Atomic theory

"Atomic model" redirects here. For the unrelated term in mathematical logic, see atomic model (mathematical logic).
This article is about the historical development of understanding the existence and behavior of atoms. For a history of the study of how atoms combine to form molecules, see history of molecular theory. For the modern view of the atom which developed from atomic theory, see atomic physics.

The current theoretical model of the atom involves a dense nucleus surrounded by a probabilistic "cloud" of electrons

Atomic theory is the scientific theory that matter is composed of particles called atoms. The concept that matter is composed of discrete particles is an ancient idea, but gained scientific credence in the 18th and 19th centuries when scientists found it could explain the behaviors of gases and how chemical elements reacted with each other. By the end of the 19th century, atomic theory had gained widespread acceptance in the scientific community.

The term "atom" comes from the Greek word atomos, which means "uncuttable". John Dalton applied the term to the basic units of mass of the chemical elements under the mistaken belief that chemical atoms are the fundamental particles in nature; it was another century before scientists realized that Dalton's so-called atoms have an underlying structure of their own. Particles which are truly indivisible are now referred to as "elementary particles".

History

Philosophical atomism

Main article: Atomism
See also: Prima materia

The idea that matter is made up of discrete units is a very old idea, appearing in many ancient cultures, including Greece and India. The word "atom" (Greek: ἄτομος; atomos), meaning "uncuttable", was coined by the Pre-Socratic Greek philosophers Leucippus and his pupil Democritus (c.460–c.370 BC).[1][2][3][4] Democritus taught that atoms were infinite in number, uncreated, and eternal, and that the qualities of an object result from the kind of atoms that compose it.[2][3][4] Democritus's atomism was refined and elaborated by the later Greek philosopher Epicurus (341–270 BC), and by the Roman Epicurean poet Lucretius (c.99–c.55 BC).[3][4] During the Early Middle Ages, atomism was mostly forgotten in western Europe. During the 12th century, it became known again in western Europe through references to it in the newly-rediscovered writings of Aristotle.[3] The opposing view of matter upheld by Aristotle was that matter was continuous and infinite and could be subdivided without limit.[5][6]

In the 14th century, the rediscovery of major ancient works describing atomist teachings, including Lucretius's De rerum natura and Diogenes Laërtius's Lives and Opinions of Eminent Philosophers, led to increased scholarly attention on the subject. Nonetheless, because atomism was associated with the philosophy of Epicureanism, which contradicted orthodox Christian teachings, belief in atoms was not considered acceptable by most European philosophers.[3] The French Catholic priest Pierre Gassendi (1592–1655) revived Epicurean atomism with modifications, arguing that atoms were created by God and, though extremely numerous, are not infinite in number. He was the first person who used the term "molecule" to describe aggregation of atoms.[3][4] Gassendi's modified theory of atoms was popularized in France by the physician François Bernier (1620–1688) and in England by the natural philosopher Walter Charleton (1619–1707). The chemist Robert Boyle (1627–1691) and the physicist Isaac Newton (1642–1727) both defended atomism and, by the end of the 17th century, the idea of an atomistic foundation of nature had become accepted by portions of the scientific community.[3]

Dalton's law of multiple proportions

From A New System of Chemical Philosophy, 1808.

Near the end of the 18th century, two laws about chemical reactions emerged without referring to the notion of an atomic theory. The first was the law of conservation of mass, closely associated with the work of Antoine Lavoisier, which states that the total mass in a chemical reaction remains constant (that is, the reactants have the same mass as the products).[7] The second was the law of definite proportions. First established by the French chemist Joseph Proust in 1797 this law states that if a compound is broken down into its constituent chemical elements, then the masses of the constituents will always have the same proportions by weight, regardless of the quantity or source of the original substance.[8]

John Dalton studied data gathered by himself and other scientists and noticed a pattern that later came to be known as the law of multiple proportions. In compounds which all contain a particular element, the content of that element will differ across these compounds by ratios of small whole numbers. Dalton concluded from all this that elements react with each other in discrete and consistent units of weight. Borrowing the word from the philosophical tradition, Dalton called these units atoms.

