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Process optimization for producing hierarchical porous bamboo-derived carbon materials with ultrahigh specific surface area for lithium-sulfur batteries.

Benefiting from the merits of low cost, non‐flammability and high operational safety, aqueous rechargeable batteries have emerged as promising candidates for large‐scale energy storage applications. Among various metal‐ion/non‐metallic charge carriers, proton (H+) as a charge carrier possesses numerous unique properties such as a fast proton diffusion dynamics, a low molar mass and a small hydrated ion radius, which endow aqueous proton batteries (APBs) with a salient rate capability, a long‐term life span and an excellent low‐temperature electrochemical performance. In addition, redox‐active organic molecules, with the advantages of structural diversity, rich proton‐storage sites and abundant resources, are considered as attractive electrode materials for APBs. However, as far as application is concerned, the charge storage and transport mechanisms of organic electrodes in APBs is still in infancy. Therefore, finding suitable electrode materials and uncovering the H+ storage mechanisms are significant for the applications of organic materials in APBs. Herein, the latest research progresses on organic materials such as small molecules and polymers for APBs are reviewed. Furthermore, a comprehensive summary and evaluation of APBs employing organic electrodes as anode and/or cathode is provided, especially on their low‐temperature and high‐power performances, along with systematic discussions for guiding the rational design and the construction of APBs based on organic electrodes.This article is protected by copyright. All rights reserved

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Summary Carbon aerogel (CA), possessing abundant pore structures and excellent electrical conductivity, have been utilized as conductive sulfur hosts for lithium‐sulfur (Li‐S) batteries. However, a serious shuttle effect resulted from polysulfide ions has not been effectively suppressed yet due to the weak absorption nature of CA, resulting in rapid decay of capacity as the cycle number increases. Herein, ultrafine (~3 nm) gadolinium oxide (Gd2O3) nanoparticles (with upper redox potential of ~ 1.58 V versus Li+/Li) are uniformly in‐situ integrated with CA through directly sol‐gel polymerization and high‐temperature carbonization. The Gd2O3 modified CA composites (named as Gdx‐CA, where x means molar ratio of Gd2O3 nanoparticles to carbon) are incorporated with S. Then, the products (S/Gdx‐CA) are acted as sulfur host materials for Li‐S batteries. The results demonstrate that adding ultrafine Gd2O3 nanoparticles can dramatically improve the electrochemical properties of the composite cathodes. The S/Gd2‐CA electrode (loading with 58.9 wt% of S) possesses the best electrochemical properties, including a high initial capacity of 1210 mAh g−1 and a relatively high capacity of 555 mAh g−1 after 50 cycles at 0.1 C. It is noteworthy that the performance of long‐term cycle (350 cycles) for the S/Gd2‐CA (317 mAh g−1 after 100 cycles and 233 mAh g−1 after 350 cycles at 1 C) is improved significantly than that of S/CA (150 mAh g−1 after 150 cycles at 1 C). Overall, the enhancement of electrochemical performances can be due to the strong polar nature of the ultrafine Gd2O3 nanoparticles, which provide strong adsorption sites to immobilize S and polysulfide. Furthermore, the Gd2O3 nanoparticles present a catalytic effect. Our research suggests that adding Gd2O3 nanoparticles into S/CA composite cathode is an effective and novelty method for improving the electrochemical performances of Li‐S batteries.

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