As the world moves towards sustainable and renewable energy sources, there is a need for reliable energy storage systems. A good candidate for such an application could be to improve secondary aqueous zinc–manganese dioxide (Zn-MnO₂) batteries. For this reason, different aqueous Zn-MnO₂ battery technologies are discussed in this short review, focusing on how electrolytes with different pH affect the battery. Improvements and achievements in alkaline aqueous Zn-MnO₂ batteries the recent years have been briefly reviewed. Additionally, mild to acidic aqueous electrolyte employment in Zn-MnO₂ batteries has been described, acknowledging their potential success, as such a battery design can increase the potential by up to 2 V. However, we have also recognized a novel battery electrolyte type that could increase even more scientific interest in aqueous Zn-MnO₂ batteries. Consisting of an alkaline electrolyte in the anode compartment and an acidic electrolyte in the cathode compartment, this dual (amphoteric) electrolyte system permits the extension of the battery cell potential above 2 V without water decomposition. In addition, papers describing pH immobilization in aqueous zinc–manganese compound batteries and the achieved results are reported and discussed.

Laser-induced periodic surface structures (LIPSS) enable advanced surface functionalization with broad applications in various fields such as micro- and nanoelectronics, medicine, microbiology, tribology, anti-icing systems, and more. This study demonstrates the possibility of achieving anisotropy in the tribological behavior of C45-grade steel structured by nanosecond laser radiation using the LIPSS method. The lateral surface of the steel roller was irradiated with a pulsed Nd:YAG laser at an optimum intensity I = 870 MW/cm² for the formation of LIPSS. Two sets of samples were formed with LIPSS that were perpendicular and parallel to the roller’s rotational motion direction. The Raman intensity maps revealed that the LIPSS structure consisted of periodically arranged oxides at the top of hills. At the same time, the valleys of the LIPSS structures were almost not oxidized. These results correlated well with scanning electron microscopy energy dispersive X-ray spectroscopy mapping and atomic force microscopy measurements. A comparison of Raman and X-ray photoelectron spectroscopy spectra revealed that both the magnetite phase and traces of the hematite phase were present on the surface of the samples. Tribological tests were performed in two cycles with periodic changes in the normal clamping force and sliding speed. It was found that the LIPSS structures which were formed perpendicularly to the sliding direction on the roller had a significantly greater impact on the friction processes. Structures oriented perpendicular to the direction of motion had a positive influence on reducing the energy consumption of a friction process as well as increasing the wear resistance compared to LIPSS formed parallel to the direction of motion or ones having a non-texturized surface. Laser texturing to produce LIPSS perpendicular to the direction of motion could be recommended for friction pairs operating under low-load conditions.

In this work, reactions between 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-diones with different benzohydrazides were studied. Nucleophilic substitution at C(6) was followed by isomerization and led to α-hydroxy-p-quinone imine derivatives. Synthesized compounds represent a combination of several structural motifs: a benzimidazole core fused with α-hydroxy-p-quinone imine, which contains a benzamide fragment. X-ray crystallography analysis revealed the formation of dimers linked through OH···O interactions and stabilization of the imine form by strong intramolecular NH···N hydrogen bonds. The protonation/deprotonation processes were investigated in a solution using UV–Vis spectroscopy and a ¹H NMR titration experiment. Additionally, the electrochemical properties of 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione and its α-hydroxy-p-quinone imine derivative as cathode materials were investigated in acidic and neutral environments using cyclic voltammetry measurements. Cathode material based on 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione could act as a potentially effective active electrode in aqueous electrolyte batteries; however, further optimization is required.

Reactions of quinones with compounds containing an amino group can produce a wide variety of addition or substitution products that depend on reactivity of both quinone and amino derivative. 6,7-Dichloropyrido[1,2-a]benzimidazole-8,9-diones undergo selective nucleophilic substitution reaction with different benzohydrazides and α-hydroxy-p-quinone imine derivatives stabilized by strong intramolecular hydrogen bond were isolated. Synthesized compounds represent a combination of several structural motifs: benzimidazole core fused with α-hydroxy-p-quinone imine which contains a benzamido fragment. The protonation/deprotonation processes were investigated in a solution using UV-Vis spectroscopy and 1H NMR titration experiment. X-ray crystallography analysis revealed a set of weak non-covalent interactions such as intra- and intermolecular hydrogen bonds and π-π stacking. Additionally, the redox behavior of 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione and its p-imino derivative was investigated in acidic and neutral environment using cyclic voltammetry measurements. Cathode material based on 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione could act as potential effective active electrode in aqueous electrolyte batteries, however further optimization is required.

Non-rechargeable alkaline Zn-MnO2 batteries are dominating the primary battery market and are a promising candidate for secondary battery storage systems as well. However, these batteries suffer from low potential and poor rechargeability. Here, we report a rechargeable membrane-less amphoteric aqueous Zn-MnO2 battery with a 2.4 V open circuit potential. We have employed alkaline (KOH), acidic (H2SO4) and neutral (K2SO4) Pluronic F-127 hydrogels as electrolytes. By placing the anode in an alkaline environment but the cathode in an acidic environment, we have successfully widened the potential window in an aqueous medium avoiding hydrogen and oxygen evolution reactions. The obtained open circuit potential of as prepared amphoteric battery is stable for more than 25 hours and 200 charge-discharge cycles.