Engineering g-C3N4 with CuAl-layered double hydroxide in 2D/2D heterostructures for visible-light water splitting

被引:8
|
作者
Boumeriame, Hanane [1 ,2 ,3 ,4 ]
Cherevan, Alexey [4 ]
Eder, Dominik [4 ]
Apaydin, Dogukan H. [4 ]
Chafik, Tarik [3 ]
Da Silva, Eliana S. [1 ,2 ]
Faria, Joaquim L. [1 ,2 ]
机构
[1] Univ Porto, Fac Engn, LSRE LCM Lab Separat & React Engn, Lab Catalysis & Mat, Rua Dr Roberto Frias S-N, P-4200465 Porto, Portugal
[2] Univ Porto, Fac Engn, ALiCE Associate Lab Chem Engn, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[3] Univ Abdelmalek Essaadi, Fac Sci & Tech, Lab Chem Engn & Valorizat Resources LGCVR UAE L01F, Tangier, Morocco
[4] Tech Univ Wien TU Wien, Inst Mat Chem, Getreidemarkt 9, A-1060 Vienna, Austria
基金
奥地利科学基金会;
关键词
Graphitic carbon nitride; CuAl layered double hydroxide; S-scheme heterojunction; 2D/2D heterostructure; Photocatalytic water splitting; HYDROGEN-PRODUCTION; CARBON NITRIDE; PHOTOCATALYTIC PROPERTY; STRUCTURAL STABILITY; ELECTRONIC-STRUCTURE; ENHANCED EFFICIENCY; ENERGY; OXIDATION; DRIVEN; NI;
D O I
10.1016/j.jcis.2023.08.159
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
CuAl layered double hydroxide (LDH) and polymeric carbon nitride (g-C3N4, GCNN) were assembled to construct a set of novel 2D/2D CuAl-LDH/GCNN heterostructures. These materials were tested towards H-2 and O-2 generation from water splitting using visible-light irradiation. Compared to pristine materials, the heterostructures displayed strongly enhanced visible-light H-2 evolution, dependent on the LDH content, which acts as a cocatalyst, replacing the benchmark Pt. The optimal LDH loading was achieved for 0.2CuAl-LDH/GCNN that exhibited an increased number of active sites and showed a trade-off between charge separation efficiency and light shading, resulting in a 32-fold increase in the amount of evolved H-2 compared with GCNN. In addition, the 0.2CuAl-LDH/GCNN heterostructure generated 1.5 times more O-2 than GCNN. The higher photocatalytic performance was due to efficient charge carriers' separation at the heterojunction interface via an S-scheme (corroborated by work function, steady-state and time-resolved photoluminescence studies), enhanced utilisation of longer-wavelength photons (>460 nm) and higher surface area available for the catalytic reactions.
引用
收藏
页码:2147 / 2158
页数:12
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