1,3,5-Triphenylbenzene Based Porous Conjugated Polymers for Highly Efficient Photoreduction of Low-Concentration CO2 in the Gas-Phase System

被引:14
|
作者
Dai, Chunhui [1 ]
Zhong, Lixiang [2 ]
Wu, Wei [1 ]
Zeng, Chao [3 ]
Deng, Yue [1 ]
Li, Shuzhou [2 ]
机构
[1] East China Univ Technol, Jiangxi Key Lab Mass Spectrometry & Instrumentat, Sch Chem Biol & Mat Sci, Nanchang 330013, Jiangxi, Peoples R China
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[3] Jiangxi Normal Univ, Inst Adv Mat IAM, Nanchang 330022, Jiangxi, Peoples R China
来源
SOLAR RRL | 2022年 / 6卷 / 04期
基金
美国国家科学基金会;
关键词
1,3,5-triphenylbenzene; CO2; photoreduction; gas-phase systems; porous conjugated polymers; METAL-ORGANIC FRAMEWORK; MICROPOROUS POLYMERS; CARBON-DIOXIDE; CAPTURE; DESIGN;
D O I
10.1002/solr.202100872
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Herein, three 1,3,5-triphenylbenzene based porous conjugated polymers (PCPs) are designed for photochemical reduction of CO2 in simulated flue gas in the mild gas-solid reaction system. By tuning the nature of the comonomers, the PCPs present high surface areas, high CO2/N-2 selectivity, and broad visible light absorptions with bandgaps of 1.81-2.07 eV. At 1 bar and 273 K, the CO2 uptake capacity of PCPs is enhanced from 1.28 to 2.18 mmol g(-1), with an increase in CO2 adsorption heat from 21.8 to 28.3 KJ mol(-1). In the presence of gaseous water, SO-TPB demonstrates the highest CO production rate of 40.12 mu mol h(-1) g(-1) and nearly 100% product selectivity without using organic sacrificial reagent and additional cocatalyst (>420 nm). Moreover, SO-TPB can be recovered while well retaining the photocatalytic activity and reused at least five runs, indicating good recyclability.
引用
收藏
页数:8
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