MICROCHEMICAL JOURNAL
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2022
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IF 5.304
Ziyu Xue,Dehong Bai,Yu Li,Qiankun Zhang,Tao shao,Peiqing Guo,Dongxia Zhang,Xibin Zhou
In this work, a simple strategy for the rapid detection of Ag + based on nitrogen, sulfur doped graphene quantum dots (N, S-GQDs) decorated platinum nanoclusters (PtNCs) was proposed for the first time. N, S-GQDs decorated PtNCs (N, S-GQDs@PtNCs) were prepared by a reduction method using ascorbic acid (AA) as reducing agent and N, S-GQDs as a stabilizer and morphology directing reagent, respectively. The N, S-GQDs@PtNCs have an excellent peroxidase activity, which could catalyze the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) by H 2 O 2 to lead to an obvious color change. However, Ag + could be reduced to Ag 0 by N,S-GQDs, and the Ag 0 covered the surface of N, S-GQDs@PtNCs causing its peroxidase activity to decrease. Ag + concentration could be quantified by measuring the maximum absorption signal at 652 nm for oxidized TMB with a wide linear range of 0.5–300.0 nM and a limit of detection (LOD) as low as 0.2 nM. In addition, satisfactory results were obtained for the detection of Ag + in actual water samples. The prepared colorimetric sensor had advantages such as simple operation, cost-effective, fast response, and visualization, and had great potential in detecting toxic Ag + in environmental.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Xiaoqing Yang,Huimin Xiang,Jianying Huang,Chuan Zhou,Ran Ran,Wei Wang,Wei Zhou,Zongping Shao
Lead-free inorganic Cs 2 AgBiBr 6 double perovskites have emerged as promising materials in perovskite solar cells (PSCs) to tackle the inferior stability and toxicity issues of organic–inorganic hybrid PSCs. However, the power conversion efficiencies (PCEs) of Cs 2 AgBiBr 6 solar cells are remarkably restricted by the intrinsic and extrinsic defects of Cs 2 AgBiBr 6 films. More specifically, the fast crystallization process in the formation of Cs 2 AgBiBr 6 films strongly prevents the homogeneous growth of perovskite crystals, leading to inferior Cs 2 AgBiBr 6 film quality. This work introduces a facile strategy to retard the crystallization of Cs 2 AgBiBr 6 perovskites by introducing Lewis base additives into the precursor solution. The incorporation of a strongly coordinated thiourea additive with a sulfur donor leads to the generation of a Lewis acid base adduct, which retards the crystallization process for Cs 2 AgBiBr 6 crystals, improves the quality of the Cs 2 AgBiBr 6 film, decreases the defect density and inhibits charge carrier recombination. After optimization, the cell delivers a superior PCE of 3.07%, surpassing that reported for most Cs 2 AgBiBr 6 -based solar cells in the literature, and exhibits outstanding stability with a PCE retention rate of 95% after 20 days of storage in air. This work provides an effective strategy for further improvements in the performance of inorganic lead-free Cs 2 AgBiBr 6 -based photovoltaic cells .
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
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IF 9.965
Xi Chen,Songrong Li,Peizhen Yang,Yunfeng Chen,Cheng Xue,Yuhan Long,Jiayan Han,Jianming Su,Wenli Huang,Dongfang Liu
Peroxymonosulfate (PMS) heterogeneous catalysis dominated by nonradical pathway showed excellent adaptability for pollutant removal in complex water matrixes. Herein, ultra-small Fe-doped MoS 2 nanosheets with N-doped carbon intercalation (CF-MoS 2 ) were synthesized via a one-step hydrothermal method to treat high salinity organic wastewater. CF-MoS 2 exhibited an expanded interlayer spacing by 1.63 times and the specific surface area by 9 times compared with Fe-doped MoS 2 (F-MoS 2 ), substantially increasing the active sites. Homogeneous Fe 2+ catalytic experiments confirmed that the promotion of carbon intercalated MoS 2 (C-MoS 2 ) on Fe 3+ /Fe 2+ redox cycle was much higher than pure MoS 2 . Besides, the considerable removal of tetracycline (TC) under high salinity conditions (0–7.1%) was attributed to the dominant role of PMS nonradical oxidation pathways, including 1 O 2 and surface-bound radicals. The catalytic sites included Fe 3+ /Fe 2+ , Mo 4+ /Mo 5+ /Mo 6+ , C=O, pyridine N, pyrrolic N and hydroxyl groups . Finally, density functional theory (DFT) was employed to get the radical electrophilic attack sites and nucleophile attack sites of TC, and the results were consistent with the TC degradation products determined by HPLC-MS. This work would broaden the application of MoS 2 -based catalysts, especially for PMS catalytic removal of organic pollutants from high salinity wastewater.