Example 1 — tin oxides: Dalton identified two oxides of tin. One is a grey powder (which Dalton referred to as the "protoxide") in which for every 100 parts of tin there is 13.5 parts of oxygen. The other oxide is a white powder (which Dalton referred to as the "deutoxide") in which for every 100 parts of tin there are 27 parts of oxygen.[9] 13.5 and 27 form a ratio of 1:2. Dalton concluded that in the grey oxide, there is one oxygen atom for every tin atom, and in the white oxide there are two oxygen atoms for every tin atom. These oxides are today known as tin(II) oxide (SnO) and tin(IV) oxide (SnO2) respectively.

Example 2 — iron oxides: Dalton identified two oxides of iron. One is a black powder in which for every 100 parts of iron there are about 28 parts of oxygen. The other is a red powder in which for every 100 parts of iron there are 42 parts of oxygen.[10] 28 and 42 form a ratio of 2:3. These oxides are today known as iron(II) oxide (better known as wüstite) and iron(III) oxide (the major constituent of rust). Their modern formulas are Fe2O2 and Fe2O3 respectively.

Example 3 — nitrogen oxides: Dalton was aware of three oxides of nitrogen: "nitrous oxide", "nitrous gas", and "nitric acid"[11] (these compounds are known today as nitrous oxide, nitric oxide, and nitrogen dioxide respectively). Dalton understood that "Nitrous oxide" is 63.3% nitrogen and 36.7% oxygen, which means it has 80 g of oxygen for every 140 g of nitrogen. "Nitrous gas" is 44.05% nitrogen and 55.95% oxygen, which means there are 160 g of oxygen for every 140 g of nitrogen. "Nitric acid" is 29.5% nitrogen and 70.5% oxygen, which means it has 320 g of oxygen for every 140 g of nitrogen. 80 g, 160 g, and 320 g form a ratio of 1:2:4. Dalton's formulas for these compounds were N2O, NO, and NO2, essentially the same as today's.

Dalton's atomic theory

From the evidence provided by the law of multiple proportions Dalton developed his atomic theory. A central problem for the theory was to determine the relative weights of the atoms of various elements. The atomic weight of an element is the weight an atom of that element is compared to the weights of atoms of the other elements. Dalton and his contemporaries could not measure the absolute weight of atoms—i.e. their weight in grams—because atoms were far too small to be directly measured with the technologies that existed in the 19th century. Instead, they measured how heavy atoms of various elements were relative to atoms of hydrogen, which chemists of Dalton's day knew was the lightest element in nature.

Dalton estimated the atomic weights according to the mass ratios in which they combined, with the weight of the hydrogen atom taken conventionally as unity. However, Dalton did not realize that some elements exist as molecules in their natural pure form—-e.g. pure oxygen exists as O2. He also mistakenly believed that the simplest compound between any two elements is always one atom of each (so he thought water was HO, not H2O).[12] This, in addition to the limitations of his apparatus, flawed his results. For instance, in 1803 he believed that oxygen atoms were 5.5 times heavier than hydrogen atoms, because in water he measured 5.5 grams of oxygen for every 1 gram of hydrogen and believed the formula for water was HO. Adopting better data, in 1806 he concluded that the atomic weight of oxygen must actually be 7 rather than 5.5, and he retained this weight for the rest of his life. Others at this time had already concluded from more precise measurements that the oxygen atom must weigh 8 relative to hydrogen equals 1, if one assumes Dalton's formula for the water molecule (HO), or 16 if one assumes the modern water formula (H2O).[13]

