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It has been claimed by R. Sietmann that the attribution of the discovery of the so-called 'Auger' effect to Pierre Auger was a false attribution and that Lise Meitner should have got the credit for that discovery. However Sietmann himself recognised that Meitner's description of this effect was 'buried in' two larger papers whose primary concern was nuclear physics. Sietmann only mentioned Auger's 1925 article and did not mention his 1923 article, an omission now found in many places. We examine again L. Meitner's and P. Auger's contributions to the description of the 'Auger' effect. Meitner's concern was the exact nature of the (nuclear) beta radiations about which she opposed Ch. D. Ellis, and this had been the subject of an intense Berlin-Cambridge controversy where Ellis' description eventually prevailed. Auger's observations were the central theme of his PhD thesis at the J. Perrin's laboratory on the composed photoelectric effect. We thus believe that while L. Meitner should have shared the Nobel Prize with O. Hahn, the Auger effect has rightly been attributed to Auger.
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Olivier Hardouin Duparc
LSI, École Polytechnique, Palaiseau, France
Pierre Auger Lise Meitner:
Comparative contributions to the Auger effect
It has been claimed by R. Sietmann that the attribution of
the discovery of the so-called ‘Auger’ effect to Pierre
Auger was a false attribution and that Lise Meitner should
have got the credit for that discovery. However Sietmann
himself recognised that Meitner’s description of this effect
was ‘buried in’ two larger papers whose primary concern
was nuclear physics. Sietmann only mentioned Auger’s
1925 article and did not mention his 1923 article, an omis-
sion now found in many places. We examine again L. Meit-
ner’s and P. Auger’s contributions to the description of the
‘Auger’ effect. Meitner’s concern was the exact nature of
the (nuclear) beta radiations about which she opposed
Ch. D. Ellis, and this had been the subject of an intense Ber-
lin–Cambridge controversy where Ellis’ description even-
tually prevailed. Auger’s observations were the central
theme of his PhD thesis at the J. Perrin’s laboratory on the
composed photoelectric effect. We thus believe that while
L. Meitner should have shared the Nobel Prize with
O. Hahn, the Auger effect has rightly been attributed to
Auger.
Keywords: History of Sciences; Auger Effect; Nuclear
beta decay; Secondary electronic emission in solids
1. Introduction
AES is a well-known acronym for all surface scientists and
stands for Auger Electron Spectroscopy. It is one of the
most commonly employed surface analytical techniques
for determining the composition of the surface layers of
materials, and a large amount of research on surfaces and
interfaces has been performed using AES in the last three
or four decennia. Pierre Auger is a French physicist also
well-known for his contributions to cosmic ray physics.
Twenty years ago, however, it has been claimed by Richard
Sietman that “Lise Meitner [was] the person who really
should have taken the credits for discovering the so-called
‘Auger’ effect” and the freelance author explained the
background in a two-page article [1]. Favourably impressed
by the idea of doing justice to someone who, “as a woman
in the male dominated world of physics, was an outsider,”
I enthusiastically shared the news with Siegfried Hofmann,
a respected German specialist of AES, who expressed some
skepticism. I thus decided to re-examine the background by
myself, and found a background even more complicated
than I first thought.
The present paper is organised as follows: Lise Meitner’s
contributions, within the context of the so-called b-ray
controversy with the Briton Charles Drumond Ellis, then
Pierre Auger’s contribution, in the context of his PhD the-
sis, then the developing recognition of the effect, first in
Germany then worldwide. Conclusions are eventually
drawn.
2. Lise Meitner, and Charles Drumond Ellis
Several good books have been written on Lise Meitner [2
4]. Born in 1878, she went to Berlin in 1907 to study with
Max Planck and started her research work with Otto Hahn
on the radioactivity of the b-ray emitters, in a woodshop at
the Chemical Institute of the Berlin University. Other teams
naturally tried to do the same and, mainly due to the
subtlety of these b-rays, divergences soon arose. This fasci-
O. H. Duparc: Pierre Auger Lise Meitner: Comparative contributions to the Auger effect
1162 Int. J. Mat. Res. (for merly Z. Metallkd.) 100 (2009) 9
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nating and complex story has already been described [5 8],
beautifully at length by Carl Jensten [7]. I shall sum up the
matter here, the beginning and the end, and develop the part
about the so-called internal conversions (of whi ch the
Auger effects are now the most useful examples), which
needs to be put into context.
