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Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China.

Donor-acceptor-type conjugated polymers are widely used in memristors due to their unique push-pull electron structures and charge transfer mechanisms. However, the inherently inhomogeneous microstructure of polymer films and their low crystallinity produce randomness that destabilizes formed conductive channels, giving polymer-based memristors unstable switching behavior. In this contribution, we prepared a synaptic device based on PM6-MoS QD (molybdenum disulfide quantum dot) nanocomposites.

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The propulsion of photocatalytic hydrogen (H ) production is limited by the rational design and regulation of catalysts with precise structures and excellent activities. In this work, the [MoOS ] unit is introduced into the Cu clusters to form a series of atomically-precise Mo -Cu bimetallic clusters of [Cu (MoOS ) (C H (CH )S) (P(C H -R) ) ] ⋅ xCH CN (R=H, CH , or F), which show high photocatalytic H evolution activities and excellent stability. By electron push-pull effects of the surface ligand, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels of these Mo -Cu clusters can be finely tuned, promoting the resultant visible-light-driven H evolution performance.

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We have prepared and characterized a series of unprecedented group 6-group 11, N-bridged, heterobimetallic [ML(η-N)(μ-η:η-N)Au(NHC)] complexes (M = Mo, W, L = diphosphine) by treatment of -[ML(N)] with a cationic gold(I) complex [Au(NHC)]. The adducts are very labile in solution and in the solid, especially in the case of molybdenum, and decomposition pathways are likely initiated by electron transfers from the zerovalent group 6 atom to gold. Spectroscopic and structural parameters point to the fact that the gold adducts are very similar to Lewis pairs formed out of strong main-group Lewis acids (LA) and low-valent, end-on dinitrogen complexes, with a bent M-N-N-Au motif.

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Coal seam gas (CSG) extraction generates large volumes of coproduced water. Injection of the excess water into deep aquifers is often the most sustainable management option. However, such injection risks undesired sediment-water interactions that mobilize metal(loid)s in the receiving aquifer.

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