Article(id=1319969648032989523, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1319969627665445134, articleNumber=null, orderNo=null, doi=10.14062/j.issn.0454-5648.20230368, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1685289600000, receivedDateStr=2023-05-29, revisedDate=1693843200000, revisedDateStr=2023-09-05, acceptedDate=null, acceptedDateStr=null, onlineDate=1792634887941, onlineDateStr=2026-10-22, pubDate=1705680000000, pubDateStr=2024-01-20, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792634887941, onlineIssueDateStr=2026-10-22, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792634887941, creator=13701087609, updateTime=1792634887941, updator=13701087609, issue=Issue{id=1319969627665445134, tenantId=1146029695717560320, journalId=1263187385517883426, year='2024', volume='52', issue='1', pageStart='1', pageEnd='370', issueExtLink='null', onlineDate='null', pubDate='1705680000000', pubDateStr='2024-01-20', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792634883085, creator='13701087609', updateTime=1792641944622, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319999245965443838, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1319969627665445134, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319999245965443839, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1319969627665445134, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=122, endPage=132, ext={EN=ArticleExt(id=1319969648272064852, articleId=1319969648032989523, tenantId=1146029695717560320, journalId=1263187385517883426, language=EN, title=Enhanced Photocatalytic Performance of Amorphous Carbon/g-C
3N
4/Bi
2WO
6 Ternary Z-Scheme Heterojunction Photocatalyst, columnId=1319726165087077079, journalTitle=Journal of the Chinese Ceramic Society, columnName=Research Article, runingTitle=null, highlight=null, articleAbstract=
Introduction Photocatalysis is one of the most potential techniques to solve energy crisis and environmental pollution problems, and how to obtain photocatalysts with a greater catalytic efficiency is always a research hotspot in the photocatalysis. The heterogeneous photocatalyst is proved as a promising efficient strategy to address this issue. The heterojunction photocatalysts can be utilized to expedite the separation of photo-induced electron-hole pairs. In particular, Z-scheme heterojunctions exhibit the dual advantages of suppression of recombination of electron-hole pairs, reserving a high redox ability for both semiconductors. The visible-light-driven photocatalysts Bi2WO6 and g-C3N4 exhibit a poor photocatalytic activity because of their fast recombination of photo-generated carriers. It is advisable to choose the g-C3N4 and Bi2WO6 to form an all-solid-state Z-scheme photocatalytic system to obtain the higher photocatalytic performance. It is reported that carbon materials often put up a low work function when they modify the electronic and optical properties of hybrids. In this paper, a novel amorphous carbon/g-C3N4/Bi2WO6 (C/C3N4/Bi2WO6) Z-scheme heterojunction with a visible light response was synthesized. The performance of C/C3N4/Bi2WO6 was measured by photo-degrading TC under the visible light (i.e., ≥420 nm). The as-synthesized composites played an enhanced visible-light photoactivity than the pure g-C3N4 and Bi2WO6. Furthermore, the possible mechanism of the enhanced performance of the C/C3N4/Bi2WO6 composite was discussed.
Methods All reagents with analytical grade were used without further purification. First, the C/C3N4 sample was prepared by a milling/roasting method. When a mass ratio of glucose to urea was 0.1%, the as-fabricated C/C3N4 composite exhibited an optimum photocatalytic performance. The C/C3N4/Bi2WO6 nanocomposites were prepared through a facile hydrothermal method. The obtained products were denoted as C/C3N4/Bi2WO6-1, C/C3N4/Bi2WO6-2, C/C3N4/Bi2WO6-3 and C/C3N4/Bi2WO6-4, when the mass ratios of C/C3N4∶Bi2WO6 were 1.0∶0.1, 1.0∶0.4, 1.0∶0.7 and 1∶1, respectively. For the comparison, a pure Bi2WO6 sample was synthesized through the same procedur without introducing C/C3N4.
The crystal structure was detected by X-ray diffraction with Cu Kα radiation (λ=0.154 06 nm). The morphology and microstructures of the synthesized samples were investigated on high-resolution transmission electron microscopy (HRTEM). The ultraviolate-visible (UV-Vis) diffuse reflectance spectra (DRS) were taken on UV-Vis-near infrared (NIR) spectrophotometry with BaSO4 as a reference. The chemical composition and chemical state of C/C3N4/Bi2WO6 were analyzed by X-ray photoelectron spectroscopy (XPS) with Al Kα excitation source. The photocurrent response under simulated solar light irradiation was recorded with an electrochemical workstation in a sandwich-type configuration, a Pt slice as a counter electrode, a saturated calomel electrode (SCE) as ae reference, and 0.1 mol/L Na2SO4 solution as electrolyte. A 300 W xenon arc lamp equipped with a simulated solar light filter calibrated to 100 mW/cm2, which was measured with a radiometer, employed as a light source. Electrochemical impedance spectroscopy (EIS) Nyquist plots were obtained at 0.6 V with a small alternating current amplitude of 5 mV in a frequency range of 0.1 Hz-105 Hz.
