Qian-Cheng Zhu, Xu- Bo Xin, Shi-Huan Zhou, Zi-Yuan Wang, De- Yu Mao, Ai-Jun Fu
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引用次数: 0
Abstract
Li–CO2 batteries (LCBs) stand out as promising candidates for high-energy-density storage solutions, capturing widespread interest and research focus. However, the high charging voltage and poor cycling stability owing to the sluggish reaction kinetics of carbon dioxide reduction seriously limit the commercialization of LCBs. Herein, a composite of cobalt and molybdenum carbide nanoparticles decorated three-dimensional N-doped graphene was fabricated as an efficient cathode catalysts for LCBs . The porous structure and large specific surface area of graphene substrate provide abundant catalytic active sites and sufficient deposition space for discharge products. The co-catalytic effect of cobalt-molybdenum carbide bimetal greatly enhances the CO2 reaction kinetics. The assembled LCBs exhibited a ultrahigh discharge capacity of 27,886 mAh g−1 at 100 mA g−1, a long cycle life of 248 cycles (limited capacity of 500 mAh g−1), and a low overpotential of 1.56 V. This research presents a practical approach to developing highly effective cathode catalysts, aiming to enhance the operational efficiency of LCBs.
锂-二氧化碳电池(LCBs)作为高能量密度存储解决方案的有前途的候选者脱颖而出,引起了广泛的兴趣和研究焦点。然而,由于二氧化碳还原反应动力学缓慢,充电电压高,循环稳定性差,严重限制了lcb的商业化。本文制备了一种由钴和碳化钼纳米颗粒修饰的三维n掺杂石墨烯的复合材料,作为lcb的高效阴极催化剂。石墨烯衬底的多孔结构和较大的比表面积为放电产物提供了丰富的催化活性位点和充足的沉积空间。钴-碳化钼双金属的共催化作用大大提高了CO2反应动力学。所制备的lcb在100 mA g−1时具有27,886 mAh g−1的超高放电容量,248次的长循环寿命(限定容量为500 mAh g−1)和1.56 V的低过电位。本研究提出了一种开发高效阴极催化剂的实用方法,旨在提高lcb的运行效率。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.