ChemNanoMat
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2018
·Vol. 4
·期 5
·487-495
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IF 3.173
Zhinian Li,Shenliang Wang,Wei Hong,Shihui Zou,Liping Xiao,Jie Fan
Graphical Smart screens : An intelligent approach was developed to screen Na−Mn−W/SiO 2 catalysts for the oxidative coupling of methane (OCM). Effective composition regions other than the standard composition were successfully excavated. The wide range of the optimal composition allowed a fluctuation of composition during the reaction, which secured its excellent stability in the OCM reaction. Optimizing the performance and understanding the mechanism of metal oxide catalysts in the oxidative coupling of methane (OCM) is one of the most important projects in industrial catalysis. Here, we report an intelligent approach to screen Na−Mn−W/SiO 2 catalysts for the OCM reaction via ink-jet printing and multidimensional group testing. The ink-jet-printing-assisted (IJP-A) synthetic methodology ensured a fast synthesis of 1536 catalysts that were evaluated in 24 tests via a multidimensional group testing strategy (m-GT). After two-round synthesis-and-screening processes, several excellent groups with different composition space were screened out. Among the excellent catalysts, the OCM performance of Na−Mn−W/SiO 2 catalyst with higher Na, Mn and W content (G3 and G7) was less sensitive to its constituent than that of Na−Mn−W/SiO 2 catalyst with lower Na, Mn and W content (G1). These results indicated the sensitivity of performance to its Na, Mn and W content decreased in larger Na, Mn and W spaces, consistent with the complex homogeneous/heterogeneous reaction mechanism and multi-active sites. A series of Na−Mn−W/SiO 2 formulas with good performance also provide a reasonable explanation to its excellent stability for the OCM reaction. In addition, this intelligent optimization in total space offers a pathway to study the multicomponent metal oxide catalyst in the OCM reaction.
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高影响因子
MATERIALS CHEMISTRY AND PHYSICS
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2018
·
IF 2.21
Zhixiang Jiang,Yue Zhao,Ping Yang
Wire-in-tube and tube-in-tube structures have been prepared using single-spinneret electrospinning method through adjusting the preparation parameters of precursors and subsequent calcined process. Cobalt ferrite (CoFe 2 O 4 ) samples revealed wire-in-tube morphology using a Co/Fe molar ratio of 1/2. In the case of other a Co/Fe molar ratio, belt and porous fiber morphologies were created. Manganese ferrite (MnFe 2 O 4 ) sample exhibited tube-in-tube structure while nickel ferrite (NiFe 2 O 4 ) sample just exhibited tube structure. Because of no template in electrospun polymer composite nanofibers , the precursor diffusion process during calcination plays an important role for morphology controlling. The magnetic properties of samples were examined. The cobalt ferrite (CoFe 2 O 4 ) wire-in-tube sample revealed the highest saturation magnetization (60 emu/g). After growing with AlOOH on the surface, CoFe 2 O 4 wire-in-tube sample revealed a high efficiency for the removal of Congo red pollutant. These nanostructures are particularly attractive for use in the field of nano-fluidic and nano-energy harvesting devices.
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ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Qiujun Li,Hua Yao,Feng Liu,Zitao Gao,Yangyi Yang
A new Mn-doped coordination supramolecular network (CSN) was synthesized on nickel foam directly by a simple one-step hydrothermal method . Compared with the pure CSN electrode (∼2.46 C cm −2 at 10 mA cm −2 ), this Mn-doped binder-free electrode showed an ultrahigh areal capacity (∼8.12 C cm −2 at 10 mA cm −2 ). In addition, when the current density increased from 10 mA cm −2 to 50 mA cm −2 , it had a good rate capability with 73.33% capacitance retention. For practicality, an asymmetrical supercapacitor (ASC) was assembled by Activated Carbon (AC) electrode and the Mn-doped CSN electrode. The device not only could achieve a maximum energy density of 3.41 mW h cm −3 at the power density of 44.98 mW cm −3 , but also could exhibit excellent stability after 4000 cycles, with the capacitance retention of 90.14%. The above results indicate that the Mn-doped CSNs are promising electrode materials for supercapacitors in energy storage.
