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Catalytic reduction of nitrate over bimetallic catalysts has emerged as a technology for sustainable treatment of nitrate-containing groundwater. However, the structure of bimetallic has been much less investigated for catalyst optimization. Herein, two main types of Pd-Cu bimetallic nanocrystal structures, heterostructure and intermetallic, were prepared and characterized using high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The results show that two individual Pd and Cu nanocrystals with a mixed interface exist in the heterostructure nanocrystals, while Pd and Cu atoms are uniformly distributed across the intermetallic Pd-Cu nanocrystals. The catalytic nitrate reduction experiments were carried out in a semibatch reactor under constant hydrogen flow. The nitrate conversion rate of the heterostructure Pd-Cu nanocrystals supported on α-Al2O3, γ-Al2O3, SBA-15, and XC-72R exhibited 3.82-, 6.76-, 4.28-, 2.44-fold enhancements relative to the intermetallic nanocrystals, and the nitrogen and nitrite were the main products for the heterostructure and intermetallic Pd-Cu nanocrystals, respectively. This indicates that the catalytic nitrate reduction over Pd-Cu catalyst is sensitive to the bimetallic structures of the catalysts, and heterostructure bimetallic nanocrystals exhibit better catalytic performances on both the activity and selectivity, which may provide new insights into the design and optimization of catalysts to improve catalytic activity and selectivity for nitrate reduction in water.

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Precise control over the size, species, and breakthrough of the activity-selectivity trade-off are great challenges for sub-nano non-noble metal catalysts. Here, for the first time, a "multiheteroatom induced SMSI + in situ P activation" strategy that enables high stability and effective construction of sub-2 nm metal sites for optimizing selective hydrogenation performance is developed. It is synthesized the smallest metal phosphide clusters (<2 nm) including from unary to ternary non-noble metal systems, accompanied by unprecedented thermal stability. In the proof-of-concept demonstration, further modulation of size and species results in the creation of a sub-2 nm site platform, directionally achieving single atom (Ni1), Ni1+metal cluster (Ni1+Nin), or novel Ni1+metal phosphide cluster synergistic sites (Ni1+Ni2Pn), respectively. Based on thorough structure and mechanism investigation, it is found the Ni1+Ni2Pn site is motivated to achieve electronic structure self-optimizing through synergistic SMSI and site coupling effect. Therefore, it speeds up the substrate adsorption-desorption kinetics in semihydrogenation of alkyne and achieves superior catalytic activity that is 56 times higher than the Ni1 site under mild conditions. Compared to traditional active sites, this may represent the highly effective integration of atom utilization, thermal stability, and favorable site requirements for chemisorption properties and reactivities of substrates.

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Developing an efficient electrocatalyst that enables the efficient electrochemical conversion from CO2 to CH4 across a wide potential range remains a formidable challenge. Herein, we introduce a precatalyst strategy that realizes the in situ electrochemical reconstruction of ultrafine Cu2O nanodomains, intricately coupled on the CeO2 surface (Cu2O/CeO2), originating from the heterointerface comprised of ultrafine CuO nanodomains on the CeO2 surface (CuO/CeO2). When served as the electrocatalyst for the electrochemical CO2 reduction reaction, Cu2O/CeO2 delivers a selectivity higher than 49 % towards CH4 over a broad potential range from -1.2 V to -1.7 V vs. RHE, maintaining negligible activity decay for 20 h. Notably, the highest selectivity for CH4 reaches an impressive 70 % at -1.5 V vs. RHE. Through the combination of comprehensive analysis including synchrotron X-ray absorption spectroscopy, spherical aberration-corrected high-angle annular dark field scanning transmission electron microscope as well as the density functional theoretical calculation, the efficient production of CH4 is attributed to the coherent interface between Cu2O and CeO2, which could converted from the original CuO and CeO2 interface, ensuring abundant active sites and enhanced intrinsic activity and selectivity towards CH4.

