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Rechargeable aqueous batteries are regarded as promising candidates for large-scale energy storage with the advantages of cost-effectiveness, environmentally friendliness, and innate safety. However, to date, most of the aqueous ion batteries that have been reported are equipped with metal cation charge carriers and encounter either poor sustainability or low reaction activity. Here, we first reported an aqueous imidazolium-ion battery with MMZ-H/H as co-intercalated ions. In detail, we configured an almost neutral electrolyte with a wide electrochemical window of 2.66 V by adding an appropriate amount of alkaline 1-methylimidazole (MMZ) to 0.5 M HSO, and named it 50M-10S electrolyte. Due to the strong binding energy between MMZ and H, MMZ-H as an entire unit can be inserted into or extracted from the HATN-3CN (hexaazatrinaphthalene-2,8,14-tricarbonitrile) electrode. The MMZ-H and H co-insertion increases the capacity by 40% compared to pure H insertion in this proton battery (287.6 mAh g in 50M-10S electrolyte 206.8 mAh g in 0.5 M HSO electrolyte, 0.1 A g). Theoretical calculations illustrated that the insertion of MMZ-H can further activate the unreacted N active sites due to their enhanced nucleophilicity derived from stronger electron-donating ability of ionized nitrogen sites than the protonated one. Moreover, the assembled full batteries also exhibit ultra-high specific capacity (266.6 mAh g, 1 A g) and ultra-slow degradation (capacity retention of 97%, 1 A g, 1000 cycles). This research further enriches the library of inserted ions and will help to understand and enhance proton storage in near-neutral electrolytes and build new battery models.
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http://dx.doi.org/10.1039/d5sc02677f | DOI Listing |
Chem Sci
July 2025
Beijing Institute of Nanoenergy & Nanosystems, Chinese Academy of Sciences Beijing 101400 China
Rechargeable aqueous batteries are regarded as promising candidates for large-scale energy storage with the advantages of cost-effectiveness, environmentally friendliness, and innate safety. However, to date, most of the aqueous ion batteries that have been reported are equipped with metal cation charge carriers and encounter either poor sustainability or low reaction activity. Here, we first reported an aqueous imidazolium-ion battery with MMZ-H/H as co-intercalated ions.
View Article and Find Full Text PDFSci Rep
September 2022
Department of Chemistry, Faculty of Science, University of Birjand, P.O. Box 97175-615, Birjand, Iran.
A novel ecofriendly heterogeneous catalyst containing Schiff base coordinated Cu(II) covalently attached to FeO@SiO nanoparticles through imidazolium linker [FeO@SiO-Im(Br)-SB-Cu (II)] was synthesized and characterized by using various techniques. The catalytic efficiency of this nano-catalyst was tested in water in the synthesis of tetrazole derivatives using two one-pot multicomponent reaction (MCR) models: The synthesis of 1-aryl 1H-tetrazole derivatives from the reaction of aniline, triethyl orthoformate, and sodium azide and the synthesis of 5-aryl 1H-tetrazole derivatives from the reaction of benzaldehyde, hydroxy amine hydrochloride, and sodium azide. The investigation showed that (i) The catalyst is highly efficient in the synthesis of tetrazole derivatives with high yield (97%) in aqueous medium and mild temperatures; (ii) The catalytic effectiveness is due to the synergy between the metallic center and the imidazolium ion and (iii) The reuse advantage of the catalyst without contamination or significant loss (12% of loss range) in the catalytic activity.
View Article and Find Full Text PDFPhys Chem Chem Phys
October 2015
Corporate Research & Development Center, Toshiba Corporation, Kawasaki, 212-8582, Japan.
Imidazolium ion-terminated self-assembled monolayer (SAM)-modified electrodes achieve CO2 conversion while suppressing hydrogen evolution. Immobile imidazolium ion on gold (Au) electrodes reduce CO2 at low overpotential. The distance between electrode and imidazolium ion separated by alkane thiol affects CO2 reduction activity.
View Article and Find Full Text PDFOrg Biomol Chem
June 2003
University Chemical Laboratory, Canterbury, Kent, UK CT2 7NH.
The reaction of imidazole in aqueous solution with toluene-4-sulfonate salts of substituted phenyl N-methylpyridinium-4-carboxylate esters obeys the rate law: k(obs) - k(background) = k2[Im] + k3[Im]2 where [Im] is the imidazole concentration present as free base. The parameters k2 and k3 fit Brønsted type free energy correlations against the pKa of the leaving phenol with betaLg values of -0.65 and -0.
View Article and Find Full Text PDFBiochim Biophys Acta
March 2003
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Japan.
Kinetic analysis of hydrolytic stability of 2',5'- and 3',5'-linked dinucleoside monophosphate (N(2)'pN and N(3)'pN) was successfully performed in aqueous solution at 175-240 degrees C using a new real-time monitoring method for rapid hydrothermal reactions. The half-lives of NpN were in the range 2-8 s at 240 degrees C and apparent activation energy decreases in the order U(2)'pU>A(2)'pA>G(2)'pG>U(3)pU approximately C(3)'pC>A(3)pA. The stability of phosphodiester bond was dependent on the types of base moiety and phosphodiester linkages, but no systematic correlation was found between the structure and stability.
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