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APPLIED CATALYSIS A-GENERAL · 2021 · IF 5.706

Efficient conversion of cellulose to lactic acid over yttrium modified siliceous Beta zeolites

Juan Ye,Chenyu Chen,Ying Zheng,Dan Zhou,Yunzhen Liu,Denglong Chen,Liufang Ni,Gang Xu,Fanan Wang

The selective one-pot synthesis of lactic acid (LA) from cellulose, and further the raw biomass, on heterogeneous catalysts is the key point for the development of biorefinery technology. Herein, we reported an yttrium (Y) modified siliceous Beta zeolites catalyst via two-step post-synthesis for highly efficient conversion of cellulose to LA. Under condition of 220 °C and 2 MPa N 2 , the cellulose could be transformed to LA with a yield of 49.2 % within 30 min, and the substrate can be extended to various raw biomass. It was demonstrated that the dealumination and modification of Y can efficiently modulate the acidity on the surface of zeolite. The dehydration products HMF and other derivatives were suppressed, and the yield of LA was correlated in line with the acid amount, which were attributed to the increased Lewis acidity originated by Y incorporation. These results contribute to the development of the green and efficient synthesis of bio-chemicals.

研究领域: 生物化学 · 催化化学 · 可再生资源
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COMPOSITES PART B-ENGINEERING · 2024 · IF 12.7

Regulation of charge transfer direction and key steps via Y modification of redox-active sites on borocarbonitride for photocatalytic CO2 reduction

Xianghui Zeng,Xuelin Bu,Hui Chen,Zhaohui Huang,Wei Fang,Daheng Wang,Xuan He,Xing Du,Weixin Li,Haijun Zhang,Lei Zhao

Hexagonal borocarbonitride (h-BCN) have garnered significant attention for their unique optoelectronic properties in solar-to-fuel conversions. However, the efficiency of h-BCN in the field of photocatalytic CO 2 reduction is limited by high reaction energy barriers and serious charge recombination. Here, a Y-modified h-BCN were synthesized through an organic-inorganic hybrid precursor pyrolysis method. Both theoretical simulation and experimental analysis demonstrated that the Y-modified sample exhibits an inhomogeneous charge distribution that favours rapid charge transfer and can decrease the reaction barrier of the rate-control step. Further investigations indicated that adding Y changes the electronic structure of BCN, which leads to rapid charge transfer/separation and an increased lifespan for photoinduced electrons. As a result, 2.5%Y/BCN exhibited improved CO 2 photoreduction activity with a fuel yield of 50.35 μmol g −1 . Notably, this outstanding performance was achieved without the use of any cocatalyst or sacrificial agent. In the meanwhile, cycle test shows the photocatalyst's great stability. The findings provide a useful suggestions for BCN-based photocatalysts.

CAS / MDL: 13494-98-9
研究领域: 材料科学 · 环境科学 · 化学工程
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Catalysis Science & Technology · 2022 ·Vol. 12 ·期 15 ·4871-4883 · IF 6.177

Highly active and stable cobalt catalysts with a tungsten carbide-activated carbon support for dry reforming of methane: effect of the different promoters

Yu Zhang,Zhoujie Liang,Guojie Zhang,Jun Liu,Ying Wang,Yuqing Zhao,Guoqiang Li,Yongkang Lv

Greenhouse effect has become one of the serious issues in the human development. Greenhouse gases are mainly composed of methane and carbon dioxide. Dry methane reforming (DMR) is an excellent technology owing to the direct utilization of greenhouse gases. However, there are severe catalyst sintering and coke deposits in the process of DMR. Therefore, it is necessary to synthesize catalysts with fantastic properties. Here, a series of cobalt catalysts modified by different transition metals (Y, Gd, and Mn) were synthesized applying the impregnation method. The Y-modified catalyst shows excellent catalytic activity and anti-coking ability. Under the reaction condition of 800 °C, the catalyst exhibits not only the highest CH4 conversion (83%) but also stable CO2 conversion (94%) after 10 h of reaction. N2 physisorption, TG, H2-TPR, XPS, XRD and TEM were applied to research the crystal phase, microstructure and texture characteristics of the catalysts. The results show that the Mn-modified catalyst exhibited a negative influence for the DMR reaction although the catalyst shows a large specific surface area. Gd- and Y-modified catalysts exhibited superior interaction between the metal and carrier, which improves the stability of active metal Co during DMR. Simultaneously, the introduction of Y maintains more number of oxygen vacancies and improves the dispersion of the active metal. The study found that both the activity and coke resistance of the catalyst can be concurrently enhanced due to the addition of Y through promoting the dispersion of the metal and the activation of CO2. Most noteworthily, after a 50 h stability test, the CH4 and CO2 conversion on the Y-modified catalyst dropped from 91% and 95% to 83% and 94%, respectively.

研究领域: 化学工程 · 环境科学
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Structural Regulation Enables High Interfacial Functionality for Ni-Rich Single-Crystalline Cathodes

Pei Liu,Haoran Wei,Tao Huang,Zhencheng Huang,Lingli Chen,Xuanlong He,Yuying Liu,Hongkai Yang,Mijie Liu,Shenghua Ye,Xuming Yang,Zhanhua Wu,Yaming Liu,Qingqing Jia,XiaoBai Ma,Jing Chen,Xiangzhong Ren,Xiaoping Ouyang,Jianhong Liu,Qianling Zhang,Jiangtao Hu

Ni-rich single-crystalline layered cathodes have garnered significant attention due to their high energy density and thermal stability. However, they experience severe capacity degradation caused by lattice strain and interfacial side reactions during practical applications. In this study, an effective yttrium modification method is employed to stabilize the structure of Ni-rich single-crystalline LiNi0.83Mn0.05Co0.12O2 (SC-NMC83) to solve these issues. This innovative approach successfully immobilizes oxygen within the material, preventing crack formation while simultaneously broadening the diffusion path of Li+. The yttrium-modified sample (SC-NMC83-Y) exhibits a superior capacity retention compared to the SC-NMC83 sample, with values of 90% and 76.1% after 100 cycles, respectively. This work demonstrates the promising potential of a doping strategy for Ni-rich single-crystalline cathodes and paves a pathway for its practical implementation, such as all-solid-state batteries.

CAS / MDL: 872-50-4
研究领域: 材料科学 · 电化学
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