Effects of Genetic Relatedness of Kin Pairs on Univariate ACE Model Performance.

The current study explored the impact of genetic relatedness differences (ΔH) and sample size on the performance of nonclassical ACE models, with a focus on same-sex and opposite-sex twin groups. The ACE model is a statistical model that posits that additive genetic factors (A), common environmental factors (C), and specific (or nonshared) environmental factors plus measurement error (E) account for individual differences in a phenotype. By extending Visscher's (2004) least squares paradigm and conducting simulations, we illustrated how genetic relatedness of same-sex twins (HSS) influences the statistical power of additive genetic estimates (A), AIC-based model performance, and the frequency of negative estimates. We found that larger HSS and increased sample sizes were positively associated with increased power to detect additive genetic components and improved model performance, and reduction of negative estimates. We also found that the common solution of fixing the common environment correlation for sex-limited effects to .95 caused slightly worse model performance under most circumstances. Further, negative estimates were shown to be possible and were not always indicative of a failed model, but rather, they sometimes pointed to low power or model misspecification. Researchers using kin pairs with ΔH less than .5 should carefully consider performance implications and conduct comprehensive power analyses. Our findings provide valuable insights and practical guidelines for those working with nontwin kin pairs or situations where zygosity is unavailable, as well as areas for future research.

Molecularly Confined Topochemical Transformation of MXene Enables Ultrathin Amorphous Metal-Oxide Nanosheets.

Two-dimensional (2D) amorphous nanosheets with ultrathin thicknesses have properties that differ from their crystalline counterparts. However, conventional methods for growing 2D materials often produce either crystalline flakes or amorphous nanosheets with an uncontrollable thickness. Here, we report that ultrathin amorphous metal-oxide nanosheets featuring superior flatness can be realized through the molecularly confined topochemical transformation of MXene. Using MXene Ti2CTx as an example, we show that surface modification of Ti2CTx nanosheets with molecular ligands, such as oleylamine (OAm) and oleic acid (OA), not only imparts notable colloidal dispersity to Ti2CTx nanosheets in nonpolar organic solvents but also confines their subsequent oxidation to in-plane configurations. We demonstrate that unlike the drastic oxidation conventionally observed for pristine MXene, hydrophobizing MXene with OAm and OA ligands enables individual Ti2CTx nanosheets to undergo independent oxidation in a nondestructive manner, resulting in amorphous titanium oxide (am-TiO2) nanosheets that faithfully retain the dimension and flatness of pristine MXene. These am-TiO2 nanosheets exhibit exceptional activity as substrates for surface-enhanced Raman scattering. Importantly, this molecular confinement strategy can be extended to other MXene materials, providing a versatile approach for synthesizing ultrathin amorphous metal-oxide nanosheets with tailored compositions and functionalities.

A universal, green, and self-reliant electrolytic approach to high-entropy layered (oxy)hydroxide nanosheets for efficient electrocatalytic water oxidation.

The development and exploration of high-entropy materials with tunable chemical compositions and unique structural characteristics, although challenging, have attracted increasingly greater attention over the past few years. Here, we report a universal and green method to prepare high-entropy layered (oxy)hydroxide (HE-LH) nanosheets under ambient conditions. This method is based on a self-reliant electrochemical process, utilizing only low-cost metal foils and electrolytes as reactant, with no need of involving extra alkali salts and/or organic reagents. Importantly, the composition of HE-LH nanosheets is widely tunable by simply adjusting the combination of metal foils. As a representative example, quinary layered (oxy)hydroxide (CoFeNiCrV-LH) nanosheets are rationally designed, which exhibit superior electrocatalytic activity and long-term durability towards the electrocatalytic oxygen evolution reaction, outperforming both CoFe layered double hydroxides and most previously reported transition-metal-based electrocatalysts. Comprehensive characterization and analysis reveal that the high-entropy effects play a significant role in forming the defect-rich, low-crystalline microstructures, along with large specific surface areas and optimized electronic configurations, thus enabling the boosted electrocatalytic performance. This electrochemical synthetic approach is generally applicable to the scalable synthesis of diverse HE-LH materials towards versatile promising applications.

Mismatched ligand density enables ordered assembly of mixed-dimensional, cross-species materials.

The ordered coassembly of mixed-dimensional species-such as zero-dimensional (0D) nanocrystals and 2D microscale nanosheets-is commonly deemed impracticable, as phase separation almost invariably occurs. Here, by manipulating the ligand grafting density, we achieve ordered coassembly of 0D nanocrystals and 2D nanosheets under standard solvent evaporation conditions, resulting in macroscopic, freestanding hybrid-dimensional superlattices with both out-of-plane and in-plane order. The key to suppressing the notorious phase separation lies in hydrophobizing nanosheets with molecular ligands identical to those of nanocrystals but having substantially lower grafting density. The mismatched ligand density endows the two mixed-dimensional components with a molecular recognition-like capability, driving the spontaneous organization of densely capped nanocrystals at the interlayers of sparsely grafted nanosheets. Theoretical calculations reveal that the intercalation of nanocrystals can substantially reduce the short-range repulsions of ligand-grafted nanosheets and is therefore energetically favorable, while subsequent ligand-ligand van der Waals attractions induce the in-plane order and kinetically stabilize the laminate superlattice structure.