Rujun MaLihui DongBin LiTongming SuXuan LuoZuzeng QinHongbing Ji
Abstract g‐C 3 N 4 /BiYO 3 composites were prepared by an electrostatic self‐assembly of g‐C 3 N 4 and BiYO 3 and were used as photocatalysts for photocatalytic hydrogen evolution. The UV‐vis DRS revealed that the band gaps of BiYO 3 and g‐C 3 N 4 were 2.58 eV and 2.96 eV, respectively, and the g‐C 3 N 4 /BiYO 3 composites showed stronger visible light absorption than that of g‐C 3 N 4 because the composite with BiYO 3 served as a narrow bandgap catalyst. Electrochemical impedance spectroscopy (EIS) proved that the g‐C 3 N 4 /BiYO 3 composites exhibited a better electronic transmission capacity and a larger photocurrent than that of g‐C 3 N 4 or BiYO 3 because the BiYO 3 acted as an electron acceptor in the composites. The PL spectra showed that g‐C 3 N 4 combined with BiYO 3 inhibited the recombination of photo‐generated electron holes in g‐C 3 N 4 and enhanced the photocatalytic activity for hydrogen evolution. Furthermore, the photocatalytic activities for hydrogen evolution with the g‐C 3 N 4 /BiYO 3 composites were higher than those of the individual g‐C 3 N 4 or BiYO 3 alone due to the transfer of photogenerated electrons from the conduction band of g‐C 3 N 4 to the conduction band of BiYO 3 and the transfer of photogenerated holes from the valence band of BiYO 3 to the valence band of g‐C 3 N 4 . The composite with a g‐C 3 N 4 /BiYO 3 mass ratio of 2 showed an optimal hydrogen evolution rate of 37.6 μmol⋅h –1 ⋅g cat –1 , which was 8.4‐ and 6.4‐fold higher than that of g‐C 3 N 4 and BiYO 3 , respectively.
Hideyuki KatsumataYusuke TachiT. SuzukiSatoshi Kaneco
Yuliang SunJin DiYuan SunXing MengYu GaoYohan Dall’AgneseGang ChenXiaofeng Wang
Sanmilan Jyoti KalitaSagar VaranganePurashri BasyachKaranika SonowalB. Moses AbrahamAnkur K. GuhaUjjwal PalLakshi Saikia
Haiyan XieKai WangSongling LiZhiliang Jin