The purpose of this note is to stimulate interest in measuring and characterizing the emitted ultraviolet frequencies in antimicrobial copper materials. Antimicrobial sanitizing materials are urgently needed to limit ...The purpose of this note is to stimulate interest in measuring and characterizing the emitted ultraviolet frequencies in antimicrobial copper materials. Antimicrobial sanitizing materials are urgently needed to limit the spread of COVID-19 virus. In the current pandemic, ultraviolet radiation is often used for sterilization. It is shown that 3<b><span "=""> </span></b><span>d-orbital capture in copper can result in radiation generated by copper materials. Since ultraviolet radiation is known to be effective in antimicrobial sterilization, it is logical to assume that the radiation formed by copper occurs in the ultraviolet region. Electron transitions in 3 d-orbital capture are expected to occur in this region. A description of the 3 d-orbital capture process, and the origin of the associated frequency, is given. It is shown that for Group 1B elements the strength of electron affinity in the d-orbital capture process increases with increasing Periodic Table period number, n. This is the opposite of other electron affinity properties for atoms that decrease wth an increase in n. A brief discussion of the relationship of d-orbital capture to the chemical inertness of gold is given. The same type of d-orbital capture process that occurs in antimicrobial copper occurs in high temperature superconducting cuprates.</span>展开更多
The development of high-performance non-precious metal-based robust bifunctional electrocatalyst for both hydrogen evolution reaction(HER) and oxygen evolution reactions(OER) in alkaline media is essential for the ele...The development of high-performance non-precious metal-based robust bifunctional electrocatalyst for both hydrogen evolution reaction(HER) and oxygen evolution reactions(OER) in alkaline media is essential for the electrochemical overall water splitting technologies. Herein, we demonstrate that the HER/OER performance of Co Se_(2)can be significantly enhanced by tuning the 3d-orbital electron filling degree through Mo doping. Both density functional theory(DFT) calculations and experimental results imply that the doping of Mo with higher proportion of the unoccupied d-orbital(P_(un)) could not only serve as the active center for water adsorption to enhance the water molecule activation, but also modulate the electronic structures of Co metal center leading to the optimized adsorption strength of*H. As expected, the obtained Mo-Co Se_(2)exhibits a remarkable bifunctional performance with overpotential of only 85 m V for HER and 245 m V for OER to achieve the current density of 10 m A/cm^(2)in alkaline media.This work will provide a valuable insight to design highly efficient bifunctional electrocatalyst towards HER and OER.展开更多
Electrochemical reduction of acetonitrile to ethylamine with a high selectivity is a novel approach to manufacture valuable primary amines which are important raw material in organic chemical industry. However, the po...Electrochemical reduction of acetonitrile to ethylamine with a high selectivity is a novel approach to manufacture valuable primary amines which are important raw material in organic chemical industry. However, the poor ethylamine Faradic efficiency(FE_(ethylamine)) and catalyst stability at the high current density prohibit this method from being practically used. Herein, CuNi alloy ultrafine-nano-particles based on the d-orbital coupling modulation were synthesized through the electrodeposition and their catalytic performance towards acetonitrile reduction reaction(ACNRR) has been systematically studied. The highest FE_(ethylamine)(97%) is achieved with the current density of-114 mA cm^(-2). For practical application, the current density can reach-602.8 mA cm^(-2) with 82.8% FE_(ethylamine)maintained. With the appearance of other organics which co-exist with acetonitrile in the SOHIO process, CuNi can also hydrogenate acetonitrile in it with more than 80% FE_(ethylamine). Our in-situ spectroscopy analysis and DFT calculations towards the acetonitrile hydrogenation behavior reveal that the evenly dispersed Ni in Cu modulates the dband so as to endow CuNi with the better acetonitrile adsorption, milder binding energy with the reaction intermediates, smaller barrier for *CH_3CH_2NH_2 desorption and higher ability for H_2O dissociation to provide *H.展开更多
High temperature superconductivity in cuprates is explained in terms of 3d-orbital capture in copper. In elemental Cu 3d-orbital capture abstracts an electron from the 4 s2 valence orbital, and leaves it as 4 s1. This...High temperature superconductivity in cuprates is explained in terms of 3d-orbital capture in copper. In elemental Cu 3d-orbital capture abstracts an electron from the 4 s2 valence orbital, and leaves it as 4 s1. This is known since Cu occurs in Group IB of the Periodic Table. This forms an electron vacancy, or hole, in the valence shell. Therefore, the energy of 3d-orbital capture is stronger than the energy of unpairing of a paired-spin 4 s2 orbital. In cuprates 3d-orbital capture abstracts an electron from a Cu-O covalent bond, and leaves a hole in the excited state orbital. By electron-hole migration the excited state orbital leads to a coordinate covalent bond. This leads to superconductivity. The 3d-orbital process accounts for superconductivity and insulator behavior in cuprates. These results lend credence to the statement that 3d-orbital capture in copper is the cause of high temperature superconductivity.展开更多
