TY - JOUR
T1 - Gas/solid/liquid triphase interface of carbon nitride for efficient photocatalytic H2O2 production
AU - He, Mao
AU - Peng, Xiaoying
AU - Wu, Suqin
AU - Lei, Bin
AU - Xiong, Shuai
AU - Luo, Qin
AU - Tu, Zongxing
AU - Lin, Xiaoxue
AU - Peng, Guiming
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/2/25
Y1 - 2025/2/25
N2 - Photocatalytic two-electron oxygen reduction offers a sustainable method to produce hydrogen peroxide (H2O2). However, the efficiency of carbon nitride (CN) in this process is hindered by serious charge recombination and slow diffusion of oxygen. This work reports the thermal vapor-assisted surface chemical modification of CN by 4-aminobenzoyl groups (PABA/CN), which alters the conjugation system, extends the light absorption range, and enhances charge separation and electron transfer. Besides, it tunes the CN surface to be hydrophobic, which forms a gas/solid/liquid triphase interface in photocatalytic H2O2 production, and thus significantly improves O2 diffusion and proton supply for photosynthesis of H2O2. Photocatalytic experiments revealed that PABA/CN delivered an H2O2 yield of up to 745 μmol g−1 h−1 in pure water, 8 times that of pristine CN, ranking among the top performances of CN-based photocatalysts. Moreover, its selectivity reached 70%. Mechanism studies identified a two-step one-electron oxygen reduction reaction pathway for H2O2 photoproduction. Overall, this work simultaneously addresses the issues of mass transfer of O2, light harvesting, and charge separation of CN in photosynthesis of H2O2via surface chemical modification with 4-aminobenzoyl moieties, which extends π-conjugation and imparts surface hydrophobicity.
AB - Photocatalytic two-electron oxygen reduction offers a sustainable method to produce hydrogen peroxide (H2O2). However, the efficiency of carbon nitride (CN) in this process is hindered by serious charge recombination and slow diffusion of oxygen. This work reports the thermal vapor-assisted surface chemical modification of CN by 4-aminobenzoyl groups (PABA/CN), which alters the conjugation system, extends the light absorption range, and enhances charge separation and electron transfer. Besides, it tunes the CN surface to be hydrophobic, which forms a gas/solid/liquid triphase interface in photocatalytic H2O2 production, and thus significantly improves O2 diffusion and proton supply for photosynthesis of H2O2. Photocatalytic experiments revealed that PABA/CN delivered an H2O2 yield of up to 745 μmol g−1 h−1 in pure water, 8 times that of pristine CN, ranking among the top performances of CN-based photocatalysts. Moreover, its selectivity reached 70%. Mechanism studies identified a two-step one-electron oxygen reduction reaction pathway for H2O2 photoproduction. Overall, this work simultaneously addresses the issues of mass transfer of O2, light harvesting, and charge separation of CN in photosynthesis of H2O2via surface chemical modification with 4-aminobenzoyl moieties, which extends π-conjugation and imparts surface hydrophobicity.
UR - http://www.scopus.com/inward/record.url?scp=105002688075&partnerID=8YFLogxK
U2 - 10.1039/d4qi03352c
DO - 10.1039/d4qi03352c
M3 - Article
AN - SCOPUS:105002688075
SN - 2052-1545
VL - 12
SP - 3237
EP - 3245
JO - Inorganic Chemistry Frontiers
JF - Inorganic Chemistry Frontiers
IS - 8
ER -