In nuclear physics, the island of stability is a predicted set of isotopes of superheavy elements that may have considerably longer half-lives than known isotopes of these elements. It is predicted to appear as an "island" in the chart of nuclides, separated from known stable and long-lived primordial radionuclides. Its theoretical existence is attributed to stabilizing effects of predicted "magic numbers" of protons and neutrons in the superheavy mass region. [3] [4]
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Several predictions have been made regarding the exact location of the island of stability, though it is generally thought to center near copernicium and flerovium isotopes in the vicinity of the predicted closed neutron shell at N = 184. [2] These models strongly suggest that the closed shell will confer further stability towards fission and alpha decay. While these effects are expected to be greatest near atomic number Z = 114 (flerovium) and N = 184, the region of increased stability is expected to encompass several neighboring elements, and there may also be additional islands of stability around heavier nuclei that are doubly magic (having magic numbers of both protons and neutrons). Estimates of the stability of the nuclides within the island are usually around a half-life of minutes or days; some optimists propose half-lives on the order of millions of years. [5]
Although the nuclear shell model predicting magic numbers has existed since the 1940s, the existence of long-lived superheavy nuclides has not been definitively demonstrated. Like the rest of the superheavy elements, the nuclides within the island of stability have never been found in nature; thus, they must be created artificially in a nuclear reaction to be studied. Scientists have not found a way to carry out such a reaction, for it is likely that new types of reactions will be needed to populate nuclei near the center of the island. Nevertheless, the successful synthesis of superheavy elements up to Z = 118 (oganesson) with up to 177 neutrons demonstrates a slight stabilizing effect around elements 110 to 114 that may continue in heavier isotopes, consistent with the existence of the island of stability. [2] [6]
The composition of a nuclide (atomic nucleus) is defined by the number of protons Z and the number of neutrons N, which sum to mass number A. Proton number Z, also named the atomic number, determines the position of an element in the periodic table. The approximately 3300 known nuclides [7] are commonly represented in a chart with Z and N for its axes and the half-life for radioactive decay indicated for each unstable nuclide (see figure). [8] As of 2019 [update] , 251 nuclides are observed to be stable (having never been observed to decay); [9] generally, as the number of protons increases, stable nuclei have a higher neutron–proton ratio (more neutrons per proton). The last element in the periodic table that has a stable isotope is lead (Z = 82), [a] [b] with stability (i.e., half-lives of the longest-lived isotopes) generally decreasing in heavier elements, [c] [12] especially beyond curium (Z = 96). [13] The half-lives of nuclei also decrease when there is a lopsided neutron–proton ratio, such that the resulting nuclei have too few or too many neutrons to be stable. [14]
The stability of a nucleus is determined by its binding energy, higher binding energy conferring greater stability. The binding energy per nucleon increases with atomic number to a broad plateau around A = 60, then declines. [15] If a nucleus can be split into two parts that have a lower total energy (a consequence of the mass defect resulting from greater binding energy), it is unstable. The nucleus can hold together for a finite time because there is a potential barrier opposing the split, but this barrier can be crossed by quantum tunneling. The lower the barrier and the masses of the fragments, the greater the probability per unit time of a split. [16]
Protons in a nucleus are bound together by the strong force, which counterbalances the Coulomb repulsion between positively charged protons. In heavier nuclei, larger numbers of uncharged neutrons are needed to reduce repulsion and confer additional stability. Even so, as physicists started to synthesize elements that are not found in nature, they found the stability decreased as the nuclei became heavier. [17] Thus, they speculated that the periodic table might come to an end. The discoverers of plutonium (element 94) considered naming it "ultimium", thinking it was the last. [18] Following the discoveries of heavier elements, of which some decayed in microseconds, it then seemed that instability with respect to spontaneous fission would limit the existence of heavier elements. In 1939, an upper limit of potential element synthesis was estimated around element 104, [19] and following the first discoveries of transactinide elements in the early 1960s, this upper limit prediction was extended to element 108. [17]
