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The complexity of chemical compounds in lithium‐ion batteries (LIBs) results in great difficulties in the extraction of multiple transition metals, which have similar physicochemical characteristics. Here, we propose a novel strategy for selective extraction of nickel, cobalt, and manganese from spent LiNixCoyMn1−x−yO2 (NCM) cathode through the regulation of coordination environment. Depending on adjusting the composition of ligand in transition metal complexes, a tandem leaching and separation system is designed and finally enables nickel, cobalt, and manganese to enrich in the form of NiO, Co3O4, and Mn3O4 with high recovery yields of 99.1 %, 95.1 %, and 95.3 %, respectively. We further confirm that the combination of different transition metals with well‐designed ligands is the key to good selectivity. Through our work, fine‐tuning the coordination environment of metal ions is proved to have great prospects in the battery recycling industry. [ABSTRACT FROM AUTHOR]

Electrosynthesis of hydrogen peroxide (H2O2) in the acidic environment could largely prevent its decomposition to water, but efficient catalysts that constitute entirely earth‐abundant elements are lacking. Here we report the experimental demonstration of narrowing the interlayer gap of metallic cobalt diselenide (CoSe2), which creates high‐performance catalyst to selectively drive two‐electron oxygen reduction toward H2O2 in an acidic electrolyte. The enhancement of the interlayer coupling between CoSe2 atomic layers offers a favorable surface electronic structure that weakens the critical *OOH adsorption, promoting the energetics for H2O2 production. Consequently, on the strongly coupled CoSe2 catalyst, we achieved Faradaic efficiency of 96.7 %, current density of 50.04 milliamperes per square centimeter, and product rate of 30.60 mg cm−2 h−1. Moreover, this catalyst shows no sign of degradation when operating at −63 milliamperes per square centimeter over 100 hours. [ABSTRACT FROM AUTHOR]

Although the Turing structures, or stationary reaction‐diffusion patterns, have received increasing attention in biology and chemistry, making such unusual patterns on inorganic solids is fundamentally challenging. We report a simple cation exchange approach to produce Turing‐type Ag2Se on CoSe2 nanobelts relied on diffusion‐driven instability. The resultant Turing‐type Ag2Se‐CoSe2 material is highly effective to catalyze the oxygen evolution reaction (OER) in alkaline electrolytes with an 84.5 % anodic energy efficiency. Electrochemical measurements show that the intrinsic OER activity correlates linearly with the length of Ag2Se‐CoSe2 interfaces, determining that such Turing‐type interfaces are more active sites for OER. Combing X‐ray absorption and computational simulations, we ascribe the excellent OER performance to the optimized adsorption energies for critical oxygen‐containing intermediates at the unconventional interfaces. [ABSTRACT FROM AUTHOR]

Abstract: Ultrathin nanostructures are attractive for diverse applications owing to their unique properties compared to their bulk materials. Transition‐metal chalcogenides are promising electrocatalysts, yet it remains difficult to make ultrathin structures (sub‐2 nm), and the realization of their chemical doping is even more challenging. Herein we describe a soft‐template mediated colloidal synthesis of Fe‐doped NiSe2 ultrathin nanowires (UNWs) with diameter down to 1.7 nm. The synergistic interplay between oleylamine and 1‐dodecanethiol is crucial to yield these UNWs. The in situ formed amorphous hydroxide layers that is confined to the surface of the ultrathin scaffolds enable efficient oxygen evolution electrocatalysis. The UNWs exhibit a very low overpotential of 268 mV at 10 mA cm−2 in 0.1  m KOH, as well as remarkable long‐term stability, representing one of the most efficient noble‐metal‐free catalysts. [ABSTRACT FROM AUTHOR]