The flaw in Dalton's theory was corrected in principle in 1811 by Amedeo Avogadro. Avogadro had proposed that equal volumes of any two gases, at equal temperature and pressure, contain equal numbers of molecules (in other words, the mass of a gas's particles does not affect the volume that it occupies).[14] Avogadro's hypothesis, now usually called Avogadro's law, provided a method for deducing the relative weights of the molecules of gaseous elements, for if the hypothesis is correct relative gas densities directly indicate the relative weights of the particles that compose the gases. This way of thinking led directly to a second hypothesis: the particles of certain elemental gases were not atoms, but molecules consisting of two atoms each; and when combining chemically these molecules often split in two. For instance, the fact that two liters of hydrogen will react with just one liter of oxygen to produce two liters of water vapor (at constant pressure and temperature) suggested that a single oxygen molecule must split in two in order to form two molecules of water. This also meant that the water molecule must be H2O. Thus, Avogadro was able to offer more accurate estimates of the atomic mass of oxygen and various other elements, and made a distinction between molecules and atoms. What we now call atoms Avogadro called "elementary molecules", and what we now call molecules Avogadro called "compound molecules".[15]

Opposition to atomic theory

Dalton's atomic theory was not immediately accepted by all scientists.

One problem was the lack of uniform nomenclature. The word "atom" implied indivisibility, but Dalton instead defined an atom as being the basic particle of any substance, which meant that "compound atoms" such as carbon dioxide could divided, as opposed to "elementary atoms".[16] Other scientists used their own nomenclature, which only added to the general confusion. For instance, J. J. Berzelius used the term "organic atoms" to refer to particles containing three or more elements, because he thought this only existed in organic compounds.[17]

A second problem was philosophical. Scientists in the 19th century had no way of directly observing atoms. They inferred the existence of atoms through indirect observations, such as Dalton's law of multiple proportions. Some Scientists, notably those who ascribed to the school of positivism, argued that scientists should not attempt to deduce the deeper reality of the universe, but only systemize what patterns they can directly observe. The anti-atomists argued that while atoms might be a useful abstraction for predicting how elements react, they do not reflect concrete reality.

Such scientists were sometimes known as "equivalentists", because they preferred the theory of equivalent weights, which is a generalization of Proust's law of definite proportions. For example, 1 gram of hydrogen will combine with 8 grams of oxygen to form 9 grams of water, therefore the equivalent weight of oxygen is 8 grams. This position was eventually quashed by two important advancements that happened later in the 19th century: the development of the periodic table and the discovery that molecules have an internal architecture that determines their properties.[18]

Dalton's law of multiple proportions was also shown to not be a universal law when it came to organic substances. For instance, in oleic acid there is 34 g of hydrogen for every 216 g of carbon, and in methane there is 72 g of hydrogen for every 216 g of carbon. 34 and 72 form a ratio of 17:36, which is not a ratio of small whole numbers. We know now that carbon-based substances can have very large molecules, larger than any the other elements can form. Oleic acid's formula is C18H34O2 and methane's is CH4.[19]

Isomerism

Scientists soon discovered cases of substances that have the same proportional elemental composition but different properties. For instance, in 1827, Friedrich Wöhler discovered that silver fulminate and silver cyanate are both 107 parts silver, 12 parts carbon, 14 parts nitrogen, and 12 parts oxygen (we now know their formulas as both AgCNO). Wöhler also discovered that urea and ammonium cyanate both have the same composition (we now know their formulas are CH4N2O) but different properties. In 1830, Jöns Jacob Berzelius introduced the term isomerism to describe the phenomenon. Most chemists of the 1830s and later accepted the suggestion that isomerism resulted from the differing arrangements of the same numbers and types of atoms, resulting in distinct substances. The numbers of isomers proliferated rapidly with the development of organic chemistry, especially after the introduction of atomic valence and structural theory in the 1860s. Consider, for example, pentane (C5H12). According to the theories of valence and structure, there are three possible atomic configurations for the pentane molecule, and there really are three different substances that have the same composition as pentane but different properties.[20][21]

n-pentane
isopentane
neopentane
Molecular structure based on valence of atoms correctly predicted exactly three possible isomers for pentane (C5H12).

