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A novel hybrid electrode of zeolitic imidazolate framework–derived carbon encapsulated in reduced‐TiO 2 nanotube arrays: Fabrication and photoelectrocatalytic activity
Author(s) -
Song Huihui,
Zhang Junming,
Sun Zhongqiao,
Sun Ting,
Han Yide,
Meng Hao,
Zhang Xia
Publication year - 2020
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5791
Subject(s) - photocurrent , zeolitic imidazolate framework , chemical engineering , carbon nanotube , nanotechnology , rhodamine b , x ray photoelectron spectroscopy , scanning electron microscope , electrode , nanotube , materials science , chemistry , photocatalysis , metal organic framework , composite material , optoelectronics , organic chemistry , catalysis , adsorption , engineering
Constructing high‐efficient photoelectrodes is one of the promising tasks in photoelectrocatalytic (PEC) technology. Al‐reduced TiO 2 nanotube arrays (R‐TNTAs) exhibit distinct improved visible‐light response ability in comparison with traditional TiO 2 nanomaterials. In addition, metal–organic framework (MOF)‐derived porous carbon materials possess versatile advantages partly due to preserved geometry configuration of MOF. Inspired by these characteristics, in this work, we synthesized the novel hybrid electrodes of C–N (Zn)@R‐TNTAs through the pyrolysis of ZIF‐8@R‐TNTAs at controlled temperatures, which were pre‐synthesized by coating zeolitic imidazolate frameworks (ZIF‐8) onto R‐TNTAs. The resulting hybrid electrodes were characterized using field‐emission scanning electron microscopy, powder X‐ray diffraction, X‐ray photoelectron spectra, and Fourier‐transform infrared techniques. The EC property and PEC activity of the composite electrodes were also analyzed, and the dependence of these on the pyrolysis temperature was also explored. The results showed that the pyrolyzed carbon materials were uniformly deposited in the inner TiO 2 nanotubes and thus effectively enhanced their EC and PEC activities. The best EC and PEC capacities were obtained by C–N (Zn)@R‐TNTAs (600); the maximum photocurrent density was 0.85 mA cm −2 , which is ~1.5 times that of single R‐TNTAs; and the maximum H 2 evolution rate was 58.83 μmol h −1 cm −2 , being ~2.3 times that of R‐TNTAs. In addition, C–N (Zn)@R‐TNTAs (600) exhibited the best PEC activity in the degradation of rhodamine B with excellent catalytic stability. Based on EC analyses, a possible band structure and enhanced PEC mechanism for C–N (Zn)@R‐TNTAs were proposed. There are only a few reports related to reduced TiO 2 nanotubes, and this work highlights the ideas of designing the hybrid electrodes based on reduced TNTAs and MOF‐derived carbon materials, which may find broad applications in PC and PEC processes.