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Two-dimensional (2D) bismuthene material was predicted to possess intriguing physical and electrical properties, such as high-temperature quantum-spin Hall effect, topological edge state, high carrier mobility, and tunable band gap. However, epitaxial growth of single-crystalline 2D bismuthene nanoflakes inevitably requires a high vacuum environment, primarily due to the high surface energy constraints of Bi. Herein, we report the growth of 2D single-crystalline hexagonal bismuthene nanoflakes on Cu foil substrate at atmospheric pressure by chemical vapor deposition. Based on first-principles calculations, the structural transformation of Bi on Cu foil can be suppressed by introducing the top h-BN layer, which potentially compensates for the charge transfer from Bi to the Cu (1 1 1) surface. The sandwich structure is identified by cross-sectional SEM and EDS characterization, demonstrating that bismuthene nanoflakes are sandwiched between the h-BN film and Cu foil. Benefiting from the encapsulation of the top h-BN layer, bismuthene nanoflakes also exhibit excellent thermal stability in ambient air even after annealing at 500 °C for 10 min. For further practical application, bismuthene nanoflakes are utilized for electrochemical CO2 reduction reactions (CO2RR). These bismuthene nanoflakes demonstrate remarkable ability in converting CO2 to formic acid with a Faradaic efficiency of 96.3% at ‒1.0 V (vs. RHE) and exhibit great catalytic stability with a Faradaic efficiency of over 90% in 15 h CO2RR tests. The ultrathin 2D feature of as-prepared bismuthene nanoflakes may result in abundant CO2 adsorption sites and stabilize the intermediate *OCHO, finally favoring the formation of HCOOH. We provide an effective strategy to simultaneously synthesize and passivate 2D single-crystalline bismuthene nanoflakes towards CO2RR, which is expected to be applied to other 2D materials with strong metallic growth behavior.

Nanozyme is a collection of nanomaterials with enzyme-like activity but higher environmental tolerance and long-term stability than their natural counterparts. Improving the catalytic activity and expanding the category of nanozymes are prerequisites to complement or even supersede enzymes. However, the development of hydrolytic nanozymes is still challenged by diverse hydrolytic substrates and following complicated mechanisms. Here, two strategies are informed by data to screen and predict catalytic active sites of MOF (metal–organic framework) based hydrolytic nanozymes: (1) to increase the intrinsic activity by finely tuned Lewis acidity of the metal clusters; (2) to improve the density of active sites by shortening the length of ligands. Finally, as-obtained Ce-FMA-MOF-based hydrolytic nanozyme is capable of cleaving phosphate bonds, amide bonds, glycosidic bonds, and even their mixture, biofilms. This work provides a rational methodology to design hydrolytic nanozyme, enriches the diversity of nanozymes, and potentially sheds light on future evolution of enzyme engineering.

Nanozyme is a collection of nanomaterials with enzyme-like activity but exhibits higher environmental tolerance and long-term stability than their natural counterparts. Improving the catalytic activity and expanding the category of nanozymes are prerequisites to complement or even supersede natural enzymes. Specifically, a powerful hydrolytic nanozyme is demanded to degrade the unsustainable substance which natural enzymes hardly achieve. However, the development of hydrolytic nanozymes is still hindered by diverse hydrolytic substrates and following complicated mechanisms. Here, we apply two strategies which are informed by data to screen and predict catalytic active sites of MOF (metal–organic framework) based hydrolytic nanozymes. One is to increase the intrinsic activity by finely tuned Lewis acidity of the metal clusters. The other is to adjust the volume density of the active sites by shortening the length of ligands. Finally, we construct a Ce-FMA-MOF-based hydrolytic nanozyme with robust cleavage ability towards phosphate bonds, amide bonds, glycosidic bonds whose energy ascend in order; and even their mixture, biofilms. This work provides a rational methodology to design hydrolytic nanozyme, enriches the diversity of nanozymes, and potentially sheds a light on the evolution of enzyme engineering in the future.

