Sulfur-Bridged Asymmetric CuNi Bimetallic Atom Sites for CO2 Reduction with High Efficiency.

Double-atom catalysts (DACs) with asymmetric coordination are crucial for enhancing the benefits of electrochemical carbon dioxide reduction and advancing sustainable development, however, the rational design of DACs is still challenging. Herein, this work synthesizes atomically dispersed catalysts with novel sulfur-bridged Cu-S-Ni sites (named Cu-S-Ni/SNC), utilizing biomass wool keratin as precursor. The plentiful disulfide bonds in wool keratin overcome the limitations of traditional gas-phase S ligand etching process and enable the one-step formation of S-bridged sites. X-ray absorption spectroscopy (XAS) confirms the existence of bimetallic sites with N2Cu-S-NiN2 moiety. In H-cell, Cu-S-Ni/SNC shows high CO Faraday efficiency of 98.1% at -0.65 V versus RHE. Benefiting from the charge tuning effect between the metal site and bridged sulfur atoms, a large current density of 550 mA cm-2 can be achieved at -1.00 V in flow cell. Additionally, in situ XAS, attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS), and density functional theory (DFT) calculations show Cu as the main adsorption site is dual-regulated by Ni and S atoms, which enhances CO2 activation and accelerates the formation of *COOH intermediates. This kind of asymmetric bimetallic atom catalysts may open new pathways for precision preparation and performance regulation of atomic materials toward energy applications.

Sulfur Modified Carbon-Based Single-Atom Catalysts for Electrocatalytic Reactions.

Efficient and sustainable energy development is a powerful tool for addressing the energy and environmental crises. Single-atom catalysts (SACs) have received high attention for their extremely high atom utilization efficiency and excellent catalytic activity, and have broad application prospects in energy development and chemical production. M-N4 is an active center model with clear catalytic activity, but its catalytic properties such as catalytic activity, selectivity, and durability need to be further improved. Adjustment of the coordination environment of the central metal by incorporating heteroatoms (e.g., sulfur) is an effective and feasible modification method. This paper describes the precise synthetic methods for introducing sulfur atoms into M-N4 and controlling whether they are directly coordinated with the central metal to form a specific coordination configuration, the application of sulfur-doped carbon-based single-atom catalysts in electrocatalytic reactions such as ORR, CO2RR, HER, OER, and other electrocatalytic reaction are systematically reviewed. Meanwhile, the effect of the tuning of the electronic structure and ligand configuration parameters of the active center due to doped sulfur atoms with the improvement of catalytic performance is introduced by combining different characterization and testing methods. Finally, several opinions on development of sulfur-doped carbon-based SACs are put forward.

An asymmetrically coordinated Zn-Co diatomic site catalyst for efficient hydrogen evolution reactions.

We propose an innovative preparation method, namely, a two-step pyrolysis process, to synthesize Zn-Co bimetallic catalysts with excellent hydrogen evolution performance. In the synthesized Zn1Co1-SNC catalyst, there exists a strong interaction between Zn and Co, along with synergistic effects with S/N atoms, collectively promoting the stability of the catalyst structure. Experimental results demonstrate that the overpotential of this catalyst at 10 mA cm-2 current density is only 49 mV, and it maintains excellent hydrogen evolution performance even after 5000 cycles.

Electronic Metal-Support Interactions between Copper Nanoparticles and Nitrogen-Doped Ti3C2Tx MXene to Boost Peroxidase-like Activity for Detecting Astaxanthin.

Nanozymes with high activity and stability have emerged as a potential alternative to natural enzymes in the past years, but the relationship between the electronic metal-support interactions (EMSI) and catalytic performance in nanozymes still remains unclear. Herein, a copper nanoparticle nanozyme supported on N-doped Ti3C2Tx (Cu NPs@N-Ti3C2Tx) is successfully synthesized and the modulation of EMSI is achieved by introducing N species. The stronger EMSI between Cu NPs and Ti3C2Tx, involving electronic transfer and an interface effect, is revealed by X-ray photoelectron spectroscopy, soft X-ray absorption spectroscopy, and hard X-ray absorption fine spectroscopy at the atomic level. Consequently, Cu NPs@N-Ti3C2Tx nanozyme exhibits remarkable peroxidase-like activity, surpassing its counterpart (Cu NPs, Ti3C2Tx, Cu NPs-Ti3C2Tx), suggesting that EMSI significantly enhances catalytic performance. Benefiting from the excellent performance, the colorimetric platform based on Cu NPs@N-Ti3C2Tx nanozyme for detecting astaxanthin is constructed and shows a wide linear detection range of 0.01-50 µM and a limit of detection of 0.015 µM in the sunscreens. Density functional theory is further conducted to reveal that the excellent performance is ascribed to the stronger EMSI. This work opens an avenue for studying the influence of EMSI toward catalytic performance of nanozyme.

