scholarly journals Nickel antimony oxide (NiSb2O6) nanofibers: amorphization and electrocatalytic nitrogen fixation under ambient conditions

2021 ◽  
Vol 2021 (1) ◽  
pp. 012076
Author(s):  
Wanping Xu ◽  
Meng Zhang ◽  
Lihai Cai ◽  
Yitao Liu
Nanoscale ◽  
2019 ◽  
Vol 11 (21) ◽  
pp. 10439-10445 ◽  
Author(s):  
Xiaolan Xue ◽  
Renpeng Chen ◽  
Changzeng Yan ◽  
Yi Hu ◽  
Wenjun Zhang ◽  
...  

Bi2MoO6/OV-BiOBr heterojunctions are synthesized and show good photocatalytic activities for nitrogen reduction to ammonia under ambient conditions.


2021 ◽  
Author(s):  
Luke Sibimol ◽  
Manjunath Chatti ◽  
Asha Yadav ◽  
Brittany Kerr ◽  
Jiban Kangsabanik ◽  
...  

Proton-exchange membrane water electrolysers provide many advantages for the energy-efficient production of H<sub>2</sub>, but the current technology relies on high loadings of expensive iridium at the anodes, which are often unstable in operation. To address this, the present work scrutinises the properties of antimony-metal (Co, Mn, Ni, Fe, Ru) oxides synthesised as flat thin films by a solution-based method for the oxygen evolution reaction in 0.5 M H<sub>2</sub>SO<sub>4</sub>. Among the non-noble-metal catalysts, only cobalt-antimony and manganese-antimony oxides demonstrate high stability and reasonable activity under ambient conditions, but slowly lose activity at elevated temperatures. The ruthenium-antimony system is highly active, requiring an overpotential of 0.39 ± 0.03 and 0.34 ± 0.01 V to achieve 10 mA cm<sup>-2</sup> at 24 ± 2 and 80 °C, respectively, and remaining remarkably stable during one-week tests at 80 °C. The <i>S</i>-number for this catalyst is higher than that for the high-performance benchmark Ir-based systems. Density functional theory analysis and physical characterisation reveal that this high stability is supported by the enhanced hybridisation of the oxygen p- and metal d-orbitals induced by antimony, and can arise from two distinct structural scenarios: either formation of an antimonate phase, or nanoscale intermixing of metal and antimony oxide crystallites.


2018 ◽  
Vol 57 (21) ◽  
pp. 6354-6354
Author(s):  
Chade Lv ◽  
Chunshuang Yan ◽  
Gang Chen ◽  
Yu Ding ◽  
Jingxue Sun ◽  
...  

2020 ◽  
Vol 8 (4) ◽  
pp. 1652-1659 ◽  
Author(s):  
Feili Lai ◽  
Jianrui Feng ◽  
Xiaobin Ye ◽  
Wei Zong ◽  
Guanjie He ◽  
...  

Electrochemical nitrogen-to-ammonia conversion under ambient conditions is realized by an oxygen vacancy-rich spinel structured materials, showing relatively high faradaic efficiency and yields.


2019 ◽  
Vol 55 (72) ◽  
pp. 10705-10708 ◽  
Author(s):  
Wen-Yan Gao ◽  
Yu-Chen Hao ◽  
Xin Su ◽  
Li-Wei Chen ◽  
Tong-An Bu ◽  
...  

Ag triangle-nanoplates and potassium cations can synergistically promote electrocatalytic nitrogen fixation in aqueous solutions under ambient conditions.


1993 ◽  
Vol 115 (4) ◽  
pp. 346-355 ◽  
Author(s):  
L. T. Nguyen

This paper discusses the current reliability issues involved with typical postmolded IC packages. Four major topics are presented, namely, stress, moisture permeation and corrosion-related problems, adhesion, and outgassing impurities. As the trend moves toward higher lead count, with increasingly larger dies which require more power dissipation within smaller package outlines, stress reduction will become a main concern. Methods to quantify package stresses in situ are outlined, together with the advantages and drawbacks of various schemes for decoupling the silicon die from the molding compound. Since the typical molding compound is permeable to moisture, the package collects water during stringent qualification tests (autoclave, T/H, and HAST), and even under normal ambient conditions. Any ionic impurities in the molding compound will combine with the absorbed water to form an electrolytic pool. This increases the likelihood of corrosion in the presence of passivation defects or exposed metal lines. Device structures designed to follow moisture permeation and detect water-induced damage are discussed. The integrity of the interface between the molding compound and the device components is crucial to the long term reliability of the package. Delamination at the die interface produces complex stress profiles that can result in various defects ranging from metal line shift, passivation cracking, corner die chipping, to ball bond fatigue. Poor adhesion along the leads also opens potential paths for moisture ingress. The effects of assembly conditions and various adhesion enhancing schemes on the package integrity are evaluated. Finally, outgassing of halogenated (bromine and antimony oxide) byproducts added for flame retardancy during high temperature storage life testing results in ball bond degradation. The interaction yields typically porous intermetallic structures which grow in size with exposure time, leading ultimately to bond lifting. Possible reaction mechanisms are presented.


2018 ◽  
Vol 57 (21) ◽  
pp. 6073-6076 ◽  
Author(s):  
Chade Lv ◽  
Chunshuang Yan ◽  
Gang Chen ◽  
Yu Ding ◽  
Jingxue Sun ◽  
...  

2021 ◽  
Author(s):  
Luke Sibimol ◽  
Manjunath Chatti ◽  
Asha Yadav ◽  
Brittany Kerr ◽  
Jiban Kangsabanik ◽  
...  

Proton-exchange membrane water electrolysers provide many advantages for the energy-efficient production of H<sub>2</sub>, but the current technology relies on high loadings of expensive iridium at the anodes, which are often unstable in operation. To address this, the present work scrutinises the properties of antimony-metal (Co, Mn, Ni, Fe, Ru) oxides synthesised as flat thin films by a solution-based method for the oxygen evolution reaction in 0.5 M H<sub>2</sub>SO<sub>4</sub>. Among the non-noble-metal catalysts, only cobalt-antimony and manganese-antimony oxides demonstrate high stability and reasonable activity under ambient conditions, but slowly lose activity at elevated temperatures. The ruthenium-antimony system is highly active, requiring an overpotential of 0.39 ± 0.03 and 0.34 ± 0.01 V to achieve 10 mA cm<sup>-2</sup> at 24 ± 2 and 80 °C, respectively, and remaining remarkably stable during one-week tests at 80 °C. The <i>S</i>-number for this catalyst is higher than that for the high-performance benchmark Ir-based systems. Density functional theory analysis and physical characterisation reveal that this high stability is supported by the enhanced hybridisation of the oxygen p- and metal d-orbitals induced by antimony, and can arise from two distinct structural scenarios: either formation of an antimonate phase, or nanoscale intermixing of metal and antimony oxide crystallites.


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