Guan De-Hui, Wang Xiao-Xue, Li Ma-Lin, Li Fei, Zheng Li-Jun, Huang Xiao-Lei, Xu Ji-Jing
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
International Center of Future Science, Jilin University, Changchun, 130012, P. R. China.
Angew Chem Int Ed Engl. 2020 Oct 26;59(44):19518-19524. doi: 10.1002/anie.202005053. Epub 2020 Jun 30.
A photoinduced flexible Li-CO battery with well-designed, hierarchical porous, and free-standing In S @CNT/SS (ICS) as a bifunctional photoelectrode to accelerate both the CO reduction and evolution reactions (CDRR and CDER) is presented. The photoinduced Li-CO battery achieved a record-high discharge voltage of 3.14 V, surpassing the thermodynamic limit of 2.80 V, and an ultra-low charge voltage of 3.20 V, achieving a round trip efficiency of 98.1 %, which is the highest value ever reported (<80 %) so far. These excellent properties can be ascribed to the hierarchical porous and free-standing structure of ICS, as well as the key role of photogenerated electrons and holes during discharging and charging processes. A mechanism is proposed for pre-activating CO by reducing In to In under light illumination. The mechanism of the bifunctional light-assisted process provides insight into photoinduced Li-CO batteries and contributes to resolving the major setbacks of the system.
本文展示了一种光诱导柔性锂-二氧化碳电池,该电池采用精心设计的、具有分级多孔结构且独立的硫化铟@碳纳米管/不锈钢(ICS)作为双功能光电极,以加速二氧化碳还原和析出反应(CDRR和CDER)。该光诱导锂-二氧化碳电池实现了创纪录的3.14 V高放电电压,超过了2.80 V的热力学极限,以及3.20 V的超低充电电压,往返效率达到98.1%,这是迄今为止报道的最高值(<80%)。这些优异性能可归因于ICS的分级多孔和独立结构,以及光生电子和空穴在充放电过程中的关键作用。提出了一种在光照下通过将铟还原为铟来预激活二氧化碳的机制。双功能光辅助过程的机制为光诱导锂-二氧化碳电池提供了深入了解,并有助于解决该系统的主要问题。