Isomerism was not something that could be fully explained by alternative theories to atomic theory, such as radical theory and the theory of types.[22][23]

In 1860, Louis Pasteur hypothesized that the molecules of isomers might have the same composition but different arrangements of their atoms in three dimensions.[24] In 1874, Jacobus Henricus van 't Hoff proposed that the carbon atom forms bonds to other atoms in a tetrahedral arrangement. Working from this hypothesis, he could explain cases of isomerism where the relevant molecules appeared to have the same basic skeletal structure; the two molecules differed only in their three-dimensional spatial configurations, like two otherwise identical left and right hands, or two identical spirals that wind clockwise and counterclockwise. [25]

Mendeleev's periodic table

Main article: Periodic table

Dmitrii Mendeleev noticed that when he arranged the elements in a row according to their atomic weights, there was a certain periodicity to them.[26]: 117  For instance, the second element, lithium, had similar properties to the ninth element, sodium, and the sixteenth element, potassium — a period of seven. Likewise, beryllium, magnesium, and calcium were similar and all were seven places apart from each other on Mendeleev's table (eight places apart on the modern table). Using these patterns, Mendeleev predicted the existence and properties of new elements, which were later discovered in nature: scandium, gallium, and germanium.[26]: 118  Moreover, the periodic table could predict how many atoms of other elements that an atom could bond with — e.g., germanium and carbon are in the same group on the table and their atoms both combine with two oxygen atoms each (GeO2 and CO2). Mendeleev found these patterns to confirm the hypothesis that matter is made of atoms because it showed that the elements could be categorized by their atomic weight. Inserting a new element into the middle of a period would break the parallel between that period and the next, and would also violate Dalton's law of multiple proportions.[27]

Mendeleev's periodic table from 1871.

Brownian motion

In 1827, the British botanist Robert Brown observed that dust particles inside pollen grains floating in water constantly jiggled about for no apparent reason. In 1905, Albert Einstein theorized that this Brownian motion was caused by the water molecules continuously knocking the grains about, and developed a mathematical model to describe it. This model was validated experimentally in 1908 by French physicist Jean Perrin, who used Einstein's equations to determine the size of atoms.[28]

Kinetic diameters of various simple molecules
Molecule Perrier's measurements[29] Modern measurements
Helium 1.7 × 10−10 m 2.6 × 10−10 m
Argon 2.7 × 10−10 m 3.4 × 10−10 m
Mercury 2.8 × 10−10 m 3 × 10−10 m
Hydrogen 2 × 10−10 m 2.89 × 10−10 m
Oxygen 2.6 × 10−10 m 3.46 × 10−10 m
Nitrogen 2.7 × 10−10 m 3.64 × 10−10 m
Chlorine 4 × 10−10 m 3.20 × 10−10 m

Statistical mechanics

In order to introduce the Ideal gas law and statistical forms of physics, it was necessary to postulate the existence of atoms. In 1738, Swiss physicist and mathematician Daniel Bernoulli postulated that the pressure of gases and heat were both caused by the underlying motion of molecules.

In 1860, James Clerk Maxwell, who was a vocal proponent of atomism, was the first to use statistical mechanics in physics.[30] Ludwig Boltzmann and Rudolf Clausius expanded his work on gases and the laws of Thermodynamics especially the second law relating to entropy. In the 1870s, Josiah Willard Gibbs extended the laws of entropy and thermodynamics and coined the term "statistical mechanics." Einstein later independently reinvented Gibbs' laws, because they had only been printed in an obscure American journal.[31] Einstein later commented that had he known of Gibbs' work, he would "not have published those papers at all, but confined myself to the treatment of some few points [that were distinct]."[32] All of statistical mechanics and the laws of heat, gas, and entropy took the existence of atoms as a necessary postulate.

Discovery of subatomic particles

Main articles: Electron and Plum pudding model
The cathode rays (blue) were emitted from the cathode, sharpened to a beam by the slits, then deflected as they passed between the two electrified plates.

Atoms were thought to be the smallest possible division of matter until 1897 when J. J. Thomson discovered the electron through his work on cathode rays.[33]

A Crookes tube is a sealed glass container in which two electrodes are separated by a vacuum. When a voltage is applied across the electrodes, cathode rays are generated, creating a glowing patch where they strike the glass at the opposite end of the tube. Through experimentation, Thomson discovered that the rays could be deflected by an electric field (in addition to magnetic fields, which was already known). He concluded that these rays, rather than being a form of light, were composed of very light negatively charged particles. Thomson called these "corpuscles", but other scientists called them electrons, following an 1894 suggestion by George Johnstone Stoney for naming the basic unit of electrical charge.[34] He measured the mass-to-charge ratio and discovered it was 1800 times smaller than that of hydrogen, the smallest atom. These corpuscles were a particle unlike any other previously known.

