Mario Molina
I was born in Mexico City on March 19, 1943; my parents were Roberto
Molina Pasquel and Leonor Henriquez de Molina. My father was a lawyer;
he had a private practice, but he also taught at the National University
of Mexico (Universidad Nacional Autonoma de Mexico (UNAM) ). In his
later years, after I had left Mexico, he served as Mexican Ambassador to
Ethiopia, Australia and the Philippines.
I attended elementary school and high school in Mexico City. I was
already fascinated by science before entering high school; I still
remember my excitement when I first glanced at paramecia and amoebae
through a rather primitive toy microscope. I then converted a bathroom,
seldom used by the family, into a laboratory and spent hours playing
with chemistry sets. With the help of an aunt, Esther Molina, who was a
chemist, I continued with more challenging experiments along the lines
of those carried out by freshman chemistry students in college. Keeping
with our family tradition of sending their children abroad for a couple
of years, and aware of my interest in chemistry, I was sent to a
boarding school in Switzerland when I was 11 years old, on the
assumption that German was an important language for a prospective
chemist to learn. I remember I was thrilled to go to Europe, but then I
was disappointed in that my European schoolmates had no more interest in
science than my Mexican friends. I had already decided at that time to
become a research chemist; earlier, I had seriously contemplated the
possibility of pursuing a career in music - I used to play the violin in
those days. In 1960, I enrolled in the chemical engineering program at
UNAM, as this was then the closest way to become a physical chemist,
taking math-oriented courses not available to chemistry majors.
After finishing my undergraduate studies in Mexico, I decided to obtain
a Ph.D. degree in physical chemistry. This was not an easy task;
although my training in chemical engineering was good, it was weak in
mathematics, physics, as well as in various areas of basic physical
chemistry - subjects such as quantum mechanics were totally alien to me
in those days. At first I went to Germany and enrolled at the University
of Freiburg. After spending nearly two years doing research in
kinetics of polymerizations, I realized that I wanted to have time to
study various basic subjects in order to broaden my background and to
explore other research areas. Thus, I decided to seek admission to a
graduate program in the United States. While pondering my future plans, I
spent several months in Paris, where I was able to study mathematics on
my own and I also had a wonderful time discussing all sorts of topics,
ranging from politics, philosophy, to the arts, etc., with many good
friends. Subsequently, I returned to Mexico as an Assistant Professor at
the UNAM and I set up the first graduate program in chemical
engineering. Finally, in 1968 I left for the University of California at
Berkeley to pursue my graduate studies in physical chemistry.
During my first year at Berkeley, I took courses in physics and
mathematics, in addition to the required courses in physical chemistry. I
then joined the research group of Professor George C. Pimentel, with
the goal of studying molecular dynamics using chemical lasers, which
were discovered in his group a few years earlier.
George Pimentel was also a pioneer in the development of matrix
isolation techniques, which is widely used in the study of the molecular
structure and bonding of transient species. He was an excellent teacher
and a wonderful mentor; his warmth, enthusiasm, and encouragement
provided me with inspiration to pursue important scientific questions.
My graduate work involved the investigation of the distribution of
internal energy in the products of chemical and photochemical reactions;
chemical lasers were well suited as tools for such studies. At the
beginning I had little experience with the experimental techniques
required for my research, such as handling vacuum lines, infrared
optics, electronic instrumentation, etc. I learned much of this from my
colleague and friend Francisco Tablas, who was a postdoctoral fellow at
that time. Eventually I became confident enough to generate original
results on my own: my earliest achievement consisted of explaining some
features in the laser signals - that at first sight appeared to be noise
- as "relaxation oscillations," predictable from the fundamental
equations of laser emission.
My years at Berkeley have been some of the best of my life. I arrived
there just after the era of the free-speech movement. I had the
opportunity to explore many areas and to engage in exciting scientific
research in an intellectually stimulating environment. It was also
during this time that I had my first experience dealing with the impact
of science and technology on society. I remember that I was dismayed by
the fact that high-power chemical lasers were being developed elsewhere
as weapons; I wanted to be involved with research that was useful to
society, but not for potentially harmful purposes.
After completing my Ph.D. degree in 1972, I stayed for another year at
Berkeley to continue research on chemical dynamics. Then, in the fall of
1973, I joined the group of Professor F. Sherwood (Sherry) Rowland as a
postdoctoral fellow, moving to Irvine, California. Sherry had pioneered
research on "hot atom" chemistry, investigating chemical properties of
atoms with excess translational energy and produced by radioactive
processes. Sherry offered me a list of research options: the one project
that intrigued me the most consisted of finding out the environmental
fate of certain very inert industrial chemicals - the
chlorofluorocarbons (CFCs) - which had been accumulating in the
atmosphere and which at that time were thought to have no significant
effects on the environment. This project offered me the opportunity to
learn a new field - atmospheric chemistry - about which I knew very
little; trying to solve a challenging problem appeared to be an
excellent way to plunge into a new research area. The CFCs are compounds
similar to others that Sherry and I had investigated from the point of
view of molecular dynamics; we were familiar with their chemical
properties, but not with their atmospheric chemistry.
