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Abstract Background This study aims to investigate the short-term effects and safety of adjunct Suxiao Jiuxin Pills (SJPs) on conventional therapy in chronic coronary syndrome (CCS) patients who are intolerant to the adverse effects of long-acting nitrates. Methods This was a multicenter, randomized, double-blind, placebo-controlled trial. A total of 174 CCS participants from eight clinical study centers in China were included in the modified intention-to-treat analyses. Participants with CCS and intolerance to the adverse effects of long-acting nitrates were recruited and randomized to either the SJPs or the placebo group for a duration of 4 weeks. Results Compared to the placebo group, the SJPs group showed a significant improvement in the efficacy rate after 4 weeks (OR = 2.43, 95% CI = 1.32 to 4.47, P = 0.004). Besides, individuals without a history of alcohol consumption showed a greater improvement in the SAQ summary score compared to those with a history of alcohol consumption. Conclusion Adjunctive SJPs enhance the effectiveness of short-term conventional anti-angina treatment for patients with CCS who experience intolerance to long-acting nitrates, without significant adverse effects during application. Trial registration Chinese Clinical Trials Registry Platform, ChiCTR2100050066. Registered 16 August 2021, https://www.chictr.org.cn/showproj.html?proj=131470 .

Abstract Electrochemical reduction of CO2 to syngas (CO and H2) offers an efficient way to mitigate carbon emissions and store intermittent renewable energy in chemicals. Herein, the hierarchical one‐dimensional/three‐dimensional nitrogen‐doped porous carbon (1D/3D NPC) is prepared by carbonizing the composite of Zn‐MOF‐74 crystals in situ grown on a commercial melamine sponge (MS), for electrochemical CO2 reduction reaction (CO2RR). The 1D/3D NPC exhibits a high CO/H2 ratio (5.06) and CO yield (31 mmol g−1 h−1) at −0.55 V, which are 13.7 times and 21.4 times those of 1D porous carbon (derived from Zn‐MOF‐74) and N‐doped carbon (carbonized by MS), respectively. This is attributed to the unique spatial environment of 1D/3D NPC, which increases the adsorption capacity of CO2 and promotes electron transfer from the 3D N‐doped carbon framework to 1D carbon, improving the reaction kinetics of CO2RR. Experimental results and charge density difference plots indicate that the active site of CO2RR is the positively charged carbon atom adjacent to graphitic N on 1D carbon and the active site of HER is the pyridinic N on 1D carbon. The presence of pyridinic N and pyrrolic N reduces the number of electron transfer, decreasing the reaction kinetics and the activity of CO2RR. The CO/H2 ratio is related to the distribution of N species and the specific surface area, which are determined by the degree of spatial confinement effect. The CO/H2 ratios can be regulated by adjusting the carbonization temperature to adjust the degree of spatial confinement effect. Given the low cost of feedstock and easy strategy, 1D/3D NPC catalysts have great potential for industrial application.

Abstract Electroreduction of CO2 to valuable multicarbon (C2+) products is a highly attractive way to utilize and divert emitted CO2. However, a major fraction of C2+ selectivity is confined to less than 90% by the difficulty of coupling C-C bonds efficiently. Herein, we identify the stable Cu0/Cu2+ interfaces derived from copper phosphate-based (CuPO) electrocatalysts, which can facilitate C2+ production with a low-energy pathway of OC-CHO coupling verified by in situ spectra studies and theoretical calculations. The CuPO precatalyst shows a high Faradaic efficiency (FE) of 69.7% towards C2H4 in an H-cell, and exhibits a significant FEC2+ of 90.9% under industrially relevant current density (j = −350 mA cm−2) in a flow cell configuration. The stable Cu0/Cu2+ interface breaks new ground for the structural design of electrocatalysts and the construction of synergistic active sites to improve the activity and selectivity of valuable C2+ products.

