidase 18, lymphocyte antigen 6 family member E, and MX dynamin-like GTPase 1). Some signaling pathways were identified in patients with CAE, including cell adhesion molecule, O-glycan biosynthesis, and the renin-angiotensin system. Conclusions: Abnormal methylation-modified DEGs involved in signaling pathways may be involved in CAE development.

Regulated bacterial interaction networks: A mathematical framework to describe competitive growth under inclusion of metabolite cross-feeding.

When bacterial species with the same resource preferences share the same growth environment, it is commonly believed that direct competition will arise. A large variety of competition and more general 'interaction' models have been formulated, but what is currently lacking are models that link monoculture growth kinetics and community growth under inclusion of emerging biological interactions, such as metabolite cross-feeding. In order to understand and mathematically describe the nature of potential cross-feeding interactions, we design experiments where two bacterial species Pseudomonas putida and Pseudomonas veronii grow in liquid medium either in mono- or as co-culture in a resource-limited environment. We measure population growth under single substrate competition or with double species-specific substrates (substrate 'indifference'), and starting from varying cell ratios of either species. Using experimental data as input, we first consider a mean-field model of resource-based competition, which captures well the empirically observed growth rates for monocultures, but fails to correctly predict growth rates in co-culture mixtures, in particular for skewed starting species ratios. Based on this, we extend the model by cross-feeding interactions where the consumption of substrate by one consumer produces metabolites that in turn are resources for the other consumer, thus leading to positive feedback in the species system. Two different cross-feeding options were considered, which either lead to constant metabolite cross-feeding, or to a regulated form, where metabolite utilization is activated with rates according to either a threshold or a Hill function, dependent on metabolite concentration. Both mathematical proof and experimental data indicate regulated cross-feeding to be the preferred model to constant metabolite utilization, with best co-culture growth predictions in case of high Hill coefficients, close to binary (on/off) activation states. This suggests that species use the appearing metabolite concentrations only when they are becoming high enough; possibly as a consequence of their lower energetic content than the primary substrate. Metabolite sharing was particularly relevant at unbalanced starting cell ratios, causing the minority partner to proliferate more than expected from the competitive substrate because of metabolite release from the majority partner. This effect thus likely quells immediate substrate competition and may be important in natural communities with typical very skewed relative taxa abundances and slower-growing taxa. In conclusion, the regulated bacterial interaction network correctly describes species substrate growth reactions in mixtures with few kinetic parameters that can be obtained from monoculture growth experiments.

Ullmann-Like Covalent Bond Coupling without Participation of Metal Atoms.

Ullmann-like on-surface synthesis is one of the most appropriate approaches for the bottom-up fabrication of covalent organic nanostructures and many successes have been achieved. The Ullmann reaction requires the oxidative addition of a catalyst (a metal atom in most cases): the metal atom will insert into a carbon-halogen bond, forming organometallic intermediates, which are then reductively eliminated and form C-C covalent bonds. As a result, traditional Ullmann coupling involves reactions of multiple steps, making it difficult to control the final product. Moreover, forming the organometallic intermediates will potentially poison the metal surface catalytic reactivity. In the study, we used the 2D hBN, an atomically thin sp2-hybridized sheet with a large band gap, to protect the Rh(111) metal surface. It is an ideal 2D platform to decouple the molecular precursor from the Rh(111) surface while maintaining the reactivity of Rh(111). We realize an Ullmann-like coupling of a planar biphenylene-based molecule, i.e., 1,8-dibromobiphenylene (BPBr2), on an hBN/Rh(111) surface with an ultrahigh selectivity of the biphenylene dimer product, containing 4-, 6-, and 8-membered rings. The reaction mechanism, including electron wave penetration and the template effect of the hBN, is elucidated by combining low-temperature scanning tunneling microscopy and density functional theory calculations. Our findings are expected to play an essential role regarding the high-yield fabrication of functional nanostructures for future information devices.

Screening of transition metal single-atom catalysts supported by a WS2 monolayer for electrocatalytic nitrogen reduction reaction: insights from activity trend and descriptor.