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高影响因子
CELLULOSE
·
2022
·Vol. 29
·期 15
·8133-8150
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IF 6.123
Sun Liangyun,Han Juan,Tang Chaofan,Wu Jiacong,Fang Sihan,Li Yuanyuan,Mao Yanli,Wang Lei,Wang Yun
As an effective substitute for ionic liquids (ILs), deep eutectic solvents (DESs) are known as a new generation of green solvents. In addition, DESs are considered to be the best solvents to replace traditional organic solvents and ILs due to their advantages of economy, simple preparation and biodegradability, which can be used to further break through the technical bottleneck in the field of biomass pretreatment. This study synthesized a series of choline chloride-based (ChCl-based) DESs and used them to pretreat microcrystalline cellulose (MCC) without dissolution, in order to achieve the purpose of improving the saccharification effect. DES-9 (ChCl/hydroquinone), DES-12 (ChCl/acetamide) and DES-16 (ChCl/acetic acid) were better pretreatment solvents. The optimum conditions for the pretreatment of MCC by DES-9 and DES-12 were both at 110 °C for 4 h, and the optimum condition of DES-16 was at 90 °C for 4 h. Compared with untreated MCC (26.66%), the saccharification yield of pretreated MCC with DES-16 increased by 20.5%. Finally, the structure and morphology changes of MCC before and after pretreatment were investigated in detail through the degree of polymerization (DP), SEM and enzyme adsorption. The results showed that DESs pretreatment made the surface of MCC become rough, which enhanced the accessibility of cellulose and enzymes, improving the saccharification effect. Graphical abstract
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CHINESE JOURNAL OF STRUCTURAL CHEMISTRY
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2022
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IF 0.847
Zhaoyang An,Hui Xue,Jing Sun,Niankun Guo,Tianshan Song,Jiawen Sun,Yi-Ru Hao,Qin Wang
Integrating the advantages of anion vacancies and heterostructures into the catalytic materials may increase the binding affinities to intermediates, provide more active sites, and significantly promote the activity of overall water splitting. However, the successful assembly of anion vacancies and heterostructures for high-efficiency water splitting performance is still challenging. In this work, we ingeniously present the co-construction of sulfur vacancies and heterogeneous interface into Ni 3 S 2 /MoS 2 catalysts on nickel foam (NF). The introduction of sulfur vacancies and Ni 3 S 2 /MoS 2 heterostructures can significantly improve electron and ion transport, effectively improve structural stability, and enhance overall water splitting activity. The obtained V S -Ni 3 S 2 /MoS 2 catalysts (V S stands for sulfur vacancies) exhibit superior OER and HER activities, and the overpotentials for OER and HER are 180 and 71 mV at 10 mA·cm −2 , respectively. Furthermore, a low water splitting voltage of 1.46 V is required at 10 mA·cm −2 for the V S -Ni 3 S 2 /MoS 2 catalysts, which is considerably lower than most that of water splitting electrocatalysts currently reported. This work offers an effective mean for the preparation of catalysts with both anion vacancies and heterostructures for achieving high-performance alkaline overall water splitting.
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ACS Applied Materials & Interfaces
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2022
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IF 10.383
Yanping Guo,Jichun Zhu,Dongxing Kou,Wenhui Zhou,Zhengji Zhou,Shengjie Yuan,Yafang Qi,Yuena Meng,Litao Han,Zhi Zheng,Sixin Wu
The kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cells have shown a continuous rise in power conversion efficiencies in the past years. However, the encountered interfacial problems with respect to charge recombination and extraction losses at the CdS/CZTSSe heterojunction still hinder their further development. In this work, an additional plasmonic local electric field is imposed into the CdS/CZTSSe interface through the electrostatic assembly of a two-dimensional (2D) ordered Au@SiO2 NP array onto an aminosilane-modified surface absorber. The interfacial electric properties are tuned by controlling the coverage particle distance, and the finite-difference time domain (FDTD) simulation demonstrates that the strong near-field enhancement mainly occurs near the p-n junction interface. It is shown that the imposed local electric field leads to interfacial electrostatic potential (Velec) augmentation and improves the charge extraction and recombination processes. These electric benefits enable remarkable improvements in open-circuit voltage (Voc) and short-circuit current (Jsc), leading to the cell efficiency being increased from 10.19 to 11.50%. This work highlights the dramatic role of the plasmonic local electric field and the use of the 2D Au@SiO2 NP array to modify a surface absorber instead of the extensively used ion passivation, providing a new strategy for p-n junction engineering in kesterite photovoltaics.
