Elevating Discharge Voltage of Li2CO3‐Routine Li−CO2 Battery over 2.9 V at an Ultra‐Wide Temperature Window

Author:

Zhao Ning1,Liu Limin1,Lu Xuan1,Li Yuyang1,Wu Xiaosha1,Peng Shaochen2,Wei Jingwen1,Gao Yang1,Zhang Hanqi1,Fan Yiming1,Yin Zicheng1,Feng Rongfen1,Wang Ru1,Hu Xiaofei134ORCID,Ding Shujiang134,Liu Wenfeng1

Affiliation:

1. School of Chemistry, School of Electrical Engineering and School of Aerospace Engineering Xi'an Jiaotong University ShaanXi 710061 China

2. HeBei Key Laboratory of Applied Chemistry Yanshan University Qinhuangdao 066004 China

3. Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education Xi'an Jiaotong University ShaanXi 710061 China

4. National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology Xi'an Jiaotong University ShaanXi 710061 China

Abstract

AbstractThe Li−CO2 batteries utilizing greenhouse gas CO2 possess advantages of high energy density and environmental friendliness. However, these batteries following Li2CO3‐product route typically exhibit low work voltage (<2.5 V) and energy efficiency. Herein, we have demonstrated for the first time that cobalt phthalocyanine (CoPc) as homogeneous catalyst can elevate the work plateau towards 2.98 V, which is higher than its theoretical discharge voltage without changing the Li2CO3‐product route. This unprecedented discharge voltage is illustrated by mass spectrum and electrochemical analyses that CoPc has powerful adsorption capability with CO2 (−7.484 kJ mol−1) and forms discharge intermediate of C33H16CoN8O2. Besides high discharge capacity of 18724 mAh g−1 and robust cyclability over 1600 hours (1000 mAh g−1 cut‐off) at a current density of 100 mA g−1, the batteries show high temperature adaptability (−30–80 °C). Our work is paving a promising avenue for the progress of high‐efficiency Li−CO2 batteries.

Publisher

Wiley

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