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Journal of Materials Chemistry C
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2024
·
IF 5.7
Tonghui Zhao,Yuqing Zhang,Lifei Wu,Qitong Zhong,Wei Xie,Bo Li,Dongling Geng,Haibo Zeng
In this research, we present an innovative, environmentally friendly, and cost-effective alcohothermal method for synthesizing Mn2+ and Mn2+–Cu+ doped 0D Cs3ZnCl5, a green luminescent material, marking the first time this approach has been reported. An exhaustive analysis of the luminescence properties of both undoped and doped Cs3ZnCl5 was conducted, with a particular emphasis on the energy transfer mechanisms in the Mn2+ mono-doped and Mn2+–Cu+ co-doped systems. The results demonstrate the successful construction of an efficient energy transfer pathway that significantly enhances the luminescence efficiency of Cs3ZnCl5:Mn2+. Specifically, the photoluminescence quantum yield of Mn2+ within the Cs3ZnCl5 matrix has been improved from 51.6% to 71.1%, thanks to the Cu+ codopant acting as an effective energy transfer mediator. A mechanism for the luminescence and energy transfer phenomena observed in the Mn2+–Cu+ co-doped Cs3ZnCl5 system has been also proposed. Furthermore, to assess the practical applicability of the synthesized materials, their structural and photoluminescent stability were evaluated. In essence, our study presents a promising solution to current challenges in the synthesis of advanced luminescent materials and opens up new possibilities for harnessing the potential of Mn2+-activated 0D metal halides in optoelectronic applications.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
He Ma,Dashuai Li,Yingying Li,Yuanyuan Li,Changhua Wang,Xintong Zhang
While photocatalytic technology has been recognized as an effective means for removing low-concentration NOx in ambient atmosphere, it still faces the challenge of the deep oxidation in high efficiency. In many cases, the release of more toxic NO 2 byproduct appeared to be inevitable during the photocatalytic oxidation of NO. Herein we report that the atomically dispersed MnO x cocatalyst on TiO 2 (B) microspheres could significantly enhance the deep oxidation of NOx under mild photocatalytic conditions (1 mW/cm 2 UV-A light, 1 L/min flow rate). At an initial NO concentration of 0.35 ppm, ca. 67.15% of NO is oxidized on the MT-0.5 sample, which is 2.76 times higher than the pristine TiO 2 (B) sample. More importantly, the release of NO 2 is suppressed by 2.11 times. Comprehensive spectral analyses suggest that atomically dispersed MnO x effectively promotes the charge separation of photogenerated carriers in TiO 2 (B), even better than MnO x nanoparticles-loaded TiO 2 (B). EPR and in-situ FTIR analyses illustrate that atomically dispersed MnO x -loaded TiO 2 (B) sample exhibits excellent low concentration NOx abatement performance, thus providing a rational mechanism for the NO deep oxidation pathway. This study not only provides a unique approach for preparing non-noble metal atomically dispersed co-catalysts, but also affords an effective means for efficient photocatalytic NO degradation.
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CRYSTENGCOMM
·
2016
·Vol. 18
·期 8
·1384-1392
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IF 3.849
S. Ding,X. F. Yang,T. T. Deng,E. H. Song,Z. J. Ma,S. Ye,M. M. Wu,Q. Y. Zhang
Solid-solution phase K(Mn,Zn)F3 mesoporous microspheres have been successfully prepared via a simple one-pot hydrothermal method by using citrate ions as a chelating agent. Effects of the reaction time on the phase transformation and morphological evolution of the K(Mn,Zn)F3 microspheres have been carefully investigated. The results revealed that the hierarchical mesoporous spherical structures with a solid-solution phase were formed from a core–shell structure with mixed phases via the nanoscale Kirkendall effect. It is noted that Yb3+/Er3+-codoped K(Mn,Zn)F3 microspheres exhibit intense single-band red up-conversion emission with environmental responsivity upon excitation using a 980 nm laser diode, indicating a promising potential biomedical application for drug delivery.
