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RSC Advances · 2014 ·Vol. 4 ·期 52 ·27259-27266 · IF 3.708

Continuous heterogeneous cyclohexanone ammoximation reaction using a monolithic TS-1/cordierite catalyst

Libin Yang,Feng Xin,Junzhong Lin,Zhuang Zhuang,Rui Sun

In this study, a hydrothermal synthesis was developed to prepare a thin titanium silicalite-1 catalyst layer in the internal channels of the honeycomb cordierite support, which was used in a continuous heterogeneous reaction. The as-prepared thin TS-1 catalyst layer was characterized by SEM, XRD, UV-vis and ATR-FTIR methods. Multiple hydrothermal syntheses were used for controlling the crystalline growth to optimize catalytic activity and lifetime. Moreover, a monolithic TS-1/cordierite reactor with external looping was utilized to investigate the characteristics of the continuous heterogeneous ammoximation reaction without the organic solvent tert-butanol (TBA). The reaction results showed that the conversion of cyclohexanone and selectivity of oxime approached more than 0.96 and 0.98, respectively. When compared with the reaction using TBA as the reaction solvent, the activity of the monolithic TS-1/cordierite showed no differences except for a longer lifetime.

研究领域: 化学工程 · 催化化学 · 材料科学 · 工业化学 · 绿色化学
✓ 已验证 DOI 高影响因子
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Science China-Materials · 2023 ·Vol. 66 ·期 5 ·1810-1819 · IF 8.1

Anchoring palladium nanoparticles on CsPbBr3 perovskite nanocrystals for enhanced photocatalytic CO2 reduction

Xiao Hongbin,Qian Qingkai,Zang Zhigang

Recently, all-inorganic cesium lead halide (CsPbX 3 (X = Cl, Br, and I) perovskite nanocrystals (NCs) have been extensively investigated for photocatalytic carbon dioxide (CO 2 ) reduction reaction (CO 2 RR). However, because the pristine CsPbX 3 NCs suffer from severe radiative recombination, it is imperative to elaborately design heterostructures to separate electron-hole pairs for achieving efficient CO 2 RR. Herein, palladium (Pd) nanoparticles (NPs) are anchored on CsPbBr 3 NCs by a photo-assisted approach for the first time. The as-prepared CsPbBr 3 @Pd NCs not only build Schottky junctions at the CsPbBr 3 /Pd interfaces that promote the carrier separation and suppress the radiative recombination, but also exhibit lower energy barriers for photocatalytic CO 2 RR than pristine CsPbBr 3 NCs according to the density functional theory calculations. The electron consumption rate reaches a striking peak of 46.2 µmol g −1 h −1 by using CsPbBr 3 @Pd NCs as photocatalysts for CO 2 RR, which is 4.8-fold of the counterpart of pristine CsPbBr 3 NCs. This work not only presents a photo-assisted strategy for anchoring Pd NPs on CsPbBr 3 NCs, but also demonstrates the great potential of using CsPbBr 3 @Pd NCs for photocatalytic CO 2 RR.

研究领域: 材料化学 · 光催化 · 纳米材料 · 环境化学 · 能源化学 · 半导体物理 · 催化化学
✓ 已验证 DOI 高影响因子
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CHEMOSPHERE · 2020 · IF 5.778

Efficient removal of 2,2′,4,4′-tetrabromodiphenyl ether with a Z-scheme Cu2O-(rGO-TiO2) photocatalyst under sunlight irradiation

Kexin Chen,Xi Wang,Pengfei Xia,Jinxin Xie,Jing Wang,Xukai Li,Yiming Tang,Laisheng Li

Z-scheme Cu 2 O-(rGO-TiO 2 ) photocatalyst was successfully synthesized via a simple three-step approach for 2,2′,4,4′-tretrabromodiphenyl ether (BDE47) reductive removal under simulated solar irradiation. Unlike the traditional heterojunction , the addition of reduced graphene oxide (rGO) enhanced the redox ability of Cu 2 O-TiO 2 by increasing charge transfer. When modifying Cu 2 O films by adding 1% rGO and coating with 70% TiO 2 , the resulting Cu 2 O-(rGO-TiO 2 ) exhibited the best photocatalytic activity for BDE47 removal. The charge transfers of Cu 2 O-(rGO-TiO 2 ) were proven to follow a Z-scheme pathway through the electron paramagnetic resonance analysis. The degradation pathways of BDE47 were elucidated by identifying intermediate products via gas chromatography-mass spectrometry (GC-MS) and gas chromatography (GC). Photo-electrons (e − ) generated from the conduction band of Cu 2 O and hydrogen protons (H 0 ) reduced from H + in water were the main contributing elements for the removal of BDE47, which response to the ortho and para debromination . Ortho-Br of BDE47 was attacked by e − and BDE28 was the dominant debromination product on the first stage. Then e − and H 0 attacked ortho-Br and para-Br of BDE28 to form BDE15 and BDE8, respectively. The concentration of BDE8 was higher than that of BDE15, suggesting that H 0 played the most important role on the second debromination stage. An effective Cu 2 O-(rGO-TiO 2 )-based Z-scheme system for BDE47 debromination was proposed in this study, which may contribute to the development of novel green technologies.