In the development of lithium-sulfur (Li-S) batteries, various approaches have been adopted to enhance the electronic conductivity of the sulfur cathode and alleviate the shuttle effect of polysulfides; however, the strategies providing efficient solutions are still limited. To further improve the electrochemical performance of Li-S batteries, in this work we propose a new strategy involving the incorporation of a three-dimensional functional spongy framework as polysulfide reservoir layer, with strong absorbability and electrocatalytic activity towards sulfur species. The spongy framework has a hierarchical architecture composed of highly conductive Ni foam/graphene/carbon nanotubes/MnO2 nanoflakes (NGCM). The strongly interconnected Ni foam, graphene, and carbon nanotubes of the NGCM sponge facilitate electron transfer during discharge/charge processes; moreover, the superlyophilic properties of the NGCM sponge ensure good wettability and interface contact with the Li-S electrolyte, and the porous MnO2 nanoflakes provide strong chemisorptive and electrocatalytic effects on polysulfides (as confirmed theoretically and experimentally). The NGCM sponge, serving as a polysulfide reservoir layer attached on a conventional sulfur-mixed carbon nanotubes (S/CNTs) cathode, can provide improved reversible capacity, rate capability (593 mAh·g–1 at 3.0 C), and cycling stability. In addition, the self-discharge rate is greatly reduced, owing to the efficient conservation of polysulfides in the NGCM spongy framework.

Although silver nanoparticles are considered as promising antibacterial agents because of their antibacterial activity, the acute cytotoxicity of Ag+ released from Ag nanoparticles restricts their potential practical applications. Herein, porous Ag@Au nanoplates, which could balance the Ag+ release and the toxicity of Ag naoparticles, were fabricated by stepwise seed-mediated growth and oxidation. Laser irradiation further boosted their antimicrobial activity, and significantly accelerated the curing rate of wound. Comparing with Ag nanoplates, the irradiated porous Ag@Au nanoplates showed the similar antibiotic ability against S. aureus strains and lower cytotoxicity in vitro. When the porous Ag@Au nanoplates were applied to treat S. aureus-infected wound, they had the best curing effect. Thus, these porous Ag@Au nanoplates could act as promising antibacterial agents for wound healing applications.

Considerable efforts have been devoted on the design and fabrication of non-platinum electrocatalysts with high performance and low cost for hydrogen evolution reaction (HER). However, the catalytic activity of existing electrocatalysts usually subjects to the limited amount of exposed active sites. Herein, we propose that self-assembled ultrathin NiCo2S4 nanoflakes grown on nickel foam (NiCo2S4/Ni foam) can serve as excellent electrocatalyst for HER in alkaline solution with high activity and stability. The NiCo2S4/Ni foam electrodes were prepared by the complete sulfidation of networked ultrathin NiCo-layered double hydroxide nanoflakes grown on Ni foam (NiCo-LDH/Ni foam). The advantages of this unique architecture are that the ultrathin and porous NiCo2S4 nanoflakes can provide a huge number of exposed active sites, the highly-conductive Ni foam can promote the transfer of electrons, and the three-dimensional-networked structure can facilitate the diffusion and penetration of electrolyte. Electrochemical measurements reveal that NiCo2S4/Ni foam electrodes exhibit greatly improved performance than NiCo-LDH/Ni foam for HER in alkaline solution with low onset overpotential (17 mV), small Tafel slope (84.5 mV/dec) and excellent long-duration cycling stability (maintaining an onset overpotential of ~20 mV and an overpotential of 155 mV at 50 mA/cm2 after testing for 100,000 s). In addition, the highly-flexible NiCo2S4/Ni foam electrodes show no obvious catalytic degradation after bending for 200 times, confirming the high flexibility and robustness under severe conditions.

Correction for ‘Pitaya-like microspheres derived from Prussian blue analogues as ultralong-life anodes for lithium storage’ by Lianbo Ma et al., J. Mater. Chem. A, 2016, 4, 15041–15048.

We investigated the effects of solvents on the intrinsic propensity of peptide backbone conformations based on molecular dynamics simulations. The results show that compared with pure water, aqueous urea decreases the helix propensity. In comparison, methanol decreases the polyproline II (PPII) propensity. Such a solvent dependence of the intrinsic propensity of the backbone conformation is correlated with the solvent dependence of the hydration of the backbone groups and the formation probability of the local intrapeptide hydrogen bonds. Aqueous urea which has low ability to stabilize the local intrapeptide hydrogen bonds disfavors the helical conformation. Whereas, methanol which has low ability to hydrate the backbone groups disfavors the polyproline II conformation. In addition, the solvent effects can be further modulated by the side chains of the peptides. The solvent effects of the intrinsic propensity of peptide backbone conformations observed in this work suggest that changing the intrinsic propensity of the protein backbone conformations can partly contribute to the solvent-induced protein structure and dynamics variations. These results will be useful in understanding the solvent dependence of the conformational distributions of the unfolded proteins or peptides (or intrinsically disordered proteins) in which the global tertiary interactions are less important than that in the well-folded proteins.