The electrocatalytic nitrogen reduction reaction (NRR), as an alternative green technology to the Haber-Bosch process, can efficiently synthesize ammonia under ambient conditions and has a reduced carbon footprint. Here we systematically investigate the NRR activity and selectivity of transition metal (TM) single-atom catalyst (SAC) anchored WS2 monolayers (TM@WS2) by means of first-principles calculations and microkinetic modeling. The construction of the reaction activity trend and the identification of an activity descriptor, namely *N2H adsorption energy, facilitate the efficient screening and rational design of SACs with high activity. Manipulating the adsorption strength of the pivotal *N2H intermediate is a potential strategy for enhancing NRR activity. Utilizing the limiting potential difference of NRR and the hydrogen evolution reaction (HER) as a selectivity descriptor, we screen three SACs with excellent activity and selectivity toward NRR, i.e., Re@WS2, Os@WS2 and Ir@WS2 with favorable limiting potentials of -0.44 V, -0.38 V and -0.69 V. By using the explicit H9O4+ model, the kinetic barriers of the rate-determining steps (0.47 eV-1.15 eV) of the solvated proton transfer on the screened SACs are found to be moderate, indicative of a kinetically feasible process. Microkinetic modeling shows that the turnover frequencies of N2 reduction to NH3 on Re@WS2, Os@WS2 and Ir@WS2 are 1.52 × 105, 8.21 × 102 and 4.17 × 10-4 per s per site at 400 K, achieving fast reaction rates. The coexistence of empty and occupied 5d orbitals of candidate SACs is beneficial for σ donation and π* backdonation, endowing them with extraordinary N2 adsorption and activation. Moreover, the screened SACs possess good dispersity and thermodynamic stability. Our work provides a promising solution for the efficient screening and rational design of high-performance electrocatalysts toward the NRR.

Recent Developments of Cathode Materials for Thermal Batteries.

Big progress has been made in batteries based on an intercalation mechanism in the last 20 years, but limited capacity in batteries hinders their further increase in energy density. The demand for more energy intensity makes research communities turn to conversion-type batteries. Thermal batteries are a special kind of conversion-type battery, which are thermally activated primary batteries composed mainly of cathode, anode, separator (electrolyte), and heating mass. Such kinds of battery employ an internal pyrotechnic source to make the battery stack reach its operating temperature. Thermal batteries have a long history of research and usage in military fields because of their high specific capacity, high specific energy, high thermal stability, long shelf life, and fast activation. These experiences and knowledge are of vital importance for the development of conversion-type batteries. This review provides a comprehensive account of recent studies on cathode materials. The paper covers the preparation, characterization of various cathode materials, and the performance test of thermal batteries. These advances have significant implications for the development of high-performance, low-cost, and mass production conversion-type batteries in the near future.

BN cluster-doped graphdiyne as visible-light assisted metal-free catalysts for conversion CO2 to hydrocarbon fuels.

Carbon dioxide electrochemical reduction reaction (CO2RR) under ambient conditions provides an intriguing picture for conversion of CO2 to useful fuels and chemicals. Here by means of density functional theory (DFT) computations, the formation configuration and CO2RR catalytic activity of boron nitrogen cluster-doped graphdiyne (BN-doped GDY) were systematically investigated. The band structure and optical adsorption spectra reveal that BN-doped GDY exhibits semiconductor with the band gap of 0.902 eV and shows photothermal effect under visible and even infrared light irradiation. The BN-doped GDY could act as a hot spot to enhance CO2RR. The adsorption configurations of various reaction intermediates indicate that boron atoms are active sites, which can be further confirmed by charge analysis. Based on thermodynamic analysis, the reaction pathways and onset potentials were studied as compared with Cu(111) surface. For the production of CO, the onset potential for BN-doped GDY (-1.06 V) is higher than that for Cu(111) surface. While for the reduction of CO2 to HCOOH, CH4, CH3OH, and C2H4 on BN-doped GDY, the onset potentials are lower than that on Cu(111) surface, which are -0.57 V, -0.62 V, -0.57 V, and -0.82 V, respectively. Moreover, the onset potential of competitive hydrogen evolution reaction on BN-doped GDY is high to -0.82 V, which shows us a good selectivity towards to CO2RR rather than HER. Our results may pave a new avenue for the conversion of CO2 into high-value fuels and chemicals.

Graphdiyne coordinated transition metals as single-atom catalysts for nitrogen fixation.

