Shedding light on the light- driven lithium ion deinsertion reaction: towards the design of a photorechargeable battery

被引:52
作者
Nguyen, O. [1 ]
Courtin, E. [1 ]
Sauvage, F. [2 ]
Krins, N. [1 ]
Sanchez, C. [1 ]
Laberty-Robert, C. [1 ]
机构
[1] UPMC, Lab Chim Mat Condensee Paris, UMR 7574, Coll France, 4 Pl Jussieu, F-75005 Paris, France
[2] UPJV, LRCS, CNRS, UMR 7314, 33 Rue St Leu, F-80039 Amiens, France
关键词
ELECTROCHEMICAL ENERGY-STORAGE; MESOPOROUS THIN-FILMS; ANATASE TIO2; ELECTRON-TRANSPORT; INTERCALATION; INSERTION; NANOCRYSTALS; LIXTIO2;
D O I
10.1039/c7ta00493a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Li-ion batteries need to be charged by being plugged into the grid, limiting their autonomy. Charging a battery consists of applying an external load to reverse the spontaneous electrochemical reactions during discharge. A strategy to improve their autonomy is to design nanostructured electrodes whose composition and architecture allow for these reactions to be driven by light. Classical electrochemical experiments (in the dark and under light) demonstrate that light promotes the de-insertion reaction of 3D LixTiO2 mesoporous thin films due to the participation of photogenerated holes (h(+)). These holes allow the oxidation of Ti3+ into Ti4+, simultaneously giving rise to Li-ion extraction. Galvanostatic experiments performed on Li-rich TiO2 mesoporous films show that competition between ion insertion and de-insertion occurs, leading to electrodes with potentially infinite capacity. This work constitutes a proof of concept that low potential Li-ion batteries (TiO2//Li-0) can solely be recharged by exposure to light.
引用
收藏
页码:5927 / 5933
页数:7
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