In this work, we synthesized MoS2 catalyst via one-step hydrothermal method, and systematically investigated the catalytic effect of MoS2 on the hydrogen storage properties of MgH2. The MgH2-5MoS2 composite milled for 5 h starts to release hydrogen at 259 °C. Furthermore, it can desorb 4.0 wt.% hydrogen within 20 min at 280 °C, and absorb 4.5 wt.% hydrogen within 5 min at 200 °C. Mo and MoS2 coexisted in the ball milled sample, whereas only Mo was kept in the sample after dehydrogenation and rehydrogenation, which greatly weakens the Mg-H bonds and facilitates the dissociation of MgH2 on the surface of Mo (110). The comparative study show that the formed MgS has no catalytic effect for MgH2. We believed that the evolution and the catalytic mechanism of MoS2 will provide the theoretical guidance for the application of metal sulfide in hydrogen storage materials.

Abstract Direct seawater electrolysis is promising for sustainable hydrogen gas (H2) production. However, the chloride ions in seawater lead to side reactions and corrosion, which result in a low efficiency and poor stability of the electrocatalyst and hinder the use of seawater electrolysis technology. Here we report a corrosion-resistant RuMoNi electrocatalyst, in which the in situ-formed molybdate ions on its surface repel chloride ions. The electrocatalyst works stably for over 3000 h at a high current density of 500 mA cm−2 in alkaline seawater electrolytes. Using the RuMoNi catalyst in an anion exchange membrane electrolyzer, we report an energy conversion efficiency of 77.9% and a current density of 1000 mA cm−2 at 1.72 V. The calculated price per gallon of gasoline equivalent (GGE) of the H2 produced is $ 0.85, which is lower than the 2026 technical target of $ 2.0/GGE set by the United Stated Department of Energy, thus, suggesting practicability of the technology.

Electroreduction of CO2 into formic acid (HCOOH) is of great economical value and potential for industrialization. However, it is still a substantial challenge due to the lack of efficient catalysts with simultaneously high activity, selectivity, and durability. Herein, a single‐atom bismuth loaded on N‐doped hollow carbon sphere (Bi–SA/NHCS) catalyst is reported and its catalytic activity and selectivity are modulated by changing the coordination structure of Bi center. The obtained Bi–SA/NHCS with a Bi–N3 site exhibits significantly enhanced electrocatalytic activity and selectivity of HCOOH synthesis from CO2 reduction. The HCOOH production rate achieves 16.2 mmol L−1 h−1 cm−2 at a current density of 20 mA cm−2, and its Faradaic efficiency remains 100% during a long‐term reaction. The HCOOH production rate normalized by catalyst loading is at a molar level of nearly 1.5 mol h−1 gcat−1. The production rate and Faradaic efficiency of HCOOH electrosynthesis on Bi–SA/NHCS are significantly boosted as compared with other catalysts reported in the literature. Experimental and density‐functional theory results demonstrate that the boosted activity and selectivity of HCOOH synthesis owe to the electronic structure modulation to the Bi center via threefold coordinated N‐ligands, leading to a proper binding energy of HOCO* intermediates.

Partial oxidation of methane is a promising alternative strategy for methanol production under mild reaction conditions; however, significant challenges hinder the development of appropriate catalysts. In this study, based on first-principles calculations, we demonstrate that a single Fe atom supported on anatase TiO2(001) provides double active sites (Fe and Ti5C) to activate gas-phase O2 and form O-assisted intermediates. The triple state Fe-O/TiO2(001) system exhibited better activity for methane activation (ΔGmax = 1.02 eV). Our findings offer new insights into the design of non-noble-3d transition metal single-atom catalysts on TiO2(001) for partial methane oxidation via an inexpensive O2 oxidant under mild reaction conditions.

Catalysed oxidative C-C bond formation reactions are important in the synthesis of natural products, but poorly tolerated by polyphenolic flavones. Here the authors report the reactivity of molecular oxygen in alkaline water without added catalyst for the synthesis of a collection of flavone dimers and trimers.