研究领域: 环境科学 · 光催化化学 · 环境污染与控制 · 材料科学 · 绿色技术 · 有机污染物降解
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International Journal of Electrochemical Science · 2023 ·Vol. 12 ·期 6 ·5421-5430 · IF 1.5

Membrane Separators Coated by TiO2-PMMA with Low Thermal Shrinkage Rate for Lithium-Ion Batteries

Yangyang Xi,Peng Zhang,Haining Zhang,Zhaohui Wan,Wenmao Tu,Haolin Tang

Composite membrane separators are fabricated by coating one side of microporous polyethylene membrane with poly(methyl methacrylate) modified titanate nanoparticles that are synthesized through emulsifier-free emulsion polymerization of methacrylate-functionalized titanate nanoparticles. The formed composite membrane separators exhibit great thermal-shrinking resistance due to the introduction of thermal resistant titanate nanoparticles. After immersed into electrolyte solution, the swelling poly(methyl methacrylate) microspheres leads to the formation of gel electrolyte, thus stabilizing the electrolyte. Moreover, the porous structure of the coated layer can facilitate the swelling of electrolyte and the transport of lithium ions. The thus-assembled lithium ion battery shows an improved cycle performance and rate capability.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子纳米复合材料 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2016 · IF 6.333

Efficient and stable iron based perovskite La0.9Ca0.1Fe0.9Nb0.1O3-δ anode material for solid oxide fuel cells

Xiaowei Kong,Xiaoliang Zhou,Yu Tian,Xiaoyan Wu,Jun Zhang,Wei Zuo,Xiaobo Gong,Zhanhu Guo

A novel La 0.9 Ca 0.1 Fe 0.9 Nb 0.1 O 3-δ (LCFNb) perovskite for solid oxide fuel cells (SOFCs) anode is prepared by means of the citrate-nitrate route and composited with Ce 0.8 Sm 0.2 O 1.9 (SDC) by impregnation method to form nano-scaled LCFNb/SDC anode catalytic layers. The single cells with LCFNb and LCFNb/SDC impregnated anodes both achieve relatively high power output with maximum power densities (MPDs) reaching up to 610, 823 mW·cm −2 in H 2 at 800 °C, respectively, presenting a high potential of LCFNb for use as SOFCs anode. The power outputs of the single cells with LCFNb/SDC composite anode in CO and syngas (CO H 2 mixture) are almost identical to that in H 2 at each testing temperature. This composite anode also presents excellent durability in both H 2 and CO for as long as 50 h, showing desirable anti-reduction and carbon deposition resistance abilities. Besides, the cell output is stable in 100 ppm H 2 S H 2 atmospheres for 20 h at a current density of 600 mA·cm −2 with negligible sulfur accumulation on the anode surface . Hence, a novel iron based perovskite LCFNb anode with remarkable cell performance, carbon deposition resistance and sulfur poisoning tolerance for SOFCs is successfully obtained.

研究领域: 材料科学 · 电化学 · 能源材料 · 无机非金属材料 · 功能陶瓷 · 清洁能源技术
✓ 已验证 DOI 高影响因子
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DYES AND PIGMENTS · 2021 · IF 4.889

Tetrakis (N-phenothiazine) spirobifluorene-based hole-transporting material towards high photovoltage perovskite photovoltaics for driving electrochromic devices

You Liu,Fang Liu,Jungan Wang,Hongyan Huang,Suhao Yan,Song Gao,Lin Wang,Wei Huang,Tianshi Qin

Wide-bandgap photovoltaics (WBPV) could not only provide electrical energy by photoelectronic conversion of the invisible part of the solar spectrum, but also usually had the unique advantage of high open circuit voltage ( V oc). In this work, we reported a novel HTM based on tetrakis (N-phenothiazine) Spirobifluorene (Spiro-PT), its HOMO energy level could be well matched with MAPbBr 3 perovskite HOMO energy level. This HTM could effectively suppress nonradiative recombination, which leads to an increase in the photovoltage of WBPV to more than 1.41 V. As a result, the n-i-p mesoscopic structured WBPV achieved a champion PCE of 7.36% as well as excellent operational stability exhibiting 91% of initial efficiency after 500 h continuous illumination without encapsulation. Based on the high V oc of the MAPbBr 3 /Spiro-PT device, the photovoltaic electrochromic device showed a response speed (the average coloring time was 40 s and the bleaching time was 272 s) and high average visible light transmittance contrast (about 37% in 450–780 nm), the corresponding electrochromic device with maximum dynamic contrast up to 46% at 600 nm between bleached and colored states. This WBPV-powered electrochromic system could provide a pathway towards stand-alone smart window technique for future energy-saving buildings.

