Manganese dioxide cathodes are inexpensive and have high theoretical capacity (based on two electrons) of 617 mAh g, making them attractive for low-cost, energy-dense batteries. They are used in non-rechargeable batteries with anodes like zinc. Only ∼10% of the theoretical capacity is currently accessible in rechargeable alkaline systems. Attempts to access the full capacity using additives have been unsuccessful. We report a class of Bi-birnessite (a layered manganese oxide polymorph mixed with bismuth oxide (BiO)) cathodes intercalated with Cu that deliver near-full two-electron capacity reversibly for >6,000 cycles. The key to rechargeability lies in exploiting the redox potentials of Cu to reversibly intercalate into the Bi-birnessite-layered structure during its dissolution and precipitation process for stabilizing and enhancing its charge transfer characteristics. This process holds promise for other applications like catalysis and intercalation of metal ions into layered structures. A large prismatic rechargeable Zn-birnessite cell delivering ∼140 Wh l is shown.
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http://dx.doi.org/10.1038/ncomms14424 | DOI Listing |
Dalton Trans
January 2025
College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi Province, China.
The physical separation of CH from CO on metal-organic frameworks (MOFs) has received a substantial amount of research interest due to its advantages of simplicity, security, and energy efficiency. However, the exploitation of ideal MOF adsorbents for CH/CO separation remains a challenging task due to their similar physical properties and molecular sizes. Herein, we report a unique CH nano-trap constructed using accessible oxygen and nitrogen sites, which exhibits energetic favorability toward CH molecules.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Fudan University, Laboratory of Advanced Materials, Shanghai, 200433, Shanghai, CHINA.
Tellurium (Te), with its rich valence states (-2 to +6), could endow aqueous batteries with potentially high specific capacity. However, achieving complete and stable hypervalent Te0/Te4+ electrochemistry in an aqueous environment poses significant challenges, owing to the sluggish reduction kinetics, the easy dissolution of Te4+ species, and a controversial energy storage mechanism. Herein, for the first time, we demonstrate an amorphous strategy for robust aqueous TeO2/Te electrochemistry.
View Article and Find Full Text PDFInorg Chem
January 2025
School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, China.
The recycling of low-concentration coal-bed methane (CBM) is environmentally beneficial and plays a crucial role in optimizing the energy mix. In this work, we present a strategy involving pore chemical modification to synthesize a series of bimetallic diamond coordination networks, namely CuIn(ina), CuIn(3-ain), and CuIn(3-Fina) (where ina = isonicotinic acid, 3-ain = 3-amino-isonicotinic acid, and 3-Fina = 3-fluoroisonicotinic acid). Among these, the amino-functionalized CuIn(3-ain) exhibits excellent CH adsorption capacity (1.
View Article and Find Full Text PDFMicrobiome
January 2025
Key Laboratory of Environment Remediation and Ecological Health, Ministry of Education, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, China.
Background: The widespread selective pressure of antibiotics in the environment has led to the propagation of antibiotic resistance genes (ARGs). However, the mechanisms by which microbes balance population growth with the enrichment of ARGs remain poorly understood. To address this, we employed microcosm cultivation at different antibiotic (i.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Key Laboratory for High Efficiency Energy Conversion Science and Technology of Henan Province, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, School of Physics and Electronics, Henan University, Kaifeng, 475004, P. R. China.
Multimode luminescent materials exhibit tunable photon emissions under different excitation or stimuli channels, endowing them high encoding capacity and confidentiality for anti-counterfeiting and encryption. Achieving multimode luminescence into a stable single material presents a promising but remains a challenge. Here, the downshifting/upconversion emissions, color-tuning persistent luminescence (PersL), temperature-dependent multi-color emissions, and hydrochromism are integrated into Er ions doped CsNaYbCl nanocrystals (NCs) by leveraging shallow defect levels and directed energy migration.
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