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Interview: Chemistry's gain
31 July 2008
Ryong Ryoo tells Rachel Cooper how he took a risk and became an expert in mesoporous materials
![]() | Ryong Ryoo is professor of chemistry at Korea Advanced Institute of Science and Technology and has been on the Chemical Communications editorial board since 2006. He has received numerous awards and was named Korea's national scientist by the Korean government in 2007. |
What first attracted you to science?
In the second year of high school in Korea, students are divided into two groups. One group is taught science and engineering and the other is taught an advanced level of literature (such as English). I belonged to the non-science group, so I never thought I would become a scientist. When I was almost at the end of my high school studies, I realised that my ability was science-based, so I decided to risk taking the entrance exam for science at Seoul National University.
Was this unusual?
What made you choose chemistry as a career?
At university, I liked chemistry much more than chemical engineering so I chose to study chemistry. I took the entrance exam for KAIST [Korea Advanced Institute of Science and Technology], a university that gave special exemption from military service. People graduating from KAIST could instead take a job in industry, a research institute or even in a university, with three years' regular salary. I would never have thought about being a chemist otherwise, as my parents could not afford to pay for my graduate studies. Korea was totally different 30 years ago - ordinary people couldn't think about sending their children to study. It cost too much.
KAIST was established several years before I entered; tuition was free and students got scholarships. So that was my opportunity, my chance. I entered KAIST and I saw many senior students going abroad for study, and I thought, 'yes, this is the way - I like chemistry, and I can do chemistry research very well.'
Which area of chemistry did you work in?
Initially, I chose computational chemistry, calculating thermodynamic properties of liquid helium and other liquids. After working at a national lab, the Korea Atomic Energy Research Institute, for three years, I went to Stanford University for my PhD. There, I chose more practical chemistry - heterogenous catalysis. I learnt about xenon gas NMR, and its use on porous materials, such as zeolites, but I didn't learn how to synthesise porous materials at that time. I returned to Korea after a one-year post-doctoral stay at the University of California, Berkeley and I did the same kind of research as I had done in the US. I used zeolites as supports for platinum. I used xenon NMR, extended X-ray absorption fine structure and other physical tools to characterise porous zeolites and supported metal nanoparticles, at that time called clusters.
What is your favourite piece of research?
At a conference in Japan in 1993, I happened to hear about mesoporous silica MCM-41. I was fascinated by its structure and large pores. I wanted to use the material as a support for metal nanoparticles, but I couldn't obtain it then. Although I knew nothing about the chemistry of silica, I decided to synthesise it in my laboratory. I struggled for several years, and somehow became an expert in mesoporous materials. Because I hadn't been trained how to do it, I used my own ideas and this is what brings the field forwards. In 1999, I published a very important paper on the synthesis of ordered mesoporous carbon, using mesoporous silica as a template. Before that, there were no carbon materials showing ordered porosity, so my synthesis of the first ordered mesoporous carbon, named CMK (carbon metastructure at KAIST), was very surprising. It was the first material to exhibit Bragg X-ray diffraction peaks (due to the structural order) with porosity. People were fascinated by the material; they began to use it and to follow the synthesis. So that was my favourite, and best, work.
What do you see as the most important future applications for mesoporous materials?
The reason for this improvement is not yet well understood, but we believe that it may be due to the facile diffusion of the reactants and products. I think particularly in the case of the intermediate products, it removes the intermediate or product quickly out of the micropores, so that the deactivation of the catalyst (which is caused by the accumulation of the polymeric carbonaceous species forming by an interaction between intermediate species) is reduced. Hierarchical zeolites show increasing lifetimes in a number of reactions, so I am working on that. I am also trying to further develop the synthesis method for hierarchical zeolites.
If you had to completely change your area of research, which topic would you like to investigate?
I would do research in biology. When I was a child, I enjoyed watching birds and insects, and I liked to grow plants in the garden, so biology was my dream. But somehow, I became a chemist. Biologists couldn't find jobs so easily. I think I could do better in biology, but I think it's too late now.
What do you like to do in your spare time?
I like to watch nature and walk. I also like gardening. I have a garden that is quite big for Korea. I have been constructing it for several years. Next year, I plan to have a house built, but before that, I will finish the garden. I believe that people who love plants and animals are suited to do science.
Related Links
Ryoo's page at Korea Advanced Institute of Science and Technology
Read more about Ryong Ryoo's work here
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Also of interest
ChemComm Editorial Board member named Korea's National Scientist
The 2007 Korean National Scientist prize has been awarded to Ryong Ryoo.
High temperature treatment of ordered mesoporous carbons prepared by using various carbon precursors and ordered mesoporous silica templates
Kamil P. Gierszal, Mietek Jaroniec, Tae-Wan Kim, Jeongnam Kim and Ryong Ryoo, New J. Chem., 2008, 32, 981
DOI: 10.1039/b716735k
Mesoporous carbons with KOH activated framework and their hydrogen adsorption
Minkee Choi and Ryong Ryoo, J. Mater. Chem., 2007, 17, 4204
DOI: 10.1039/b704104g

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