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RADIATION PHYSICS AND CHEMISTRY · 2023 · IF 2.9

Enhanced degradation performance and mineralization of ciprofloxacin by ionizing radiation combined with g-C3N4/CDs

Junhui He,Qi Ye,Yi Zhu,Miao Yang,Long Zhao

In this study, the degradation of ciprofloxacin (CIP) was investigated in the synergetic system of electron beam irradiation (EBI) combined with graphite carbon nitride/carbon nanodots (g-C 3 N 4 /CDs). The results suggested that the presence of g-C 3 N 4 /CDs could not only promote the degradation of CIP but also significantly enhanced the mineralization ratio. At 25 kGy, the mineralization ratio increased from 18.1% to 69.0% while g-C 3 N 4 /CDs was added. Regeneration experiments revealed that the g-C 3 N 4 /CDs composite possessed good reusability. In addition to finding that the presence of CO 3 2− , HCO 3 − , NO 3 − and NO 2 − obviously restrained the radiolysis process of CIP, the adding of Cl − and SO 4 2− could also have slight inhibitory effects. The effect of various water matrices in EBI&g-C 3 N 4 /CDs systems suggested that the degradation efficiency decreased in lake and tap water. Moreover, the studies in the presence of different radical scavengers suggested that ·OH was the main reactive species in the degradation process. The possible degradation pathway of CIP was proposed in the light of intermediate products using Liquid chromatograph-mass spectrometer (LC–MS) analysis coupled with DFT calculations.

CAS / MDL: 5949-29-1 57-13-6
研究领域: 环境科学 · 辐射生物学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2022 · IF 4.326

Ti3+ Defective TiO2/CdS Z-Scheme Photocatalyst for Enhancing Photocatalytic CO2 Reduction to C1–C3 Products

Yunxia Bai,Mei Li,Xuemei Liu,Jinyu Han,Xinli Zhu,Qingfeng Ge,Hua Wang

Photocatalytic CO2 reduction is a promising route to simultaneously address two critical issues related to the energy and environment. Herein, a direct Z-scheme photocatalytic system, Ti3+ defective TiO2/CdS nanoflowers, was fabricated to enhance the production of C1–C3 products from CO2 reduction. First, nanoflower-like TiO2 (NF-TiO2) is prepared using a TiB2 precursor to build in Ti3+ defects. Then, the NF-TiO2/CdS heterojunctions are constructed via the sulfurization of TiO2/Cd-MOF. Importantly, the optimal heterojunction photocatalyst NF-TiO2/CdS0.6 exhibits a highly promoted CO2 reduction activity not only for CO and CH4 but also for C2–C3 hydrocarbons. The cumulative yields of CO and CH4 are 1007.0 μmol/g and 83.5 μmol/g (2.5 h), respectively, and a yield of 55.3 μmol/g (2.5 h) of C2–C3 hydrocarbons is obtained. This enhanced yield of C1–C3 products is attributed to the synergistic effects of abundant Ti3+ defects that increase adsorption and activation of CO2, the large surface area that provides sufficient active sites, and a direct Z-scheme heterojunction with a good intimate contact interface that effectively separates charge carriers and accumulates electrons with strong reducibility. Moreover, the photoluminescence analysis of hydroxyl radicals was conducted to provide evidence for the direct Z-scheme mechanism. This work provides a facile method for the construction of a TiO2-based direct Z-scheme photocatalytic system for improving photocatalytic performance toward CO2 reduction.

研究领域: 材料科学 · 环境科学 · 能源科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Dual interfacing with metallic cobalt boosts the electron shuttle of CdS-carbide nanoassemblies

Xujing Ji,Jiayang Zhang,Guoqing Zhang,Na Li,Ruixin Wang,Haiqiang Lin,Xinping Duan

Harnessing accelerated interfacial redox, thus boosting charge separation, is of great importance in photocatalytic solar hydrogen generation. In effect, nanoassembling non-noble metallic phases in CdS-based systems and elucidating their role in photocatalysis hold the key to eventually boosting electron shuttle in the field. Here we combine an efficient in-situ exsoluted metallic Co 0 nanoparticles on a carbides matrix (CMG) with CdS (CdS@ Co CMG) for photogeneration of hydrogen. The metallic cobalt phase exhibits strong binding at the CdS-carbide dual interfaces, forming the accelerated “electron converter” mechanism validated by charge transfer kinetics and achieving two orders of magnitude faster hydrogen production (44.42 mmol g −1  h −1 ) relative to CdS (0.43 mmol g −1  h −1 ). We propose that the unique catalyst configuration enable the directional electron-relay photocatalysis via harnessing interfaces between Co 0 phase, carbides, and CdS clusters, which eventually boosts the redox process and charge separation of the integrated system, leading to high H 2 production rates in the suspension.

