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Interview with Robert A. Freitas Jr. Part 1
Robert A. Freitas Jr. has written pioneering books on nanomedicine,
nanorobots, and molecular manufacturing. What's next? The last two books in the Nanomedicine series and a book on fundamentals of nanomechanical engineering, extending Eric Drexler's classic Nanosystems, he reveals in this interview.
Originally published on Nanotech.biz
November 4, 2005. Reprinted on KurzweilAI.net February 2, 2006.
Robert A. Freitas Jr., J.D., published the first detailed technical
design study of a mechanical nanorobot ever published in a peer-reviewed
mainstream biomedical journal and is the author of nanomedicine,
the first book-length technical discussion of the medical applications
of nanotechnology and medical nanorobotics.
Question 1: Tell us about yourself. What is your background,
and what is your current affiliation?
I received an undergraduate B.S. degree from Harvey Mudd College
(dual major, physics and psychology) in 1974 and a Juris Doctor
(J.D.) graduate degree from University of Santa Clara School of
Law in 1978. In the late 1970s and early 1980s I published
numerous editions of Lobbying for Space, the first space program
political advocacy handbook ever published, and conducted three
separate observational
SETA/SETI
programs with a colleague, using both optical and radio telescopes. I co-edited the 1980 NASA feasibility
analysis of self-replicating space factories and in 1996 authored
the first detailed technical design
study of a medical nanorobot ever published in a peer-reviewed
mainstream biomedical journal. After
a stint as Research Scientist at Zyvex
Corp. from 2000-2004, I’m now back with the Institute
for Molecular Manufacturing, my previous and current primary
affiliation, as their Senior Research Fellow.
Question 2: When and how did you first hear about molecular
nanotechnology? At what point did you decide to devote your career
to this field?
The first time I ever thought about atomic-scale engineered objects
was probably in 1977-78, when I was working on my first treatise-length
book project (Xenology).
In Chapter 16 of that book, I hypothesized that “using molecular
electronics with components on the order of 10 Å in size, 1010
microneurons could be packed into a space of a few microns” which
would be “small enough to hide inside a bacterium.”
During my NASA work on self-replicating
machines in the summer of 1980, I wondered how small machine
replicators might be made. I
briefly studied the emerging micromachine technology, but by the
time Engines of Creation
came out in 1986 I had temporarily left the field in pursuit of
more pragmatic opportunities. In early 1994 I happened to pick up and read
a copy of Unbounding
the Future. This
was my first exposure to what has come to be known as molecular
nanotechnology (MNT). I studied the detailed technical arguments presented
in Nanosystems,
which confirmed what I had already suspected based on my own knowledge—namely,
that the technical case for molecular nanotechnology was very solid.
Having fully absorbed the MNT paradigm, I immediately realized
that medicine would be the single most important application area
of this new technology. In
particular, nanomedicine offered a chance for significant healthspan
(healthy lifespan) extension. It
also appeared that this objective could possibly be achieved within
the several decades of life actuarially remaining to me and others
of my generation. But was anyone pushing it forward? I contacted the Foresight Institute and learned
that nobody had yet written any systematic treatment of this area,
nor was anyone planning to do so in the near future. So I took up the challenge of writing Nanomedicine, the
first book-length technical discussion of the potential medical
applications of molecular nanotechnology and medical nanorobotics.
I’ve been writing the Nanomedicine book
series since 1994. This technical book is my attempt
to rationally assess various possible nanorobotic capabilities
and medical systems to determine which ones might be plausible (and
which ones not) if we could build nanorobots at some point in the
future. The first volume (I) was published by Landes Bioscience
in 1999 and is freely available online at http://www.nanomedicine.com/NMI.htm.
The second volume (IIA) was also published by Landes Bioscience,
in 2003, and is also freely available online at http://www.nanomedicine.com/NMIIA.htm.
I’m still writing the last 2 volumes (IIB, III) of this
book series, an ongoing effort that will continue during 2005-2010.
Question 3: Recently, the Foresight community has de-emphasized
molecular assemblers in favor of a desktop manufacturing paradigm.
What brought about this shift? How will this change affect the field?
While I’m not involved in the decisions of the Foresight Institute,
I believe the shift occurred primarily as an attempt to redirect
the often rancorous scientific debate away from the growing fears
of runaway motile free-range replicators, and away from the seeming
impossibility of building self-replicating machines (a prejudice
common to many ill-informed scientists), and towards a more rational
consideration of the underlying technologies and their benefits.
