An in situ coupling approach is developed to create a new highly efficient and durable cobalt-based electrocatalyst for the oxygen evolution reaction (OER). Using a novel cyclotetramerization, a task-specific bimetallic phthalocyanine-based nanoporous organic framework is successfully built as a precursor for the carbonization synthesis of a nonprecious OER electrocatalyst. The resultant material exhibits an excellent OER activity with a low overpotential of 280 mV at a current density of 10 mA cm and high durability in an alkaline medium. This impressive result ranks among the best from known Co-based OER catalysts under the same conditions. The simultaneous installation of multiple diverse cobalt-based active sites, including FeCo alloys and Co N nanoparticles, plays a critical role in achieving this promising OER performance. This innovative approach not only enables high-performance OER activity to be achieved but simultaneously provides a means to control the surface features, thereby tuning the catalytic property of the material.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.201704091 | DOI Listing |
J Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering, Central South University, Changsha 410083, Hunan, China. Electronic address:
Heterointerface engineering is an effective strategy to design and construct high-performance photocatalysts. Herein, polyaniline (PANI) nanoparticles and ZnTi layered double hydroxide (ZnTi-LDH) nanosheets were integrated to form organic-inorganic heterostructure (PANI/LDH) via d-π electronic coupling using in-situ polymerization for photocatalytic oxidation/reduction towards tetracycline (TC) and Cr(VI). The photocatalytic activity was closely related to feed amount of aniline (Ani) in the polymerization process, which the abundant PANI nanoparticles were evenly distributed on the surface of ZnTi-LDH nanosheets at the proper Ani feed amount, and thus reinforced d-π electronic coupling at the organic-inorganic interfaces more efficiently.
View Article and Find Full Text PDFChem Asian J
January 2025
University of Queensland, School of Chemical Engineering, AUSTRALIA.
The activation mechanism of Li-rich cathode has been discussed for many years, yet there is still debate on different theories. Potassium doping can assist the investigation on activation mechanism through its unique function in terms of blocking TM migration during activation. K-doping works by occupying Li sites even after Li has been extracted, increasing stability by blocking transition metals from migrating into these sites, which can help us distinguish the pathway of activation.
View Article and Find Full Text PDFChemSusChem
January 2025
Dalian University of Technology, State Key Laboratory of Fine Chemicals, 2 Ligong Rd., 116024, Dalian, CHINA.
Understanding the impact of surface copper valence states on the distribution of electrochemical carbon dioxide products is critical. Herein, CuO@Cu2O with a Cu2+/Cu+ interface was fabricated using wet chemical etching approach. The hollow shape offered a large region for gas adsorption, while the interfacial mixed chemical state of Cu2+/Cu+ with tunable control ratio raised the local density of CHO* and accelerated the carbon-carbon coupling reaction.
View Article and Find Full Text PDFDoping strategies have been recognized as effective approaches for developing cost-effective and durable catalysts with enhanced reactivity and selectivity in the electrochemical synthesis of value-added compounds directly from CO. However, the reaction mechanism and the specific roles of heteroatom doping, such as N doping, in advancing the CO reduction reaction are still controversial due to the lack of precise control of catalyst surface microenvironments. In this study, we investigated the effects of N doping on the performances for electrochemically converting CO to CO over Ni@NCNT/graphene hybrid structured catalysts (Ni@NCNT/Gr).
View Article and Find Full Text PDFChemistry
January 2025
University of Victoria, Chemistry, 3800 Finnerty Rd, V8P 5C2, Victoria, CANADA.
We report the synthesis, characterization, and catalytic applications of N,N'-diaryl diazabutadiene (DAB) Ni(0) complexes stabilized by alkene ligands. These complexes are soluble and stable in several organic solvents, making them ideal candidates for in situ catalyst formation during high-throughput experimentation (HTE). We used HTE to evaluate these Ni(0) precatalysts in a variety of Suzuki and C-N coupling reactions, and they were found to have equal or better performance than the still-standard Ni(0) source, Ni(COD)2.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!