Potassium Molten Salt-Mediated In Situ Structural Reconstruction of a Carbon Nitride Photocatalyst

被引:24
作者
Gupta, Akanksha [1 ,2 ]
Bhoyar, Toshali [3 ]
Abraham, B. Moses [4 ]
Kim, Dong Jin [5 ]
Pasupuleti, Kedhareswara Sairam [6 ]
Umare, Suresh S. [3 ]
Vidyasagar, Devthade [3 ,7 ]
Gedanken, Aharon [1 ,2 ]
机构
[1] Bar Ilan Univ, Bar Ilan Inst Nanotechnol & Adv Mat BINA, IL-5290002 Ramat Gan, Israel
[2] Bar Ilan Univ, Dept Chem, IL-5290002 Ramat Gan, Israel
[3] Visvesvaraya Natl Inst Technol VNIT, Dept Chem, Mat & Catalysis Lab, Nagpur 440010, Maharashtra, India
[4] Indian Inst Technol Kanpur, Dept Chem Engn, Kanpur 208016, India
[5] Kyungpook Natl Univ, Sch Energy Engn, Daegu 41566, South Korea
[6] Chungnam Natl Univ, Dept Phys, Daejeon 34134, South Korea
[7] Korea Univ, Dept Mat Sci & Engn, Seoul 02841, South Korea
关键词
polymeric carbon nitride; molten salts; surface sites; chromium reduction; CRYSTALLINE; NANOSHEETS;
D O I
10.1021/acsami.3c00239
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Metal-free polymeric carbon nitride (PCN) materials are at the forefront of photocatalytic applications. Nevertheless, the overall functionality and performance of bulk PCN are limited by rapid charge recombination, high chemical inertness, and inadequate surface-active sites. To address these, here, we employed potassium molten salts (K+X-, where X- is Cl-, Br-, and I-) as a template for the in situ generation of surface reactive sites in thermal pyrolyzed PCN. Theoretical calculations imply that addition of KX salts to PCN-forming monomers causes halogen ions to be doped into C or N sites of PCN with a relative trend of halogen ion doping being Cl < Br < I. The experimental results show that reconstructing C and N sites in PCN develops newer reactive sites that are beneficial for surface catalysis. Interestingly, the photocatalytic H2O2 generation rate of KBr-modified PCN was 199.0 mu mol h-1, about three times that of bulk PCN. Owing to the simple and straightforward approach, we expect molten salt-assisted synthesis to have wide exploration in modifying PCN photocatalytic activity.
引用
收藏
页码:18898 / 18906
页数:9
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