Thomson suggested that atoms were divisible, and that the corpuscles were their building blocks.[35] To explain the overall neutral charge of the atom, he proposed that the corpuscles were distributed in a uniform sea of positive charge.[36] This became known as the plum pudding model as the electrons were embedded in the positive charge like bits of fruit in a dried-fruit pudding, though Thomson thought the electrons moved about within the atom.[37]

Discovery of the nucleus

Main article: Geiger–Marsden experiments
The Geiger–Marsden experiment
Left: Expected results: alpha particles passing through the plum pudding model of the atom with negligible deflection.
Right: Observed results: a small portion of the particles were deflected by the concentrated positive charge of the nucleus.

Thomson's plum pudding model was disproved in 1909 by one of his former students, Ernest Rutherford, who discovered that most of the mass and positive charge of an atom is concentrated in a very small fraction of its volume, which he assumed to be at the very center.

Ernest Rutherford and his colleagues Hans Geiger and Ernest Marsden came to have doubts about the Thomson model after they encountered difficulties when they tried to build an instrument to measure the charge-to-mass ratio of alpha particles (these are positively-charged particles emitted by certain radioactive substances such as radium). The alpha particles were being scattered by the air in the detection chamber, which made the measurements unreliable. Thomson had encountered a similar problem in his work on cathode rays, which he solved by creating a near-perfect vacuum in his instruments. Rutherford didn't think he'd run into this same problem because alpha particles are much heavier than electrons. According to Thomson's model of the atom, the positive charge in the atom is not concentrated enough to produce an electric field strong enough to deflect an alpha particle, and the electrons are so lightweight they should be pushed aside effortlessly by the much heavier alpha particles. Yet there was scattering, so Rutherford and his colleagues decided to investigate this scattering carefully.[38]

Between 1908 and 1913, Rutherford and his colleagues performed a series of experiments in which they bombarded thin foils of metal with alpha particles. They spotted alpha particles being deflected by angles greater than 90°. To explain this, Rutherford proposed that the positive charge of the atom is not distributed throughout the atom's volume as Thomson believed, but is concentrated in a tiny nucleus at the center. Only such an intense concentration of charge could produce an electric field strong enough to deflect the alpha particles as observed.[38] Rutherford's model is sometimes called the "planetary model".[39] However, Hantaro Nagaoka was quoted by Rutherford as the first to suggest a planetary atom in 1904.[40] And planetary models had been suggested as early as 1897 such as the one by Joseph Larmor.[41] Probably the earliest solar system model was found in an unpublished note by Ludwig August Colding in 1854 whose idea was that atoms were analogous to planetary systems that rotate and cause magnetic polarity.[42]

First steps toward a quantum physical model of the atom

Main article: Bohr model

The planetary model of the atom had two significant shortcomings. The first is that, unlike planets orbiting a sun, electrons are charged particles. An accelerating electric charge is known to emit electromagnetic waves according to the Larmor formula in classical electromagnetism. An orbiting charge should steadily lose energy and spiral toward the nucleus, colliding with it in a small fraction of a second. The second problem was that the planetary model could not explain the highly peaked emission and absorption spectra of atoms that were observed.