As early as 1914, the possible existence of superheavy elements with atomic numbers well beyond that of uranium—then the heaviest known element—was suggested, when German physicist Richard Swinne proposed that superheavy elements around Z = 108 were a source of radiation in cosmic rays. Although he did not make any definitive observations, he hypothesized in 1931 that transuranium elements around Z = 100 or Z = 108 may be relatively long-lived and possibly exist in nature. [22] In 1955, American physicist John Archibald Wheeler also proposed the existence of these elements; [23] he is credited with the first usage of the term "superheavy element" in a 1958 paper published with Frederick Werner. [24] This idea did not attract wide interest until a decade later, after improvements in the nuclear shell model. In this model, the atomic nucleus is built up in "shells", analogous to electron shells in atoms. Independently of each other, neutrons and protons have energy levels that are normally close together, but after a given shell is filled, it takes substantially more energy to start filling the next. Thus, the binding energy per nucleon reaches a local maximum and nuclei with filled shells are more stable than those without. [25] This theory of a nuclear shell model originates in the 1930s, but it was not until 1949 that German physicists Maria Goeppert Mayer and Johannes Hans Daniel Jensen et al. independently devised the correct formulation. [26]
The numbers of nucleons for which shells are filled are called magic numbers. Magic numbers of 2, 8, 20, 28, 50, 82 and 126 have been observed for neutrons, and the next number is predicted to be 184. [6] [27] Protons share the first six of these magic numbers, [28] and 126 has been predicted as a magic proton number since the 1940s. [29] Nuclides with a magic number of each—such as 16O (Z = 8, N = 8), 132Sn (Z = 50, N = 82), and 208Pb (Z = 82, N = 126)—are referred to as "doubly magic" and are more stable than nearby nuclides as a result of greater binding energies. [30] [31]
In the late 1960s, more sophisticated shell models were formulated by American physicist William Myers and Polish physicist Władysław Świątecki, and independently by German physicist Heiner Meldner (1939–2019 [32] [33] ). With these models, taking into account Coulomb repulsion, Meldner predicted that the next proton magic number may be 114 instead of 126. [34] Myers and Świątecki appear to have coined the term "island of stability", and American chemist Glenn Seaborg, later a discoverer of many of the superheavy elements, quickly adopted the term and promoted it. [29] [35] Myers and Świątecki also proposed that some superheavy nuclei would be longer-lived as a consequence of higher fission barriers. Further improvements in the nuclear shell model by Soviet physicist Vilen Strutinsky led to the emergence of the macroscopic–microscopic method, a nuclear mass model that takes into consideration both smooth trends characteristic of the liquid drop model and local fluctuations such as shell effects. This approach enabled Swedish physicist Sven Nilsson et al., as well as other groups, to make the first detailed calculations of the stability of nuclei within the island. [34] With the emergence of this model, Strutinsky, Nilsson, and other groups argued for the existence of the doubly magic nuclide 298Fl (Z = 114, N = 184), rather than 310 Ubh (Z = 126, N = 184) which was predicted to be doubly magic as early as 1957. [34] Subsequently, estimates of the proton magic number have ranged from 114 to 126, and there is still no consensus. [6] [21] [36] [37]
Element | Atomic number | Most stable isotope | Half-life [d] | |
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Publications [38] [39] | NUBASE 2020 [40] | |||
Rutherfordium | 104 | 267Rf | 48 min [41] | 2.5 h |
Dubnium | 105 | 268Db | 16 h [42] | 1.2 d |
Seaborgium | 106 | 269Sg | 14 min [43] | 5 min |
Bohrium | 107 | 270Bh [e] | 2.4 min [45] | 3.8 min |
Hassium | 108 | 269Hs | 9.7 s [46] | 16 s |
Meitnerium | 109 | 278Mt [f] [g] | 4.5 s | 6 s |
Darmstadtium | 110 | 281Ds [f] | 12.7 s | 14 s |
Roentgenium | 111 | 282Rg [f] [h] | 1.7 min | 2.2 min |
Copernicium | 112 | 285Cn [f] | 28 s | 30 s |
Nihonium | 113 | 286Nh [f] | 9.5 s | 12 s |
Flerovium | 114 | 289Fl [f] [i] | 1.9 s | 2.1 s |
Moscovium | 115 | 290Mc [f] | 650 ms | 840 ms |
Livermorium | 116 | 293Lv [f] | 57 ms | 70 ms |
Tennessine | 117 | 294Ts [f] | 51 ms | 70 ms |
Oganesson | 118 | 294Og [f] | 690 μs | 700 μs |
Interest in a possible island of stability grew throughout the 1960s, as some calculations suggested that it might contain nuclides with half-lives of billions of years. [48] [5] They were also predicted to be especially stable against spontaneous fission in spite of their high atomic mass. [34] [49] It was thought that if such elements exist and are sufficiently long-lived, there may be several novel applications as a consequence of their nuclear and chemical properties. These include use in particle accelerators as neutron sources, in nuclear weapons as a consequence of their predicted low critical masses and high number of neutrons emitted per fission, [50] and as nuclear fuel to power space missions. [36] These speculations led many researchers to conduct searches for superheavy elements in the 1960s and 1970s, both in nature and through nucleosynthesis in particle accelerators. [23]
