离子
溴化物
吸附
水溶液
选择性
离子交换
电极
材料科学
电场
空位缺陷
化学
纳米技术
无机化学
物理化学
催化作用
有机化学
物理
量子力学
结晶学
作者
Jie Wang,Xiao Du,Xiaoqiong Hao,Jinhua Luo,Xiaogang Hao,Qing Cao,Guoqing Guan,Jun Li,Zhong Liu,Yongguo Li,Abuliti Abudula
标识
DOI:10.1016/j.cej.2021.131693
摘要
Effective recovery of high-value-added bromide ion (Br−) from aqueous solutions is significant because of its high application value. Electrochemically switched ion exchange (ESIX) has been proven as a valid method for the selective capture and recovery of target ions. As the photocatalysts are also used as the electroactive materials in the ESIX process, the light illumination could promote the excitation of electrons for the improvement of ion capture capacity. Herein, taking advantage of synergetic effect between photo and electric field we propose a novel photo-assisted electrochemically switched ion exchange (P-ESIX) strategy for the first time. As a try, Br−-vacancy BiOBr film is used as an ideal electrode material in P-ESIX system for the recovery of Br−, which not only possesses photo/electron bi-activity, but also exhibits high selectivity towards Br−. Compared with the traditional ESIX, this P-ESIX displays superior capture performances with a photo-assisted adsorption capacity growth rate of 23.09% with 1.23 times higher Br− adsorption capacity at 0.8 V applied potential. The capture capacity of Br− in P-ESIX reaches 106.80 mg g−1 with excellent stability. Meanwhile, P-ESIX working mechanism is deeply analyzed based on experiments and DFT calculations. This novel technology provides a new direction in separation field to achieve higher capture efficiency for the target ions.
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