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Photoinduced DNA cross-linking process showed advantages of high spatio-temporal resolution and control. We have designed, synthesized, and characterized several 4,4'-dibromo binaphthalene analogues (1a-f) that can be activated by 350 nm irradiation to induce various DNA damage, including DNA interstrand cross-links (ICL) formation, strand cleavages, and alkaline labile DNA lesions. The degree and types of DNA damage induced by these compounds depend on the leaving groups of the substrates, pH value of the buffer solution, and DNA sequences. The DNA ICL products were produced from the carbocations formed via the oxidation of free radicals photo-generated from 1a-f. Most of these compounds alone exhibited minimum cytotoxicity towards cancer cells while 350 nm irradiation greatly improved their anticancer effects (up to 40-fold enhancement) because of photo-induced cellular DNA damage. This work provides guidance for further design of photo-inducible DNA cross-linking agents as potent photo-activated anticancer prodrugs with good control over toxicity and selectivity.

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The release of wastewaters containing relatively low levels of nitrate (NO3-) results in sufficient contamination to induce harmful algal blooms and to elevate drinking water NO3- concentrations to potentially hazardous levels. In particular, the facile triggering of algal blooms by ultra-low concentrations of NO3- necessitates the development of efficient methods for NO3- destruction. However, promising electrochemical methods suffer from weak mass transport under low reactant concentrations, resulting in long treatment times (on the order of hours) for complete NO3- destruction. In this study, we present flow-through electrofiltration via an electrified membrane incorporating nonprecious metal single-atom catalysts for NO3- reduction activity enhancement and selectivity modification, achieving near-complete removal of ultra-low concentration NO3- (10 mg-N L-1) with a residence time of only a few seconds (10 s). By anchoring Cu single atoms supported on N-doped carbon in a carbon nanotube interwoven framework, we fabricate a free-standing carbonaceous membrane featuring high conductivity, permeability, and flexibility. The membrane achieves over 97% NO3- removal with high N2 selectivity of 86% in a single-pass electrofiltration, which is a significant improvement over flow-by operation (30% NO3- removal with 7% N2 selectivity). This high NO3- reduction performance is attributed to the greater adsorption and transport of nitric oxide under high molecular collision frequency coupled with a balanced supply of atomic hydrogen through H2 dissociation during electrofiltration. Overall, our findings provide a paradigm of applying a flow-through electrified membrane incorporating single-atom catalysts to improve the rate and selectivity of NO3- reduction for efficient water purification.

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Electrochemical nitrogen reduction reaction (eNRR) is promising in place of the Haber-Bosch process for artificial N2 fixation. However, the high activity and selectivity of eNRR are challenging to achieve simultaneously due to the scaling relations. Such "leverage" between activity and selectivity has severely restricted eNRR. To overcome this bottleneck, the complementary design of electronic structures in multicomponent electrocatalysts has been recently pursued, aiming to maximize the advantages of each component and optimize the multistep reactions, which has stood at the cutting edge in this aspect. Here, we present a minireview of the design, performance, and mechanism of multicomponent electrocatalysts with complementary electronic structures. We particularly emphasize the interactions between N2 and elements from d-, p-, and s-blocks, which are essential for understanding how these electrocatalysts are beyond the "leverage" between activity and selectivity.

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1,2-Dichloroethane (1,2-DCE) is a toxic volatile organic compound, which is harmful to the environment and human health. Herein, we develop a single-atom Ru catalyst anchored on the mesoporous schistose γ-Al2O3 (Ru SACs/m-γ-Al2O3) to enhance the catalytic activity and selectivity toward 1,2-DCE degradation. The Ru SACs/m-γ-Al2O3 shows low T50 and T90 (the temperature for 50 and 90% conversion) of 215 and 289 °C, which are lower than those for Ru NPs/m-γ-Al2O3 (291 and 374 °C) and pristine m-γ-Al2O3 (323 and 386 °C). The degradation products are mainly CO2 (>94%) and HCl (>90%) by using the Ru SACs/m-γ-Al2O3 catalyst, and almost no byproducts are detected. Furthermore, Ru SACs/m-γ-Al2O3 also presents excellent anti-chlorine poisoning effect and water resistance during the stability test. This work may shed light on the development of efficient single-atom catalysts for the degradation of industrial pollutants.