The Bohr model of the atom

Quantum theory revolutionized physics at the beginning of the 20th century, when Max Planck and Albert Einstein postulated that light energy is emitted or absorbed in discrete amounts known as quanta (singular, quantum). This led to a series of quantum atomic models such as the quantum model of Arthur Erich Haas in 1910 and the 1912 John William Nicholson quantum atomic model that quantized angular momentum as h/2π.[43][44] In 1913, Niels Bohr incorporated this idea into his Bohr model of the atom, in which an electron could only orbit the nucleus in particular circular orbits with fixed angular momentum and energy, its distance from the nucleus (i.e., their radii) being proportional to its energy.[45] Under this model an electron could not spiral into the nucleus because it could not lose energy in a continuous manner; instead, it could only make instantaneous "quantum leaps" between the fixed energy levels.[45] When this occurred, light was emitted or absorbed at a frequency proportional to the change in energy (hence the absorption and emission of light in discrete spectra).[45]

Bohr's model was not perfect. It could only predict the spectral lines of hydrogen, not those of multielectron atoms.[46] Worse still, it could not even account for all features of the hydrogen spectrum: as spectrographic technology improved, it was discovered that applying a magnetic field caused spectral lines to multiply in a way that Bohr's model couldn't explain. In 1916, Arnold Sommerfeld added elliptical orbits to the Bohr model to explain the extra emission lines, but this made the model very difficult to use, and it still couldn't explain more complex atoms.[47][48]

Discovery of isotopes

Main article: Isotope

While experimenting with the products of radioactive decay, in 1913 radiochemist Frederick Soddy discovered that there appeared to be more than one variety of some elements.[49] The term isotope was coined by Margaret Todd as a suitable name for these varieties.[50]

That same year, J. J. Thomson conducted an experiment in which he channeled a stream of neon ions through magnetic and electric fields, striking a photographic plate at the other end. He observed two glowing patches on the plate, which suggested two different deflection trajectories. Thomson concluded this was because some of the neon ions had a different mass.[51] The nature of this differing mass would later be explained by the discovery of neutrons in 1932: all atoms of the same element contain the same number of protons, while different isotopes have different numbers of neutrons.[52]

Discovery of nuclear particles

Main articles: Atomic nucleus and Discovery of the neutron

In 1917 Rutherford bombarded nitrogen gas with alpha particles and observed hydrogen nuclei being emitted from the gas (Rutherford recognized these, because he had previously obtained them bombarding hydrogen with alpha particles, and observing hydrogen nuclei in the products). Rutherford concluded that the hydrogen nuclei emerged from the nuclei of the nitrogen atoms themselves (in effect, he had split a nitrogen).[53]

From his own work and the work of his students Bohr and Henry Moseley, Rutherford knew that the positive charge of any atom could always be equated to that of an integer number of hydrogen nuclei. This, coupled with the atomic mass of many elements being roughly equivalent to an integer number of hydrogen atoms - then assumed to be the lightest particles - led him to conclude that hydrogen nuclei were singular particles and a basic constituent of all atomic nuclei. He named such particles protons. Further experimentation by Rutherford found that the nuclear mass of most atoms exceeded that of the protons it possessed; he speculated that this surplus mass was composed of previously-unknown neutrally charged particles, which were tentatively dubbed "neutrons".

In 1928, Walter Bothe observed that beryllium emitted a highly penetrating, electrically neutral radiation when bombarded with alpha particles. It was later discovered that this radiation could knock hydrogen atoms out of paraffin wax. Initially it was thought to be high-energy gamma radiation, since gamma radiation had a similar effect on electrons in metals, but James Chadwick found that the ionization effect was too strong for it to be due to electromagnetic radiation, so long as energy and momentum were conserved in the interaction. In 1932, Chadwick exposed various elements, such as hydrogen and nitrogen, to the mysterious "beryllium radiation", and by measuring the energies of the recoiling charged particles, he deduced that the radiation was actually composed of electrically neutral particles which could not be massless like the gamma ray, but instead were required to have a mass similar to that of a proton. Chadwick now claimed these particles as Rutherford's neutrons.[54] For his discovery of the neutron, Chadwick received the Nobel Prize in 1935.[55]

Quantum physical models of the atom

Main article: Atomic orbital
The five filled atomic orbitals of a neon atom separated and arranged in order of increasing energy from left to right, with the last three orbitals being equal in energy. Each orbital holds up to two electrons, which most probably exist in the zones represented by the colored bubbles. Each electron is equally present in both orbital zones, shown here by color only to highlight the different wave phase.