研究领域: 材料科学 · 能源化学
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ACS Sustainable Chemistry & Engineering · 2019 · IF 6.97

Carbonized MoS2: Super-Active Co-Catalyst for Highly Efficient Water Splitting on CdS

Mengmeng Shao,Yangfan Shao,Shengjie Ding,Rui Tong,Xiongwei Zhong,Lingmin Yao,Weng Fai Ip,Baomin Xu,Xing-Qiang Shi,Yi-Yang Sun,Xuesen Wang,Hui Pan

Searching photocatalysts for efficient hydrogen production has been a challenging issue for solar-energy harvesting. Using co-catalyst is proven to be an effective approach to improve the efficiency of photocatalyst in water-splitting. Here, we report that carbonized MoS2 (MoS2/Mo2C) can be a superactive co-catalyst in solar-driven hydrogen production. We show that MoS2/Mo2C decorated CdS achieves a high photocatalytic hydrogen evolution rate (34 mmol/h/g, ∼112 times higher than pure CdS) and excellent apparent quantum efficiency (41.4% at 420 nm). The outstanding photocatalytic performance of MoS2/Mo2C/CdS is attributed to the metallic characteristic of MoS2/Mo2C and suitable Gibbs free energy of hydrogen adsorption, leading to enhanced light absorption, fast separation and transportation of photoinduced carriers, and optimal activity in hydrogen evolution reaction (HER). We further show that MoS2/Mo2C as co-catalyst can also dramatically improve the photocatalytic activity of g-C3N4. Our findings demonstrate that the carbonized transition metal disulfide can be active as co-catalyst in photocatalysis, providing guidance on exploring novel photocatalysts for energy harvesting.

研究领域: 材料科学 · 能源科学 · 催化化学
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Nanoscale Research Letters · 2014 ·Vol. 9 ·期 1 ·1-7 · IF 2.481

Graphene-enhanced visible-light photocatalysis of large-sized CdS particles for wastewater treatment

Lü Wei,Chen Jie,Wu Yao,Duan Lianfeng,Yang Yue,Ge Xin

The hybrid composites of graphene decorated by large-sized CdS particles (G/M-CdS) were prepared by a one-pot solvothermal route in which the reduction of graphite oxide into graphene was accompanied by the generation of microsized CdS particles. The structure and composition of the obtained nanocomposites were studied by means of X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The CdS particles with the average sizes of approximately 640 nm were formed on graphene sheets. The as-prepared composite was used as adsorbent to remove dye from wastewater using the organic dye Rhodamine B as the adsorbate. The G/M-CdS composite reveals a high photodegradation rate under visible light irradiation. Our results demonstrate that the G/M-CdS is very promising for removing organic dyes from wastewater.

CAS / MDL: 10102-17-7 7790-78-5
研究领域: 材料科学 · 环境科学 · 化学工程
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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING · 2021 ·Vol. 127 ·期 7 ·1-8 · IF 2.584

Research on FTO/CBD-CdS: Cl thin film photodetector with a vertical structure

Zhang Junlin,Wang Yunfan,Zhou Biao,Cao Hongyuan,Yang Xiutao,Li Bing,Zhang Jingquan,Feng Lianghuan,Zeng Guanggen,Zhong Zhengxiang,Ghali Mohsen,Karazhanov Smagul

In this work, CdS thin films were deposited on glass/fluorine-doping tin oxide (FTO) substrates by low-cost chemical bath deposition (CBD), followed by annealing with CdCl 2 -doping (Cl-doping) to fabricate resistive-type photodetectors (PDs) with a vertical structure of glass/FTO/CBD-CdS:Cl/electrode. The effect of annealing with Cl-doping (AwCl) on the various properties of films and the photodetection performance of PDs were systematically characterized by special testing methods. The results revealed that the surface morphology and crystal structure of CBD-CdS:Cl films were improved, accompanied by an enhancement of hexagonal phase (002) crystal plane (wurtzite structure), and the optical bandgap of films can be adjusted between 2.43 and 2.26 eV while the electron activation energy of the films was reduced from 75.9 to 10.3 meV after AwCl. Furthermore, the light responsivity of CBD-CdS:Cl PDs were 0.57, 0.59 and 1.67 A/W under 365, 400 and 530 nm illumination at a bias of −2.0 V, respectively, and the detectivity of photons at corresponding wavelengths were 3.7 × 10 8 , 3.9 × 10 8 and 1.08 × 10 9 Jones. Meanwhile, the PDs showed optimized repeatability and improved sensitivity under periodic illumination. The above results demonstrated that the CBD-CdS:Cl PDs with a vertical structure developed in this work had good detection performance at certain characteristic wavelengths.