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Rational phase engineering of reduction cocatalyst offers a promising route to modulate the photocatalytic activity and selectivity in the conversion of CO2 to chemical feedstocks. However, it remains a great challenge to choose a suitable phase given that high-crystallinity phase is more conducive to the charge transfer and separation, while amorphous phase is more favorable for the adsorption and activation of CO2 molecules. To resolve this dilemma, herein, with Pd as a well-defined model, a surface amorphization strategy has been developed to fabricate crystalline@amorphous semi-core-shell cocatalysts based on the transformation of outer layer atoms of crystalline cocatalysts to disorder phase. According to the theoretical and experimental analysis, in the heterostructured cocatalysts, crystalline core shuttles the photoexcited electrons from light-harvesting semiconductor to amorphous shell due to its strong electronic coupling with both components. Meanwhile, amorphous shell provides efficient active sites for preferential activation and conversion of CO2 and suppression of undesirable proton reduction. Benefiting from the synergistic effects between crystalline core and amorphous shell, the optimized heterophase cocatalyst with suitable thickness of amorphous shell achieves superior CO (22.2 µmol gcat-1 h-1 ) and CH4 (38.1 µmol gcat-1 h-1 ) formation rates with considerable selectivity and high stability in comparison with crystalline and amorphous counterparts.

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Tuning bimetallic effects is a promising strategy to guide catalytic properties. However, the nature of these effects can be difficult to assess and compare due to the convolution with other factors such as the catalyst surface structure and morphology and differences in testing environments. Here, we investigate the impact of atomic-scale bimetallic effects on the electrochemical CO2 reduction performance of Cu-based catalysts by leveraging a systematic approach that unifies protocols for materials synthesis and testing and enables accurate comparisons of intrinsic catalytic activity and selectivity. We used the same physical vapor deposition method to epitaxially grow Cu(100) films decorated with a small amount of noble or base metal atoms and a combination of experimental characterization and first-principles calculations to evaluate their physicochemical and catalytic properties. The results indicate that the metal atoms segregate to under-coordinated Cu sites during physical vapor deposition, suppressing CO reduction to oxygenates and hydrocarbons and promoting competing pathways to CO, formate, and hydrogen. Leveraging these insights, we rationalize bimetallic design principles to improve catalytic selectivity for CO2 reduction to CO, formate, oxygenates, or hydrocarbons. Our study provides one of the most extensive studies on Cu bimetallics for CO2 reduction, establishing a systematic approach that is broadly applicable to research in catalyst discovery.

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Enveloped viruses such as SARS-CoV-2 frequently have a highly infectious nature and are considered effective natural delivery systems exhibiting high efficiency and specificity. Since simultaneously enhancing the activity and selectivity of lipopeptides is a seemingly unsolvable problem for conventional chemistry and pharmaceutical approaches, we present a biomimetic strategy to construct lipopeptide-based mimics of viral architectures and infections to enhance their antimicrobial efficacy while avoiding side effects. Herein, a surface-nanoengineered antimicrobial liposome (SNAL) is developed with the morphological features of enveloped viruses, including a moderate size range, lipid-based membrane structure, and highly lipopeptide-enriched bilayer surface. The SNAL possesses virus-like infection to bacterial cells, which can mediate high-efficiency and high-selectivity bacteria binding, rapidly attack and invade bacteria via plasma membrane fusion pathway, and induce a local "burst" release of lipopeptide to produce irreversible damage of cell membrane. Remarkably, viral mimics are effective against multiple pathogens with low minimum inhibitory concentrations (1.6-6.3 µg mL-1), high bactericidal efficiency of >99% within 2 h, >10-fold enhanced selectivity over free lipopeptide, 99.8% reduction in skin MRSA load after a single treatment, and negligible toxicity. This bioinspired design has significant potential to enhance the therapeutic efficacy of lipopeptides and may create new opportunities for designing next-generation antimicrobials.

