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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Photoelectrochemical water splitting improved by a cucurbit[7]uril-induced ternary heterojunction

Hong-Si Guo,Wenfeng Zhao,Qingmei Ge,Nan Jiang,Mao Liu,Hang Cong

A promising method for producing hydrogen from solar energy and converting it into chemical fuels is photoelectrochemical (PEC) water splitting. In this paper, a novel photoanode is prepared by hydrothermal growing of nanorod CdS/g-C 3 N 4 /Q[7] heterojunction on FTO substrate for photoelectrochemical water splitting to produce hydrogen. In this method, Q[7]-doped g-C 3 N 4 is tightly combined with CdS composite and substrate, which significantly improves the separation and migration of photogenerated carriers in g-C 3 N 4 /Q[7] and CdS, and effectively reduces the internal resistance of the photoanode. Compared with the free CdS NRs, the PEC performance of the heterojunction CdS/g-C 3 N 4 /Q[7]-10 is significantly enhanced with the improved photocurrent density of 1049.7 μA/cm 2 under AM 1.5 G (100 mW/cm 2 ) simulated sunlight, which is 3.6 times that of pristine CdS and 2.6 times that of FTO-CdS/g-C 3 N 4 under the same conditions. The external bias photocurrent conversion efficiency and photohydrogen conversion efficiency of CdS/g-C 3 N 4 /Q[7]-10 photoanode at 0.7 V (relative to RHE) are measured to be both 0.31 %, as 3.1 times high as that of the original CdS NRs (0.10 %), and 2.07 times high as that of FTO-CdS/g-C 3 N 4 (0.15 %). The generation of heterostructure with interfacial interaction reduces the recombination of photogenerated electron-hole pairs, to enhance the charge transfer of water oxidation kinetics, allowing electrons to quickly transfer through the external circuit to the counter electrode for H + reduction to produce H 2 . A schematic diagram of the photoelectrochemical water splitting hydrogen evolution process with the heterojunction CdS/g-C 3 N 4 /Q[7]-10 is systematically proposed.

研究领域: 材料科学 · 能源转换 · 光电化学
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ANALYTICAL SCIENCES · 2022 ·Vol. 38 ·期 9 ·1181-1188 · IF 1.967

A label-free electrochemical sensor constructed with layer-by-layer assembly of GCE-AuNPs-Q[7]·HAuCl4 for detection of diphenylamine

Wang Cheng-Yan,Ge Qingmei,Jiang Nan,Cong Hang,Tao Zhu,Liu Mao,Fan Ying

Metal–organic frameworks (MOFs) including cucurbit[7]uril block (Q[7]·HAuCl 4 ) were employed to develop a diphenylamine (DPA) sensor in electrochemical method, the presence of HAuCl 4 improved the conductivity of the macrocyclic compound. To further enhance of the sensitivity, Au nanoparticles were inserted between the surface of glassy carbon electrode and Q[7]·HAuCl 4 MOFs (GCE-AuNPs-Q[7]·HAuCl 4 ). Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV) were applied for evaluation on the electrochemical behavior. For the electrochemical inertness of DPA, a label-free electrochemical sensor in 5 mM K 3 [Fe(CN) 6 ] solution was achieved, to produce a limit of detection as low as 4.6 µM in a linear range of 5–1000 µM with good reproducibility, high stability and acceptable anti-interference ability. Application of the proposed electrode for the quantitative determination of DPA in tap water and apple juice confirms its real value. Graphical abstract

研究领域: 分析化学 · 材料科学 · 电化学
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