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CdS
Chem · 2021 · IF 22.804

Partially reduced Pd single atoms on CdS nanorods enable photocatalytic reforming of ethanol into high value-added multicarbon compound

Peng Zhou,Qinghua Zhang,Yuguang Chao,Liang Wang,Yiju Li,Hui Chen,Lin Gu,Shaojun Guo

Photocatalytic co-production of high value-added multicarbon compounds and hydrogen from renewable bioethanol is an environmental and long-term approach to industrial activities and remains a great challenge because of the difficulty in bioethanol dehydrogenation. Guided by first-principle simulation, we first synthesized a partially reduced Pd–P 3 single atom (PdPSA) on CdS nanorods with an unoccupied hybrid state of Pd 4d and P 3p via both metal-support interaction effect and Pd–P coordination effect. This unique electronic structure of PdPSA is totally different from highly reduced S-coordinated Pd single atoms or nanoparticles and allows PdPSA-CdS to exhibit a visible-light photocatalytic activity of 35.1 mmol g −1 h −1 for the co-production of high-value-added 1,1-diethoxyethane and H 2 with a selectivity of 100%. Mechanism studies revealed that the unoccupied hybrid states of Pd 4d and P 3p in PdPSA not only greatly promoted the dehydrogenation of ethanol but also promised PdPSA with a high H 2 -production activity.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Insight into synergistic effect of Ti3C2 MXene and MoS2 on anti-photocorrosion and photocatalytic of CdS for hydrogen production

Chao Wu,Weixin Huang,Huanmin Liu,Kangle Lv,Qin Li

Facing the increasingly serious issues of energy crisis and environmental pollution, it is vital to develop efficient and durable photocatalysis systems for hydrogen (H 2 ) production from water splitting. However, for the famous CdS-based systems, the bottleneck of poor efficiency and low stability arisen from photocorrosion has not been broken through yet. In this study, a ternary composite of CdS , MoS 2 and Ti 3 C 2 MXene with intimately contact interfaces was successfully constructed via an in situ growth method, which exhibited reinforced photocatalytic H 2 -production activity and increased photocorrosion resistant capability. Both of experimental characterizations and density functional theory (DFT) calculations well proved that the photogenerated holes and electrons of CdS timely migrated to Ti 3 C 2 and MoS 2 , respectively. As a consequence, the optimal sample displayed a high H 2 production rate of 14.88 mmol·h −1 ·g −1 with a lifetime of up to 78 h, and the component and structure of the composite were kept intact during the photocatalysis reaction. This work highlights the synergistic effect of the Ti 3 C 2 MXene and MoS 2 as redox dual cocatalysts on the promoted photocatalytic performance and durability of CdS, which can be anticipated to significantly enhance the commercial availability of CdS and even boost its incorporation into industrial applications.

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ANALYST · 2020 ·Vol. 146 ·期 4 ·1295-1302 · IF 3.978

A novel signal amplified electrochemiluminescence biosensor based on MIL-53(Al)@CdS QDs and SiO2@AuNPs for trichlorfon detection

Defen Feng,Fucun Wei,Yeyu Wu,Xuecai Tan,Fang Li,Yongkuai Lu,Gaochao Fan,Heyou Han

An ultrasensitive electrochemiluminescence (ECL) biosensor was developed based on MIL-53(Al)@CdS QDs and SiO2@AuNPs for trichlorfon detection. Metal–organic frameworks (MOFs) were used as a loading platform that provided a large surface area to load targets and modified materials onto the electrode. At the same time, SiO2@AuNPs loaded plenty of AuNPs which effectively increased the ECL resonance energy transfer between the CdS QDs, so that the ECL signal was strongly quenched and resulted in an amplified response. In the range of 10−11–10−4 M, the ECL response showed a linear relationship with the concentration (logarithm) of trichlorfon, and the detection limit was 5.1 × 10−12 M (S/N = 3). When the biosensor was applied to detect trichlorfon in lettuce, broccoli, cucumber, and chives, the recoveries obtained from the spiked samples were 97%–105%, 102%–104%, 100%–104%, and 98%–104%, respectively. Thus, this novel ECL biosensor has potential applications for the analysis of trichlorfon in food samples.

