2020
DOI: 10.1039/d0cy00656d
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2D MXene-derived Nb2O5/C/Nb2C/g-C3N4 heterojunctions for efficient nitrogen photofixation

Abstract: Due to the rather high 940.95 kJ mol-1 thermodynamically cleavage energy of N-N triple bond, developing a robust catalytic process for the N2 reduction under mild conditions is a continuing...

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Cited by 61 publications
(25 citation statements)
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“…However, only a few metal oxide semiconductors can be synthesized through the in situ oxidation, such as TiO 2 /Ti 3 C 2 T x and Nb 2 O 5 /Nb 2 CT x composites, due to the limitation of the kinds of transition metal elements in MXenes. [117][118][119] Considering the unique structure of MXenes, they could be better supporting materials than graphene for constructing heterojunction photocatalysts with 0D, 1D, and 2D semiconductors, [120][121][122] as shown in Figure 10d. [123] Through the aforementioned three synthetic routes, various and c) in situ oxidation of Ti 3 C 2 MXene precursor for the preparation of TiO 2 /Ti 3 C 2 heterojunction.…”
Section: In Situ Oxidation For Preparing Heterostructured Photocatalystsmentioning
confidence: 99%
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“…However, only a few metal oxide semiconductors can be synthesized through the in situ oxidation, such as TiO 2 /Ti 3 C 2 T x and Nb 2 O 5 /Nb 2 CT x composites, due to the limitation of the kinds of transition metal elements in MXenes. [117][118][119] Considering the unique structure of MXenes, they could be better supporting materials than graphene for constructing heterojunction photocatalysts with 0D, 1D, and 2D semiconductors, [120][121][122] as shown in Figure 10d. [123] Through the aforementioned three synthetic routes, various and c) in situ oxidation of Ti 3 C 2 MXene precursor for the preparation of TiO 2 /Ti 3 C 2 heterojunction.…”
Section: In Situ Oxidation For Preparing Heterostructured Photocatalystsmentioning
confidence: 99%
“…Furthermore, Bian and co-workers developed a Nb 2 O 5 /C/ Nb 2 C/g-C 3 N 4 catalyst used for photocatalytic N 2 reduction in water under mild conditions through in situ partial oxidation of Nb 2 CT x MXene and subsequent combination with g-C 3 N 4 . [118] In comparison with the Nb 2 O 5 /g-C 3 N 4 composite, the nitrogen reduction rate on Nb 2 O 5 /C/Nb 2 C/g-C 3 N 4 sample increased by 9.1 times to 0.365 mmol g À1 h À1 (Figure 17c), due to the formation of Schottky junctions and the close interface between Nb 2 O 5 and Nb 2 C, which is beneficial to the separation of photoinduced electron-hole pairs and the transfer of charge carriers (Figure 17d). The research on MXene/semiconductor composites for photocatalytic nitrogen fixation is just beginning and there are lots of problems under debate, such as the N 2 adsorption model on the surface of MXenes and the N 2 photofixation process.…”
Section: Nitrogen Photofixationmentioning
confidence: 99%
“…In order to acquire a deeper understanding of the role of light in the reaction, we investigated the effect of wavelength on one-pot hydrogenation and N-alkylation. The catalytic activity was generally maintained with the irradiation of UV, white or green LEDs (Table 1, entries [17][18][19]. However, the chemoselectivity of E1 was significantly decreased to 46.3% with UV.…”
Section: Resultsmentioning
confidence: 99%
“…Aromatic nitro compounds having different substituents could be reacted with benzyl alcohol to prepare N-alkylamines or N-benzylideneanilines on the irradiated 3%Pt/D-TiO 2 /Ti 3 C with good to excellent activity and chemoselectivity. In comparison with nitrobenzene, aromatic nitro compounds with different substituents generally had a good catalytic activity; the electron-donating group on the aromatic nitro compound was more favorable for catalytic activity than the electron-withdrawing group (Table 2, entries 3-12 vs. [13][14][15][16][17][18]. When the aromatic nitro compounds had methyl substituent (Table 2, entries 3-8), the reactivity order, onitrotoluene < m-nitrotoluene < p-nitrotoluene, should be owing to the steric hindrance effect.…”
Section: Resultsmentioning
confidence: 99%
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