5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A rechargeable aqueous phenazine-Prussian blue proton battery with long cycle life

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We report a high-performance rechargeable aqueous battery that operates with protons commuting between a fused-ring phenazine derivative anode and a Prussian blue analogue cathode.

          Abstract

          Aqueous proton batteries (APBs) are one of the most attractive technologies for grid-scale storage of renewable energy due to their unique merits of a proton as a charge carrier, such as light weight, small ionic radius, and the ability to bind covalently or ionically to various organic/inorganic moieties. Although various types of electrode materials have been employed in APBs, their full cells still show unsatisfactory performance with limited energy density and cycle durability. Herein, we report a novel high-performance APB that operates in a sulfuric acid electrolyte with protons commuting between a Cu–Fe Prussian blue analogue cathode and a fused-ring phenazine derivative anode. The fabricated APB full cell exhibits an energy density of up to 52 W h kg −1, excellent rate performance, and stable cycle life for 10 000 cycles with a capacity retention of ∼65.2% and a round-trip energy efficiency of 87.1%. The proton storage mechanism is studied by ex situ Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). This work indicates a potential direction to rationally design high-performance APBs.

          Related collections

          Most cited references37

          • Record: found
          • Abstract: found
          • Article: not found

          High-rate electrochemical energy storage through Li+ intercalation pseudocapacitance.

          Pseudocapacitance is commonly associated with surface or near-surface reversible redox reactions, as observed with RuO2·xH2O in an acidic electrolyte. However, we recently demonstrated that a pseudocapacitive mechanism occurs when lithium ions are inserted into mesoporous and nanocrystal films of orthorhombic Nb2O5 (T-Nb2O5; refs 1,2). Here, we quantify the kinetics of charge storage in T-Nb2O5: currents that vary inversely with time, charge-storage capacity that is mostly independent of rate, and redox peaks that exhibit small voltage offsets even at high rates. We also define the structural characteristics necessary for this process, termed intercalation pseudocapacitance, which are a crystalline network that offers two-dimensional transport pathways and little structural change on intercalation. The principal benefit realized from intercalation pseudocapacitance is that high levels of charge storage are achieved within short periods of time because there are no limitations from solid-state diffusion. Thick electrodes (up to 40 μm thick) prepared with T-Nb2O5 offer the promise of exploiting intercalation pseudocapacitance to obtain high-rate charge-storage devices.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Copper hexacyanoferrate battery electrodes with long cycle life and high power.

            Short-term transients, including those related to wind and solar sources, present challenges to the electrical grid. Stationary energy storage systems that can operate for many cycles, at high power, with high round-trip energy efficiency, and at low cost are required. Existing energy storage technologies cannot satisfy these requirements. Here we show that crystalline nanoparticles of copper hexacyanoferrate, which has an ultra-low strain open framework structure, can be operated as a battery electrode in inexpensive aqueous electrolytes. After 40,000 deep discharge cycles at a 17 C rate, 83% of the original capacity of copper hexacyanoferrate is retained. Even at a very high cycling rate of 83 C, two thirds of its maximum discharge capacity is observed. At modest current densities, round-trip energy efficiencies of 99% can be achieved. The low-cost, scalable, room-temperature co-precipitation synthesis and excellent electrode performance of copper hexacyanoferrate make it attractive for large-scale energy storage systems.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Diffusion-free Grotthuss topochemistry for high-rate and long-life proton batteries

                Bookmark

                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                March 28 2023
                2023
                : 11
                : 13
                : 7152-7158
                Affiliations
                [1 ]Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, China
                [2 ]College of Energy Science and Engineering, Nanjing Tech University, Nanjing 211816, China
                [3 ]Jiangsu Key Laboratory of Materials Surface Science and Technology, Changzhou 213164, China
                [4 ]Key Laboratory of Excited-State Materials of Zhejiang Province, Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, China
                Article
                10.1039/D2TA09749D
                b10a7d40-ef0a-4c71-b0f7-2f51468423a8
                © 2023

                http://rsc.li/journals-terms-of-use

                History

                Comments

                Comment on this article