Engineering MXene-based photocatalyst for efficient NADH regeneration and photoenzymatic CO2 reduction without electron mediator

被引:10
作者
Wei, Ping [1 ]
Zhang, Yue [2 ,3 ]
Dong, Jinfeng [1 ]
Cao, Yunhao [1 ]
Lee, Simon Ming-Yuen [4 ]
Lou, Wenyong [5 ]
Peng, Chao [2 ,3 ,6 ]
机构
[1] Wuyi Univ, Sch Pharm & Food Engn, Jiangmen 529020, Guangdong, Peoples R China
[2] Wuyi Univ, Sch Environm & Chem Engn, Jiangmen Key Lab Synthet Chem & Cleaner Prod, Jiangmen 529020, Guangdong, Peoples R China
[3] Wuyi Univ, Inst Carbon Peaking & Carbon Neutralizat, Jiangmen 529020, Guangdong, Peoples R China
[4] Hong Kong Polytech Univ, Dept Food Sci & Nutr, Hung Hom, Kowloon, Hong Kong 999077, Peoples R China
[5] South China Univ Technol, Sch Food Sci & Engn, Lab Appl Biocatalysis, Guangzhou 510640, Guangdong, Peoples R China
[6] Jieyang Ctr, Guangdong Lab Chem & Fine Chem Ind, Jieyang 515200, Guangdong, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 357卷
基金
中国国家自然科学基金;
关键词
Photoenzyme cascade catalysis; 1; 4-NADH regeneration; CO2; reduction; MXene-based photocatalyst; Without electron mediator; SOLAR FUEL PRODUCTION; INTERFACE; METHANOL; COMPOSITE; DIOXIDE; ANATASE; LAYER; TI3C2;
D O I
10.1016/j.apcatb.2024.124257
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
In this study, an MXene-based photocatalyst, ARTM to regenerate NADH without electron mediator is reported. The ARTM was able to achieve a regenerated NADH yield of 65 % within 50 min in the absence of electron mediator, with a 1,4-NADH selectivity of 90.8 %. The turnover frequency (TOF) of 1,4-NADH was as high as 0.148 h(-1), which was 74 and 148 times higher than that of A-TiO2 and R-TiO2, respectively. The synergetic effect between anatase/rutile TiO2 phase junction (ART-PJ) and TiO2@Ti3C2Tx heterojunction (TM-HJ) facilitates the efficient carriers separation and NADH regeneration. Enzymatic assay and HNMR revealed that the incorporation of Ti3C2Tx promoted the highly selective generation of 1,4-NADH. DFT calculation elucidated that this could be attributed to the end-on adsorption of the nicotinamide ring of NAD(+). Subsequently, an electron mediator free photoenzyme cascade catalysis system was constructed, which could effectively promote CO2 photoreduction to formate (594 mu mol g(-1) h(-1)).
引用
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页数:13
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