研究领域: 材料科学 · 光伏技术 · 纳米能源 · 智能窗技术 · 器件物理
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2016 · IF 6.333

Integrated plasmonic and upconversion starlike Y2O3:Er/Au@TiO2 composite for enhanced photon harvesting in dye-sensitized solar cells

Fanli Meng,Yi Luo,Yali Zhou,Jinwen Zhang,Yanzhen Zheng,Guozhong Cao,Xia Tao

A plasmon-enhanced upconversion composite Y 2 O 3 :Er/Au@TiO 2 (SYE/A@T) with a three-dimensional starlike morphology is prepared and then mixed with submicron TiO 2 (200 nm) to form a multifunctional scattering layer in TiO 2 -based dye-sensitized solar cells (DSSCs). In such starlike micronsized upconverter, Au nanoparticle-assisted plasmon effect can intensify the upconversion emission of Y 2 O 3 :Er, and simultaneously TiO 2 coating can improve the charge transport within SYE/A@T. Therefore, the SYE/A@T shows extended light-absorbing range to near-infrared region and improved light-scattering ability, leading to an improved photovoltaic performance of DSSCs. With the optimum mixing ratio, a conversion efficiency of 8.62% is attained, which is a significant improvement of 27.6% compared with the cell without adding SYE/A@T. Our work provides a feasible strategy to prepare an upconversion composite with plasmon-enhanced emission and enable this composite to accommodate the DSSCs system and improve the conversion efficiency of DSSCs.

研究领域: 材料科学 · 光伏技术 · 纳米光学 · 能源材料 · 表面等离激元
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2020 ·Vol. 8 ·期 28 ·14162-14170 · IF 11.301

A SmBaCo2O5+δ double perovskite with epitaxially grown Sm0.2Ce0.8O2−δ nanoparticles as a promising cathode for solid oxide fuel cells

Zhihong Du,Keyun Li,Hailei Zhao,Xu Dong,Yang Zhang,Konrad Świerczek

Modified by Sm0.2Ce0.8O2−δ (SDC) nanoparticles (NPs), SmBaCo2O5+δ (SBCO) double perovskite oxide is evaluated as a promising cathode material for intermediate temperature solid oxide fuel cells. The SDC NPs are epitaxially grown on the surface of SBCO with (220) planes of SDC aligning smoothly to (020) or (100) planes of SBCO, forming a tight, coherent connection at the interface. The influence of this modification on thermal expansion, oxygen diffusion, electrical conductivity and electrochemical properties is investigated thoroughly in this work. The designed SBCO–SDC cathode material demonstrates a lower thermal expansion coefficient (TEC), ∼16.4 × 10−6 K−1, than that of the unmodified SBCO, ∼20.9 × 10−6 K−1. While SDC coating results in a decreased total electrical conductivity, it facilitates oxygen bulk diffusion and improves the surface exchange reaction kinetics. Coating with SDC NPs can accelerate the rate-determining process of dissociation of the absorbed molecular oxygen, especially at intermediate temperatures. Accordingly, the constructed symmetrical cell with the La0.8Sr0.2Ga0.8Mg0.2O3−δ (LSGM) electrolyte shows lower polarization resistance values, if the SBCO–SDC cathode is utilized. Also, the LSGM electrolyte-supported (300 μm) full cell is found to deliver a high power density of 800 mW cm−2 at 800 °C. Owing to the strong and coherent interfacial connection, the developed cathode demonstrates a relatively steady electrochemical performance.

研究领域: 材料科学 · 能源化学 · 电化学 · 无机功能材料 · 燃料电池技术
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Science China-Materials · 2016 ·Vol. 59 ·期 10 ·833-841 · IF 0

Ultrathin ALD coating on TiO2 photoanodes with enhanced quantum dot loading and charge collection in quantum dots sensitized solar cells

Shen Ting,Tian Jianjun,Li Bo,Cao Guozhong

TiO 2 nanocrystals are widely used in photoanodes for quantum dot solar cells (QDSCs) owing to their chemical stability and suitable energy band structure. However, surface defects and grain boundaries of TiO 2 nanocrystals photoanodes allow high surface charge recombination, which limits the performance of QDSCs. In this work, an ultrathin TiO 2 layer is introduced to the surface of TiO 2 photoanodes by atomic layer deposition (ALD). The ultrathin layer not only reduces the surface defects of TiO 2 nanoparticles and strengthens the connection between adjacent nanoparticles to suppress the charge recombination for improving the electron collection efficiency (η cc ), but also increases the surface energy of photoanodes to load more quantum dots (QDs) for enhancing the light harvesting efficiency (LHE). As a result, the solar cell based on CdS/CdSe QDs with ALD treatment exhibits an efficiency of 5.07% that is much higher than that of the cells without modification (4.03%).

