阳极
三碘化物
光电子学
电池(电)
材料科学
电化学
储能
电极
插层(化学)
纳米技术
电压
化学
电气工程
电解质
色素敏化染料
无机化学
物理
工程类
功率(物理)
物理化学
量子力学
作者
Arvind Pujari,Byung‐Man Kim,Hooman Abbasi,Myeong‐Hee Lee,Neil C. Greenham,Michaël De Volder
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-07-23
卷期号:9 (8): 4024-4031
标识
DOI:10.1021/acsenergylett.4c01350
摘要
The demand for autonomous off-grid devices has led to the development of "photobatteries", which integrate light-energy harvesting and electrochemical energy storage in the same architecture. Despite several photobattery chemistries and designs being reported recently, there have been few insights into the physical conditions necessary for charge transfer between the photoelectrode and counter electrode. Here, we use a three-electrode photobattery with a dye-sensitized TiO2 photoelectrode, triiodide (I–/I3–) catholyte, and anodes with varying intercalation potentials to confirm that photocharging is only feasible when the conduction band quasi-Fermi level (EFc) is positioned above the anode intercalation/plating potential. We also show that parasitic reactions after the battery is fully charged can be accelerated if the voltage of the battery and solar cell are not matched. The integration of multiple anodes in the same photobattery ensures well-controlled measurement conditions, allowing us to demonstrate the physical conditions necessary for charge transfer in photobatteries, which has been a topic of controversy in the field.
科研通智能强力驱动
Strongly Powered by AbleSci AI