During the 1970s, many searches for long-lived superheavy nuclei were conducted. Experiments aimed at synthesizing elements ranging in atomic number from 110 to 127 were conducted at laboratories around the world. [51] [52] These elements were sought in fusion-evaporation reactions, in which a heavy target made of one nuclide is irradiated by accelerated ions of another in a cyclotron, and new nuclides are produced after these nuclei fuse and the resulting excited system releases energy by evaporating several particles (usually protons, neutrons, or alpha particles). These reactions are divided into "cold" and "hot" fusion, which respectively create systems with lower and higher excitation energies; this affects the yield of the reaction. [53] For example, the reaction between 248Cm and 40Ar was expected to yield isotopes of element 114, and that between 232Th and 84Kr was expected to yield isotopes of element 126. [54] None of these attempts were successful, [51] [52] indicating that such experiments may have been insufficiently sensitive if reaction cross sections were low—resulting in lower yields—or that any nuclei reachable via such fusion-evaporation reactions might be too short-lived for detection. [j] Subsequent successful experiments reveal that half-lives and cross sections indeed decrease with increasing atomic number, resulting in the synthesis of only a few short-lived atoms of the heaviest elements in each experiment; [55] as of 2022 [update] , the highest reported cross section for a superheavy nuclide near the island of stability is for 288Mc in the reaction between 243Am and 48Ca. [42]
Similar searches in nature were also unsuccessful, suggesting that if superheavy elements do exist in nature, their abundance is less than 10−14 moles of superheavy elements per mole of ore. [56] Despite these unsuccessful attempts to observe long-lived superheavy nuclei, [34] new superheavy elements were synthesized every few years in laboratories through light-ion bombardment and cold fusion [k] reactions; rutherfordium, the first transactinide, was discovered in 1969, and copernicium, eight protons closer to the island of stability predicted at Z = 114, was reached by 1996. Even though the half-lives of these nuclei are very short (on the order of seconds), [40] the very existence of elements heavier than rutherfordium is indicative of stabilizing effects thought to be caused by closed shells; a model not considering such effects would forbid the existence of these elements due to rapid spontaneous fission. [19]
Flerovium, with the expected magic 114 protons, was first synthesized in 1998 at the Joint Institute for Nuclear Research in Dubna, Russia, by a group of physicists led by Yuri Oganessian. A single atom of element 114 was detected, with a lifetime of 30.4 seconds, and its decay products had half-lives measurable in minutes. [57] Because the produced nuclei underwent alpha decay rather than fission, and the half-lives were several orders of magnitude longer than those previously predicted [l] or observed for superheavy elements, [57] this event was seen as a "textbook example" of a decay chain characteristic of the island of stability, providing strong evidence for the existence of the island of stability in this region. [59] Even though the original 1998 chain was not observed again, and its assignment remains uncertain, [44] further successful experiments in the next two decades led to the discovery of all elements up to oganesson, whose half-lives were found to exceed initially predicted values; these decay properties further support the presence of the island of stability. [6] [47] [60] However, a 2021 study on the decay chains of flerovium isotopes suggests that there is no strong stabilizing effect from Z = 114 in the region of known nuclei (N = 174), [61] and that extra stability would be predominantly a consequence of the neutron shell closure. [37] Although known nuclei still fall several neutrons short of N = 184 where maximum stability is expected (the most neutron-rich confirmed nuclei, 293Lv and 294Ts, only reach N = 177), and the exact location of the center of the island remains unknown, [62] [6] the trend of increasing stability closer to N = 184 has been demonstrated. For example, the isotope 285Cn, with eight more neutrons than 277Cn, has a half-life almost five orders of magnitude longer. This trend is expected to continue into unknown heavier isotopes in the vicinity of the shell closure. [63]
Though nuclei within the island of stability around N = 184 are predicted to be spherical, studies from the early 1990s—beginning with Polish physicists Zygmunt Patyk and Adam Sobiczewski in 1991 [65] —suggest that some superheavy elements do not have perfectly spherical nuclei. [66] [67] A change in the shape of the nucleus changes the position of neutrons and protons in the shell. Research indicates that large nuclei farther from spherical magic numbers are deformed, [67] causing magic numbers to shift or new magic numbers to appear. Current theoretical investigation indicates that in the region Z = 106–108 and N ≈ 160–164, nuclei may be more resistant to fission as a consequence of shell effects for deformed nuclei; thus, such superheavy nuclei would only undergo alpha decay. [68] [69] [70] Hassium-270 is now believed to be a doubly magic deformed nucleus, with