In 1924, Louis de Broglie proposed that all moving particles—particularly subatomic particles such as electrons—exhibit a degree of wave-like behavior. Erwin Schrödinger, fascinated by this idea, explored whether or not the movement of an electron in an atom could be better explained as a wave rather than as a particle. Schrödinger's equation, published in 1926,[56] describes an electron as a wave function instead of as a point particle. This approach elegantly predicted many of the spectral phenomena that Bohr's model failed to explain. Although this concept was mathematically convenient, it was difficult to visualize, and faced opposition.[57] One of its critics, Max Born, proposed instead that Schrödinger's wave function did not describe the physical extent of an electron (like a charge distribution in classical electromagnetism), but rather gave the probability that an electron would, when measured, be found at a particular point.[58] This reconciled the ideas of wave-like and particle-like electrons: the behavior of an electron, or of any other subatomic entity, has both wave-like and particle-like aspects, and whether one aspect or the other is more apparent depends upon the situation.[59]

A consequence of describing electrons as waveforms is that it is mathematically impossible to simultaneously derive the position and momentum of an electron. This became known as the Heisenberg uncertainty principle after the theoretical physicist Werner Heisenberg, who first published a version of it in 1927.[60] (Heisenberg analyzed a thought experiment where one attempts to measure an electron's position and momentum simultaneously. However, Heisenberg did not give precise mathematical definitions of what the "uncertainty" in these measurements meant. The precise mathematical statement of the position-momentum uncertainty principle is due to Earle Hesse Kennard, Wolfgang Pauli, and Hermann Weyl.[61][62]) This invalidated Bohr's model, with its neat, clearly defined circular orbits. The modern model of the atom describes the positions of electrons in an atom in terms of probabilities. An electron can potentially be found at any distance from the nucleus, but, depending on its energy level and angular momentum, exists more frequently in certain regions around the nucleus than others; this pattern is referred to as its atomic orbital. The orbitals come in a variety of shapes—sphere, dumbbell, torus, etc.—with the nucleus in the middle.[63] The shapes of atomic orbitals are found by solving the Schrödinger equation; however, analytic solutions of the Schrödinger equation are known for very few relatively simple model Hamiltonians including the hydrogen atom and the dihydrogen cation. Even the helium atom—which contains just two electrons—has defied all attempts at a fully analytic treatment.[64][65][66]

