Kim Yun-Jung, Lee Hongkyung, Lee Dong Jin, Park Jung-Ki, Kim Hee-Tak
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, Daejeon (Republic of Korea).
ChemSusChem. 2015 Aug 10;8(15):2496-502. doi: 10.1002/cssc.201500520. Epub 2015 Jul 14.
The problem of high charge polarization is one of the most significant challenges in current nonaqueous Li-O2 batteries. The development of an electrode for the oxygen evolution reaction (OER) at reduced overpotential is thus essential. Here, we suggest a binder-free electrode based on Co nanoparticles embedded in carbon nanofibers (Co-CNFs), which simultaneously reduces the charge and discharge polarization and extends cycling stability. Co-CNF gives rise to a lower discharge polarization because of an enhanced oxygen reduction reaction activity compared to Co-free CNF. Although the embedment of Co does not enhance the OER activity, it significantly reduces charge overvoltage by forming easily decomposable amorphous Li2 O2 . A mechanism for the formation of amorphous Li2 O2 is suggested in terms of charge localization induced by the Co NPs. The findings suggest a new electrode design strategy of combining inexpensive metals and carbon materials for modulating the phase of the discharge product.
高电荷极化问题是当前非水锂氧电池面临的最重大挑战之一。因此,开发一种在较低过电位下用于析氧反应(OER)的电极至关重要。在此,我们提出一种基于嵌入碳纳米纤维(Co-CNFs)中的钴纳米颗粒的无粘结剂电极,它能同时降低充放电极化并延长循环稳定性。与不含钴的碳纳米纤维相比,Co-CNFs由于增强的氧还原反应活性而产生较低的放电极化。尽管钴的嵌入并没有增强OER活性,但它通过形成易于分解的非晶态Li2O2显著降低了充电过电压。从钴纳米颗粒引起的电荷局域化角度提出了非晶态Li2O2的形成机制。这些发现提出了一种将廉价金属和碳材料相结合以调节放电产物相的新电极设计策略。