Suppr超能文献

将超细钌纳米颗粒锚定在棉衍生的自支撑碳纤维上作为锂-二氧化碳电池的高效阴极催化剂。

Anchoring ultrafine Ru nanoparticles on cotton-derived self-standing carbon fibers as efficient cathode catalyst for Li-CO battery.

作者信息

Sun Jingchun, Tan Deshan, Li Xingyu, Han Xiaole, Liu Yi, Zhou Tengfei, Jiang Qingqing, Hu Juncheng

机构信息

School of Chemistry and Materials Science, Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education, South-Central Minzu University, Wuhan 430074, China.

Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, China.

出版信息

J Colloid Interface Sci. 2025 Dec;699(Pt 1):138131. doi: 10.1016/j.jcis.2025.138131. Epub 2025 Jun 8.

Abstract

Li-CO batteries could capture and convert CO into a valuable energy storage medium. The slow kinetics and high activation barrier associated with the breakdown cleavage of discharge products pose a significant hurdle in the advancement of reversible Li-CO batteries. Herein, cotton-derived self-standing carbon fibers were utilized to disperse Ru nanoparticles which could avoid depletion of active sites caused by stacking of graphite-based supports. Consequently, CBRu cathode presents small voltage polarization of 1.41 V at high current density of 200 μA cm, and high energy efficiency of 76.0 % at 20 μA cm as well as long-term cyclability over 1000 h. According to in/ex-situ characterizations and theoretical calculations, the unique cross-linked structure of the carbon fibers offers ample space for the deposition of discharge products while these ultrafine Ru nanoparticles regulate the growth path of LiCO and accelerate reaction kinetics. This study offers a novel perspective on the selection of self-standing cathode carbon matrix for Li-CO batteries.

摘要

锂-二氧化碳电池可以捕获二氧化碳并将其转化为一种有价值的储能介质。与放电产物的分解裂解相关的缓慢动力学和高活化能垒是可逆锂-二氧化碳电池发展的重大障碍。在此,利用源自棉花的自立式碳纤维来分散钌纳米颗粒,这可以避免因石墨基载体堆叠而导致的活性位点耗尽。因此,CBRu阴极在200 μA cm的高电流密度下呈现出1.41 V的小电压极化,在20 μA cm下具有76.0%的高能量效率以及超过1000小时的长期循环稳定性。根据原位/非原位表征和理论计算,碳纤维独特的交联结构为放电产物的沉积提供了充足的空间,而这些超细钌纳米颗粒则调节了Li₂CO₃的生长路径并加速了反应动力学。这项研究为锂-二氧化碳电池自立式阴极碳基体的选择提供了新的视角。

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