deformed magic numbers Z = 108 and N = 162. [71] It has a half-life of 9 seconds. [40] This is consistent with models that take into account the deformed nature of nuclei intermediate between the actinides and island of stability near N = 184, in which a stability "peninsula" emerges at deformed magic numbers Z = 108 and N = 162. [72] [73] Determination of the decay properties of neighboring hassium and seaborgium isotopes near N = 162 provides further strong evidence for this region of relative stability in deformed nuclei. [49] This also strongly suggests that the island of stability (for spherical nuclei) is not completely isolated from the region of stable nuclei, but rather that both regions are instead linked through an isthmus of relatively stable deformed nuclei. [72] [74]
The half-lives of nuclei in the island of stability itself are unknown since none of the nuclides that would be "on the island" have been observed. Many physicists believe that the half-lives of these nuclei are relatively short, on the order of minutes or days. [62] Some theoretical calculations indicate that their half-lives may be long, on the order of 100 years, [2] [55] or possibly as long as 109 years. [5]
The shell closure at N = 184 is predicted to result in longer partial half-lives for alpha decay and spontaneous fission. [2] It is believed that the shell closure will result in higher fission barriers for nuclei around 298Fl, strongly hindering fission and perhaps resulting in fission half-lives 30 orders of magnitude greater than those of nuclei unaffected by the shell closure. [34] [75] For example, the neutron-deficient isotope 284Fl (with N = 170) undergoes fission with a half-life of 2.5 milliseconds, and is thought to be one of the most neutron-deficient nuclides with increased stability in the vicinity of the N = 184 shell closure. [43] Beyond this point, some undiscovered isotopes are predicted to undergo fission with still shorter half-lives, limiting the existence [m] and possible observation [j] of superheavy nuclei far from the island of stability (namely for N < 170 as well as for Z > 120 and N > 184). [14] [19] These nuclei may undergo alpha decay or spontaneous fission in microseconds or less, with some fission half-lives estimated on the order of 10−20 seconds in the absence of fission barriers. [68] [69] [70] [75] In contrast, 298Fl (predicted to lie within the region of maximum shell effects) may have a much longer spontaneous fission half-life, possibly on the order of 1019 years. [34]
In the center of the island, there may be competition between alpha decay and spontaneous fission, though the exact ratio is model-dependent. [2] The alpha decay half-lives of 1700 nuclei with 100 ≤ Z ≤ 130 have been calculated in a quantum tunneling model with both experimental and theoretical alpha decay Q-values, and are in agreement with observed half-lives for some of the heaviest isotopes. [68] [69] [70] [79] [80] [81]
The longest-lived nuclides are also predicted to lie on the beta-stability line, for beta decay is predicted to compete with the other decay modes near the predicted center of the island, especially for isotopes of elements 111–115. Unlike other decay modes predicted for these nuclides, beta decay does not change the mass number. Instead, a neutron is converted into a proton or vice versa, producing an adjacent isobar closer to the center of stability (the isobar with the lowest mass excess). For example, significant beta decay branches may exist in nuclides such as 291Fl and 291Nh; these nuclides have only a few more neutrons than known nuclides, and might decay via a "narrow pathway" towards the center of the island of stability. [1] [2] The possible role of beta decay is highly uncertain, as some isotopes of these elements (such as 290Fl and 293Mc) are predicted to have shorter partial half-lives for alpha decay. Beta decay would reduce competition and would result in alpha decay remaining the dominant decay channel, unless additional stability towards alpha decay exists in superdeformed isomers of these nuclides. [82]
Considering all decay modes, various models indicate a shift of the center of the island (i.e., the longest-living nuclide) from 298Fl to a lower atomic number, and competition between alpha decay and spontaneous fission in these nuclides; [83] these include 100-year half-lives for 291Cn and 293Cn, [55] [78] a 1000-year half-life for 296Cn, [55] a 300-year half-life for 294Ds, [75] and a 3500-year half-life for 293Ds, [84] [85] with 294Ds and 296Cn exactly at the N = 184 shell closure. It has also been posited that this region of enhanced stability for elements with 112 ≤ Z ≤ 118 may instead be a consequence of nuclear deformation, and that the true center of the island of stability for spherical superheavy nuclei lies around 306 Ubb (Z = 122, N = 184). [20] This model defines the island of stability as the region with the greatest resistance to fission rather than the longest total half-lives; [20] the nuclide 306Ubb is still predicted to have a short half-life with respect to alpha decay. [2] [70] The island of stability for spherical nuclei may also be a "coral reef" (i.e., a broad region of increased stability without a clear "peak") around N = 184 and 114 ≤ Z ≤ 120, with half-lives rapidly decreasing at higher atomic number, due to combined effects from proton and neutron shell closures. [86]