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Zhuo-Rui Jiang,Pengfei Wang,Yu-Xiao Zhou,Changhua Wang,Jiwen Jiang,Yeqing Lan,Cheng Chen
An elastic and 3D-blocky catalyst (CoMnO x @sponge) was successfully prepared via uniform growth and distribution of Co-Mn bimetallic oxide inside the sponge for the activation of peroxymonosulfate (PMS). The results showed that 30 mg/L sulfisoxazole (SIZ) could be completely degraded by PMS (1 mM) activated with CoMnO x @sponge (0.1 g/L) within 5 min. The pseudo-first-order rate constant was calculated to be 1.83 min −1 , which was much larger than those from previous reports. The excellent stability and reusability of CoMnO x @sponge were confirmed through 20 recycle runs with more than 90% degradation of SIZ and less than 0.9 mg/L leached metal ions. Singlet oxygen ( 1 O 2 ), hydroxyl radicals ( • OH) and sulfate radicals (SO 4 •− ) were determined to be the dominating reactive oxygen species (ROS) responsible for the degradation of SIZ. The possible pathways of SIZ degradation as well as underlying catalytic mechanism were deduced. The bio-toxicity declined obviously after the mineralization of SIZ and the removal of TOC at 5 mg/L SIZ was high up to 90.4%. Furthermore, the system of CoMnO x @sponge/PMS also exhibited the strong anti-interference ability in natural water and the universal degradation capacity towards other common organic pollutants. More remarkably, the 3D-catalyst possessing an elasticity and extremely high porosity could be easily assembled with a column to realize the consecutive degradation of pollutants. The labor- and time-saving removal of pollutants based on a combination of CoMnO x @sponge with PMS makes it great potential in practical application.
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
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2022
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IF 5.141
Wenjing Wang,Xin Xin,Ke An,Yao Chen,Zhanfeng Zhao,Jiangdan Tan,Dong Yang,Zhongyi Jiang
Graphite carbon nitride (g-C 3 N 4 ) has a huge application potential in the photocatalysis field due to its unique conjugated structure. Inspired by the mussel adhesion protein, the cPTA/CNT/CNU (cPTA, carbonized poly(tannic acid); CNT, g-C 3 N 4 prepared by thiourea); CNU, g-C 3 N 4 prepared by urea) nanorod was synthesized by using PTA as the adhesive and template, and thiourea and urea as g-C 3 N 4 precursors. The CNT/CNU isotype heterojunction is assembled on the surface of porous cPTA nanorod, which effectively solves the problem of high photogenerated electron-hole recombination of pure g-C 3 N 4 . The optimal cPTA/CNT/CNU photocatalyst can degrade 95% of rhodamine B (RhB) within 1 h under visible light, which is much higher than CNT, CNU and CNT/CNU. With the conduction band potential difference of cPTA, CNT and CNU, a multistep electron transfer path forms in the cPTA/CNT/CNU, which can accelerate the electron transfer through the interface, thereby increasing the photocatalytic activity.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2022
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IF 6.371
Ya Xiong,Teng Liu,Xinyu Wang,Wendi Liu,Yanjun Xue,Xiaoli Zhang,Can Xiong,Jian Tian
Ultrathin CdS nanosheets (NSs) are intriguing in photocatalytic hydrogen evolution . Severe photo-corrosion and rapid recombination of electrons and holes, however, impair their applications. To solve this problem, a novel step-scheme (S-scheme) 2D CdS/W 18 O 49 heterostructure with strong interfacial interactions and large contact interface has been successfully designed. Due to the ultrathin structure of CdS, defect-rich W 18 O 49 NSs-assembled network, unique 2D heterostructure and state-of-the-art S-scheme mode, 40 wt% CdS/W 18 O 49 (CW40) shows a prominent photocatalytic H 2 production rate of 15.4 mmol g −1 h −1 . Besides, the apparent quantum efficiency of CW40 is up to 15.4 % under light at λ = 370 nm. Besides, the as-prepared CW40 can protect CdS from photo-corrosion, exhibiting outstanding stability over 24 h circular reaction. Our work provides an out-of-box solution to broaden the application potential of certain catalysts with inherent drawbacks and offers fresh insight into the design and preparation of highly-efficient 2D heterostructures for versatile applications.