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ELECTROCHIMICA ACTA
·
2016
·
IF 4.803
Ting Shen,Jianjun Tian,Lili Lv,Chengbin Fei,Yajie Wang,Tönu Pullerits,Guozhong Cao
Mn-doping into CdS quantum dots (QDs) has been demonstrated a useful way to enhance the power conversion efficiency (PCE) of quantum dot sensitized solar cells (QDSCs), the detailed systematic study is needed to get a better fundamental understanding. This work focuses on the study of the effects of Mn dopant on light harvesting, charge transfer, and charge collection of the solar cells. The results indicate that the Mn-doping into CdS QDs increases the light absorbance and extends the light absorption range, which results in the enhancement of the photo-generated current density. In addition, both the electron transport rate and the electron diffusion length are also increased with the introduction of Mn dopant. So the charge collection efficiency ( η cc ) of the solar cell increases from 89.9% for CdS sample to 96.7% for Mn/CdS sample. As a result, the PCE of Mn/CdS QDSC reaches 3.29%, which is much higher than that of CdS QDSC (2.01%).
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CRYSTENGCOMM
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2012
·Vol. 14
·期 24
·8440-8445
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IF 3.842
Tingting Yao,Shufang Kou,Yanghui Sun,Qing Zhao,Jian Yang
Transition-metal doping in semiconductors is an important way to modulate their intrinsic properties or bring out new functionalities for applications. Here, elongated Mn-doped ZnSe1−xSx nanocrystals are synthesized through a facile one-pot reaction under mild conditions. These ZnSe1−xSx nanocrystals with a diameter of 2–4 nm have a cubic phase structure. EPR and PL spectra confirm the successful doping of Mn2+ into the ZnSe1−xSx nanocrystals, based on the corresponding hyperfine splitting constants and emission bands. The temporal evolution of UV-vis absorption and PL spectra indicates the growth-doping mechanism for the formation of the doped nanocrystals. Surface coating of these nanocrystals with a shell increases the quantum yield up to 35%. And the dual-function role of 1-dodecanethiol is confirmed in the formation of the elongated Mn-doped ZnSe1−xSx nanocrystals.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2013
·Vol. 25
·期 2
·754-759
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IF 1.486
Liu Lu,Huang Miaoliang,Lan Zhang,Wu Jihuai,Shang Guanglu,Liu Guijing,Lin Jianming
Mn-doped CdS quantum dot sensitized solar cells based on SnO 2 microsphere photoelectrodes are prepared with successive ionic layer adsorption and reaction method. It is found that with Mn-doped CdS quantum dot sensitizers, the photovoltaic performance of the cells based on SnO 2 microsphere photoelectrodes can obviously be enhanced. The reasons are owing to the improved light absorption and the expanded light absorption edge by doping Mn in CdS quantum dots. The electrochemical impedance spectroscopy analysis found that the cells with Mn-doped CdS quantum dot sensitized SnO 2 microsphere photoelectrodes can efficiently suppress dark reaction, owing to the increased related resistance. Moreover, it is also found that the Mn-doped CdS quantum dot sensitized SnO 2 microsphere photoelectrode can increase the electron diffusion lifetime in the cell. The power conversion efficiency of the cell with 4 wt% Mn-doped CdS quantum dot sensitizers can attain to 2.80 %, with 53 % enhancement compared with that of the CdS quantum dot sensitized cell (1.83 %).