Inspired by the apparently quite reasonable idea of a sim-
ple analogy a-rays and b-rays, Lise Meitner, with Otto
Hahn, first thought they had demonstrated that b-rays were
purely mono-energetic by using a magnetic spectrometer
and photographic plates. In 1913, however, James Chad-
wick (1891 1974) showed, using Geiger point counters in-
stead of photographic plates, that b-particles have a range
of energies, with a continuous spectrum (up to a maximum
energy) rather than just a set of discrete lines (J. Chadwick
had been recommended by Ernest Rutherford Manchester
to work with Hans Wilhelm Geiger in his Radioactivity
Laboratory at the Physikalisch-Technische Reichsanstalt
in Berlin-Charlottenburg Geiger had previously been
Rutherford’s assistant in Manchester. There were very pri-
vileged relations between Germany and Great Britain be-
fore World War I, see [9]). Research on b-rays went on after
1918, with Lise Meitner in Berlin, and with Rutherford’s
group in Cambridge. The beginning 1920’s saw the rise of
the so-called b-ray controversy, with bitter exchanges in
1922. Charles Drumond Ellis (18951980), who was
Rutherford’s student, pragmatically wrote that while the
discrete b-lines could more or less be exp lained by the ac-
tion of internal (nuclear) c-rays on the orbital electrons
(i.e. some internal photoelectric effect), the continuous b-
spectrum certainly was of nuclear origin, with a continuous
distribution probably from the start, once they leave the nu-
cleus, even if he had no theory to explain it. Meitner tried to
save her original assumption of mo nochromatic nuclear b-
rays, and, while she successfully attributed the discrete b-
lines to various internal effects, including the now called
Auger effect, she dev eloped the rather ad hoc idea that the
continuous b-spectrum was to be explained by some per-
turbing effects on the purely monochromatic primary (nu-
clear) b-rays.
Let us be more precise about the discrete b-lines. Ellis
had for the first time in 1921 proposed some mechanism to
explain the b-ray discrete line spectrum [10]. He attributed
this mechanism to his mentor Rutherford (Nobel Prize
1908, knighted 1914): “According to his view the primary
phenomenon is the emission of a b-particle from the
nucleus. It may happen, through some mechanism at pres-
ent unknown, that this b-particle gives rise to a c-ray. This
c-ray in traversing the electronic system of the atom may
be absorbed and eject a high speed electron. It is these last
electrons which constitute the b-ray line spectrum.” And
more explicitly again in 1922 [11]: “Sir Ernest Rutherford
has shown that the lines in the b-ray spectrum were due in
some way to the conversion of monochromatic c-rays in
the same radio-active atom that emitted them.” This was
clearly stated but not clearly substantiated (‘in some
way’). Meitner developed apparently similar ideas in two
articles published in 1922 to explain the discrete b lin es
[12, 13]. In the second article she even went a little further:
“A primary (nuclear-) b-ray turns itself into a c-ray in the
nucleus. The c-ray either goes through unchanged, or ejects
secondary b-rays from the electron shells. The characteris-
tic Röntgen-ray [X-ray] of the atom is thus excited. It, in
turn, can of course eject again electrons, from lower energy
levels.” She described the process with more details in a
1923 article, received in June [14] , where she wrote: “The
primary b-rays eject K-electrons, thus exciting the K
a
-ra-
diation, which in turn disperses L-, M- or N-electrons, the
whole process, from the emission of the primary b-ray re-
lated to the nucleus disintegration to the dispersion of an
L-, M-, or N-electron, occuring within the same atom.”
She further insisted that the whole story must occur within
the same atom, and not with neighbouring atoms. The ex-
pression “in the same atom” explicitly appeared in Ellis
1922 and in Meitner 1923 where it was connected to some
conceptual (and even somewhat handwaving by today’s
standards) argument developed by Svein Rosseland on the
possibility of internal conversion [15].
One does of course recognize a primitive description of
what is now known as the Auger effect. Most unfortunately
however, Meitner’s articles are actually more concerned
with the determination of the characteristics of the primary,
(nuclear-) b-rays, than with the characteristics of the sec-
ondary (shell-) b-rays. Reading the articles from both sides,
one deeply feels a strong opposition between her and Ellis.
Although they kept on improving the accuracy of their
apparatus, with magnetic spectrometers and Geiger coun-
ters, the two teams would not change their mind on the in-
terpretation of the continuous part of the spectrum [4 8].