Abstract Pure titanium is widely used in clinical implants, but its bioinert properties (poor strength and mediocre effect on bone healing) limit its use under load‐bearing conditions. Modeling on the structure of collagen fibrils and specific nanocrystal plane arrangement of hydroxyapatite in the natural bone, a new type of titanium (Ti) with a highly aligned fibrous‐grained (FG) microstructure is constructed. The improved attributes of FG Ti include high strength (≈950 MPa), outstanding affinity to new bone growth, and tight bone‐implant contact. The bone‐mimicking fibrous grains induce an aligned surface topological structure conducive to forming close contact with osteoblasts and promotes the expression of osteogenic genes. Concurrently, the predominant Ti(0002) crystal plane of FG Ti induces the formation of hydrophilic anatase titanium oxide layers, which accelerate biomineralization. In conclusion, this bioinspired FG Ti not only proves to show mechanical and bone‐regenerative improvements but it also provides a new strategy for the future design of metallic biomaterials.

Article highlights Crawfish-shell biochar (CSB) pyrolyzed at 350°C showed the highest Sb(III) adsorption and oxidation. DFT calculations highlighted complexation, H-bonding and π–π interactions as key removal mechanisms. Sb(III) oxidation was mainly governed by persistent free radicals and electron transfer capacity of biochar.

Water electrolysis is a promising hydrogen production technique but is restricted from large-scale application due to poor performance and high cost. Here, the authors report a mechanically stable monolith electrocatalyst that achieves superior hydrogen evolution at large current densities.

High-resolution neutron radiography provides novel and stirring opportunities to investigate the structures of light elements encased by heavy elements. For this study, a series of Gd2O2S:Tb, F particles were prepared using a high-temperature solid phase method and then used as a scintillation screen. Upon reaching 293 nm excitation, a bright green emission originated from the Tb3+ luminescence center. The level of F doping affected the fluorescence intensity. When the F doping level was 8 mol%, the fluorescence intensity was at its highest. The absolute quantum yield of the synthesized particles reached as high as 77.21%. Gd2O2S:Tb, F particles were applied to the scintillation screen, showing a resolution on the neutron radiograph as high as 12 μm. These results suggest that the highly efficient Gd2O2S:Tb, F particles are promising scintillators for the purposes of cold neutron radiography.

Selective methane conversion to alcohol derivatives remains an open challenge. Here, bimetallic catalyst, AuPd@ZIF-8, has been synthesized and demonstrated as an excellent catalyst in the presence of H2O2 and O2 under mild condition. Specifically, the yield for liquid oxygenated and methanol are 83.0 and 21.7 mmol gAuPd−1 h−1, with selectivity up to 89.5% and 21.9%, respectively. This high productivity may be due to the synergistic effect between AuPd nanoparticles and ZIF-8 framework. Oxygen-based isotopic tests reveal that oxygen serve as oxidants for this oxidation process. Methyl hydroperoxide is the primary product at early stage, which can be further oxidized.

Polyoxyanion compounds are alternative cathodes to conventional oxides, but their reliance on the transition metal redox limits the performance. Here the authors report an oxalate system which possesses additional polyanionic redox reactivity, suggesting a new direction for cathode materials design.

Through computational calculations, CuO(001) has been identified as an active surface for methane oxidation. Experimental validation with CuO nanobelts comprised of predominantly (001) surfaces has been performed and it is confirmed that the performance of such nanobelts is much higher than normal nanoparticles and nanowires. First principle calculations further clarified that two-coordinated oxygen plays a key role for methane adsorption and oxidation.

With the advancement of ultra-fast and high-energy pulsed laser output, lasers have caused serious harm to precision instruments and human eyes. Therefore, the development of optical limiting materials with a fast response, low optical limiting threshold, and high damage threshold are important. In this work, for the first time, it is reported that phosphors Gd2O2S:Tb3+(GOS) displays exceptional functionality in laser protection. GOS with sizes of 11 μm, 1 μm, and 0.45 μm are prepared. Based on the optical limiting and Z-scan technology systems under 532 nm and 1064 nm nanosecond laser excitation, the nonlinear optical properties of GOS are investigated. It is found that GOS exhibits outstanding optical limiting properties. In addition, the optical limiting response of GOS is size-dependent. Concerning the largest particle size, GOS has the best nonlinear optical response, while the precursor shows no nonlinear optical performance. Meanwhile, GOS doped gel glass also displays excellent optical limiting properties with high transmittance, which preliminarily validates the application of GOS and other scintillators in nonlinear optics and encourages more research to better realize the potential of GOS.