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LUMINESCENCE
·
2013
·Vol. 29
·期 2
·151-157
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IF 1.273
Wei Bian,Jing Ma,Qiaoling Liu,Yanli Wei,Yingfu Li,Chuan Dong,Shaomin Shuang
N -acetyl- l -cysteine-capped Mn-doped ZnS quantum dots (QDs) were prepared by hydrothermal methods. It could emit phosphorescence at 583 nm with the excitation wavelength at 315 nm. The phosphorescence intensity of QDs could be quenched dramatically by increasing the concentration of Co 2+ ion. The novel phosphorescence sensor based on N -acetyl- l -cysteine-capped QDs was developed for detecting Co 2+ ion with a linear dynamic range of 1.25 × 10 –6 –3.25 × 10 –5 m . The limit of detection and RSD were 6.0 × 10 –8 m and 2.3%, respectively. Interference experiments showed excellent selectivity over numerous cations such as alkali, alkaline earth and transitional metal ions. The possible quenching mechanism was also examined by phosphorescence decays. The proposed phosphorescence method was further applied to the trace determination of Co 2+ ion in tap and pond water samples with recoveries of 97.75–103.32%. Copyright © 2013 John Wiley & Sons, Ltd.
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PubMed
高影响因子
JOURNAL OF ENVIRONMENTAL MANAGEMENT
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2025
·
IF 8.4
Mei Lin,Miao Wang,Jianwang Wu,Ming Liu,Zuliang Chen
Since the widespread use of antibiotics, the residues of antibiotics have frequently been detected in various water sources, making antibiotic pollution an urgent environmental issue. In this paper, one-step green synthetic reduced graphene/manganese nanoparticles (rGO/Mn NPs) composites have been utilized as a novel environmentally-friendly catalyst for tetracycline (TC) removal. The results demonstrated that rGO/Mn NPs exhibit excellent adsorption performance for TC, and can efficiently activate sodium persulfate (PDS) to oxidize and degrade TC. Furthermore, the rGO/Mn NPs adsorption-oxidation system (85.2%) was more effective than the adsorption process (70.9%) in removing TC (50 mg L −1 ). Free radical quenching experiments and EPR results elucidated that singlet oxygen ( 1 O 2 ) and superoxide radicals (·O 2 − ) are the primary reactive species responsible for the degradation of TC in the oxidation system. Based on the characterization results, a mechanism of oxidative degradation of TC by rGO/Mn NPs has been proposed. To further elucidate the degradation pathway of TC, the degradation products were identified by high performance liquid chromatography-mass spectrometry (HPLC-MS). This analysis provides a foundation for understanding how the rGO/Mn NPs composites activate PDS to degrade TC. Additionally, the ecological structure-activity relationship analysis revealed that TC is converted into intermediates with lower toxicity.
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PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Ganghua Zhou,Yun Chen,Gaoran Chen,Hangmin Xu,Weiqin Yin,Bin Wang,Xingwang Zhu,Xin Ning,Paul K. Chu,Xiaozhi Wang,Hui Xu
Metal-organic frameworks (MOFs) with abundant pores are excellent adsorbents for metal ions. However, the subsequent treatment of used MOFs and their reutilization still lack promising solutions. Herein, the surface-restructured Mn-doped Cu 2 O (RM-Cu 2 O) catalyst containing asymmetric Mn−Cu sites is prepared by glucose reduction using the spent Cu-based MOF (HKUST-1) as the precursor. The RM-Cu 2 O catalyst shows good potential in tunable photocatalytic syngas (CO and H 2 ) production in a pure water system. The syngas ratios can be tuned from ∼1:2 to ∼1:1 by increasing CO production. DFT calculations and photoelectrochemical tests confirm that the asymmetric Mn−Cu sites on the RM-Cu 2 O catalyst accelerate the photogenerated charge transport and optimize CO 2 adsorption and activation. In situ irradiation X-ray photoelectron spectroscopy is conducted to investigate the dynamic charge transport and reactions on the RM-Cu 2 O catalyst. Based on in situ Fourier transform infrared spectroscopy and simulations, the mechanism of photocatalytic syngas production is elucidated. This work provides a promising solution for the resource utilization of the spent MOFs-based adsorbents and photocatalytic energy development.
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