The reduction of N2 molecules to NH3 is a very challenging task in chemistry. The electrocatalytic nitrogen reduction reaction (NRR) is a promising technology for NH3 synthesis. By using first-principles calculation, a new class of single-atom catalysts (SACs), graphdiyne coordinated single transition metal atoms (TM@GDY, TM = Sc-Zn, Y-Cd, and La-Hg) were designed, and the NRR catalytic character of TM@GDY was systematically investigated. The results demonstrated that some TM@GDY (TM = Ti, V, Fe, Co, Zr, Rh, and Hf) monolayers exhibit better NRR activities than a Ru(0001) stepped surface. There is an obvious linear correlation between the limiting potential and the atomic N adsorption energy, which confirms that the N adsorption energy may be a descriptor for evaluation of the NRR catalytic performance. The V@GDY monolayer possesses the best NRR catalytic character with the lowest limiting potential of -0.67 V and the potential-limiting step (PLS) of *N2→ *NNH for both alternating and distal mechanisms. Our results highlight a new family of efficient and stable TM@GDY catalysts and provide useful guidelines for SAC development and practical applications.

Charge-compensated co-doping of graphdiyne with boron and nitrogen to form metal-free electrocatalysts for the oxygen reduction reaction.

The development of metal-free catalysts for the oxygen reduction reaction (ORR) is critical for rechargeable metal-air batteries and full cells. Various light non-metallic-atom-doped graphdiyne (GDY) materials have been designed based on density functional theory and evaluated as efficient ORR electrocatalysts. Volcano curve correlations between the overpotential and Gibbs adsorption free energies of oxygenated intermediates have been derived for the ORR. Optimized compensated B,N co-doped GDY monolayers exhibit the lowest ORR overpotential of 0.57 V. In compensated B,N co-doped GDY, the B atoms are positioned in the benzene rings, and the N atoms are positioned in the acetylene linkages. Moreover, some B,N co-doped GDYs have two active sites with almost the same catalytic activity: the B atom and the C atom bearing an effective positive charge nearest to the doped N atom. Based on the theoretical analysis, ideal doped GDY monolayers are expected to exhibit comparable catalytic activity to Pt-based catalysts.

Molecule-level graphdiyne coordinated transition metals as a new class of bifunctional electrocatalysts for oxygen reduction and oxygen evolution reactions.

Single-atom catalysts (SACs) are highly desired for maximizing the efficiency of metal atoms and can entail high selectivity and activity. Bifunctional catalysts enable higher performance and lower cost than two single-function catalysts. Supported single-atom bifunctional catalysts are therefore of great economic interest and scientific importance. Density functional theory calculations are used to design SACs, isolated transition metal anchored on graphdiyne (TM@GDY), for oxygen reduction (ORR) and oxygen evolution (OER) reactions in alkaline media. A dual-volcano plot is constructed to thoroughly describe and predict the catalytic activity toward ORR and OER processes on TM@GDY materials. The results demonstrate that GDY could provide a unique platform for synthesizing uniform SACs with high catalytic activity toward ORR and OER. The theoretical evaluations show that Ni@GDY and Pt@GDY catalysts possess comparable electrocatalytic activity for ORR and OER in alkaline media. The study not only provides deep insights into the catalytic activity of TM@GDY, but also guides the design of GDY based SACs.

Graphdiyne doped with sp-hybridized nitrogen atoms at acetylenic sites as potential metal-free electrocatalysts for oxygen reduction reaction.

Exploring metal-free electrocatalysts with high efficiency and lower cost for oxygen reduction reaction (ORR) is necessary to realize the commercialization of fuel cells. In this paper, the ORR mechanisms on nitrogen-doped graphdiyne (GDY) are investigated using the first principles calculations. It is found that the GDY doped with sp-hybridized N at acetylenic sites can activate molecular oxygen (O2). The kinetically most favorable reaction pathway is O2 → OOH → O + H2O → OH → H2O, which is an efficient four-electron ORR process. The first reaction step O2 → OOH is the rate determining step (RDS), and the energy barrier is 0.61 eV. The energy barrier of RDS is smaller than that of pure Pt (0.80 eV). Therefore, these results illustrate that sp-hybridized N-doped GDY is a promising carbon-based metal-free ORR catalyst.

Effect of toxic ligands on O2 binding to heme and their toxicity mechanism.