Only the use of some detector based on an entirely different
principle could perhaps help to convince one of the two
teams, one way or another. (The use of Geiger point coun-
ters by Chadwick had helped to reveal the deceptive effects
of the photographic plate technique previously used). Ellis
thus thought of using a calorimeter thick enough to measure
the total amount of energy released by the nuclear electrons
emitted by a radioactive source. Practical problems of accu-
racy were enormous and it took two years to Ellis and
Wooster to achieve this experiment (1925 1927). It cor-
roborated Ellis’ contention that the nuclear electrons are in-
deed emitted with continu ously varying energies the way
the continuous spectrum shows it. Meitner still argued
about the estimation of the possible energy loss via the c-
rays (and Wolfgang Pauli, in a letter to Ehrenfest in May
1929, even wrote that the Ellis–Wooster experiment was
completely harmless). Meitner repeated the experiment in
Berlin with a student of her and an improved calorimeter
and confirmed Ellis and Wooster’s result. This time Meit-
ner gave up and just said that she could absolutely not un-
derstand the results. The Ellis and Wooster’s calorimeter
experiment thus proved to be crucial, even if it just turned
out to be consistent with the spectrum analysis (and no
new theory was simultaneously proposed. It took a few
more years, and some desperately wild ideas, to find the so-
lution of that conundrum: the actual nuclear b-reaction is
neutron ! proton + electron + antineutrino, and (anti)neu-
trinos, although they do carry out energy, are very difficult
to detect only in 1956).
Thus, in a way, on Lise Meitner’s side as a nuclear ex-
perimental physicist, she had gone wrong on the nature of
the nuclear b -rays, and she certainly felt frustrated about it
even if she got several rewards in these years (to only men-
tion the University of Berlin, she had got a Dozentur (uni-
versity lectureship) position in 1922 and became Nicht-
beamteter Außero rdentlicher Professor in 1926, which
roughly translates to “unofficial, extraordinary Professor”,
O. H. Duparc: Pierre Auger Lise Meitner: Comparative contributions to the Auger effect
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some way to bypass the administration rigidity. The mathe-
matician Amalie (Emmy) Noether had already got a similar
title in 1922 at the University of Göttingen. Lise Meitner
was a paid Professor in the Kaiser-Wilhelm-Institut (KWI)
since 1919).
3. Pierre Auger
Born in 1899, Pierre Victor Auger entered the École Nor-
male Supérieure in Paris in 1919 in a biology group but
with interest in atomic physics [16,17]. During his last years
as a graduate student, when getting ready for the final com-
petition called the “Agrégation” he had to perform some la-
boratory work. This was in 1922 and he had been fascinated
by the cloud chamber pictures published by C.T.R. Wilson
a few years earl ier, featuring the tracks of otherwise invisi-
ble alpha particles and of photo-electrons. He decided, with
his best friend at the École, Francis Perrin, to build the first
cloud chamber “made in France” and they succeeded in
producing some reasonably accurate alpha particle tracks.
He wanted to go on with the cloud chamber and having got
a fellowship he stayed in the laboratory of Professor Jean
Perrin, in the old Sorbonne, and started work towards the
production of a doctoral thesis. His intention was to try to
visualize the whole story of an atomic photoexcitation:
first, the production of a photoelectron, then the consequent
emission of a radiation quantum, and the absorption of this
quantum, with produ ction of another photoelectron all in
the same cloud chamber.
Although first proposed in 1911, it was not until 1923
that the cloud chamber was brought to a reasonable state
of perfection. To quote C.T.R. (Charles Thomas Rees) Wil-
son himself almost verbatim in 1923 [18], the ionising rays
are made to pass through moist air, or other gas, in which
the water-vapour has been brought into the super-saturated
state by sudden expansion of the gas. Each ion liberated be-
comes at once the nucleus for the condensation of a visible
droplet of water; the clouds of drops thus formed are imme-
diately photographed. Very sharply defined pictures of the
tracks of ionising particles may be obt ained in this way.
This of course demanded a lot of skillfulness because many
conditions needed to be suitably arranged so that the photo-
graphs of the paths of the ionising particles could be consid-
ered as genuine and free from instrumental distortion.