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BIOSENSORS & BIOELECTRONICS · 2013 · IF 5.437

Ultrasensitive photoelectrochemical immunoassay of indole-3-acetic acid based on the MPA modified CdS/RGO nanocomposites decorated ITO electrode

Bing Sun,Lijian Chen,Yan Xu,Min Liu,Huanshun Yin,Shiyun Ai

A novel ultrasensitive photoelectrochemical immunosensor was fabricated based on 3-mercaptopropionic acid stabilized CdS/reduced graphene oxide (MPA-CdS/RGO) nanocomposites for indole-3-acetic acid (IAA) detection. The MPA-CdS/RGO nanocomposites were synthesized by in situ solvothermal growth of triangulated pyramidal CdS nanoparticles on the RGO sheet. 3-Mercaptopropionic acid (MPA) was employed as the modifier and bridge to immobilize the antibody. The nanocomposites were characterized by X-ray diffraction, transmission electron microscopy , scanning electron microscopy and UV/vis spectra. The results showed that the MPA-CdS/RGO nanocomposites revealed enhanced photocurrent response due to excellent electron transport properties of RGO and the improved assembly of CdS nanoparticles onto RGO sheet with the introduction of MPA. Based on the dependence of the photocurrent decline on the concentration of IAA, the proposed photoelectrochemical immunosensor for IAA depicted a linear range from 0.1 to 1000   ng/mL with a lower detection limit (0.05   ng/mL). The high sensitivity, reproducibility and specificity of the method permitted the method suitable to be used in real samples.

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CATALYSIS LETTERS · 2018 ·Vol. 148 ·期 9 ·2765-2776 · IF 2.911

In Situ Formation of Leaf-Like Ag2S/CdS Heterojunction Photocatalyst Harnessing Vis–NIR Light for Photodegradation of Organic Pollutants

Chang Libin,Zhu Gangqiang,Lu Huan,Hojamberdiev Mirabbos,Zhang Zengping,Gao Jianzhi,Wang Chenghui,Yang Woochul

Abstract The Ag 2 S/CdS composite photocatalyst with a leaf-like structure was synthesized by loading the Ag 2 S nanoparticles on the surface of the hydrothermally synthesized CdS particles. The UV–Vis–NIR absorption spectroscopy results reveal that the Ag 2 S/CdS composite photocatalyst exhibits a wide-spectrum response from ultraviolet (UV) to near-infrared (NIR), demonstrating its potential for effective utilization of solar energy. The scanning and transmission electron microscopic observations show that Ag 2 S nanoparticles with the size of about 20 nm are successfully embedded on the surface of leaf-like structure of CdS. Among the samples loaded with different molar percentages of Ag 2 S nanoparticles, the 5%-Ag 2 S/CdS composite photocatalyst exhibits a higher photocatalytic efficiency than the individually synthesized CdS and Ag 2 S for the degradation of Rhodamine B (RhB) and methyl orange (MO) under LED visible light irradiation. Furthermore, the 5%-Ag 2 S/CdS composite photocatalyst also exhibits a photocatalytic activity for the degradation of RhB under 850 and 940 nm monochromatic light irradiation. The results of the photocatalytic activity tests performed with various scavengers confirm that ·O 2 − plays a key role in the photodegradation of RhB. An enhanced photocatalytic performance of the Ag 2 S/CdS composite photocatalyst is directly attributed to the formation of a heterojunction between Ag 2 S and CdS. The developed composite photocatalyst can harness a greater share of the solar spectrum from visible to near infrared region and generate the photoinduced charge carriers more efficiently. Graphical Abstract

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TALANTA · 2020 · IF 5.339

Molecularly imprinted photo-electrochemical sensor for hemoglobin detection based on titanium dioxide nanotube arrays loaded with CdS quantum dots

Bowen Gao,Zhishan Liang,Dongxue Han,Fangjie Han,Wencai Fu,Wei Wang,Zhenbang Liu,Li Niu

A novel molecularly imprinted photo-electrochemical sensor based on CdS/TiO 2 nanocomposites was constructed for precisely detection of hemoglobin under visible light irradiation . CdS quantum dots were decorated on the surface of TiO 2 nanorod arrays to form a heterojunction, which could enhance the charge-transfer efficiency for visible light and further increase the photo-generated current of the sensor. The molecularly imprinted polymer film assembled by dopamine monomer had achieved excellent performance for specifically binding with human hemoglobin. The hemoglobin bound on the sensor could catalyze the oxidation reaction of 4-chloro-1-naphthol by H 2 O 2 , generating insoluble product on the sensor surface and triggering an obviously decrease on photocurrent . The molecularly imprinted photo-electrochemical sensor exhibited excellent sensitivity, selectivity and stability for the detection of human hemoglobin. The sensor had a linear range from 0.01 to 100 ng mL −1 with a detection limit of 0.53 pg/mL (S/N = 3). Furthermore, the sensor was successfully applied on the analysis of human hemoglobin in the urine samples.

