Ultrahigh-rate and ultralong-life aqueous batteries enabled by special pair-dancing proton transfer.

The design of Faradaic battery electrodes with high rate capability and long cycle life comparable to those of supercapacitors is a grand challenge. Here, we bridge this performance gap by taking advantage of a unique ultrafast proton conduction mechanism in vanadium oxide electrode, developing an aqueous battery with untrahigh rate capability up to 1000 C (400 A g-1) and extremely long life of 0.2 million cycles. The mechanism is elucidated by comprehensive experimental and theoretical results. Instead of slow individual Zn2+ transfer or Grotthuss chain transfer of confined H+, the ultrafast kinetics and excellent cyclic stability are enabled by rapid 3D proton transfer in vanadium oxide via the special pair dance switching between Eigen and Zundel configurations with little constraint and low energy barriers. This work provides insight into developing high-power and long-life electrochemical energy storage devices with nonmetal ion transfer through special pair dance topochemistry dictated by hydrogen bond.

Growth of single-crystal imine-linked covalent organic frameworks using amphiphilic amino-acid derivatives in water.

A core feature of covalent organic frameworks (COFs) is crystallinity, but current crystallization processes rely substantially on trial and error, chemical intuition and large-scale screening, which typically require harsh conditions and low levels of supersaturation, hampering the controlled synthesis of single-crystal COFs, particularly on large scales. Here we report a strategy to produce single-crystal imine-linked COFs in aqueous solutions under ambient conditions using amphiphilic amino-acid derivatives with long hydrophobic chains. We propose that these amphiphilic molecules self-assemble into micelles that serve as dynamic barriers to separate monomers in aqueous solution (nodes) and hydrophobic compartments of the micelles (linkers), thereby regulating the polymerization and crystallization processes. Disordered polyimines were obtained in the micelle, which were then converted into crystals in a step-by-step fashion. Five different three-dimensional COFs and a two-dimensional COF were obtained as single crystals on the gram scale, with yields of 92% and above.

Structural origin of the high-voltage instability of lithium cobalt oxide.

Layered lithium cobalt oxide (LiCoO2, LCO) is the most successful commercial cathode material in lithium-ion batteries. However, its notable structural instability at potentials higher than 4.35 V (versus Li/Li+) constitutes the major barrier to accessing its theoretical capacity of 274 mAh g-1. Although a few high-voltage LCO (H-LCO) materials have been discovered and commercialized, the structural origin of their stability has remained difficult to identify. Here, using a three-dimensional continuous rotation electron diffraction method assisted by auxiliary high-resolution transmission electron microscopy, we investigate the structural differences at the atomistic level between two commercial LCO materials: a normal LCO (N-LCO) and a H-LCO. These powerful tools reveal that the curvature of the cobalt oxide layers occurring near the surface dictates the structural stability of the material at high potentials and, in turn, the electrochemical performances. Backed up by theoretical calculations, this atomistic understanding of the structure-performance relationship for layered LCO materials provides useful guidelines for future design of new cathode materials with superior structural stability at high voltages.

Adsorption of Nitrogen Dioxide in a Redox-Active Vanadium Metal-Organic Framework Material.

Nitrogen dioxide (NO2) is a toxic air pollutant, and efficient abatement technologies are important to mitigate the many associated health and environmental problems. Here, we report the reactive adsorption of NO2 in a redox-active metal-organic framework (MOF), MFM-300(V). Adsorption of NO2 induces the oxidation of V(III) to V(IV) centers in MFM-300(V), and this is accompanied by the reduction of adsorbed NO2 to NO and the release of water via deprotonation of the framework hydroxyl groups, as confirmed by synchrotron X-ray diffraction and various experimental techniques. The efficient packing of {NO2·N2O4}∞ chains in the pores of MFM-300(VIV) results in a high isothermal NO2 uptake of 13.0 mmol g-1 at 298 K and 1.0 bar and is retained for multiple adsorption-desorption cycles. This work will inspire the design of redox-active sorbents that exhibit reductive adsorption of NO2 for the elimination of air pollutants.

Processing Natural Wood into an Efficient and Durable Solar Steam Generation Device.

Harvesting solar energy for water desalination is one of the most promising ways to produce clean water. Because of the absorber detachment and base material degradation, the solar steam generator still suffers from drastic energy loss even when using absorber materials with high photothermal conversion efficiency. We herein propose a practical desalination design that can maintain both the working efficiency and operating life. This device is made from the Paulownia wood covalently bonded with MXene on the top. Paulownia wood, as a natural heat insulator, servers as an excellent transport and customized evaporator. This heat absorber-Paulownia wood system achieved an evaporation rate of 1.465 kg m-2 h-1 at 1 sun irradiation, corresponding to 96% solar conversion efficiency. This method is proved to be universal, and the other two implemented materials, graphene oxide and the active carbon, on Paulownia wood were also demonstrated. The theoretical model based on two-phase flow in porous media further suggests this design can accelerate the distillate rate. In this article, the covalently bonded device shows a high solar-thermal conversion efficiency, excellent evaporation rate, and long-time durability, making it a superior candidate for water desalination.