I now quote P. Auger in his first article communicated at
the French Academy of Sciences in July 1923 [1 9]: “When
the first [atomic] electron leaves [the atom, ejected by an in-
cident X-ray], as a secondary b-ray, there is a vacancy left
in the electronic system of the excited atom. The drop of a
more peripheral electron on that level is accompanied by
the emission of a characteristic radiation quantum. This
quantum may be absorbed in the atom itself, and produce,
at the expense of the peripheral levels [the outer electronic
shells], a tertiary b-ray (. ..). The repetition of that process
must lead to the production of a fourth order ray; and I in-
deed believe I have observed such rays in the case of [gas-
eous] iodine.”
P. Auger kept on publishing several times on that subject
although only in French [20 23] since it has been the
subject of his three year thesis the manuscript of which ap-
peared as a seventy-one page article (+ 18 figures) in the
French Annales de Physique in 1926 [22]. The same year,
his laboratory supervisor Jean Perrin got the Nobel prize
and his sister Col ette married Francis Perrin, Jean’s son.
Pierre Auger clearly mastered the different aspects, experi-
mental as well as theoretical, of what he called the com-
posed photoelectric effect. In his synthesis he drew compar-
isons with other works, Wilson, Barkla, Maurice de Broglie
(Louis’ elder brother), Holweck, Ellis, Meitner, Klein and
Rosseland, never in a polemical way. For instance he just
said that Barkla’s observations could be simply interpreted
and did not insist on the fact that Barkla had used them to
imply that the Einsteinian quantum of rad iation, in the
sense of an indivisible bundle of radiant energy, does not
exist.
4. Recognition
In a review she wrote on nuclear structure in 1926 for the
XXII
nd
volume of the famous Hans Geiger and Karl Scheel
“Handbuch der Physik” series, Lise Meitner, on the matter
of internal absorption, i.e. absorption of a b-orac-ray in
the very atom which emitted that ray, cited herself [14],
Rosseland [15], Wilson [18] and Auger [20]. In the next
volume of the same series, published the same year, Walter
Bothe, who had just defended his thesis entitled ‘Über den
Elementarprozess der photoelektrischen Elektronenauslö-
sung’ wrote a long chapter on the emission and diffusion
of X-rays [25] where he cited Rosseland [15], Meitner [14]
and Auger [2022]. The following year, Gregor Wentzel,
just named extraordinary professor of mathematical physics
at the Leipzig university, mentioned that Auger had ob-
served in a cloud chamber photoelectric effects with emis-
sion of a second electron, and spoke of Auger-Elektronen
[26]. Still in 1927, but in the U.K., two experimentalists
measuring cathode ray lines, Harold Roper Robinson and
A.M. Cassie wrote that the most direct evidence of the fre-
quency of internal absorption is that deduced by Auger
from examination of the Wilson tracks produced by homo-
O. H. Duparc: Pierre Auger Lise Meitner: Comparative contributions to the Auger effect
1164 Int. J. Mat. Res. (for merly Z. Metallkd.) 100 (2009) 9
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Review
Fig. 1. Pierre Victor Auger. Courtesy of the French Academy of
Sciences Institut de France.
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geneous X-rays in heavy gases [27]. They also mentioned
the general summary given by Bothe. In 1931, Hartmut
Kallmann and Boris Rosen, from the Kaiser-Wilhelm-Insti-
tut (KWI) r Chemie und Elektrochemie (Meitner was at
the KWI für Chemie) , spoke of Auger-Prozesse in a review
article on elementary ionisation processes and their article
got simultaneously translated in Russian [28]. In 1933,
when she wrote the second version of her review chapter
on nuclear structure for the Geiger–Scheel series, Lise
Meitner, in the Innere Absorption section, simply added a
sentence saying that one designates such occurences as
“Rosseland–Augereffekt” [29]. In 1935, the Australian
physicist Eric Henry Stoneley Burhop wrote a 13-page arti-
cle entitled “The Auger Effect”, in the Proceedings of the
Royal Society of London [30].
Then came into play engineers and physicists concerned
with electronic devices and secondary electron emission in
solids. They used solid-state physics concepts and it worked
rather well, see [31], at least apparently until 1950, when
one could read in a short letter to the Editor published in
Phys. Rev.: “Present theories of secondary emission are
based on the Fermi gas or Bloch model of a metal. (.. .)