The civility of the public discourse may improve as a result,
and to the extent that the mainstream scientific community begins
to pay attention, it is possible that the research funding situation
might also improve. I’m all
for it.
However, the change probably won’t much affect the actual research
in the field, nor the achievement of useful results per dollar spent,
because in truth the distinction between “molecular
assemblers” and “nanofactories”
is largely cosmetic. That
is, if you possess either one, you can use it either to replicate
itself or to build the other in very short order.
Either one can be used equally well to build life-saving
medical nanorobots or life-denying nanoweapons, including everyone’s
favorite bugaboo, the marauding ecophages. Both assemblers and nanofactories are examples
of molecular
manufacturing, which depends at its core on some form of replicative
or massively-parallel fabrication and assembly capability in order
to be able to economically generate macroscale quantities of useful
end products. The two approaches differ mainly in their technical
design/performance
tradeoffs. Each approach
has different strengths and weaknesses (as manufacturing systems)
that can be readily enumerated.
I’ve been writing about both
approaches since the 1980 NASA
replicating factory study – wherein I was actually the main
proponent for the factory
approach. The key thing is that molecular assemblers and
nanofactories are both molecular manufacturing systems. Each requires almost exactly the same set of
enabling technologies. Developing
those enabling technologies as soon as possible should be our primary
focus right now.
Question 4: Do you agree with those who claim that the desktop
manufacturing paradigm could become a reality by 2020?
I would not be surprised if the fabrication of medical nanorobots
(and other useful nanorobotic systems) via molecular manufacturing
– whether via molecular assemblers or nanofactories – arrives during
the decade of the 2020s.
As noted earlier, I undertook the Nanomedicine
book series in an attempt to establish a solid foundation for the
single most important future application of MNT.
The book introduces a long-term vision for nanorobotic medicine
and articulates the technical underpinnings of that vision, so that
when the day arrives that we have the technology to build such devices,
we’ll have a clearer idea what can be done with them, and how.
More recently, to answer those who remain skeptical of the entire
MNT enterprise, including the possibility of medical nanorobotics,
I’ve turned my attention to figuring out how to build the nanorobots
– the issue of implementation of the long-term vision. My
early work on diamond mechanosynthesis is described in a lecture
I gave at the 2004 Foresight Conference in Washington DC, the text
of which (plus many images) is available online. I’m now involved
in 6 research collaborations with various university and corporate
groups in the U.S, U.K. and Russia in an effort to push forward
the technology in this area as fast as possible.
These collaborations include a variety of computational chemistry
simulations of plausible mechanosynthetic tooltips and reaction
sequences, coupled with a nascent experimental effort that is just
starting up. I have several new papers on diamond mechanosynthesis nearing completion
for journal submission, for publication in 2006. Earlier this year I also filed the first-ever
U.S. patent on diamond mechanosynthesis
that describes a specific process for achieving molecularly precise
diamond structures in a practical way.
Ralph Merkle and I are also writing an entire book-length discussion
of diamond mechanosynthesis, entitled Diamond Surfaces
and Diamond Mechanosynthesis (DSDM), to be published
in 2006 or 2007. The first half of this book is an extensive
review of all that is presently known about diamond surfaces, and
has been mostly written for several years.
The second half describes specific tools and reaction pathways
for building those surfaces using positionally controlled mechanosynthetic
tools, and methods for building those tools.
This part has been about 50% written for several years.
But finishing this part has been put on hold because our
many current research collaborations involving ab initio
and DFT-based quantum chemistry simulations are providing so much
new information that we think it’s better to wait and incorporate
this new material into the book. (Otherwise we could’ve published DSDM
in 2005.) Until then, I’ve put together a brief technical
bibliography of research on positional mechanosynthesis (including
diamond). Watch the Molecular Assembler
website for updates and further news about DSDM.
Question 5: Tell us about your latest book, Kinematic Self-Replicating
Machines. Was this book written with the specific aim of convincing
skeptics of the feasibility of molecular manufacturing?
Yes it was, though of course the subject of self-replicating machines
has been a long-standing professional interest of mine, across 3
decades. For instance, I
published the first
quantitative closure analysis for a self-replicating machine
system in 1979-1980 and participated in (and edited) the first comprehensive
technical analysis of a self-replicating
lunar factory for NASA
in 1980.
