Yang Xu

Abstract Potassium-ion batteries are a promising alternative to lithium-ion batteries. However, it is challenging to achieve fast charging/discharging and long cycle life with the current electrode materials because of the sluggish potassiation kinetics. Here we report a soft carbon anode, namely highly nitrogen-doped carbon nanofibers, with superior rate capability and cyclability. The anode delivers reversible capacities of 248 mAh g –1 at 25 mA g –1 and 101 mAh g –1 at 20 A g –1 , and retains 146 mAh g –1 at 2 A g –1 after 4000 cycles. Surface-dominated K-storage is verified by quantitative kinetics analysis and theoretical investigation. A full cell coupling the anode and Prussian blue cathode delivers a reversible capacity of 195 mAh g –1 at 0.2 A g –1 . Considering the cost-effectiveness and material sustainability, our work may shed some light on searching for K-storage materials with high performance.

Potassium‐ion batteries (KIBs) in organic electrolytes hold great promise as an electrochemical energy storage technology owing to the abundance of potassium, close redox potential to lithium, and similar electrochemistry with lithium system. Although carbon materials have been studied as KIB anodes, investigations on KIB cathodes have been scarcely reported. A comprehensive study on potassium Prussian blue K 0.220 Fe[Fe(CN) 6 ] 0.805 ⋅4.01H 2 O nanoparticles as a potential cathode material is for the first time reported. The cathode exhibits a high discharge voltage of 3.1–3.4 V, a high reversible capacity of 73.2 mAh g −1 , and great cyclability at both low and high rates with a very small capacity decay rate of ≈0.09% per cycle. Electrochemical reaction mechanism analysis identifies the carbon‐coordinated Fe III /Fe II couple as redox‐active site and proves structural stability of the cathode during charge/discharge. Furthermore, for the first time, a KIB full‐cell is presented by coupling the nanoparticles with commercial carbon materials. The full‐cell delivers a capacity of 68.5 mAh g −1 at 100 mA g −1 and retains 93.4% of the capacity after 50 cycles. Considering the low cost and material sustainability as well as the great electrochemical performances, this work may pave the way toward more studies on KIB cathodes and trigger future attention on rechargeable KIBs.

Organic sodium-ion batteries (SIBs) are potential alternatives of current commercial inorganic lithium-ion batteries for portable electronics (especially wearable electronics) because of their low cost and flexibility, making them possible to meet the future flexible and large-scale requirements. However, only a few organic SIBs have been reported so far, and most of them either were tested in a very slow rate or suffered significant performance degradation when cycled under high rate. Here, we are focusing on the molecular design for improving the battery performance and addressing the current challenge of fast-charge and -discharge. Through reasonable molecular design strategy, we demonstrate that the extension of the π-conjugated system is an efficient way to improve the high rate performance, leading to much enhanced capacity and cyclability with full recovery even after cycled under current density as high as 10 A g(-1).

In this work, we report the crystalline structure, morphology, and optical properties of novel metastable hexagonal phase MoO3 (h-MoO3) nanobelts prepared by a simple hydrothermal route from peroxomolybdate solution with the presence of sodium nitrate as a mineralizer. During the reaction process, NaNO3 has been proposed to influence the deoxidation, condensation, and further dehydration of the water-soluble peroxomolybdate precursor for connecting the [MoO6] octahedra with vertex sharing and edge sharing arrangements on determining the generation of metastable phase. The present work comparatively investigates the photochromic and electrochromic behaviors of the resultant hexagonal h-MoO3 nanobelts and the common thermodynamically stable orthorhombic α-MoO3 nanobelts. The performances concerning photochromism on two types of MoO3 nanobelt suspensions show that the photochemical efficiency of h-MoO3 is more excellent than that of α-MoO3 under UV light irradiation based on a remarkable coloration phenomenon. And the as-obtained h-MoO3 nanobelt coated film exhibits a steady electrochromic property in quick response to electrical impulse. Higher structure openness degree in the tunnel structure of h-MoO3, which could lead to an efficient electron−hole separation and provid larger spatial locations for cation insertion/extraction and diffusion, is suggested to be responsible for its enhanced coloration properties.

Mg-doped hematite (α-Fe2O3) was synthesized by atomic layer deposition (ALD). The resulting material was identified as p-type with a hole concentration of ca. 1.7 × 1015 cm–3. When grown on n-type hematite, the p-type layer was found to create a built-in field that could be used to assist photoelectrochemical water splitting reactions. A nominal 200 mV turn-on voltage shift toward the cathodic direction was measured, which is comparable to what has been measured using water oxidation catalysts. This result suggests that it is possible to achieve desired energetics for solar water splitting directly on metal oxides through advanced material preparations. Similar approaches may be used to mitigate problems caused by energy mismatch between water redox potentials and the band edges of hematite and many other low-cost metal oxides, enabling practical solar water splitting as a means for solar energy storage.