The simple correlation of [the maximum value of the true
secondary electron yield of an element] with [its] position
in the periodic system would seem to indicate that a satis-
factory theory of secondary emission must take into ac-
count atomic electrons more firmly bound than the valence
or conduction electrons in a metal” [32]. James Joseph
Lander was to solve the difficulty two years later at the Bell
Telephone Laboratories, in an article the title of which ex-
plicitly invoked Auger electrons: Auger Peaks in the En-
ergy Spectra of Secondary Electrons from Various Materi-
als [33]. J.J. Lander simultaneously developed an electron
gun generating a beam of low-velocity electrons of high
quality and stability. It provided a very interesting and reli-
able technique for surface analysis. Surface Auger Electron
Spectroscopy rocketed and Auger only had to write down
his recollections, in English that time, in 1975 in a Surface
Science issue [17].
5. Conclusions
Apart for her numerous wonderful achievements, with Otto
Hahn and later on, Lise Meitner had gone wrong on a fun-
damental aspect of the nuclear b-ray story and she probably
kept some frustration about it, as she was a nuclear physi-
cist at heart, and not an atomic physicist. She may also have
thought that on the theoretical side, Svein Rossel and had
provided some fundamenta l concept, whereas on the ex-
perimental side, Pierre Auger had “seen” the multiple elec-
tron events, at least their tracks, perfectly understanding
and analysing what he was seeing. Indeed Pierre Auger
proved most successful in his thesis work. Although he only
published in French papers at that time but it was not in a
war time it probably explains why atomic physicists and
chemists adopted the appellation of Auger effect, Auger
electrons, Auger peaks. In the meantime Pierre Auger used
the cloud chambers to detect cosmic rays and he is also
known for the Auger showers which he first discovered
not far from the Panthéon in Paris. He also was an excellent
professor and got involved in the administration of French
universities and the administration of research at the French
as well as at the international level. Last but not least, he
sculpted, bronzes, wr ote a book on the philosophy of phy-
sics and biology The microscopic Man. An Essay in Mon-
adism [33] and also wrote some poems. He died at the age
of 94 in 1993. Lise Meitner had died at the age of 90, in
1968.
I wish to thank the library department of the École Polytechnique.
References
[1]
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[2] F. Krafft: Lise Meitner: Eine Biographie, Berlin (1980).
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O. H. Duparc: Pierre Auger Lise Meitner: Comparative contributions to the Auger effect
Int. J. Mat. Res. (formerly Z. Metallkd.) 100 (2009) 9 1165
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Review
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(Received September 2, 2008; accepted October 27, 2008)
Bibliography
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Correspondence address
O. Hardouin Duparc
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91128 Palaiseau, France
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E-mail: olivier.hardouinduparc@polytechnique.edu
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Appendices
A. Original texts
Lise Meitner 1922 [12], p. 147:
Ein primärer (Kern-) b-Strahl verwandelt sich im Kern in
einen c-Strahl. Der c-Strahl geht entweder unverändert als
c-Strahl durch, oder wirft aus den Elektronenringen sekun-
däre b-Strahlen heraus. Dadurch wird aber die charakteris-
tische Röntgenstrahlung des Atoms angeregt, die natürlich
auch ihrerseits wieder Elektronen aus nied rigen Energie-
niveaus herauswerfen kann.
Lise Meitner 1923 [14], p. 61:
Die primären b-Strahlen werfen K-Elektronen hera us, da-
durch wird die K
a
-Strahlung angeregt, die ihrerseits wieder
L-, M- oder N-Elektronen auslöst, wobei sich der ganze
Vorgang von der mit dem Kernzerfall verknüpften Aussen-
dung des primären b-Strahls an bis zur Auslösung eines L-,
M- oder N-Elektrons im selben Atom abspielt.
Lise Meitner 1923 [14], p. 62:
(.. .) die von mir vertretene Meinung , daß die b-Strahlen
ebenso wie die a-Strahlen primär mit einer definierten für
den Kern charakteristischen Geschwindigkeit emittiert wer-
den. Daß die primären b-Strahlen ein etwas verwaschenes
(.. .) Band bilden, ist durch sekundär e Prozesse bedingt.
(.. .) Rosselan d geht auch von der Annahme aus, daß die
b-Strahlen beim Austritt aus dem Kern eine ganz bestimmte
Geschwindigkeit besitzen.