CsTaWO6 is a typical AMWO6-type compound and the photocatalysis of the pure and doped phases has been extensively studied experimentally. In this work, the electronic structures of sulphur (S) and nitrogen (N) co-doped CsTaWO6 have been studied in the framework of density functional theory, in particular the S/N co-doping effect has been investigated. It is found that, (i) S/N co-dopants prefer to be separated; (ii) middle-gap states are introduced by N and S-dopant at the edges of valence band and conduction band; and (iii) Co-doping not only narrows the band gap, but also promotes the separation of photo-excited electrons and holes. Feature (iii) has been identified as a key reason why S/N co-doped CsTaWO6 is more efficient in photocatalytic water-splitting. A general doping strategy has been further suggested: co-dopants which can dominate the frontier states and favour to be separated can offer excellent photocatalysis performance.

Herein, we present a systematic study on the preparation of polydopamine (PDA) hollow capsules by templating silica particles which were subsequently removed by a PDA mediated water dissolution process without using any harsh chemical treatment. It was found that the time required for silica removal varied depending on the PDA coating and dissolution conditions. Factors that could influence the core removal process including the PDA thickness and coating temperature, silica calcination duration and the availability of water were then examined in detail. Additionally, catalase was used as a model enzyme to be encapsulated into PDA hollow capsules and its bio-functionality was found to remain active. The bioactivity test results also indicated that the as-synthesized PDA capsules possessed a porous structure, which allows the penetration of small molecules such as H2O2. This study offers a better insight into silica dissolution process that mediated by PDA and contributes to the development of an eco-friendly approach for the fabrication of hollow capsules that have promising applications in drug delivery systems.

Simple but robust growth of spherical BaTiO3 nanoparticles with uniform nanoscale sizes is of great significance for the miniaturization of BaTiO3-based electron devices. This paper reports a TiO2-seeded hydrothermal process to synthesize spherical BaTiO3 nanoparticles with a size range of 90−100 nm using TiO2 (Degussa) and Ba(NO3)2 as the starting materials under an alkaline (NaOH) condition. Under the optimum conditions ([NaOH] = 2.0 mol L−1, RBa/Ti = 2.0, T = 210 °C and t = 8 h), the spherical BaTiO3 nanoparticles obtained exhibit a narrow size range of 91 ± 14 nm, and the corresponding BaTiO3/polymer/Al film is of a high dielectric constant of 59, a high break strength of 102 kV mm−1, and a low dielectric loss of 0.008. The TiO2-seeded hydrothermal growth has been proved to be an efficient process to synthesize spherical BaTiO3 nanoparticles for potential capacitor energy-storage applications.

Biomarkers are important biochemical indicators, which could be used for identification, early diagnosis and monitoring of diseases during the course of treatment. However, biomarker diagnosis has some shortcomings such as requiring a large amount of samples, long test time and high cost, which seriously influences the correctness and timely treatment to patients. Here, a relatively fast and efficient plasmonic hot spot-localized surface imprinting of Ag spheres using biomarker template immobilization and hydrogel copolymerization is described. The technique takes a fine control of the imprinting process at the nanometre scale and provides a biosensor with high sensitivity. Proof of the opinion is established by detection of biomarker using surface-enhanced Raman scattering (SERS) spectroscopy. This work represents a valuable step towards SERS with biomarkers for cost-saving and time-saving diagnostic assay. It is expected that the new surface imprinted hydrogel plasmonic material can drive possibilities in advancing application of biomarkers in plasmonic biosensors.