CAS / MDL: 10108-64-2
研究领域: 材料科学 · 光电技术
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Molecular Catalysis · 2024 · IF 3.9

Photocatalytic selective oxidation of HMF to DFF based on hollow CdS QDs/MIL-101 composites under visible light

Yuwei Liang,Chunling Hu,Peng Chen,Qi Li,Jianning Wu,Zhiyong Liu,Jichang Liu,Yanlong Tai

5-hydroxymethylfurfural (HMF) can catalyte into 2,5-diformylfuran (DFF) which had received much attention as a potential biomass resource. Here, we used a simple and effective method to construct hollow CdS quantum dot (CdS QDs)/MIL-101 heterostructures with high contact area and multiple active sites. The structure of heterostructures could improve photocatalytic activity by charge transfer, photogenerated carrier separation and the multiple refractions of light supported within the hollow-structured CdS QDs. The detailed catalytic mechanism was illustrated by trap agent experiments and electron paramagnetic resonance (EPR) spectroscopy, in which superoxide radicals (·O 2 - ) play a decisive role in the catalytic oxidation of HMF to DFF. Furthermore, the large specific surface area of MIL-101 adsorbs O 2 from the reaction system thereby accelerating the ·O 2 - formation process. Under environmental conditions, 70 % CdS QDs/MIL-101 exhibited optimal catalytic performance. Comparing with pure CdS QDs, the photocurrent enhances 1.8 times, HMF conversion is 1.5 times and DFF selectivity is 1.2 times. This work provide a useful way to improve the conversion of biomass by Z-heterostructures under ambient conditions.

研究领域: 化学工程 · 材料科学 · 环境科学
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JOURNAL OF SOLID STATE CHEMISTRY · 2019 · IF 2.291

Facile synthesis of ternary Ti3C2–OH/ln2S3/CdS composite with efficient adsorption and photocatalytic performance towards organic dyes

Hongjun Fang,Yusong Pan,Minyun Yin,Linfeng Xu,Yuan Zhu,Chengling Pan

Ternary Ti 3 C 2 –OH/ln 2 S 3 /CdS composites with an efficient visible-light-driven photocatalytic performance have been prepared via a facile hydrothermal synthesis method. The photo-degradation experiments verified that Ti 3 C 2 –OH/ln 2 S 3 /CdS composite with a large surface area of 68.2 m 2 /g exhibited an enhanced photocatalytic activity and adsorption capacity towards Rhodamine B under visible light irradiation , which was higher than that of the naked CdS and ln 2 S 3 , respectively. Furthermore, Ti 3 C 2 –OH/ln 2 S 3 /CdS composite showed robust degradation efficiency for mixture dyes of RhB and Methyl Orange (MO), and its catalytic ability was superior to that of ternary GO/ln 2 S 3 /CdS composite. The trapping experiments for active species revealed that hole (h + ) and • O 2 − species played a critical role in the removal of organic pollutants. In summary, the enhanced photocatalytic performance of Ti 3 C 2 –OH/ln 2 S 3 /CdS photocatalyst was derived from an excellent charge carrier separation and transfer of Ti 3 C 2 –OH MXene and the synergistic effect between CdS and ln 2 S 3 which resulting in strong visible light response.

研究领域: 材料科学 · 环境科学
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

One-step hydrothermal preparation of Dy2O3-CdS nanomaterials for n-butanol sensing

Jiayi Qu,Yujun Guo,Xingtai Chen,Xiaoning Wang,Davoud Dastan,Xi-Tao Yin,Xiaoguang Ma

Dy 2 O 3 -CdS nanomaterials was firstly prepared by a one-step hydrothermal method for the rapid detection of n-butanol. In comparison with the sensor solely based on CdS, the integrated gas sensitivity performance of the sensor S 2 (containing 10 mol % Dy 2 O 3 ) for n-butanol was significantly improved, with a response value of up to 130, 3.25 times higher than that of the pristine CdS for 100 ppm n-butanol gas at an optimal operating temperature of 200 °C, this represents a substantial enhancement in the sensitivity of n-butanol detection, outperforming many existing sensing materials. Secondly, the sensor not only demonstrates excellent selectivity and long-term stability towards n-butanol but also enables highly precise detection within the wide concentration range of 5-300 ppm, Additionally, it possesses a fast response/recovery time of 25/18 s, significantly improving the detection efficiency. After a sequence of characterization utilizing XRD (X-ray diffraction), SEM (scanning electron microscope), TEM (transmission electron microscope), XPS (X-Ray photoelectron spectroscopy), the study reveals that the superior gas-sensing performance is attributed to the formation of n-n type heterojunctions, the interconnection of CdS nanomicrospheres by Dy 2 O 3 nanorods that facilitates gas transport, and the unique 4f electrons of Dy 2 O 3 . These findings provide new insights into the design of high-performance gas sensors, distinguishing this work from previous studies and making it a valuable contribution to the field of n-butanol detection.

