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Rechargeable aqueous Zn-ion batteries (ZIBs) have obtained extensive attention owing to their high safety, low-cost, environmental friendliness and high energy density. Nevertheless, developing suitable cathode materials remains challenging due to requirements for appropriate microstructure. We present a porous N-doped carbon nanosheet/MnO2 (NCS/MnO2) derived from bacterial cellulose (BC) by a simple route. BC chunks were soaked in urea solution and then carbonized under Ar flow at 900 °C. N-doped carbon nanosheets were obtained and MnO2 was added by reaction with NaMnO4. Benefiting from both the conductivity and porosity of the NCS support, the NCS/MnO2 composite delivers a high capacity and long cycling stability (114 mA h g−1 at 2 A g−1 after 1800 cycles). The electrode reaction mechanism was further investigated and the MnO2 dissolution/deposition mechanism was confirmed, with a critical role of zinc sulfate hydroxide (ZSH) to assist the deposition of MnO2. [ABSTRACT FROM AUTHOR]

A versatile method based on the matrix assisted pulsed laser evaporation (MAPLE) technique was used for the fabrication of graphene-based electrodes for application in supercapacitors. The simultaneous deposition and chemical transformation of graphene oxide (GO) and GO–NiO nanoparticles was attained by including nitrogen-containing chemically reactive compounds (ammonia, urea and melamine) in aqueous MAPLE targets. Morphological analyses reveal the formation of hundreds of nanometres to tens of micrometres thick porous films on both plastic and metallic flexible substrates. Structural and compositional studies, carried out by transmission electron microscopy, and Raman and X-ray photoelectron spectroscopies, disclose significant deoxidation and nitrogen doping of the GO material. The electrodes reveal remarkable electrochemical performance, showing a maximum volumetric capacitance of 350 F cm−3 (9 mF cm−2 areal capacitance) in aqueous electrolyte. Symmetric supercapacitors fabricated with these electrodes reveal excellent long-term stability at high specific intensities. From the obtained results, it can be asserted that the reactive inverse MAPLE method stands out as a promising technology not only for the adaptable fabrication of flexible graphene-based composite electrodes but also for a wide variety of advanced functional materials for diverse applications. [ABSTRACT FROM AUTHOR]

The Keggin-type polyoxometalate α-SiW12O404− increases the discharge capacity and potential of lithium–oxygen batteries, by facilitating the reduction of O2 to Li2O2, as confirmed by in situ electrochemical pressure measurements and XRD. Compared to organic redox mediators, polyoxometalates have higher chemical and structural stability, which could lead to longer cycling lithium–oxygen batteries. [ABSTRACT FROM AUTHOR]

In pursuit of high capacitance and high energy density storage devices, hybrid materials have quickly garnered well-deserved attention based on their power to merge complementary components and properties. Here, we report the fabrication of all-solid state symmetric supercapacitors (ASSSC) based on a double hybrid approach combining a hybrid electrode (reduced graphene oxide–phoshomolybdate, rGO–PMo12) and a hybrid electrolyte (hydroquinone doped gel-electrolyte). To begin with, a high-performance hybrid electrode based on H3PMo12O40 nanodots anchored onto rGO was prepared (rGO–PMo12). Later, an all-solid state symmetric cell based on these rGO–PMo12 electrodes, and making use of a polymer gel-electrolyte was assembled. This symmetric cell showed a significant improvement in cell performance. Indeed, it allowed for an extended potential window by 0.3 V that led to an energy density of 1.07 mW h cm−3. Finally, we combined these hybrid electrodes with a hybrid electrolyte incorporating an electroactive species. This is the first proof-of-design where a redox-active solid-state gel-electrolyte is applied to rGO–PMo12 hybrid supercapacitors to accomplish a significant enhancement in the capacitance. Strikingly, a further excellent increase in the device performance (energy density of 1.7 mW h cm−3) was realized with the hybrid electrode–hybrid electrolyte combination cell as compared to that of the conventional electrolyte cell. Thus, this unique symmetric device outclasses the high-voltage asymmetric counterparts under the same power and represents a noteworthy advance towards high energy density supercapacitors. [ABSTRACT FROM AUTHOR]

In this work, different electrodes consisting of a layer of nanostructured binderless carbon supported on a stainless steel (SS) mesh have been developed and tested as cathodes for Li–air batteries. Inverse opal (IO) carbons were developed using poly(styrene-co-methacrylic acid) (PS-MAA) spheres of different sizes as templates via a resorcinol–formaldehyde sol–gel process. The resulting electrodes, which were mechanically stable and easy to manipulate, were electrochemically tested at both 25 and 60 °C by galvanostatic cycling in an ionic liquid-based electrolyte (0.3 M LiTFSI in PYR14TFSI). Different ratios of co-monomers used in the preparation of the template polymeric spheres to control their size significantly influenced the resulting surface area, pore volume and pore distribution in IO carbons of different macropore size. From the electrochemical characterisation, transverse trends in reversibility and rate capability were identified depending on the macropore size of the inverse opal carbon. Smaller pores favor a better charge–discharge reversibility. Large pores contribute to an improved rate capability and large capacity, which are likely due, respectively, to deeper oxygen diffusion into the electrode, and to larger pore bottlenecks. [ABSTRACT FROM AUTHOR]

Synchrotron radiation based techniques are powerful tools for battery research and allow probing a wide range of length scales, with different depth sensitivities and spatial/temporal resolutions. Operando experiments enable characterization during functioning of the cell and are thus a precious tool to elucidate the reaction mechanisms taking place. In this perspective, the current state of the art for the most relevant techniques (scattering, spectroscopy, and imaging) is discussed together with the bottlenecks to address, either specific for application in the battery field or more generic. The former includes the improvement of cell designs, multi-modal characterization and development of protocols for automated or at least semi-automated data analysis to quickly process the huge amount of data resulting from operando experiments. Given the recent evolution in these areas, accelerated progress is expected in the years to come, which should in turn foster battery performance improvements., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)