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CHINESE JOURNAL OF CATALYSIS · 2020 · IF 6.146

Construction of LSPR-enhanced 0D/2D CdS/MoO3−x S-scheme heterojunctions for visible-light-driven photocatalytic H2 evolution

Jinjun Peng,Jun Shen,Xiaohui Yu,Hua Tang,Zulfiqar,Qinqin Liu

Plasmonic nonmetal semiconductors with localized surface plasmon resonance (LSPR) effects possess extended light-response ranges and can act as highly efficient H 2 generation photocatalysts. Herein, an LSPR-enhanced 0D/2D CdS/MoO 3− x heterojunction has been synthesized by the growth of 0D CdS nanoparticles on 2D plasmonic MoO 3− x elliptical nanosheets via a simple coprecipitation method. Taking advantage of the LSPR effect of the MoO 3− x elliptical nanosheets, the light absorption of the CdS/MoO 3− x heterojunction was extended from 600 nm to the near-infrared region (1400 nm). Furthermore, the introduction of 2D plasmonic MoO 3− x elliptical nanosheets not only provided a platform for the growth of CdS nanoparticles, but also contributed to the construction of an LSPR-enhanced S-scheme structure due to the interface between the MoO 3− x and CdS, accelerating the separation of light-induced electrons and holes. Therefore, the CdS/MoO 3− x heterojunction exhibited higher photocatalytic H 2 generation activity than pristine CdS under visible light irradiation, including under 420, 450, 550, and 650 nm monochromic light, as well as improved photo-corrosion performance.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

ZIF-L-derived porous C-doped ZnO/CdS graded nanorods with Z-scheme heterojunctions for enhanced photocatalytic hydrogen evolution

Shuang Liang,Guozhe Sui,Jinlong Li,Dongxuan Guo,Ze Luo,Rongping Xu,Hong Yao,Chao Wang,Shijie Chen

This study presents a novel approach for synthesizing C–ZnO/CdS graded nanorods derived from metal–organic frameworks (MOFs) that can be applied as a catalyst for photocatalytic hydrogen evolution from pure water. Porous C-doped ZnO was prepared by a self-template method using imidazole-like metal–organic backbone (ZIF-L) as a precursor through a two-step calcination method. CdS nanoparticles were deposited on ZIF-L surface by chemical deposition . The two-step calcination method introduced elemental C, and the unique architecture of ZIF-L played an essential role in forming the hierarchical structure of the porous ZnO nanorods. Compared with other ZnO/CdS catalysts, the C-doped ZnO/CdS graded nanorods exhibited remarkable photocatalytic activity for hydrogen production . The highest hydrogen production rate of 20.25 mmol g −1  h −1 with an apparent quantum yield (AQY) of 24.7% at 365 nm obtained over C–ZnO/CdS with Pt as co-catalyst, which was 24.4 and 65.3 times higher than that over CdS (0.83 mmol g −1  h −1 ) and ZnO (0.31 mmol g −1  h −1 ), respectively. This outcome was attributed to (i) the formation of Z-scheme heterojunction that significantly promoted the separation and migration of photogenerated electron–hole pairs; (ii) C doping that reduced the bandgap of ZnO and broadened its spectral response range; and (iii) the ordered arrangement of porous nanorods that effectively reduced the recombination rate of the electron–hole pairs.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Construction of mechanically robust and recyclable photocatalytic hydrogel based on nanocellulose-supported CdS/MoS2/Montmorillonite hybrid for antibiotic degradation

Yiying Yue,Shuting Shen,Wanli Cheng,Guangping Han,Qinglin Wu,Jianchun Jiang

A novel photocatalytic hydrogel was prepared by the direct coagulation casting of CdS/MoS 2 /Montmorillonite (CMMt) and TEMPO-oxidized cellulose nanofiber (TOCN)-mediated polyacrylamide (PAM). The extremely high specific surface area of CdS/MoS 2 /Mt and the three-dimensional network-structured PAM-TOCN matrix contributed to the adsorption of tetracycline (TC) in wastewater treatment . The effect of the initial pH on the degradation of TC by PAM-TOCN-CMMt was analyzed, and its degradation rate reached 90.03% in 120 min at pH 7.5. In addition to being a visible-light-driven catalyst, CdS/MoS 2 /Mt acts as a reinforcing agent, and the tensile stress of PAM-TOCN-CMMt increased by 41% compared with that of PAM-TOCN. The compressive strength of TOCN-PAM-CMMt at an 80% strain level was 65% higher than that of PAM-TOCN. Thus, PAM-TOCN-CMMt, with high mechanical strength , offers multiple separations and recycling, and the TC removal rate is still more than 70.5% after five cycles. Moreover, the mechanism of TC degradation was proposed based on the photoelectric performance. The strong interaction between the CdS/MoS 2 heterojunction and the electronegative Mt is conducive to the effective separation and transportation of photogenerated electrons. The prepared nanocomposite hydrogels with a desirable catalytic degradation rate, mechanical strength, environmental friendliness , and recyclability are promising for the photodegradation of antibiotics.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Facile synthesis of magnetically retrievable Fe3O4/BiVO4/CdS heterojunction composite for enhanced photocatalytic degradation of tetracycline under visible light