研究领域: 材料科学 · 传感器技术 · 化学工程
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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Efficient SnO2/CdS double electron transport layer for Sb2S3 film solar cell

Mingzhu Su,Zitong Feng,Zheng Feng,Hanxiao Chen,Xingyun Liu,Jian Wen,Hongri Liu

Sb 2 S 3 has been proven to be a very promising light absorbing material for photovoltaic applications due to its low cost, high stability, non-toxicity, and abundant elemental storage. Electron transport layer (ETL) is a very crucial factor to the performances of Sb 2 S 3 solar cells. Here we developed a simple chemical solution process method to synthesize SnO 2 colloidal and fabricated SnO 2 ETL at low-temperature first, and then SnO 2 /CdS double ETL was prepared by combining SnO 2 and CdS. The power conversion efficiency of Sb 2 S 3 solar cell is 5.3% based on the SnO 2 /CdS double ETL, whereas the device based on CdS ETL only exhibites a PCE of 4.3%. Experimental analyses revealed that the introduction of SnO 2 ETL enhanced the grain size of Sb 2 S 3 films and passivated interfacial defects thus enhancing device efficiency. Our results show the potential application of SnO 2 in the planar Sb 2 S 3 solar cell.

研究领域: 材料科学 · 光伏技术
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 21 ·26810-26816 · IF 3.056

Defected graphene as effective co-catalyst of CdS for enhanced photocatalytic activities

Chen Ying,Wang Yue,Zhou Xiaohan,Zhao Yang,Peng Wenchao

Synthesis of highly efficient photocatalysts for energy and environment catalysis is still a big challenge in the materials field. Cadmium sulfide (CdS) is a promising visible light-driven photocatalyst, which can be composited with co-catalysts to increase its photo-activity and stability. In this study, a kind of graphene material with abundant structure defects (D-rGO) is synthesized by a two-step annealing process with nitrogen-doped rGO (N-rGO) as an intermediate. The high-temperature annealing could remove the doped heteroatoms to form structure defects with five or seven carbon atoms. The D-rGO is then used as co-catalyst for the modification of CdS nanoparticles, and enhanced photocatalytic activities could be obtained. A large hydrogen evolution rate of 102.7 μmol h −1 g −1 is achieved, which is also effective for 4-nitrophenol reduction with a rate constant of 0.168 min −1 . The novel CdS/D-rGO composite contains no noble metals and could be used as multi-functional photocatalysts, thus should has great potential in the photocatalysis field.

研究领域: 材料科学 · 能源催化 · 环境科学
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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 55 ·期 25 ·11167-11176 · IF 3.553

Umbrella-like CdS single crystal: exposed (002) facets and enhanced photocatalytic properties

Zhang Jiyun,Song Yanyan,Dong Xianhui,Jiang Haoyang,Tang Jianguo,Li Haidong

We, herein, report the synthesis of umbrella-like CdS single crystal with exposed high-activity (002) facets first time by using a one-step hydrothermal method with cadmium acetate dihydrate (Cd(CH 3 COO) 2 ·2H 2 O) and ammonium thiocyanate (NH 4 SCN), and its possible growth mechanism was discussed. As a contrast, CdS nanoparticles with different morphologies were also synthesized. The morphology, composition and photocatalytic property of as-synthesized samples were determined by XRD, SEM, TEM, UV–Vis DRS, PL and photocurrent tests, respectively. The results show that umbrella-like CdS under UV (20 min) and visible light (80 min) irradiation, the removal rate of rhodamine B was as high as 99.1% and 99.3%, respectively. Moreover, even though the particle size of umbrella-like CdS particle is larger than as-synthesized CdS nanospheres, it still shows excellent photocatalytic degradation activity due to its exposed high-energy (002) facets. And its excellent application prospects are conceivable. The current work provides a new paradigm in material morphology design, especially in the construction of highly active surfaces for photocatalysis and photoelectric conversion.

研究领域: 材料科学 · 光催化领域
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