TY - JOUR
T1 - Iodine nanotrap for highly efficient iodine capture under high temperature
AU - Shui, Feng
AU - Lei, Qiong
AU - Dong, Xinglong
AU - Pan, Tingting
AU - Zhang, Zhiyuan
AU - Li, Jinli
AU - Yi, Mao
AU - Zhang, Laiyu
AU - Liu, Xiongli
AU - You, Zifeng
AU - Yang, Shiqi
AU - Yang, Rufeng
AU - Zhang, Hongbo
AU - Li, Jixin
AU - Shi, Zhan
AU - Yin, Jun
AU - Li, Baiyan
AU - Bu, Xian He
N1 - KAUST Repository Item: Exported on 2023-06-06
Acknowledgements: The authors acknowledge the National Science Foundation of China (NO. 21978138 and 22035003), the Fundamental Research Funds for the Central Universities (Nankai University) and the Haihe Laboratory of Sustainable Chemical Transformations (YYJC202101), the Ph. D. Candidate Research Innovation Fund of NKU School of Materials Science and Engineering for financial support of this work.
PY - 2023/5/26
Y1 - 2023/5/26
N2 - Covalent organic frameworks have been recognized as promising porous materials for the radioactive iodine capture. However, most COFs often suffer from low adsorption capacity under practical conditions (typically ≥ 150 °C, ≤ 150 ppmv I2) due to the lack of strong binding sites and low affinity toward iodine, which restricts their application in industrial relevant conditions. Here, we develop a strategy of constructing highly efficient I2 nanotraps by manipulating two kinds of adsorption sites (ionic binding sites and Lewis binding sites) located at adjacent spatial positions, thereby realizing the synergistic binding toward I2. The obtained I2 nanotrap 4F-iCOF-TpBpy-I- delivers a remarkable I2 uptake capacity of 37 wt% at 150 °C and 150 ppmv of I2, which illustrate a record-high value for all COFs reported so far. This work opens a new avenue for the rational design of COF materials toward highly efficient I2 capture and related application.
AB - Covalent organic frameworks have been recognized as promising porous materials for the radioactive iodine capture. However, most COFs often suffer from low adsorption capacity under practical conditions (typically ≥ 150 °C, ≤ 150 ppmv I2) due to the lack of strong binding sites and low affinity toward iodine, which restricts their application in industrial relevant conditions. Here, we develop a strategy of constructing highly efficient I2 nanotraps by manipulating two kinds of adsorption sites (ionic binding sites and Lewis binding sites) located at adjacent spatial positions, thereby realizing the synergistic binding toward I2. The obtained I2 nanotrap 4F-iCOF-TpBpy-I- delivers a remarkable I2 uptake capacity of 37 wt% at 150 °C and 150 ppmv of I2, which illustrate a record-high value for all COFs reported so far. This work opens a new avenue for the rational design of COF materials toward highly efficient I2 capture and related application.
UR - http://hdl.handle.net/10754/692373
UR - https://linkinghub.elsevier.com/retrieve/pii/S1385894723022568
UR - http://www.scopus.com/inward/record.url?scp=85160414926&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2023.143525
DO - 10.1016/j.cej.2023.143525
M3 - Article
SN - 1385-8947
VL - 468
SP - 143525
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -