Abstract： Mn/Ba/Al2O3 catalyst for NO oxidation-storage and Pt/Ba/Al2O3 catalyst mixed with Mn/Ba/Al2O3 for NOx storage-reduction by hydrogen were investigated. The results showed that Mn/Ba/Al2O3 had large nitrogen ...Abstract： Mn/Ba/Al2O3 catalyst for NO oxidation-storage and Pt/Ba/Al2O3 catalyst mixed with Mn/Ba/Al2O3 for NOx storage-reduction by hydrogen were investigated. The results showed that Mn/Ba/Al2O3 had large nitrogen oxides storage capacity （397.9 μmolg^-1） under lean burn condition. When Pt/Ba/Al2O3 catalyst was mixed with Mn/Ba/Al2O3 in equal weight proportion, the NOx conversion increased between 250 ℃ and 500 ℃ under the dynamic lean-rich burn conditions, and the maximum NOx conversion increased from 95.4% to 98.2%. Mn/Ba/Al2O3 has promoted NOx storing in the lean stage and improved NOx reduction efficiency in the rich stage, these might result in higher NOx conversion over the low Pt loading content catalyst.展开更多
The ineluctable introduction of lithium salt to polymer solid-state electrolytes incurs a compromise between strength,ionic conductivity,and thickness.Here,we propose Al_(2)O_(3)-coated polyimide(AO/PI)porous film as ...The ineluctable introduction of lithium salt to polymer solid-state electrolytes incurs a compromise between strength,ionic conductivity,and thickness.Here,we propose Al_(2)O_(3)-coated polyimide(AO/PI)porous film as a high-strength substrate to support fast-ion-conducting polymer-in-salt(PIS)solid-state electrolytes,aiming to suppress lithium dendrite growth and improve full-cell performance.The Al_(2)O_(3)coating layer not only refines the wettability of polyimide porous film to PIS,but also performs as a high modulus protective layer to suppress the growth of lithium dendrites.The resulting PI/AO@PIS exhibits a small thickness of only 35μm with an outstanding tensile strength of 11.3 MPa and Young's modulus of 537.6 MPa.In addition,the PI/AO@PIS delivers a high ionic conductivity of 0.1 m S/cm at 25°C.As a result,the PI/AO@PIS enables symmetric Li cells to achieve exceptional cyclability for over 1000 h at 0.1 m A/cm2without noticeable lithium dendrite formation.Moreover,the PI/AO@PIS-based LiFePO4||Li full cells demonstrate outstanding rate performance(125.7 m Ah/g at 5 C)and impressive cycling stability(96.1%capacity retention at 1 C after 200 cycles).This work highlights the efficacy of enhancing the mechanical properties of polymer matrices and extending cell performance through the incorporation of a dense inorganic interface layer.展开更多
In this investigation, Pt–Ba–Ce/c-Al2O3 catalysts were prepared by incipient wetness impregnation and experiments were performed to evaluate the influence of H2 on the evolution mechanism of nitrogen oxides (NOx) st...In this investigation, Pt–Ba–Ce/c-Al2O3 catalysts were prepared by incipient wetness impregnation and experiments were performed to evaluate the influence of H2 on the evolution mechanism of nitrogen oxides (NOx) storage and reduction (NSR). The physical and chemical properties of the Pt–Ba–Ce/c- Al2O3 catalysts were studied using a combination of characterization techniques, which showed that PtOx, CeO2, and BaCO3, whose peaks were observed in X-ray diffraction (XRD) spectra, dispersed well on the c-Al2O3, as shown by transmission electron microscope (TEM), and that the difference between Ce3+ and Ce4+, as detected by X-ray photoelectron spectroscopy (XPS), facilitated the migration of active oxygen over the catalyst. In the process of a complete NSR experiment, the NOx storage capability was greatly enhanced in the temperature range of 250–350℃, and reached a maximum value of 315.3μmol·gcat^-1 at 350℃, which was ascribed to the increase in NO2 yield. In a lean and rich cycling experiment, the results showed that NOx storage efficiency and conversion were increased when the time of H2 exposure (i.e., 30, 45, and 60 s) was extended. The maximum NOx conversion of the catalyst reached 83.5% when the duration of the lean and rich phases was 240 and 60 s, respectively. The results revealed that increasing the content of H2 by an appropriate amount was favorable to the NSR mechanism due to increased decomposition of nitrate or nitrite, and the refreshing of trapping sites for the next cycle of NSR.展开更多
Dehydrogenation of propane on Pt or Pt Sn catalyst over Al2O3 or SBA-15 support was investigated. The catalysts were characterized by CO-pulse chemisorption, thermogravimetry, temperature-programmed-reduction of H2,an...Dehydrogenation of propane on Pt or Pt Sn catalyst over Al2O3 or SBA-15 support was investigated. The catalysts were characterized by CO-pulse chemisorption, thermogravimetry, temperature-programmed-reduction of H2,and diffuse reflectance infrared Fourier transform spectroscopy of absorbed CO. The results show that the platinum species is in oxidation state in the catalyst on Al2O3 support, so the catalyst must be reduced in H2 before dehydrogenation reaction. Addition of Sn improves the Pt dispersion, but the catalyst deactivates rapidly because of the coke formation. The interaction of Pt and Al2O3 is strong. On SBA-15 support, the platinum species is completely reduced to Pt0 in the calcination process, so the reduction is not needed. Addition of Sn improves the activity and selectivity of the catalyst. The interaction of Pt and SBA-15 is weak, so it is easy for Pt particles to sinter.展开更多
NOx storage and reduction(NSR)technology has been regarded as one of the most promising strategies for the removal of nitric oxides(NOx)from lean-burn engines,and the potential of the plasma catalysis method for NOx r...NOx storage and reduction(NSR)technology has been regarded as one of the most promising strategies for the removal of nitric oxides(NOx)from lean-burn engines,and the potential of the plasma catalysis method for NOx reduction has been confirmed in the past few decades.This work reports the NSR of nitric oxide(NO)by combining non-thermal plasma(NTP)and Co/Pt/Ba/γ-Al2O3(Co/PBA)catalyst using methane as a reductant.The experimental results reveal that the NOx conversion of NSR assisted by NTP is notably enhanced compared to the catalytic efficiency obtained from NSR in the range of 150°C–350°C,and NOx conversion of the 8%Co/PBA catalyst reaches 96.8%at 350°C.Oxygen(O_(2))has a significant effect on the removal of NOx,and the NOx conversion increases firstly and then decreases when the O_(2)concentration ranges from 2%to 10%.Water vapor reduces the NOx storage capacity of Co/PBA catalysts on account of the competition for adsorption sites on the surface of Co/PBA catalysts.There is a negative correlation between sulfur dioxide(SO_(2))and NOx conversion in the NTP system,and the 8%Co/PBA catalyst exhibits higher NOx conversion compared to other catalysts,which shows that Co has a certain SO_(2)resistance.展开更多
基金The National Natural Science Foundation of China （No. 20476032）Natural Science Foundation of Guangdong Province （No. 030951） are gratefully acknowledged for financial support for this project.
文摘Abstract： Mn/Ba/Al2O3 catalyst for NO oxidation-storage and Pt/Ba/Al2O3 catalyst mixed with Mn/Ba/Al2O3 for NOx storage-reduction by hydrogen were investigated. The results showed that Mn/Ba/Al2O3 had large nitrogen oxides storage capacity （397.9 μmolg^-1） under lean burn condition. When Pt/Ba/Al2O3 catalyst was mixed with Mn/Ba/Al2O3 in equal weight proportion, the NOx conversion increased between 250 ℃ and 500 ℃ under the dynamic lean-rich burn conditions, and the maximum NOx conversion increased from 95.4% to 98.2%. Mn/Ba/Al2O3 has promoted NOx storing in the lean stage and improved NOx reduction efficiency in the rich stage, these might result in higher NOx conversion over the low Pt loading content catalyst.
基金the financial support from the 261Project of MIIT and Natural Science Foundation of Jiangsu Province(No.BK20240179)。
文摘The ineluctable introduction of lithium salt to polymer solid-state electrolytes incurs a compromise between strength,ionic conductivity,and thickness.Here,we propose Al_(2)O_(3)-coated polyimide(AO/PI)porous film as a high-strength substrate to support fast-ion-conducting polymer-in-salt(PIS)solid-state electrolytes,aiming to suppress lithium dendrite growth and improve full-cell performance.The Al_(2)O_(3)coating layer not only refines the wettability of polyimide porous film to PIS,but also performs as a high modulus protective layer to suppress the growth of lithium dendrites.The resulting PI/AO@PIS exhibits a small thickness of only 35μm with an outstanding tensile strength of 11.3 MPa and Young's modulus of 537.6 MPa.In addition,the PI/AO@PIS delivers a high ionic conductivity of 0.1 m S/cm at 25°C.As a result,the PI/AO@PIS enables symmetric Li cells to achieve exceptional cyclability for over 1000 h at 0.1 m A/cm2without noticeable lithium dendrite formation.Moreover,the PI/AO@PIS-based LiFePO4||Li full cells demonstrate outstanding rate performance(125.7 m Ah/g at 5 C)and impressive cycling stability(96.1%capacity retention at 1 C after 200 cycles).This work highlights the efficacy of enhancing the mechanical properties of polymer matrices and extending cell performance through the incorporation of a dense inorganic interface layer.
基金the National Natural Science Foundation of China (51676090)the Natural Science Foundation of Jiangsu Province (BK20150513), and the Six Talent Peaks Project in Jiangsu Province.
文摘In this investigation, Pt–Ba–Ce/c-Al2O3 catalysts were prepared by incipient wetness impregnation and experiments were performed to evaluate the influence of H2 on the evolution mechanism of nitrogen oxides (NOx) storage and reduction (NSR). The physical and chemical properties of the Pt–Ba–Ce/c- Al2O3 catalysts were studied using a combination of characterization techniques, which showed that PtOx, CeO2, and BaCO3, whose peaks were observed in X-ray diffraction (XRD) spectra, dispersed well on the c-Al2O3, as shown by transmission electron microscope (TEM), and that the difference between Ce3+ and Ce4+, as detected by X-ray photoelectron spectroscopy (XPS), facilitated the migration of active oxygen over the catalyst. In the process of a complete NSR experiment, the NOx storage capability was greatly enhanced in the temperature range of 250–350℃, and reached a maximum value of 315.3μmol·gcat^-1 at 350℃, which was ascribed to the increase in NO2 yield. In a lean and rich cycling experiment, the results showed that NOx storage efficiency and conversion were increased when the time of H2 exposure (i.e., 30, 45, and 60 s) was extended. The maximum NOx conversion of the catalyst reached 83.5% when the duration of the lean and rich phases was 240 and 60 s, respectively. The results revealed that increasing the content of H2 by an appropriate amount was favorable to the NSR mechanism due to increased decomposition of nitrate or nitrite, and the refreshing of trapping sites for the next cycle of NSR.
文摘Dehydrogenation of propane on Pt or Pt Sn catalyst over Al2O3 or SBA-15 support was investigated. The catalysts were characterized by CO-pulse chemisorption, thermogravimetry, temperature-programmed-reduction of H2,and diffuse reflectance infrared Fourier transform spectroscopy of absorbed CO. The results show that the platinum species is in oxidation state in the catalyst on Al2O3 support, so the catalyst must be reduced in H2 before dehydrogenation reaction. Addition of Sn improves the Pt dispersion, but the catalyst deactivates rapidly because of the coke formation. The interaction of Pt and Al2O3 is strong. On SBA-15 support, the platinum species is completely reduced to Pt0 in the calcination process, so the reduction is not needed. Addition of Sn improves the activity and selectivity of the catalyst. The interaction of Pt and SBA-15 is weak, so it is easy for Pt particles to sinter.
基金by the National Engineering Laboratory for Mobile Source Emission Control Technology(No.NELMS2019A13)the National Key Research and Development Project of China(No.2019YFC1805505)+2 种基金the Shanxi Province Bidding Project(No.20191101007)the Major Science and Technology Projects of Shanxi Province(No.20181102017)State Key Laboratory of Organic Geochemistry(No.SKLOG-201909)。
文摘NOx storage and reduction(NSR)technology has been regarded as one of the most promising strategies for the removal of nitric oxides(NOx)from lean-burn engines,and the potential of the plasma catalysis method for NOx reduction has been confirmed in the past few decades.This work reports the NSR of nitric oxide(NO)by combining non-thermal plasma(NTP)and Co/Pt/Ba/γ-Al2O3(Co/PBA)catalyst using methane as a reductant.The experimental results reveal that the NOx conversion of NSR assisted by NTP is notably enhanced compared to the catalytic efficiency obtained from NSR in the range of 150°C–350°C,and NOx conversion of the 8%Co/PBA catalyst reaches 96.8%at 350°C.Oxygen(O_(2))has a significant effect on the removal of NOx,and the NOx conversion increases firstly and then decreases when the O_(2)concentration ranges from 2%to 10%.Water vapor reduces the NOx storage capacity of Co/PBA catalysts on account of the competition for adsorption sites on the surface of Co/PBA catalysts.There is a negative correlation between sulfur dioxide(SO_(2))and NOx conversion in the NTP system,and the 8%Co/PBA catalyst exhibits higher NOx conversion compared to other catalysts,which shows that Co has a certain SO_(2)resistance.
文摘以Al_2O_3为背层(硅溶胶为粘结剂),电熔BaZrO_3作为面层材料(钇溶胶为粘结剂),1550℃烧结后制成50 mm×25 mm×5 mm的Al_2O_3/BaZrO_3双陶瓷试样。通过光学显微镜(OM)、扫描电子显微镜(SEM)、X射线衍射仪(XRD)和EDS等手段观察了BaZrO_3层和Al_2O_3/BaZrO_3界面的显微结构,研究了BaZrO_3与Al_2O_3的界面反应。结果表明,面层由BaZrO_3基体和分布其上的大小10μm左右的Y稳定的ZrO_2晶粒组成;Al_2O_3/BaZrO_3界面发生反应形成厚约300μm的过渡层,界面反应生成物有BaO Al_2O_3、ZrO_2和Ba O Al_2O_32SiO_2。界面从单纯的BaZrO_3/Al_2O_3双陶瓷结构演变为BaZrO_3、ZrO_2、BaOAl_2O_3、BaOAl_2O_32SiO_2和Al_2O_3等多种物相组成的复杂结构。反应过程中Al元素基本不迁移扩散,BaZrO_3中Ba元素向Al_2O_3所在的位置扩散形成Ba O Al_2O_3,残留物形成一层条状ZrO_2,而BaOAl_2O_32SiO_2围绕着EC95(Al_2O_3+5%SiO_2)粉体颗粒周围生成。