Engineering the Coordination Interface of Isolated Co Atomic Sites Anchored on N-Doped Carbon for Effective Hydrogen Evolution Reaction.

The regulation of the coordination environment of the central metal atom is considered as an alternative way to enhance the performance of single-atom catalysts (SACs). Herein, we design an electrocatalyst with active sites of isolated Co atoms coordinated with four sulfur atoms supported on N-doped carbon frameworks (Co1-S4/NC), confirmed by high-angle annular dark-field scanning transmission electron microscope (HADDF-STEM) and synchrotron-radiation-based X-ray absorption fine structure (XAFS) spectroscopy. The Co1-S4/NC possesses higher hydrogen evolution reaction (HER) catalytic activity than other Co species and exceptional stability, which exhibits a small Tafel slope of 60 mV dec-1 and a low overpotential of 114 mV at 10 mA cm-2 during the HER in 0.5 M H2SO4 solution. Furthermore, through in situ X-ray absorption spectrum tests and density functional theory (DFT) calculations, we reveal the catalytic mechanism of Co1-S4 moieties and find that the increasing number of sulfur atoms in the Co coordination environment leads to a substantial reduction of the theoretical HER overpotential. This work may point a new direction for the synthesis, performance regulation, and practical application of single-metal-atom catalysts.

Hierarchical mesoporous NiCo2O4 hollow nanocubes for supercapacitors.

In the present work, mesoporous NiCo2O4 hollow nanocubes are synthesized using a "coordinating etching & precipitating" (CEP) route. The hollow nanocubes are characterized using SEM, TEM, XRD, XPS and BET methods. The hollow nanocubes have a uniform morphology of 300-500 nm, a high surface area of 134.52 m(2) g(-1) and a mesoporous structure of 2.4-6 nm. These mesoporous NiCo2O4 hollow nanocubes exhibit the specific capacitance of 795.6 F g(-1) at a constant discharge current density of 1 A g(-1). The high specific capacitance and the stability of the NiCo2O4 hollow nanocube electrode are attributed to its large specific surface area and mesoporous structure. The specific capacity retention is 97.5% at a current density of 1 A g(-1) and 96.1% at a current density of 2 A g(-1) over 2000 charge-discharge cycles. The high specific capacitance and excellent cyclic stability indicate that NiCo2O4 hollow nanocubes are excellent supercapacitor electrode materials.

Microwave-assisted and gram-scale synthesis of ultrathin SnO2 nanosheets with enhanced lithium storage properties.

The rational design and fabrication of SnO2-based anode materials could offer a powerful way of effectively alleviating their large volume variation and guaranteeing excellent reaction kinetics for electrochemical lithium storage. Herein, we present an ultrarapid, low-cost, and simple microwave-assisted synthesis of ultrathin SnO2 nanosheets at the gram-scale. The two-dimensional (2D) anisotropic growth depends on microwave dielectric irradiation coupled with surfactant structural direction, and is conducted under low-temperature atmospheric conditions. The ultrathin 2D nanostructure holds a great surface tin atom percentage with high activity, where the electrochemical reaction processes could be facilitated that highly dependent on the surface. Compared with 1D SnO2 nanorods, the ultrathin SnO2 nanosheets exhibit remarkably improved electrochemical lithium storage properties with a high reversible capacity of 757.6 mAh g(-1) at a current density of 200 mA g(-1) up to 40 cycles as well as excellent rate capability and cycling stability. Specifically, the ultrathin 2D nanosheet could significantly reduce ion diffusion paths, thus allowing faster phase transitions, while the sufficient external surface interspace and interior porous configuration could successfully accommodate the huge volume changes. Even more importantly, we develop a promising strategy to produce ultrathin SnO2 nanosheets to tackle their intrinsic problems for commercial applications.