解吸
电解质
电化学
氧气
吸附
材料科学
电极
阴极
电容
电池(电)
化学工程
分析化学(期刊)
纳米技术
化学
物理化学
热力学
有机化学
色谱法
工程类
功率(物理)
物理
作者
Marta Haro,Nuria Vicente,Germà García-Belmonte
标识
DOI:10.1002/admi.201500369
摘要
Li‐O 2 batteries are claimed to be one of the future energy storage technologies. Great number of scientific and technological challenges should be solved first to transform Li‐O 2 battery from a promise to real practical devices. Proposed mechanisms for oxygen reduction assume a reservoir of solved Li + ions in the electrolyte. However, the role that adsorbed Li + on the electrode surface might have on the overall oxygen reduction reaction (ORR) has not deserved much attention. Adsorbed Li + consumption is monitored here using impedance measurements from extended electrochemical double layer capacitance, which depends on the carbon matrix surface area. The presence of O 2 drastically reduces the amount of adsorbed Li + , signaling the kinetic competition between Li + surface adsorption and its consumption, only for potentials corresponding to the oxygen reduction reaction. Noticeably double layer capacitance remains unaltered after cycling. This fact suggests that the ORR products (Li 2 O 2 and Li 2 CO 3 ) are not covering the internal electrode surface, but deposited on the outer electrode‐contact interface, hindering thereby the subsequent reaction. Current results show new insights into the discharge mechanism of Li‐O 2 batteries and reveal the evidence of Li + desorption from the C surface when the ORR starts.
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