文摘The purpose of this note is to stimulate interest in measuring and characterizing the emitted ultraviolet frequencies in antimicrobial copper materials. Antimicrobial sanitizing materials are urgently needed to limit the spread of COVID-19 virus. In the current pandemic, ultraviolet radiation is often used for sterilization. It is shown that 3<b><span "=""> </span></b><span>d-orbital capture in copper can result in radiation generated by copper materials. Since ultraviolet radiation is known to be effective in antimicrobial sterilization, it is logical to assume that the radiation formed by copper occurs in the ultraviolet region. Electron transitions in 3 d-orbital capture are expected to occur in this region. A description of the 3 d-orbital capture process, and the origin of the associated frequency, is given. It is shown that for Group 1B elements the strength of electron affinity in the d-orbital capture process increases with increasing Periodic Table period number, n. This is the opposite of other electron affinity properties for atoms that decrease wth an increase in n. A brief discussion of the relationship of d-orbital capture to the chemical inertness of gold is given. The same type of d-orbital capture process that occurs in antimicrobial copper occurs in high temperature superconducting cuprates.</span>
基金financially supported by the National Natural Science Foundation of China (No. 21972107)Natural Science Foundation of Jiangsu Province (No. BK20191186)Natural Science Foundation of Hubei Province (No. 2020CFA095)。
文摘The development of high-performance non-precious metal-based robust bifunctional electrocatalyst for both hydrogen evolution reaction(HER) and oxygen evolution reactions(OER) in alkaline media is essential for the electrochemical overall water splitting technologies. Herein, we demonstrate that the HER/OER performance of Co Se_(2)can be significantly enhanced by tuning the 3d-orbital electron filling degree through Mo doping. Both density functional theory(DFT) calculations and experimental results imply that the doping of Mo with higher proportion of the unoccupied d-orbital(P_(un)) could not only serve as the active center for water adsorption to enhance the water molecule activation, but also modulate the electronic structures of Co metal center leading to the optimized adsorption strength of*H. As expected, the obtained Mo-Co Se_(2)exhibits a remarkable bifunctional performance with overpotential of only 85 m V for HER and 245 m V for OER to achieve the current density of 10 m A/cm^(2)in alkaline media.This work will provide a valuable insight to design highly efficient bifunctional electrocatalyst towards HER and OER.
基金the National Natural Science Foundation of China (12025503, 12105208)the Fundamental Research Funds for the Central Universities of China (2042022kf1181)China Postdoctoral Science Foundation (2020M682469)。
文摘Electrochemical reduction of acetonitrile to ethylamine with a high selectivity is a novel approach to manufacture valuable primary amines which are important raw material in organic chemical industry. However, the poor ethylamine Faradic efficiency(FE_(ethylamine)) and catalyst stability at the high current density prohibit this method from being practically used. Herein, CuNi alloy ultrafine-nano-particles based on the d-orbital coupling modulation were synthesized through the electrodeposition and their catalytic performance towards acetonitrile reduction reaction(ACNRR) has been systematically studied. The highest FE_(ethylamine)(97%) is achieved with the current density of-114 mA cm^(-2). For practical application, the current density can reach-602.8 mA cm^(-2) with 82.8% FE_(ethylamine)maintained. With the appearance of other organics which co-exist with acetonitrile in the SOHIO process, CuNi can also hydrogenate acetonitrile in it with more than 80% FE_(ethylamine). Our in-situ spectroscopy analysis and DFT calculations towards the acetonitrile hydrogenation behavior reveal that the evenly dispersed Ni in Cu modulates the dband so as to endow CuNi with the better acetonitrile adsorption, milder binding energy with the reaction intermediates, smaller barrier for *CH_3CH_2NH_2 desorption and higher ability for H_2O dissociation to provide *H.
文摘High temperature superconductivity in cuprates is explained in terms of 3d-orbital capture in copper. In elemental Cu 3d-orbital capture abstracts an electron from the 4 s2 valence orbital, and leaves it as 4 s1. This is known since Cu occurs in Group IB of the Periodic Table. This forms an electron vacancy, or hole, in the valence shell. Therefore, the energy of 3d-orbital capture is stronger than the energy of unpairing of a paired-spin 4 s2 orbital. In cuprates 3d-orbital capture abstracts an electron from a Cu-O covalent bond, and leaves a hole in the excited state orbital. By electron-hole migration the excited state orbital leads to a coordinate covalent bond. This leads to superconductivity. The 3d-orbital process accounts for superconductivity and insulator behavior in cuprates. These results lend credence to the statement that 3d-orbital capture in copper is the cause of high temperature superconductivity.