研究领域: 材料科学 · 纳米科技 · 能源化学 · 光伏技术 · 表面工程 · 半导体物理 · 光电转换
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JOURNAL OF NANOPARTICLE RESEARCH · 2022 ·Vol. 24 ·期 3 ·69 · IF 2.533

Macro-prepared Cs4PbBr6/CsPbBr3 perovskite screen printing inks

Song Rong,Li Ying,Qian Jun

Perovskite has shown attractive optoelectronic performances and is a potential material in lighting, anti-counterfeiting, sensor, and other optoelectronic devices. Recently, spin-coating has been widely used in fabricating high-performance perovskite films, but it is difficult to process and apply in practice. In this paper, the CsPbBr 3 /Cs 4 PbBr 6 composite perovskite quantum dots with photoluminescence quantum yield of 36% and high storage stability were prepared by using room temperature ligand-assisted precipitation method and controlling the proportion of CsBr/PbBr 2 . In addition, the composite perovskite was ground and dispersed in the inks system. After adjusting the composition and ratio of the resin components, the inks were suitable for screen printing with a viscosity of 2439 mPa•s, an initial dryness of 25 mm/30 s, and a thorough dryness of 100 s/100 μm. By printing, the perovskite films exhibited high coverage, strong green emission, and outstanding fluorescence recovery ability after exposure to water. Screen printing perovskite inks have the characteristic of being patternable, which provides a solution for preparing a perovskite film in the application.

研究领域: 材料科学 · 纳米科技 · 光电子学 · 印刷电子 · 荧光材料
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OPTICAL MATERIALS · 2022 · IF 3.754

Enhancing performance of tin-based perovskite solar cells by polyvinyl pyrrolidone doping strategy

Ziang Xie,Ping Wu,Sen Chen,Shiping Zhang,Yili Pei,Li Li,Guodong Fu,Ying Xie,Haochen Guan,Yun Xing,Jianzhang Zhu,Xinran Wang

The power conversion efficiency (PCE) of tin-based perovskite solar cells (TPSCs) was significantly improved when polyvinyl pyrrolidone (PVP) was doped into the formamidinium tin iodide (FASnI 3 ) layer with an optimized doping mass. After doping, the FASnI 3 grain size, film smoothness and average carrier lifetime were largely enhanced, which demonstrate the crystallization quality improvement to FASnI 3 . The champion PCE of the enhanced TPSC was improved to 7.83%, which is relatively 27% larger than that of the control, 6.15%. After continuous storage for 15 days, the PCE of the enhanced TPSC remained 74.4% of its original value. Using the finite difference time domain (FDTD) simulation method, we demonstrated that the light absorption ratio of the FASnI 3 :PVP layer was larger than that of the FASnI 3 , and the photo-generated carrier density of the enhanced TPSC was approximately 2% ∼ 3% larger than that of the control. The ultimate efficiency of the enhanced TPSC was calculated to be 26.23%. It is potential to dope PVP into FASnI 3 to further enhance the device performance of TPSCs.

研究领域: 材料科学 · 光伏技术 · 纳米科技 · 表面化学 · 半导体器件
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Promoting effective electrochemical oxidation of CO by Cu-doping for highly active hybrid direct carbon fuel cell anode

Xiao Yang,Minjian Ma,Chunming Xu,Rongzheng Ren,Jinshuo Qiao,Wang Sun,Kening Sun,Zhenhua Wang

Hybrid direct carbon fuel cells (HDCFCs) present its inherent and unparalleled advantages in converting chemical energy from organic waste, biomass, and coal directly into clean energy with high efficiency. However, the progress of HDCFC technology continues to be hampered by the sluggish anode reaction kinetics. Herein, an effective design strategy for HDCFC anode is proposed, a Cu-modified Sr 2 Fe 1.3 Cu 0.2 Mo 0.5 O 6-δ (SFCM) perovskite oxide is developed to meet the requirements of intermediate-temperature HDCFC anode. The Cu-doping SFCM anode demonstrates excellent redox structural stability and catalytic activity. In addition, the electrolyte-supported single cell with Cu-doping SFCM anode has improved the peak power density from 285.5 mW cm −2 to 489.3 mW cm −2 at 800 °C with activated carbon as the fuel. The significantly enhanced anode catalytic activity is primarily due to the improved interfacial activity and chemical adsorption of CO. Therefore, the present work shows an effective strategy for designing and developing novel high-performance HDCFCs anode materials .

研究领域: 能源材料 · 电化学 · 燃料电池 · 功能材料 · 催化化学
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