Heme, as the cofactor and active site of Hb, enables Hb to carry out the necessary function required for O2 management for life, that is, reversible O2 binding for transport. In this paper, the microscopic mechanism of heme-associated poisoning has been elucidated from the perspective of electronic interaction by performing first-principles calculations. The results show that the functional groups (-CHO, -COOH, -NO2, -NH2) and CN exhibit a stronger affinity for heme than O2 and are more likely to occupy the O2 binding site, which results in the loss of the ability of heme to carry O2. Moreover, the addition of functional groups, CO and CN to heme at the side site can cause a pronounced enhancement toward the O2 binding characteristics of heme, which prevents heme from releasing O2 to oxygen-consuming tissues as the blood circulates. The reversible O2 binding function of heme is disrupted by the presence of these toxic ligands in the heme binding pocket, which greatly affects O2 transport in the blood. The inability of tissues to obtain O2 leads to tissue hypoxia, which is the main cause of poisoning. Based on the energy, geometry and electronic properties, the hypoxia mechanism proposed by us coincides well with experiment, and the research has the potential to provide a theoretical reference for the relevant areas of bioscience.

Enhanced degradation of isoproturon in an agricultural soil by a Sphingomonas sp. strain and a microbial consortium.

Isoproturon (IPU) degradation in an agricultural soil inoculated with an isolated IPU-degrader strain (Sphingomonas sp. strain AK1, IS) or a microbial consortium (MC) harboring this strain, with or without carrier material, were investigated in soil microcosm experiments during 46 days. Effect of the carrier material and inoculation size on IPU-degradation efficacy of the inoculants were studied. Mineralization, extractable residues and non-extractable residues of 14C-labeled IPU were analyzed. The low IPU mineralization in untreated soil (7.0%) was enhanced to different extents by inoculation of IS (17.4%-46.0%) or MC (58.9%-67.5%). Concentrations of IPU residues in soils amended with MC (0.002-0.095 µg g dry soil-1) were significantly lower than in soils amended with IS (0.02-0.67 µg g dry soil-1) and approximately 10 times lower than in the uninoculated soil (0.06-0.80 µg g dry soil-1). Less extractable residues and non-extractable residues were detected in soil with higher IPU mineralization. Inoculation size (as indicated by the volume of liquid cultures or by the number of carrier particles) determined the IPU-removal efficacy of IS in soil, but this effect was less pronounced for MC. The low sorption of IPU to soil and the decreasing IPU-mineralizing rates suggested incapability of IS to establish the IPU-mineralizing function in the soil. The thorough removal of IPU and persistent IPU-mineralizing activity of soil inoculated with MC indicated a high persistence of IPU-metabolic trait. Our results showed that microbial consortia might be more efficient than single degrader strains to enhance clean-up of organic chemicals in soil.

Bensulfuron-Methyl Treatment of Soil Affects the Infestation of Whitefly, Aphid, and Tobacco Mosaic Virus on Nicotiana tabacum.

Bensulfuron-methyl (BSM) is widely used in paddy soil for weed control. BSM residue in the soil has been known to inhibit the growth of sensitive crop plants. However, it is unknown whether BSM residue can affect the agrosystem in general. In this study, we have found significant effects of BSM on the infestation of Bemisia tabaci, Myzus persicae, and Tobacco mosaic virus (TMV) in Nicotiana tabacum. The soil was treated with BSM before the pest inoculation. The herbicide-treated tobaccos showed resistance to B. tabaci, but this resistance could not be detected until 15-day post-infestation when smaller number of adults B. tabaci appeared. In M. persicae assay, the longevity of all development stages of insects, and the fecundity of insects were not significantly affected when feeding on BSM-treated plants. In TMV assay, the BSM treatment also reduced virus-induced lesions in early infection time. However, the titer of TMV in BSM treated plants increased greatly over time and was over 40-fold higher than the mock-infected control plants after 20 days. Further studies showed that BSM treatment increased both jasmonic acid (JA) and salicylic acid (SA) levels in tobacco, as well as the expression of target genes in the JA and SA signaling pathways, such as NtWIPK, NtPR1a, and NtPAL. NtPR1a and NtPAL were initially suppressed after virus-inoculation, while NtRDR1 and NtRDR6, which play a key role in fighting virus infection, only showed up- or were down-regulated 20 days post virus-inoculation. Taken together, our results suggested that BSM residue in the soil may affect the metabolism of important phytohormones such as JA and SA in sensitive plants and consequently affect the plant immune response against infections such as whitefly, aphids, and viruses.