Correction: Mesoporous polyvalent Ni-Mn-Co-O composite nanowire arrays towards integrated anodes boosting high-properties lithium storage.

Correction for 'Mesoporous polyvalent Ni-Mn-Co-O composite nanowire arrays towards integrated anodes boosting high-properties lithium storage' by Junxiang Zhou et al., Dalton Trans., 2023, 52, 3526-3536, https://doi.org/10.1039/D3DT00211J.

Mesoporous polyvalent Ni-Mn-Co-O composite nanowire arrays towards integrated anodes boosting high-properties lithium storage.

Ternary transition metal oxides (TMOs) are potentially promising anode materials for lithium storage with high power and energy density. Designing appropriate electrode structures is an effective strategy to sufficiently exhibit the advantages of TMOs for lithium storage. Here, we present the synthetic process and electrochemical properties of carbon-coated mesoporous Ni-Mn-Co-O (NMCO) nanowire arrays (NWAs) grown on Ni foam as an integrated electrode for lithium-ion batteries (LIBs). The electrochemical measurements show that the carbon-coated NMCO integrated electrode exhibits high capacity and cycling properties. In addition, we have also developed an all one-dimensional (1D) structural full cell using an LiMn2O4 nanorod cathode and an NMCO/Ni NWAs@C-550 anode, which exhibits relatively outstanding cycling properties.

Transforming Metal-Organic Frameworks into Porous Liquids via a Covalent Linkage Strategy for CO2 Capture.

Porous liquids (PLs), an emerging kind of liquid materials with permanent porosity, have attracted increasing attention in gas capture. However, directly turning metal-organic frameworks (MOFs) into PLs via a covalent linkage surface engineering strategy has not been reported. Additionally, challenges including reducing the cost and simplifying the preparation process are daunting. Herein, we proposed a general method to transform Universitetet i Oslo (UiO)-66-OH MOFs into PLs by surface engineering with organosilane (OS) and oligomer species via covalent bonding linkage. The oligomer species endow UiO-66-OH with superior fluidity at room temperature. Meanwhile, the resulting PLs showed great potential in both CO2 adsorption and CO2/N2 selective separation. The residual porosity of PLs was verified by diverse characterizations and molecular simulations. Besides, CO2 selective capture sites were determined by grand canonical Monte Carlo (GCMC) simulation. Furthermore, the universality of the covalent linkage surface engineering strategy was confirmed using different classes of oligomer species and another MOF (ZIF-8-bearing amino groups). Notably, this strategy can be extended to construct other PLs by taking advantages of the rich library of oligomer species, thus making PLs promising candidates for further applications in energy and environment-related fields, such as gas capture, separation, and catalysis.

Effect of Pore Size on the Carbon Dioxide Adsorption Behavior of Porous Liquids Based on Hollow Silica.

Porous liquids are an expanding class of material that has huge potential in gas separation and gas adsorption. Pore size has a dramatic influence on the gas adsorption of porous liquids. In this article, we chose hollow silica nanoparticles as cores, 3-(trihydroxysilyl)-1-propanesulfonic acid (SIT) as corona, and inexpensive industrial reagent polyether amine (M2070) as canopy to obtain a new type of porous liquids. Hollow silica nanospheres with different pore sizes were chosen to investigate the influence of porosity size on CO2 adsorption capacity of porous liquids. Their chemical structure, morphology, thermal behavior and possible adsorption mechanism are discussed in detail. It was proved that with similar grafting density, porous liquid that has bigger pore size possesses a better CO2 adsorption capacity (2.182 mmol g-1 under 2.5 MPa at 298 K). More than that, this article demonstrates a more facile and low-cost method to obtain porous liquids with good CO2 adsorption capacity, recyclability, and huge variability.