Three months after I arrived at Irvine, Sherry and I developed the
"CFC-ozone depletion theory." At first the research did not seem to be
particularly interesting - I carried out a systematic search for
processes that might destroy the CFCs in the lower atmosphere, but
nothing appeared to affect them. We knew, however, that they would
eventually drift to sufficiently high altitudes to be destroyed by solar
radiation. The question was not only what destroys them, but more
importantly, what the consequences are. We realized that the chlorine
atoms produced by the decomposition of the CFCs would catalytically
destroy ozone. We became fully aware of the seriousness of the problem
when we compared the industrial amounts of CFCs to the amounts of
nitrogen oxides which control ozone levels; the role of these catalysts
of natural origin had been established a few years earlier by Paul
Crutzen. We were alarmed at the possibility that the continued release
of CFCs into the atmosphere would cause a significant depletion of the
Earth's stratospheric ozone layer. Sherry and I decided to exchange
information with the atmospheric sciences community: we went to Berkeley
to confer with Professor Harold Johnston, whose work on the impact of
the release of nitrogen oxides from the proposed supersonic transport
(SST) aircraft on the stratospheric ozone layer was well known to us.
Johnston informed us that months earlier Ralph Cicerone and Richard
Stolarski had arrived at similar conclusions concerning the catalytic
properties of chlorine atoms in the stratosphere, in connection with the
release of hydrogen chloride either from volcanic eruptions or from the
ammonium perchlorate fuel planned for the space shuttle.
We published our findings in Nature, in a paper which appeared in the
June 28, 1974 issue. The years following the publication of our paper
were hectic, as we had decided to communicate the CFC - ozone issue not
only to other scientists, but also to policy makers and to the news
media; we realized this was the only way to insure that society would
take some measures to alleviate the problem.
To me, Sherry Rowland has always been a wonderful mentor and colleague.
I cherish my years of association with him and my friendship with him
and his wife, Joan. While he was on sabbatical leave in Vienna during
the first six months of 1974, we communicated via mail and telephone.
There were many exchanges of mail during this short period of time,
which illustrated the frantic pace of our research at that time while we
continued to refine our ozone depletion theory. Soon after, Sherry and I
published several more articles on the CFC-ozone issue; we presented
our results at scientific meetings and we also testified at legislative
hearings on potential controls on CFCs emissions.
In 1975, I was appointed as a member of the faculty at the University
of California, Irvine. Although I continued to collaborate with Sherry,
as an assistant professor I had to prove that I was capable of
conducting original research on my own. I thus set up an independent
program to investigate chemical and spectroscopic properties of
compounds of atmospheric importance, focusing on those that are unstable
and difficult to handle in the laboratory, such as hypochlorous acid,
chlorine nitrite, chlorine nitrate, peroxynitric acid, etc.
Although my years at Irvine were very productive, I missed not doing
experiments myself because of the many responsibilities associated with a
faculty position: teaching courses, supervising graduate students,
meetings, etc. After spending seven years at Irvine as Assistant and
then Associate Professor, I decided to move to a non-academic position. I
joined the Molecular Physics and Chemistry Section at the Jet
Propulsion Laboratory in 1982. I had a smaller group - only a few
postdoctoral fellows - but I also had the luxury of conducting
experiments with my own hands, which I enjoyed very much. Indeed, I
spent many hours in the laboratory in those years, conducting
measurements and developing techniques for the study of newly emerging
problems. Around 1985, after becoming aware of the discovery by Joseph
Farman and his co-workers of the seasonal depletion of ozone over
Antarctica, my research group at JPL investigated the peculiar chemistry
which is promoted by polar stratospheric clouds, some of which consist
of ice crystals. We were able to show that chlorine-activation reactions
take place very efficiently in the presence of ice under polar
stratospheric conditions; thus, we provided a laboratory simulation of
the chemical effects of clouds over the Antarctic. Also, in order to
understand the rapid catalytic gas phase reactions that were taking
place over the South Pole, experiments were carried out in my group with
chlorine peroxide, a new compound which had not been reported
previously in the literature and which turned out to be important in
providing the explanation for the rapid loss of ozone in the polar
stratosphere.
In 1989 I returned to academic life, moving to the Massachusetts
Institute of Technology, where I have continued with research on global
atmospheric chemistry issues.
Although I no longer spend much time in the laboratory, I very much
enjoy working with my graduate and postdoctoral students, who provide me
with invaluable intellectual stimulus. I have also benefited from
teaching; as I try to explain my views to students with critical and
open minds, I find myself continually being challenged to go back and
rethink ideas. I now see teaching and research as complementary,
mutually reinforcing activities.
When I first chose the project to investigate the fate of
chlorofluorocarbons in the atmosphere, it was simply out of scientific
curiosity. I did not consider at that time the environmental
consequences of what Sherry and I had set out to study. I am heartened
and humbled that I was able to do something that not only contributed to
our understanding of atmospheric chemistry, but also had a profound
impact on the global environment.
One of the very rewarding aspects of my work has been the interaction
with a superb group of colleagues and friends in the atmospheric
sciences community. I truly value these friendships, many of which go
back 20 years or more, and which I expect to continue for many more
years to come. I feel that this Nobel Prize represents recognition for
the excellent work that has been done by my colleagues and friends in
the atmospheric chemistry community on the stratospheric ozone depletion
issue.
* This autobiography was provided by the Laureate in November 2007.
Addendum, May 2006
My wife is Guadalupe Alvarez; I am no
longer married to Luisa Molina. My son Felipe finished his medical
school studies and is now a physician in Boston.; In 2005 I moved
from MIT to the University of California, San Diego, and also to Mexico
City, where I created a new center for strategic studies in energy and
environment.
My current work is related to air quality and global change
issues. I collaborate
with colleagues from many other disciplines on the problem of rapidly growing
cities with serious air pollution problems. In Mexico City we have
succeeded in improving air quality significantly, although much work remains
to be done. My research group in San Diego is investigating chemical properties
of atmospheric particles. The goal is to better understand the effect of
these particles on clouds and climate.