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Journal of Pharmaceutical Analysis
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2022
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IF 14.026
Qiqin Wang,Lingjue Sun,Huihui Wu,Ning Deng,Xianglong Zhao,Jingwei Zhou,Tingting Zhang,Hai Han,Zhengjin Jiang
Zwitterionic sulfobetaine-based monolithic stationary phases have attracted increasing attention for their use in hydrophilic interaction chromatography. In this study, a novel hydrophilic polymeric monolith was fabricated through photo-initiated copolymerization of 3-(3-vinyl-1-imidazolio)-1-propanesulfonate (SBVI) with pentaerythritol triacrylate using methanol and tetrahydrofuran as the porogenic system. Notably, the duration for the preparation of this novel monolith was as little as 5 min, which was significantly shorter than that required for previously reported sulfobetaine-based monoliths prepared via conventional thermally initiated copolymerization. Moreover, these monoliths showed good morphology, permeability, porosity (62.4%), mechanical strength (over 15 MPa), column efficiency (51,230 plates/m), and reproducibility (relative standard deviations for all analytes were lower than 4.6%). Mechanistic studies indicated that strong hydrophilic and negative electrostatic interactions might be responsible for the retention of polar analytes on the zwitterionic SBVI-based monolith. In particular, the resulting monolith exhibited good anti-protein adhesion ability and low nonspecific protein adsorption. These excellent features seem to favor its application in bioanalysis. Therefore, the novel zwitterionic sulfobetaine-based monolith was successfully employed for the highly selective separation of small bioactive compounds and the efficient enrichment of N -glycopeptides from complex samples. In this study, we prepared a novel zwitterionic sulfobetaine-based monolith with good performance and developed a simpler and faster method for preparation of zwitterionic monoliths.
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CHEMICAL ENGINEERING SCIENCE
·
2022
·
IF 4.889
Zhufeng Hu,Yinxiang Xu,Wenchao Xiang,Xiaodong Guo,Yuchen Tong,Junbo Xu,Chao Yang
The oxygen evolution reaction (OER) is the key to prepare electrocatalysts for water splitting. Heteroatom doping is an effective way to improve the catalytic performance of OER by modulating the local electronic environment and stimulating the synergy. However, the complicated manufacturing methods have hindered their practical application. Herein, we demonstrate a method based on FeOOH/CC precursor to realize the preparation of Ni-P-S@FeOOH/CC catalyst through fast electrodeposition method. The overpotential of Ni-P-S@FeOOH/CC catalyst is 210 mV (10 mA cm −2 ), and still has an initial voltage of 97.35 % for 48 h. The surface area analysis shows a higher electrochemically active surface area for the amorphous structure prepared by electrodeposition method. XPS and DFT results show that the co-doping of P and S can stimulate the synergistic effect and the minimum energy of adsorption/desorption in OER process is only 0.83 eV. The strategy shows good prospects for preparing efficient OER pre-catalysts.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 29
·期 48
·73282-73291
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IF 5.19
Sun Yubing,Xiao Jingting,Huang Xinshui,Mei Peng,Wang Huihui
CdS-based composites as the highly efficient photocatalyst have been extensively investigated in recent years due to the suitable band gap and high photocatalytic efficiency. In this study, the effect of various factors (pH, U(VI) concentration, contents, and types of photocatalyst) on photocatalytic reduction of U(VI) by MoS 2 /CdS composite was investigated. The optimized experimental conditions (e.g., pH 7.0, 20 mg/g U(VI), and 1.0 g/L photocatalyst) was obtained by batch techniques. Approximately 97.5% of U(VI) was photo-catalytically reduced into U(IV) by 2.5 wt% MoS 2 /CdS composite within 15 min. After 5 cycles, 2.5 wt% MoS 2 /CdS composite still exhibited the high removal efficiency of U(VI) under 50-min irradiation, indicating the good stability. The photo-reduction mechanism of U(VI) on MoS 2 /CdS composite was attributed to the O − 2 radicals by quenching experiments, ESR, and XPS analysis. The findings indicate that CdS-based catalyst has a great potential for the photocatalytic reduction of uranyl in actual environmental remediation.
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