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Halogen redox couples offer distinct merits due to high redox potential and low cost, but they usually suffer from poor reversibility. Here, we report highly reversible [BrCl]/Br and [BrCl]/Cl redox couples via harnessing interhalogen chemistry within nanoporous Ketjenblack (KB) carbon as a host for zinc-based aqueous batteries. The tunable halogen reactions are facilitated by controllable coordinating chemistry of [ZnClBr] in a hydrated deep eutectic solvent electrolyte comprising ZnCl, ZnBr, and choline chloride (CHClNO). In an optimized electrolyte, the KB electrode delivers a high discharge capacity of 535 mAh g or 214 mAh g when the stored [BrCl] is counted at 100 mA g, with an average discharge voltage of ~1.6 V, and a record high energy density of 788 Wh kg or 315 Wh kg, when considering the mass of [BrCl] as well. Benefiting from the interhalogen coordination chemistry and KB pore host, the pouch cell delivers an areal capacity of 2.3 mAh cm at 0.5 mA cm, storing an energy density of ~80 Wh kg based on the mass of both electrodes. This work offers a new strategy to enhance the reversibility of static aqueous halogen batteries for energy storage applications.
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http://dx.doi.org/10.1002/anie.202421905 | DOI Listing |
Langmuir
September 2025
Key Laboratory of Colloid and Interface Chemistry of the Education Ministry of China, Shandong University, Jinan 250100, China.
In this paper, a phosphate buffer (0.10 M, pH 7.5)--hexadecane bicontinuous microemulsion (BME) stabilized by the nonionic surfactant CE was for the first time used as the medium to investigate its effect on the electrochemical behavior of the cobaltocene redox couple ( (III)/ (II)) as electron mediator and the -mediated electroreduction of coenzyme NAD.
View Article and Find Full Text PDFMater Today Bio
October 2025
Yunnan Key Laboratory of Breast Cancer Precision Medicine, Institute of Biomedical Engineering, Kunming Medical University, Kunming, 650500, Yunnan, China.
Achieving precise intratumoral accumulation and coordinated activation remains a major challenge in nanomedicine. Photothermal therapy (PTT) provides spatiotemporal control, yet its efficacy is hindered by heterogeneous distribution of PTT agents and limited synergy with other modalities. Here, we develop a dual-activation nanoplatform (IrO-P) that integrates exogenous photothermal stimulation with endogenous tumor microenvironment (TME)-responsive catalysis for synergistic chemodynamic therapy (CDT) and ferroptosis induction.
View Article and Find Full Text PDFACS Electrochem
September 2025
Liquid Sunlight Alliance, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Reaction rate coefficients for electron-transfer processes at the electrode-electrolyte interface are commonly estimated by using the Butler-Volmer equation, but their values are inaccurate beyond a few tenths of volts of overpotential. The Marcus-Hush-Chidsey (MHC) formalism yields correct asymptotic behavior of the rate coefficients vs applied overpotential but has complex dependencies on the redox system's intrinsic parameters, which can be difficult to model or measure. In this work, we bridge the two kinetics formalisms to estimate the reorganization energy, one of the important parameters for the MHC formalism, and investigate its dependence on other intrinsic parameters such as activation barriers, electronic coupling strength, and the density of states of the electrode surface.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518055, China.
Thermocells (TECs) represent a promising technology for sustainable low-grade waste heat (<100 °C) harvesting, offering distinct advantages such as scalability, structural versatility, and high thermopower. However, their practical applications are still hindered by low energy conversion efficiency and stability issues. In recent studies, electrolyte engineering has been highlighted as a critical strategy to enhance their thermopower by regulating the solvation structure and redox ion concentration gradient, thereby improving conversion efficiency.
View Article and Find Full Text PDFChemistry
September 2025
Kekulé Institute of Organic Chemistry and Biochemistry, University of Bonn, Gerhard-Domagk-Straße 1, 53121, Bonn, Germany.
Iron-based photocatalysis has emerged as a sustainable and versatile platform for facilitating a wide range of chemical transformations, offering an appealing alternative to precious metal photocatalysts. Among the various activation modes, ligand-to-metal charge transfer (LMCT)-driven homolysis of Fe(III)-L(ligand) bonds has garnered considerable attention due to its ability to generate reactive radical species under mild conditions, without requiring the matching of substrates' redox potentials. In this review, we present a comprehensive overview of recent developments in LMCT-driven iron photocatalysis, with a particular focus on both mechanistic insights and synthetic applications published in the last five years.
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