Pierre Auger 1923 [19], p. 171:
Lors du départ du premier électron, sous forme du rayon b
secondaire, une place est laissée libre dans le système élec-
tronique de l’atome excité. La chute d’un électron plus péri-
phérique sur ce niveau s’accompagne de l’émission d’un
quantum de rayonnement caractéristique. Ce quantum peut
être absorbé dans l’atome même, et servir à la production,
aux dépens des niveaux périphériques, d’un rayon b ter-
tiaire: les caractéristiques de ce rayon seront alors celles
qui ont été décrites précédemment. La répétition du même
processus doit aboutir à la production d’un rayon quater-
naire; et je crois en effet avoir observé de tels rayons dans
le cas de l’iode.
Lise Meitner 1933 [29], p. 150:
Man bezeichnet daher diese Erscheinung eines strahlung-
slosen Übergangs mit gleichzeitiger Emission eines Elek-
trons als Rosseland–Augereffekt.
B. Real, and not real photons
The actual quantum mechanical picture is somewhat more
subtle: when a peripheral electron falls down into an inner
vacancy, this may either i) emit a real X-ray, characteristic
of the atom, and leading to X-Ray fluorescence, or ii) in-
duce the emission out of the atom of another electron also
with an energy characteristic of the atom, leading to AES,
with an Auger yield complementary to the fluorescence
yield. The subtle point is that the second process does not
involve any real intermediate X-ray, contrary to what
Meitner’s, and Auger’s, simple picture implies. There are
indeed many instances where Auger electrons are ob-
served, corresponding to transitions which would be for-
bidden by the selection rules, were a real photon involved
in the process. Already in 1927, Robinson and Cassie
wrote [27]: “there is a general belief that the so-called “in-
ternal absorption” is not true absorption of an X-ray by an
atom in the usual sense, but rather the result of a “radia-
tionless” rearrangement of the electrons within the atomic
system.” For readers interested by a thourough and mod-
ern treatment, I refer to the very nice book by Dipankar
Chattarji: The Theory of Auger Transitions, Academic
Press, London, 1976.
O. H. Duparc: Pierre Auger Lise Meitner: Comparative contributions to the Auger effect
1166 Int. J. Mat. Res. (for merly Z. Metallkd.) 100 (2009) 9
R
Review
... Recombination Recombination effect is observed when the minority carrier of each region is higher than the equilibrium concentration in order to attribute the concentration to equilibrium. Three mechanisms of recombination are identified, Radiative recombination, Shockley-Read-Hall (SRH) recombination [15], and Auger recombination [16]. ...
... 16 Responsivity as a function of the wavelength. ...
... 16 Schematic of the vertical single-nanowire radial p-i-n device connected to a p-type doped silicon wafer. A p-type doped core is in contact with the doped silicon substrate and an n-type doped shell is in contact with the ITO. ...
... This class of phenomena is known as Auger decay (first observed independently by Pierre Auger and Lisa Meitner [113][114][115]) when the transition happens between levels with different main quantum number e.g. 3d → 2p, and Coster-Kronig decays [116] for transition between levels with the same main quantum number e.g. ...
Thesis
Full-text available
Understanding the changes that follow UV-excitation in thionucleobases is of great importance for the study of light-induced DNA lesions and, in a broader context, for their applications in medicine and biochemistry. Their ultrafast photophysical reactions can alter the chemical structure of DNA - leading to damages to the genetic code - as proven by the increased skin cancer risk observed for patients treated with thiouracil for its immunosuppressant properties. In this thesis, I present four research papers that result from an investigation of the ultrafast dynamics of 2-thiouracil by means of ultrafast x-ray probing combined with electron spectroscopy. A molecular jet in the gas phase is excited with a uv pulse and then ionized with x-ray radiation from a Free Electron Laser. The kinetic energy of the emitted electrons is measured in a magnetic bottle spectrometer. The spectra of the measured photo and Auger electrons are used to derive a picture of the changes in the geometrical and electronic configurations. The results allow us to look at the dynamical processes from a new perspective, thanks to the element- and site- sensitivity of x-rays. The custom-built URSA-PQ apparatus used in the experiment is described. It has been commissioned and used at the FL24 beamline of the FLASH2 FEL, showing an electron kinetic energy resolution of ∆E/E ~ 40 and a pump-probe timing resolution of 190 f s. X-ray only photoelectron and Auger spectra of 2-thiouracil are extracted from the data and used as reference. Photoelectrons following the formation a 2p core hole are identified, as well as resonant and non-resonant Auger electrons. At the L 1 edge, Coster-Kronig decay is observed from the 2s core hole. The UV-induced changes in the 2p photoline allow the study the electronic-state dynamics. With the use of an Excited-State Chemical Shift (ESCS) model, we observe a ultrafast ground-state relaxation within 250 f s. Furthermore, an oscillation with a 250 f s period is observed in the 2p binding energy, showing a coherent population exchange between electronic states. Auger electrons from the 2p core hole are analyzed and used to deduce a ultrafast C −S bond expansion on a sub 100 f s scale. A simple Coulomb-model, coupled to quantum chemical calculations, can be used to infer the geometrical changes in the molecular structure.