But focusing again on molecular manufacturing: Once diamond mechanosynthesis and the fabrication
of nanoparts becomes feasible, we will also need a massively parallel
molecular manufacturing capability in order to assemble nanorobots
cheaply, precisely, and in vast quantities. Kinematic Self-Replicating
Machines (KSRM) (Landes
Bioscience, 2004, and freely
available online), co-authored with Ralph Merkle, surveys all
known current work in the field of self-replication and replicative
manufacturing, including all known concepts of molecular assemblers
and nanofactories. It is intended as a general introduction to
the systems-level analysis of self-replicative manufacturing machinery. With 200+ illustrations and 3200+ literature
references, KSRM
describes all proposed and experimentally realized self-replicating
systems that were publicly disclosed as of 2004, ranging from nanoscale
to macroscale systems. The book extensively describes the
historical development of the field. It presents for the first
time a detailed 137-dimensional map of the entire kinematic replicator
design space to assist future engineering efforts. It includes
a primer on the mathematics of self-replication, and has an extensive
discussion of safety issues and implementation issues related to
molecular assemblers and nanofactories.
KSRM
has been cited in two articles appearing in Nature this year
(Zykov et al, Nature 435, 163 (12 May 2005) and Griffith
et al, Nature 437, 636 (29 September 2005)) and appears well
on its way to becoming the classic reference in this field.
Perhaps the most salutary effect of KSRM
is that it provides a number of physical examples of self-replicating
systems (beyond the relatively simple autocatalytic-type replicators
from the 1950s by Penrose,
Jacobson
and Morowitz
and the more recent related examples by Lohn
and Griffith)
that have already been built and operated in a laboratory environment. This provides a ready answer to the tedious
and recurring objection by the ill-informed that such things are
“impossible”: The machines
have actually been built. Interestingly,
one of
these experimental replicators is a fully autonomous machine
that runs around on a table and procures its own parts, which it
then assembles into a working copy of itself, a crude analog of
the molecular assembler approach. Another
of these experimental replicators is a computer-controlled manipulator
arm anchored to a surface, that grabs its parts from a “warehouse”
area and assembles these parts into a working copy of itself, a
crude analog of the nanofactory approach (where the nanofactories
are being used to make more nanofactories, rather than nonfactory
product).
Question 6: You and Dr. Hall are working on Fundamentals of
Nanomechanical Engineering. Is this book intended to serve as a
guide book for college students hoping to enter the nanotechnology
field?
Fundamentals will be
sharply focused on nanomechanical design, with a concentration on
diamondoid molecular machine systems, intended for use in a mechanical
engineering curriculum at the 2nd- or 3rd-year undergraduate level. We hope the book will be widely used in nanotechnology
courses and will help to train the first generation of nanomechanical
design engineers.
This is the primary purpose of the book. A second purpose is to extend and complement
the analyses already published in Drexler’s Nanosystems,
providing more design details and engineering analysis of how to
build structures with molecular precision, and understanding how
molecular machines might function (and the limitations on them).
Once an experimental ability to build diamondoid gears, bearings,
rods, and the like has been demonstrated in the laboratory, I think
the development of nanorobotics will move very rapidly from that
point, because the potential payoff to human welfare is so large
and the design space will have become accessible to active experimentation.
Question 7: MIT granted Eric Drexler a PhD in molecular nanotechnology.
How long do you estimate before other Universities offer undergraduate
and graduate degrees in molecular nanotechnology?
If you mean college degrees in MNT, in the sense of diamondoid
molecular machine systems, I think this will begin to occur as soon
as the field gains scientific credibility – i.e., as soon as it
becomes clear that there is a “there,” there.
The key here, in my opinion, will be the first experimental
demonstration of positionally controlled diamond mechanosynthesis
in the laboratory. Once this has been done, it will no longer be
possible for critics to deny that such a thing is possible, though
they still may claim that perhaps such a thing is not very useful
for anything important. But
with the newfound ability to tinker with real atoms, I expect legions
of graduate students to rise up and prove the critics wrong on that
score too, and the results of this revolution will rapidly trickle
down to the undergraduate level as well.
How long until the first simple experimental demonstration of
positionally controlled diamond mechanosynthesis in the laboratory? Perhaps not as far off as you might think.
