9001金沙官网

关于举行9001金沙官网“国际专家面对面”系列讲座(第三讲)的通知 发布者:夏雪峰   发布时间:2022-11-15   浏览次数:10

邀请人:李雪辉教授、曾强教授

报告时间:2022年11月19日17:00—18:45

报告地点:逸夫工程馆四楼会议室

Zoom会议链接:https://us06web.zoom.us/j/85656522595?pwd=SUt4QmRFeFZUV2ZsVzMvWWYrb0xoZz09

Zoom会议号:856 5652 2595 Zoom passcode: 336299


报告主题1:Redox Controlled Photochemistry and Photo Assisted Electrochemistry

报告人:Prof. Frantisek Hartl(英国雷丁大学化学系, University of Reading,UK)

报 告 内 容(17:00-17:45): 

1)Redox-Controlled Photo-Switching in Triethynyl Terthiophene Complexes

2)Photo-assisted Electrocatalysis of CO2 Reduction

3)ps-ns Time-resolved Infrared Spectroelectrochemistry


报告主题2:Induced Surface Frustrated Lewis Pair as Active Sites over ‘Rigid’ Materials

报告人:曾适之教授(英国牛津大学化学系)

报 告 内 容(18:00-18:45): 

In this talk, I will aim to pose more questions than answers that I could provide in some illustrations of dynamic structure-catalysis relationships. As generally known, the elucidation of active sites’ structure in solid catalysts under real reaction conditions is one of the most important challenges facing the scientific community. There is an increasing amount of evidence by the in situ/operando characterization that active sites can be generated by the interaction of substrate molecules with inorganic catalysts as akin to enzyme-substrate interaction, which can result in the significant promotion of catalytic performance. In addition, surface rearrangement could occur under reaction conditions, which may cause dynamic changes in the active sites. Therefore, the real active sites under working conditions could be significantly different from those characterized under ex situ conditions. Yet, current limitations in state-of-the-art characterization techniques regarding spatial, temporal and temperature/pressure gaps are sometimes unable to provide the answers for the understanding. In-situ/operando characterization using modern designated synchrotron offers exciting possibilities. I will give you some examples how Frustrated Lewis Pair (FLP) sites can be created and monitored, which offer to catalyse a wide range of chemical reactions. I hope this talk could stimulate new science/new instrumentation in catalysis and other disciplines in future.


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