Chapter
The idea of quantization advanced by M. Planck was resumed and relaunched in 1905 by A. Einstein, in the context of his studies on the creation and conversion of light, which include the photoelectric effect. In this chapter, we will discuss the steps that led to the discovery of the photoelectric effect, through the experimental studies conducted by H. Hertz, W. Hallwachs and A. Righi. Moreover, we will deal with what P. Lenard really measured and analyse in detail what was the interpretation of the photoelectric effect given by Einstein. Finally, we will describe the experimental validation given to Einstein’s heuristic model by R. Millikan in 1916, together with his work on the determination of electronic charge.
Chapter
The use of X-rays for material analysis has revolutionized our understanding of various materials, providing invaluable insights. This chapter delves into X-ray applications, including XRD, XRF, XPS, AES, and SIMS. It begins with X-ray production and then details the principles, operations, and applications of these techniques, offering deep insights into material properties. XRD is vital for deciphering solid crystalline structures and atomic arrangements, revealing lattice spacing, symmetry, and phases. XRF excels in elemental analysis, offering both qualitative and quantitative results by generating distinctive fluorescent X-rays when X-rays interact with a sample. XPS focus on surface analysis, determining elemental composition and chemical states. SIMS enables high-sensitivity elemental and isotopic analysis of surfaces. These techniques find diverse applications. This chapter enhances readers' understanding of these techniques, helping them choose the right approach for material characterization, fostering scientific progress and technological innovation.
Thesis
Lighting currently uses around 15% of global energy expenditure. Reducing this energy usage would be an important part of reducing the effects of global climate change. LEDs (light-emitting diodes) could be a more efficient light source than traditional incandescent or compact-fluorescent bulbs. However, they currently suffer from ‘efficiency droop’ — as the power through the device is increased, the efficiency goes down. While the exact cause of droop is not known completely, one effect is the Auger recombination process. Auger recombination involves an electron and hole recombination which transfers energy to another carrier (rather than emitting a photon as in the desired radiative process). Auger recombination comes in many forms and can be assisted by phonons and alloys which allow Auger to occur when it would otherwise be prevented by momentum conservation. Reducing the Auger recombination process in LED materials would allow for manufacturers to use fewer LEDs in their bulbs, reducing costs and encouraging widespread LED adoption. The challenge to reducing Auger is quantifying its impact. Experimental determination of Auger can be confounded by many factors and reported rates for Auger often vary over orders of magnitude. Theoretical determination of Auger recombination is also difficult because of the complexity of the equations involved. In this situation, computation can be an important tool to understand the underlying physics. In particular, this thesis focuses on first-principles calculations, which solve Schödinger’s equation directly rather than relying on existing experimental data. This allows these calculations to be predictive of experiment and can guide future research on more efficient materials. While many open-source and commercial options exist for codes that will solve Schödinger’s equation using Density Functional Theory, there is not an available code to solve for recombination rates. As part of this thesis, code used to find the Auger recombination rates was expanded and improved. This was then used to study various optoelectronic materials. The group-III nitrides are widely used for making LEDs. GaN is popular in making blue LEDs, but other materials in this family have uses. InN has a band gap in the infrared, and could be used for telecommunication purposes. We studied the Auger process in InN and found that it is dominated by the direct Auger process, as expected for its small band gap. We also found that at high carrier densities, Auger was primarily reduced by carrier screening rather than phase-space filling. On the other hand, AlGaN alloys could be used to create UV LEDs, with applications in sterilization and sensing. We studied Auger in AlGaN alloys of three compositions and modeled expanding these Auger values throughout the entire alloy spectrum. We expected to find the maximum alloy-assisted Auger at the 50/50 alloy, but found the opposite trend. This unintuitive result warrants further study. Scintillators are another type of device that emits light when struck by radiation. Auger affects these devices by suppressing light output and making it difficult to identify what the elemental source of the original radiation was. We studied Auger in NaI and found that the phonon-assisted process dominates as expected by the large gap of the material. This methodology and code has shed light on nonradiative carrier combination in optoelectronic materials and devices and can continue to be used in future studies.