Guoli Xu,Meiling Du,Tao Li,Yueping Guan,Chen Guo

Nowadays, designing photocatalysts with high activity and recyclability for the degradation of pollutants is still a challenging problem. In this paper, a novel Fe 3 O 4 /BiVO 4 /CdS (FBC) heterojunction photocatalyst was firstly fabricated by simultaneously decorating CdS on the surface of pristine Fe 3 O 4 and BiVO 4 in a low-temperature water bath system. The FBC photocatalyst can enhance the absorption range of visible light and facilitate the separation and transfer of charges. Simultaneously, it can also provide large specific surface area and excellent magnetic response. FBC-3 displayed the highest degradation rate of tetracycline (87.37%) under visible light irradiation. Moreover, the important parameters affecting the photocatalytic activity were investigated to simulate the degradation of TC in real aqueous system. More importantly, the synthesized magnetic photocatalyst exhibited good universal applicability, stability and reusability. The Z-scheme transfer pathway for improving photocatalytic performance was also proposed based on the results of radical trapping experiments, electron spin resonance (ESR) measurement, optical and photoelectrochemical analysis.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

In-situ constructing cobalt incorporated nitrogen-doped carbon/CdS heterojunction with efficient interfacial charge transfer for photocatalytic hydrogen evolution

Xuli Li,Yangqin Gao,Ning Li,Lei Ge

Designing an efficient heterojunction interface is an effective way to promote the electrons' transfer and improve the photocatalytic H 2 evolution performance. In this work, a novel hollow hybrid system of Co@NC/CdS has been fabricated and constructed. CdS nanospheres are anchored on the hollow-structured cobalt incorporated nitrogen-doped carbon (Co@NC) through a one-pot in-situ chemical deposition approach, forming an intimate interface and establishing an excellent channel to improve the electrons transfer and charge carriers separation between CdS and Co@NC cocatalyst , which immensely promotes the photocatalytic activity . The rate of photocatalytic H 2 evolution over hollow structured Co@NC/CdS heterojunction can be achieved 8.2 mmol g −1  h −1 , which is about 45 times of pristine CdS nanospheres . The photocatalytic H 2 evolution mechanism has been investigated by the techniques of photoluminescence (PL) spectra, photocurrent-time (i-t) curves, electrochemical impedance spectroscopy (EIS) etc. This work aims to provide a new way in developing of high-performance advanced 3D heterojunction for photocatalytic hydrogen evolution .

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2013 · IF 3.548

TiO2/CdS composite hollow spheres with controlled synthesis of platinum on the internal wall for the efficient hydrogen evolution

Xiaofeng Cui,Guiyuan Jiang,Ming Zhu,Zhen Zhao,Luchao Du,Yuxiang Weng,Chunming Xu,Dekai Zhang,Quanlai Zhang,Yuechang Wei,Aijun Duan,Jian Liu,Jinsen Gao

Solar driven semiconductor photocatalytic water splitting to produce hydrogen is an extremely charming process by storing photon energy in chemical bonds. In the present study, composite semiconductor TiO 2 /CdS was structured into uniform and porous double-shelled hollow sphere with cocatalyst platinum selectively loaded onto the internal wall. The SEM, TEM , STEM , XRD , BET and EDS elemental distribution etc. were employed to evidence the formation of the targeted photocatalyst . It was demonstrated that the material has a high efficiency of visible-light-driven hydrogen evolution (296 μmol·h −1 /10 mg) with an apparent quantum efficiency (QE) of 14.5% at wavelength of 420 nm. Comparative experiment analysis and time-resolved infrared absorption study suggested that the high photocatalytic activity of the catalyst is attributed to the vectorial electron transfer (CdS → TiO 2  → Pt) and the spatial separation of reduction and oxidation active surfaces achieved by the special morphology.

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