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For the electrochemical reduction of CO2, CO is a crucial single-carbon product and a major intermediate to multicarbon products. Direct dimerization of CO is the most charming channel to C2 products, although the corresponding kinetic energy barrier causes a huge gap compared with other alternative pathways. The effective CO migration among multiple catalytic sites is predominant but has not been fully explored during the C-C bond formation and further protonation processes. Herein, the entirely planar global-minimum Ni2B5 monolayer with multikinds of catalytic sites is selected as an appropriate instance, on which CO can effectively migrate among different types of sites with the highest barrier of 0.64 eV. Most importantly, the computed ultralow barrier of direct *CO dimerization (0.17 eV), the limiting potentials for CH2CH2 (-0.13 V), and CH3CH2OH (-0.17 V) reach the optimal value until now, which all happen on the p-p type of dual-CO adsorption configurations after CO migration. Moreover, the hydrogen reduction side reaction is uncompetitive with the CO electrochemical reduction on all possible adsorption sites. This study demonstrates the significance of CO migration and opens a new avenue for CO reduction to high-density multicarbon products on the surface of catalysts possessing multikinds of catalytic sites.

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Single-atom catalysts (SACs) have emerged as one of the most competitive catalysts toward a variety of important electrochemical reactions, thanks to their maximum atom economy, unique electronic and geometric structures. However, the role of SACs supports on the catalytic performance does not receive enough research attentions. Here, we report an efficient route for synthesis of single atom Zn loading on the N-doped carbon nano-onions (ZnN/CNO). ZnN/CNO catalysts show an excellent high selectivity for CO2 electro-reduction to CO with a Faradaic efficiency of CO (FECO) up to 97% at -0.47 V (vs. reversible hydrogen electrode, RHE) and remarkable durability without activity decay. To our knowledge, ZnN/CNO is the best activity for the Zn based catalysts up to now, and superior to single atom Zn loading on the two-dimensional planar and porous structure of graphene substrate, although the graphene with larger surface area. The exact role of such carbon nano-onions (CNO) support is studied systematically by coupling characterizations and electrochemistry with density functional theory (DFT) calculations, which have attributed such good performance to the increased curvature. Such increased curvature modifies the surface charge, which then changes the adsorption energies of key intermediates, and improves the selectivity for CO generation accordingly.

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Antimicrobial peptides (AMPs) are known to attack bacteria selectively over their host cells. Many attempts have been made to use them as a template for designing peptide antibiotics for fighting drug-resistant bacteria. A central concept in this endeavor is "peptide selectivity," which measures the "quality" of peptides. However, the relevance of selectivity measurements has often been obscured by the cell-density dependence of the selectivity. For instance, the selectivity can be overestimated if the cell density is larger for the host cell. Furthermore, recent experimental studies suggest that peptide trapping in target bacteria magnifies the cell-density dependence of peptide activity. Here, we propose a biophysical model for peptide activity and selectivity, which assists with the correct interpretation of selectivity measurements. The resulting model shows how cell density and peptide trapping in cells influence peptide activity and selectivity: while these effects can alter the selectivity by more than an order of magnitude, peptide trapping works in favor of host cells at high host-cell densities. It can be used to correct selectivity overestimates.