I’d be shocked if it was longer than 10 years, and 5 years
would not surprise me. It depends on how fast we’re able to push it forward.
Question 8: You are a scientific advisor to the startup nanotechnology
company Nanorex.
What role do you anticipate that Nanorex will play in the development
of nanotechnology? What is your contribution to that company?
Nanorex
is creating an incredibly cool piece of software called NanoEngineer that allows
the user to quickly and easily design molecular machine systems
of up to perhaps 100,000 atoms in size, then perform various computational
simulations on the system such as energy minimization (geometry
optimization) or a quantitative analysis of applied forces and torques.
It’s a CAD system for molecules, with a special competence
in the area of diamondoid structures.
Once this software is released, users anywhere in the world
will be able to begin creating designs for relatively complex nanomachine
components. We’d expect the
library of designed machine systems to rapidly expand from the current
1-2 dozen items (including mostly just a few bearings, gears, and
joints) into the hundreds or thousands in just a few years. The existence of this expanded library of nanoparts
will then make it easier to begin thinking about designs for more
complex systems that may be built from thousands or more of these
parts, containing millions or even billions of atoms.
It’s a big step along the molecular machine design and development
pathway.
I’m a member of the Scientific
Advisory Board of Nanorex. The Board provides feedback in the development
of the NanoEngineer software, especially including our respective
“wish lists” of what the ideal molecular machine design package
should include – most of which features were then incorporated into
the software. Thus the new software reflects the collective
experience of those few of us in the world who have ever actually
designed a molecular machine component the hard way – laboriously,
atom by atom, using some previously existing (inadequate) software
package.
Nanorex is also directly supporting the writing of Fundamentals
of Nanomechanical Engineering, which we hope will be used
to train the first generation of serious nanomechanical design engineers.
Question 9: Is the mainstream scientific establishment's assessment
of the feasibility of molecular nanotechnology changing? It appears
that the National Nanotechnology Initiative's long term forecasts
have become bolder, yet the standard response by Smalley and others
is that molecular manufacturing is inherently unworkable.
I think this feasibility assessment may be slowly changing, but
this change is probably being driven mainly by published
experimental results, especially in the field of STM/AFM(scanning
probe)-moderated single-atom chemistry.
For example, the first
experimental demonstration of pure mechanosynthesis of any kind
was reported in 2003 and is just now becoming more widely known.
Publication of credible high-accuracy theoretical results,
demonstrating the feasibility of diamond mechanosynthesis, will
also help change this assessment.
(For instance, in 2006 Merkle and I will be publishing a
key theoretical paper in diamond mechanosynthesis representing ~10,000
CPU-hours of quantum chemistry simulations on 2600+ molecular structures
to elucidate possible reaction pathways for building diamond.
Watch for it.)
Smalley has marginalized himself in this area by taking such an
extreme and indefensible position, using fallacious arguments. One by one, his arguments are slowly melting
away under the hot glare of brilliant (but hard-won) experimental
results.
Question 10: The Foresight Institute is collaborating with
Battelle
to create a nanotechnology roadmap. What do you know about this
roadmap? Will it affect the mainstream scientific community's assessment
of molecular manufacturing?
Actually, I don’t know anything about their roadmap. They haven’t consulted me at all on this, and
I have no idea what they’re up to except what I “read in the newspaper”.
I believe it is an attempt to involve mainstream players
in an assessment of possible development pathways leading toward
some flavor(s) of molecular manufacturing. Whether these flavor(s) will include some or
all of biological systems, protein systems, polymer systems, MEMS
systems, metal systems, diamondoid systems, or something else, I
cannot say.
Meanwhile, over the last two years Ralph Merkle and I have worked
hard to establish a small independent network of research (both
theoretical and experimental) collaborators with a sharp focus on
the implementation of diamondoid molecular machine systems. Last June we put together a simple draft implementation
flowchart that has about 100 boxes and lots of arrows, that starts
from where we are today and ends with the manufacturing of complex
molecular machine systems, including simple nanorobots.
The plan includes specific theoretical and experimental milestones
in a particular sequence. So
we’re in the process of simplifying (and implementing) our own “roadmap”. Perhaps this (or something like it) will eventually
be incorporated in the broader Foresight nanotechnology roadmap.
Watch the Molecular Assembler
website for more details in the months ahead.
Continued in Interview
with Robert Freitas: Part 2.
©2006 Sander
Olson. Reprinted with permission.
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