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Superposition of dual electric fields in covalent organic frameworks for efficient photocatalytic hydrogen evolution
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作者 Chao Li Shuo Wang +8 位作者 Yuan Liub Xihe Huang Yan Zhuang Shuhong Wu Ying Wang Na Wen Kaifeng Wu Zhengxin Ding Jinlin Long 《Chinese Journal of Catalysis》 SCIE CAS CSCD 2024年第8期164-175,共12页
Covalent organic frameworks(COFs)are promising materials for converting solar energy into green hydrogen.However,limited charge separation and transport in COFs impede their application in the photocatalytic hydrogen ... Covalent organic frameworks(COFs)are promising materials for converting solar energy into green hydrogen.However,limited charge separation and transport in COFs impede their application in the photocatalytic hydrogen evolution reaction(HER).In this study,the intrinsically tunable internal bond electric field(IBEF)at the imine bonds of COFs was manipulated to cooperate with the internal molecular electric field(IMEF)induced by the donor-acceptor(D-A)structure for an efficient HER.The aligned orientation of IBEF and IMEF resulted in a remarkable H_(2) evolution rate of 57.3 mmol·g^(-1)·h^(-1)on TNCA,which was approximately 520 times higher than that of TCNA(0.11 mmol·g^(-1)·h^(-1))with the opposing electric field orientation.The superposition of the dual electric fields enables the IBEF to function as an accelerating field for electron transfer,kinetically facilitat-ing the migration of photogenerated electrons from D to A.Furthermore,theoretical calculations indicate that the inhomogeneous charge distribution at the C and N atoms in TNCA not only pro-vides a strong driving force for carrier transfer but also effectively hinders the return of free elec-trons to the valence band,improving the utilization of photoelectrons.This strategy of fabricating dual electric fields in COFs offers a novel approach to designing photocatalysts for clean energy synthesis. 展开更多
关键词 Covalent organic framework Internal molecular electric field Internal bond electric field PHOTOCATALYSIS Hydrogen evolution
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Isolated Solid-State Packaging Technology of High-Temperature Pressure Sensor
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作者 张生才 金鹏 +2 位作者 姚素英 赵毅强 曲宏伟 《Transactions of Tianjin University》 EI CAS 2003年第4期264-268,共5页
The principle of miniature isolated solid-state encapsulation technology of high-temperature pressure sensor and the structure of packaging are discussed, including static electricity bonding, stainless steel diaphrag... The principle of miniature isolated solid-state encapsulation technology of high-temperature pressure sensor and the structure of packaging are discussed, including static electricity bonding, stainless steel diaphragm selection and rippled design, laser welding, silicon oil infilling, isolation and other techniques used in sensor packaging, which can affect the performance of the sensor. By adopting stainless steel diaphragm and high-temperature silicon oil as isolation materials, not only the encapsulation of the sensor is as small as 15 mm in diameter and under 1 mA drive, its full range output is 72 mV and zero stability is 0.48% F.S/mon, but also the reliability of the sensor is improved and its application is widely broadened. 展开更多
关键词 high-temperature pressure sensor static electricity bonding isolated solid-state silicon oil infilling
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Effect of Electric Current on Diffusion of Aluminum in Ti3AlC2 into Zirconium Alloy
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作者 卢博 YANG Xianjin +5 位作者 ZHOU Jie JING Lei SHEN Lu ZHOU Xiaobing DU Shiyu 黄庆 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2017年第3期645-649,共5页
The spark plasma sintering(SPS) method was used to study the mechanism of reaction interface between Zr and Ti3AlC2 with electric current going through it. It was found that electric current greatly reduced the bond... The spark plasma sintering(SPS) method was used to study the mechanism of reaction interface between Zr and Ti3AlC2 with electric current going through it. It was found that electric current greatly reduced the bonding temperature of Zr and Ti3AlC2. By the micro-structure analysis of the interface through SEM/EDS, it was found that Al atoms diffused from the Ti3AlC2 substrate into the Zr side and reacted with Zr to form the Zr-Al compounds at the interface, which is the strengthening mechanism of Ti3AlC2-Zr bonding. The thickness of reaction layers(Zr-Al alloy) was from 0.879 to 13.945 mm depending on different sintering condition. Current direction, heating rate, soaking time, pulse patterns all influenced the diffusion of Al atoms which affected the joining quality of Zr and Ti3AlC2. 展开更多
关键词 MAX phase diffusion bonding SPS electric current effect
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