Chapter
Almost half a century ago, in the first January 1973 issue of Science, the Roger Guillemin group in the Salk Institute (La Jolla, California), published a paper that proved the presence of a bioactive peptide in ovine hypothalamic extracts, with inhibitory effect in the secretion of immunoreactive growth hormone (GH). In the same paper, the structure of this 14-peptide was elucidated and its synthetic form was shown to elicit the same biological response in rats and humans, as well, hence its name: Somatostatin (SST) or Somatotropin-release inhibiting factor” (SRIF) [1]. SST belongs to the homonymous peptide family with cortistatin (CST). CST-17 is the bioactive cleavage product of a CST precursor peptide in humans, being a relatively recent addition. CST-17 shares common structural and functional features with SST (SST: SST-14 and SST-28 are the bioactive peptides, see Fig. 4.1), such as the depression of neuronal activity and some distinct properties as well, such as the activation of cation selective currents, not responsive to SST. It should be emphasized though, that these peptides (SST and CST) are the products of separate genes [3–5].
Thesis
Work into the interdigitated back contact (IBC) cell to date has shown that the geometry can produce amongst the highest efficiency silicon solar cells. These current devices have yet to become the market leading technology due to the costly and tricky fabrication processes required to keep the doped regions of the p/n junction separate from each other whilst being on the same side of the wafer. This project will demonstrate a novel approach using lasers to create deep surface grooves to allow localised doped regions on a single wafer surface. The purpose of this is to shorten the current path between the charge generation and charge collection regions, although potential benefits of this approach may be limited by increased recombination as a result of enlarging the metal-silicon contact area. Laser processing is however a very cheap and fast method that will allow a significant reduction in processing costs for IBC cells. In this project, an initial crude proof of concept device with an efficiency approaching 1% was fabricated. This served to prove that the novel geometry proposed by this project could create a working device. Technology Computer Aided Design (TCAD) modelling was carried out, showing that with further processing steps and Table of Contents iii optimisation of existing ones, devices with efficiencies exceeding 20.5% could potentially be created. Further experimental work was then performed to develop processes needed for the fabrication of the improved device design as modelled. In summary, the ability to utilise lower cost fabrication methods involving laser processing to produce highly efficient device geometries represents a promising approach to reducing the cost per watt of solar renewable energy.
Article
Multicarrier dynamics play an essential role in quantum dot photophysics and photochemistry, and they are primarily governed by nonradiative Auger processes. Auger recombination affects the performance of lasers, light-emitting diodes, and photodetectors, and it has been implicated in fluorescence intermittency phenomena which are relevant in microscopy and biological tagging. Auger cooling is an important mechanism of rapid electron thermalization. Inverse Auger recombination, known as impact ionization, results in carrier multiplication which can enhance the efficiencies of solar cells. This article first reviews the physical picture, theoretical framework and experimental data for Auger processes in bulk crystalline semiconductors. With this context these aspects are then reexamined for nanocrystal quantum dots, and we first consider fundamental features of Auger recombination in these systems. Methods for the chemical control of Auger recombination and Auger cooling are then discussed in the context of how they illuminate the underlying mechanisms, and we also examine the current understanding of carrier multiplication in quantum dots. Manifestations of Auger recombination in quantum dot devices are finally considered, and we conclude the article with a perspective on remaining unknowns in quantum dot multicarrier physics.
Article
Radiationless or auto-ionising transitions in the atomic shell structure are a familiar phenomenon to physicists. An atom in an excited state can reduce its excitation by dropping an electron from a higher shell into a vacant electronic state in a lower one and simultaneously eject another electron.
Article
Much has been written about the early history of beta-ray research and the controversy it provoked. Many prominent physicists lent their talents to the solution of this puzzling problem. One of the foremost of these was Lise Meitner, conspicuous in the fray not only because of her creative experimental work, but also because of her attachment to a physical principle-the simplicity of nature. This article reviews the sequence of events as they preceded, coincided with, and followed her work on the subject.
Article
DOI:https://doi.org/10.1103/PhysRev.80.925