Oxygen-bridging Fe, Co dual-metal dimers boost reversible oxygen electrocatalysis for rechargeable Zn-air batteries.

Rechargeable zinc-air batteries (ZABs) are regarded as a remarkably promising alternative to current lithium-ion batteries, addressing the requirements for large-scale high-energy storage. Nevertheless, the sluggish kinetics involving oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) hamper the widespread application of ZABs, necessitating the development of high-efficiency and durable bifunctional electrocatalysts. Here, we report oxygen atom-bridged Fe, Co dual-metal dimers (FeOCo-SAD), in which the active site Fe-O-Co-N moiety boosts exceptional reversible activity toward ORR and OER in alkaline electrolytes.

Conductivity-mediated electrochemical reconstruction of CuO for nitrate reduction to ammonia.

The electrocatalytic nitrate reduction reaction (NORR) is an ideal NH synthesis route with ease of operation, high energy efficiency, and low environmental detriment. Electrocatalytic cathodes play a dominant role in the NORR. Herein, we constructed a carbon fiber paper-supported CuO nanoarray catalyst (CP/CuO) by an electrochemical reconstruction method for NO-to-NH conversion.

Cu-optimized long-range interaction between Co nanoparticles and Co single atoms: Improved Fenton-like reaction activity.

The interplay between multi-atom assembly configurations and single atoms (SAs) has been gaining attention in research. However, the effect of long-term range interactions between SAs and multi-atom assemblies on the orbital filling characteristics has yet to be investigated. In this context, we introduced copper (Cu) doping to strengthen the interaction between cobalt (Co) nanoparticles (NPs) and Co SAs by promoting the spontaneous formation of Co-Cu alloy NPs that tends toward aggregation owing to its negative cohesive energy (-0.

Atomically Dispersed FeN P Motif with High Activity and Stability for Oxygen Reduction Reaction Over the Entire pH Range.

The past decade has witnessed the great potential of Fe-based single-atom electrocatalysis in catalyzing oxygen reduction reaction (ORR). However, it remains a grand challenge to substantially improve their intrinsic activity and long-term stability in acidic electrolytes. Herein, we report a facile chemical vapor deposition strategy, by which high-density Fe atoms (3.

The optimized Fenton-like activity of Fe single-atom sites by Fe atomic clusters-mediated electronic configuration modulation.

The performance optimization of isolated atomically dispersed metal active sites is critical but challenging. Here, TiO@Fe species-N-C catalysts with Fe atomic clusters (ACs) and satellite Fe-N active sites were fabricated to initiate peroxymonosulfate (PMS) oxidation reaction. The AC-induced charge redistribution of single atoms (SAs) was verified, thus strengthening the interaction between SAs and PMS.

Metal-Organic Frameworks for Ion Conduction.

Solid-state ionic conductors are compelling alternatives to liquid electrolytes in clean energy-harvesting and -storage technologies. The development of novel ionic conducting materials is one of the most critical challenges for next-generation energy technologies. Several advancements in design strategies, synthetic approaches, conducting properties, and underlying mechanisms for ionic conducting metal-organic frameworks (MOFs) have been made over the past five years; however, despite the recent, considerable expansion of related research fields, there remains a lack of systematic overviews.

Bacterial community changes and antibiotic resistance gene quantification in microbial electrolysis cells during long-term sulfamethoxazole treatment.

In this study, sulfamethoxazole served as the electron donor for microbial electrolysis cells. After 6 months of operation, the removal efficiencies of sulfamethoxazole in three microbial electrolysis cells were 77.60%, 87.

Degradation mechanisms of sulfamethoxazole and its induction of bacterial community changes and antibiotic resistance genes in a microbial fuel cell.

In this study, more than 85.1% of sulfamethoxazole (SMX) could be degraded within 60 h. The strengthening of microbial metabolisms and the sustainment of electrical stimulation contributed to the rapid removal of SMX in microbial fuel cells (MFCs).