Journal of Energy Chemistry
·
2019
·
IF 5.162
Jun Chen,F. Xu,L. Sun,Kexiang Zhang,Yongpeng Xia,Xiaolei Guo,Huanzhi Zhang,Fang Yu,Erhu Yan,Hongliang Peng,Pengru Huang,Shujun Qiu,Cuili Xiang,Yujie Sun
In this work, Ni-Bi-B alloy has been synthesized via chemical synthesis method . A new kind of Al-InCl 3 -(Ni-Bi-B) composite has been prepared by high energy mechanical ball grinding Al powder with additives. Results show that the doped Ni-Bi-B alloy can significantly improve the hydrogen generation performance of Al-InCl 3 and the catalytic activity is enhanced with the increasing content of Bi in Ni-Bi-B alloy. Under optimal conditions, the hydrogen generation yield and conversion yield of Al-InCl 3 -(Ni-Bi-B) reached 1196.8 mL g −1 and 100.0% at room temperature, respectively. Mechanism study shows five kinds of active sites, such as the fresh surface/defect of Al particle , Al-AlCl 3 , Al-In, Al-Bi/B and Al-Ni/B produced during the ball milling process. Their synergistic effect enhances the hydrogen generation performance of Al-InCl 3 -(Ni-Bi-B) remarkably. In general, the proposed Al-InCl 3 -(Ni-Bi-B) composite is possible to serve as hydrogen generation material for fuel cells.
研究领域:
材料科学
·
能源工程
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DOI
高影响因子
Small
·
2024
·
IF 13
Hanqi Wei,Qihua Yang,Guihua Li,Xuan Liu,Junben Huang,Chujie Wang,Xiaoming Li,Gemei Cai
As one type of recent emerging lead-free perovskites, Cs 2 ZrCl 6 nanocrystals are widely concerned, benefiting from the eminent designability, high X-ray cutoff efficiency, and favorable stability. Improving the luminescence performance of Cs 2 ZrCl 6 nanocrystals has great importance to cater for practical applications. In view of the surface defects frequently formed by the liquid phase method, the particle morphology and surface quality of this material are expected to be regulated if certain intervention is made in the synthesis process. In the work, differing from normal cell lattice modulation based on the ion doping, the grain size and surface morphology of Cs 2 ZrCl 6 nanocrystals are optimized via adding a certain amount of InCl 3 to the synthetic solution. The surface defects are restored to inhibit the defect-induced non-radiative transition, resulting in the improvement of the luminescence properties. Moreover, a flexible Cs 2 ZrCl 6 @polydimethylsiloxane film with excellent heat, water, and bending resistance and a light-emitting diode (LED) device are fabricated, exhibiting excellent application potential for X-ray imaging and blue LED.
研究领域:
材料科学
·
光学工程
·
医学影像
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产品关联
DOI
PubMed
高影响因子
Energy & Environmental Science
·
2025
·
IF 30.8
Ze Jin,Cheng Shen,Haotian Hu,Chengcheng Han,Yongqi Bai,Mengjin Yang,Quan Liu,Ziyi Ge
Significant advancements in research have been made in recent years, with single-junction organic solar cells achieving efficiencies exceeding 20%. However, scaling up laboratory prototypes to large-area commercial modules remains challenging due to the absence of high-quality thin-film deposition techniques, particularly for ultra-thin interfacial layers. In here, we demonstrate a fully vacuum-processed approach utilizing InCl3 as hole-contact and C60/BCP as electron-contact interlayers, respectively, which guarantees dense and uniform charge transporting layers, while also ensuring consistent batch-to-batch reproducibility of module performance. In addition, such ultra-thin InCl3 layer significantly reduces the surface free energy of ITO substrates, thereby inhibiting the coffee ring effect during the active layer deposition, and obtaining a more homogeneous film in a large-scale size. As a result, we measured a power conversion efficiency of 16.5% (certified efficiency: 15.8%) under 1-sun illumination for the best-performing organic solar modules (aperture area = 15.6 cm2) with a geometric fill factor of 95.5%, making them highly completive amongst recently reported modules at similar size. Most importantly, our vacuum-processed interlayers exhibit excellent reproducibility and scale-up ability, paving a way to accelerate the industrialization of organic photovoltaic technology.
研究领域:
材料科学
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可再生能源
·
光伏技术
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产品关联
DOI
高影响因子
Waste and Biomass Valorization
·
2016
·Vol. 8
·期 4
·1303-1311
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IF 0.915
Wei W. Q.,Wu S. B.
Conversion of eucalyptus cellulose into 5-hydroxymethylfurfural (5-HMF) by using Lewis acid catalyst in biphasic system was investigated in this study. The results show that the tetrahydrofuran/water biphasic system was more conducive to convert the eucalyptus cellulose into 5-HMF comparing to the single aqueous system. InCl 3 , a water-compatible Lewis acid, has the best catalytic effect. The highest yield of 5-HMF from eucalyptus cellulose is up to 45.05 mol%, which is a slight higher than that from microcrystalline cellulose. It can be ascribed to the lower crystallinity of isolated eucalyptus cellulose. The optimum conditions for catalytic conversion of eucalyptus cellulose into 5-HMF are at 200 °C for 2 h with 10 % InCl 3 dosage. Additionally, the effect of recycling the whole biphasic system which contains InCl 3 , NaCl, H 2 O and THF indicated that the 5-HMF yield was gradually decreased as the cycle times increased, the possible reason could be due to the loss of partial InCl 3 catalyst during the separation and distillation process.
研究领域:
化学工程
·
可再生资源与环境科学
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产品关联
DOI
高影响因子
Nature Communications
·
2023
·Vol. 14
·期 1
·1-9
·
IF 16.6
Meng Jiashen,Yao Xuhui,Hong Xufeng,Zhu Lujun,Xiao Zhitong,Jia Yongfeng,Liu Fang,Song Huimin,Zhao Yunlong,Pang Quanquan
Conventional solid-to-solid conversion-type cathodes in batteries suffer from poor diffusion/reaction kinetics, large volume changes and aggressive structural degradation, particularly for rechargeable aluminium batteries (RABs). Here we report a class of high-capacity redox couples featuring a solution-to-solid conversion chemistry with well-manipulated solubility as cathodes—uniquely allowed by using molten salt electrolytes—that enable fast-charging and long-lived RABs. As a proof-of-concept, we demonstrate a highly reversible redox couple—the highly soluble InCl and the sparingly soluble InCl 3 —that exhibits a high capacity of about 327 mAh g −1 with negligible cell overpotential of only 35 mV at 1 C rate and 150 °C. The cells show almost no capacity fade over 500 cycles at a 20 C charging rate and can sustain 100 mAh g −1 at 50 C. The fast oxidation kinetics of the solution phase upon initiating the charge enables the cell with ultrafast charging capability, whereas the structure self-healing via re-forming the solution phase at the end of discharge endows the long-term cycling stability. This solution-to-solid mechanism will unlock more multivalent battery cathodes that are attractive in cost but plagued by poor reaction kinetics and short cycle life.
研究领域:
材料科学
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电化学
·
能源存储
✓ 已验证
DOI
PubMed
高影响因子