See also

Footnotes

  1. ^ Pullman, Bernard (1998). The Atom in the History of Human Thought. Oxford, England: Oxford University Press. pp. 31–33. ISBN 978-0-19-515040-7.
  2. ^ a b Kenny, Anthony (2004). Ancient Philosophy. A New History of Western Philosophy. Vol. 1. Oxford, England: Oxford University Press. pp. 26–28. ISBN 0-19-875273-3.
  3. ^ a b c d e f g Pyle, Andrew (2010). "Atoms and Atomism". In Grafton, Anthony; Most, Glenn W.; Settis, Salvatore (eds.). The Classical Tradition. Cambridge, Massachusetts and London, England: The Belknap Press of Harvard University Press. pp. 103–104. ISBN 978-0-674-03572-0.
  4. ^ a b c d Cohen, Henri; Lefebvre, Claire, eds. (2017). Handbook of Categorization in Cognitive Science (Second ed.). Amsterdam, the Netherlands: Elsevier. p. 427. ISBN 978-0-08-101107-2.
  5. ^ "Welcome to CK-12 Foundation | CK-12 Foundation".
  6. ^ Berryman, Sylvia, "Democritus", The Stanford Encyclopedia of Philosophy (Fall 2008 Edition), Edward N. Zalta (ed.), http://plato.stanford.edu/archives/fall2008/entries/democritus
  7. ^ Weisstein, Eric W. "Lavoisier, Antoine (1743-1794)". scienceworld.wolfram.com. Retrieved 2009-08-01.
  8. ^ "Law of definite proportions | chemistry". Encyclopedia Britannica. Retrieved 2020-09-03.
  9. ^ Dalton (1817). A New System of Chemical Philosophy vol. 2, p. 36
  10. ^ Dalton (1817). A New System of Chemical Philosophy vol. 2, p. 28
  11. ^ Dalton (1808). A New System of Chemical Philosophy vol. 1, pp. 316-319
  12. ^ Johnson, Chris. "Avogadro - his contribution to chemistry". Archived from the original on 2002-07-10. Retrieved 2009-08-01.
  13. ^ Alan J. Rocke (1984). Chemical Atomism in the Nineteenth Century. Columbus: Ohio State University Press.
  14. ^ Avogadro, Amedeo (1811). "Essay on a Manner of Determining the Relative Masses of the Elementary Molecules of Bodies, and the Proportions in Which They Enter into These Compounds". Journal de Physique. 73: 58–76.
  15. ^ Hinshelwood, Cyril N.; Pauling, Linus (1956-10-19). "Amedeo Avogadro". Science. 124 (3225): 708–713. Bibcode:1956Sci...124..708H. doi:10.1126/science.124.3225.708. ISSN 0036-8075. PMID 17757602.
  16. ^ Pullman (1998). The Atom in the History of Human Thought, p. 201
  17. ^ Pullman (1998). The Atom in the History of Human Thought, p. 202
  18. ^ Pullman (1998). The Atom in the History of Human Thought, p. 226: "The first development is the establishment of the periodic classification of the elements, marking the successful climax of concerted efforts to arrange the chemical properties of elements according to their atomic weight. The second is the emergence of structural chemistry, which ousted what was a simple and primitive verbal description of the elemental composition, be it atomic or equivalentist, of substances and replaced it with a systematic determination of their internal architecture."
  19. ^ Trusted (1999). The Mystery of Matter, p. 73
  20. ^ Melsen (1952). From Atomos to Atom, pp. 147-148
  21. ^ Henry Enfield Roscoe, Carl Schorlemmer (1895). A Treatise on Chemistry, Volume 3, Part 1, pp. 121-122
  22. ^ Henry Enfield Roscoe, Carl Schorlemmer (1895). A Treatise on Chemistry, Volume 3, Part 1, pp. 121: "The radical theory and the theory of types are capable of explaining many cases of isomerism, but it was not until the doctrine of the linking of atoms was established that a clear light was thrown on this subject."
  23. ^ Adolphe Wurtz (1880). The Atomic Theory, p. 291: "It is in this manner that the theory of atomicity predicts, interprets, and limits the number of isomers; it has furnished the elements of one of the greatest advances which science has accomplished in the last twenty years. [...] The theory of atomicity has successfully attacked the problem by introducing into the discussion exact data, which have been in a great number of cases confirmed by experiment."
  24. ^ Pullman (1998). The Atom in the History of Human Thought, p. 230
  25. ^ Califano (2012). Pathways to Modern Chemical Physics, p. 31: As he [van 't Hoff] pointed out in his two-volume treatise, Ansichten uber die organische Chemie (1878-1881), discoveries made in his studies of the spatial organization of the molecules persuaded him that the chemical properties of organic molecules depended essentially on their physical structure.
  26. ^ a b Scerri, Eric R. (2020). The Periodic Table, Its Story and Its Significance (2nd ed.). New York: Oxford University Press. ISBN 978-0-190-91436-3.
  27. ^ Brito, Angmary; Rodríguez, María A.; Niaz, Mansoor (2005). "A Reconstruction of Development of the Periodic Table Based on History and Philosophy of Science and Its Implications for General Chemistry Textbooks". Journal of Research in Science Teaching. 42 (1): 84–111. Bibcode:2005JRScT..42...84B. doi:10.1002/tea.20044.
  28. ^ "The Nobel Prize in Physics 1926". NobelPrize.org. Retrieved 2023-02-08.
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  30. ^ See:
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Bibliography

  • Andrew G. van Melsen (1960) [First published 1952]. From Atomos to Atom: The History of the Concept Atom. Translated by Henry J. Koren. Dover Publications. ISBN 0-486-49584-1.
  • J. P. Millington (1906). John Dalton. J. M. Dent & Co. (London); E. P. Dutton & Co. (New York).
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Further reading

External links

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