The photocatalytic activity of the C/C3N4/Bi2WO6 sample was determined by degrading the simulated pollutant tetracycline (TC). In the experimental setup, a 300W Xe lamp was employed as a light source and a 420 nm cut-off filter was used to provide only visible-light irradiation. The photocatalyst of 100 mg was added to 100 mL of TC solution (1×10-4 mol/L). Before being irradiated, the suspensions were magnetically stirred in the dark for 3 h to reach the adsorption-desorption equilibrium between photocatalysts and TC. The solution was exposed to visible light irradiation under magnetic stirring. The aliquot of 3 mL was collected from the suspension and centrifuged immediately for every 10 min. The degradation of TC was monitored by checking the absorbance at 357 nm using an UV-Vis spectrometer.
Results and discussion The degradation ratios of TC are 25% and 50% after irradiation for 240 min by visible-light in the presence of g-C3N4 and Bi2WO6, respectively. Furthermore, it is clear that the C/C3N4 composite exhibits a higher photocatalytic activity in the degradation of TC than the g-C3N4 sample. All the C/C3N4/Bi2WO6 photocatalysts exhibit better photocatalytic performance than the C/C3N4 composite and Bi2WO6 under the same experimental condition. Specifically, the photocatalytic activities of C/C3N4/Bi2WO6 nanocomposites gradually improve as Bi2WO6 ratio increases, and the photocatalytic performance is optimal when the mass ratio of C/C3N4∶Bi2WO6 is 1.0∶0.7. The photocatalytic activities decrease when Bi2WO6 ratio continues to increase. Hence, the as-prepared C/C3N4/Bi2WO6-3 nanocomposite has the optimum photocatalytic performance, and the maximum degradation efficiency of 97.1% is attained after the irradiation for 240 min.
The improved photocatalytic performance of C/C3N4/Bi2WO6 composites is ascribed to the formed amorphous carbon-mediated Z-scheme heterojunction. When the heterojunction C/C3N4/Bi2WO6 is exposed to visible light (λ>420 nm), the electrons generated from CB of Bi2WO6 can transfer to the VB of g-C3N4 via the amorphous carbon mediator due to the good electrical conductivity of amorphous carbon, and then annihilate with the holes induces from the VB of g-C3N4, the photo-induced carriers can be effectively separated.
Conclusion We constructed Z-scheme C/C3N4/Bi2WO6 heterojunction photocatalyst with enhanced photocatalytic activities in degradation of TC. When the mass ratio of C/C3N4∶Bi2WO6 was 1.0∶0.7, the as-fabricated C/C3N4/Bi2WO6 heterojunction exhibited an optimum photocatalytic performance. The mechanism illuminated that the efficient separation of charge carriers generated by the amorphous carbon-mediated Z-scheme mechanism mainly contributed to the improved photocatalytic performance of C/C3N4/Bi2WO6 heterojunction. We anticipated that the results of this work could favor the application of solar energy in water pollution.
, authors=Jingjing ZHENG, Xili SHANG, Guoxia LIU, authorsList=Jingjing ZHENG, Xili SHANG, Guoxia LIU, authorCompany=null, correspAuthors=null, authorNote=
ZHENG Jingjing (1981-), female, Ph.D., Associate Professor. E-mail: zjj65050@163.com
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3N
4/Bi
2WO
6三元Z型异质结复合光催化材料的制备及性能, columnId=1263922770220560512, journalTitle=硅酸盐学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=
Z型异质结是提高半导体光催化性能的一种有效途径，因为Z型异质结具有抑制电子-空穴复合以及为2种半导体保留高氧化还原能力的双重优点。采用简单高温固化-水热法合成了具有可见光响应的新型无定型C/g-C3N4/Bi2WO6（C/C3N4/Bi2WO6）Z型异质结。对制备的复合催化材料进行了系统表征，并选择盐酸四环素（TC）作为目标污染物评价其光催化性能。C/C3N4/Bi2WO6复合材料的光催化活性优于g-C3N4、C/C3N4和Bi2WO6。当C/C3N4与Bi2WO6的质量比为1.0∶0.7时，复合催化材料（样品C/C3N4/Bi2WO6-3）的催化效率最高。C/C3N4/Bi2WO6复合光催化材料催化性能的提高可能是所形成的Z型异质结促进了光生电子-空穴对有效的分离和转移。
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