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Developing metal-free catalysts for reduction of CO2 into energy-rich products is a popular yet very challenging topic. Using density functional theory calculations, we investigated the electrocatalytic performance of C-doped and line-defect (Ld)-embedded boron nitride nanoribbons (BNNRs) for CO2 reduction reaction (CRR). Because of the presence of bare edge B atoms neighboring to C dopant and C2 dimer as active sites, defective BNNRs exhibit high CRR catalytic activity and selectivity. The Ld-embedded BNNR structures with C2 dimer can not only convert CO2 into CO with very low overpotential of -0.5 V versus reversible hydrogen electrode but also ensure high selectivity in deactivating the hydrogenation channel of the desorbed CO to CH4. The C-doped zigzag and armchair BNNRs bind strongly to the CO intermediate and thus promote the selective conversion of CO2 to CH4, with the lower energy cost on the armchair ribbon than the zigzag one. The presence of edge B atoms and C dopant as dual active sites in BNNRs enables effective couplings between *CH2 and CO intermediates, leading to the formation of C2 products including C2H4 and C2H5OH, with a high selectivity for C2H5OH. Importantly, unwanted hydrogen evolution reaction is suppressed during CRR catalyzed by these BNNR-based configurations. Overall, the present findings highlight a promising new class of low-cost, metal-free electrocatalysts combining high CRR activity and selectivity.

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Polymer electrolyte membrane fuel cells (PEMFCs) are one of the most prominent clean energy technologies designed to achieve hydrogen utilization and solve problems such as low efficiency and high pollution associated with fossil fuel combustion. In order to bring about PEMFC commercialization, especially for automobile applications, developing high-activity and -selectivity catalysts for the oxygen reduction reaction (ORR) is of critical importance. Based on the density functional theory, the catalytic activity of the conductive, two-dimensional metal-organic frameworks TM3(HITP)2 monolayer (where HITP = hexaiminotriphenylene; TM = Ni, Co, Fe, Pd, Rh, Ru, Pt, Ir, and Os) for ORR has been investigated systematically. Furthermore, the classical volcano curves of the ORR activity, as a function of the OH binding, are found where the Ni, Pd, and Pt located at the weak binding side suffer from the sluggish *OOH formation and prefer the inefficient 2e - mechanism, while for other elements belonging to the strong binding side, the reactions are hindered by the poison due to ORR intermediates. Based on the free energy profiles, the corresponding overpotentials µORR exhibit the inverted volcano curve as a function of the atomic number of the 3d/4d/5d TM active center in the same period. Based on the µORR data, ORR activity decreases in the order of Ir > Co ≈ Rh > Ni ≈ Pd > Pt ≈ Fe > Ru > Os. Herein, the Co, Rh, and Ir central atoms exhibit enhanced catalytic activity in combination with the desirable selectivity of the O2 reduction to H2O. This systematic work may open new avenues for the development of high-performance non-PGM catalysts for practical applications of ORR.

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ß-Sheet antimicrobial peptides (AMPs) are well recognized as promising candidates for the treatment of multidrug-resistant bacterial infections. To dissociate antimicrobial activity and hemolytic effect of ß-sheet AMPs, we hypothesize that N-methylation of the intramolecular hydrogen bond(s)-forming amides could improve their specificities for microbial cells over human erythrocytes. We utilized a model ß-sheet antimicrobial peptide, gramicidin S (GS), to study the N-methylation effects on the antimicrobial and hemolytic activities. We synthesized twelve N-methylated GS analogues by replacement of residues at the ß-strand and ß-turn regions with N-methyl amino acids, and tested their antimicrobial and hemolytic activities. Our experiments showed that the HC50 values increased fivefold compared with that of GS, when the internal hydrogen-bonded leucine residue was methylated. Neither hemolytic effect nor antimicrobial activity changed when proline alone was replaced with N-methylalanine in the ß-turn region. However, analogues containing N-methylleucine at ß-strand and N-methylalanine at ß-turn regions exhibited a fourfold increase in selectivity index compared to GS. We also examined the conformation of these N-methylated GS analogues using (1)H NMR and circular dichroism (CD) spectroscopy in aqueous solution, and visualized the backbone structures and residue orientations using molecular dynamics simulations. The results show that N-methylation of the internal hydrogen bond-forming amide affected the conformation, backbone shape, and side chain orientation of GS.

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