Another potentially significant decay mode for the heaviest superheavy elements was proposed to be cluster decay by Romanian physicists Dorin N. Poenaru and Radu A. Gherghescu and German physicist Walter Greiner. Its branching ratio relative to alpha decay is expected to increase with atomic number such that it may compete with alpha decay around Z = 120, and perhaps become the dominant decay mode for heavier nuclides around Z = 124. As such, it is expected to play a larger role beyond the center of the island of stability (though still influenced by shell effects), unless the center of the island lies at a higher atomic number than predicted. [87]
Even though half-lives of hundreds or thousands of years would be relatively long for superheavy elements, they are far too short for any such nuclides to exist primordially on Earth. Additionally, instability of nuclei intermediate between primordial actinides (232Th, 235U, and 238U) and the island of stability may inhibit production of nuclei within the island in r-process nucleosynthesis. Various models suggest that spontaneous fission will be the dominant decay mode of nuclei with A > 280, and that neutron-induced or beta-delayed fission—respectively neutron capture and beta decay immediately followed by fission—will become the primary reaction channels. As a result, beta decay towards the island of stability may only occur within a very narrow path or may be entirely blocked by fission, thus precluding the synthesis of nuclides within the island. [88] The non-observation of superheavy nuclides such as 292Hs and 298Fl in nature is thought to be a consequence of a low yield in the r-process resulting from this mechanism, as well as half-lives too short to allow measurable quantities to persist in nature. [89] [n] Various studies utilizing accelerator mass spectroscopy and crystal scintillators have reported upper limits of the natural abundance of such long-lived superheavy nuclei on the order of 10−14 relative to their stable homologs. [92]
Despite these obstacles to their synthesis, a 2013 study published by a group of Russian physicists led by Valeriy Zagrebaev proposes that the longest-lived copernicium isotopes may occur at an abundance of 10−12 relative to lead, whereby they may be detectable in cosmic rays. [63] Similarly, in a 2013 experiment, a group of Russian physicists led by Aleksandr Bagulya reported the possible observation of three cosmogenic superheavy nuclei in olivine crystals in meteorites. The atomic number of these nuclei was estimated to be between 105 and 130, with one nucleus likely constrained between 113 and 129, and their lifetimes were estimated to be at least 3,000 years. Although this observation has yet to be confirmed in independent studies, it strongly suggests the existence of the island of stability, and is consistent with theoretical calculations of half-lives of these nuclides. [93] [94] [95]
The decay of heavy, long-lived elements in the island of stability is a proposed explanation for the unusual presence of the short-lived radioactive isotopes observed in Przybylski's Star. [96]
The manufacture of nuclei on the island of stability proves to be very difficult because the nuclei available as starting materials do not deliver the necessary sum of neutrons. Radioactive ion beams (such as 44S) in combination with actinide targets (such as 248 Cm) may allow the production of more neutron rich nuclei nearer to the center of the island of stability, though such beams are not currently available in the required intensities to conduct such experiments. [63] [97] [98] Several heavier isotopes such as 250Cm and 254 Es may still be usable as targets, allowing the production of isotopes with one or two more neutrons than known isotopes, [63] though the production of several milligrams of these rare isotopes to create a target is difficult. [99] It may also be possible to probe alternative reaction channels in the same 48Ca-induced fusion-evaporation reactions that populate the most neutron-rich known isotopes, namely those at a lower excitation energy (resulting in fewer neutrons being emitted during de-excitation), or those involving evaporation of charged particles (pxn, evaporating a proton and several neutrons, or αxn, evaporating an alpha particle and several neutrons). [100] This may allow the synthesis of neutron-enriched isotopes of elements 111–117. [101] Although the predicted cross sections are on the order of 1–900 fb, smaller than when only neutrons are evaporated (xn channels), it may still be possible to generate otherwise unreachable isotopes of superheavy elements in these reactions. [100] [101] [102] Some of these heavier isotopes (such as 291Mc, 291Fl, and 291Nh) may also undergo electron capture (converting a proton into a neutron) in addition to alpha decay with relatively long half-lives, decaying to nuclei such as 291Cn that are predicted to lie near the center of the island of stability. However, this remains largely hypothetical as no superheavy nuclei near the beta-stability line have yet been synthesized and predictions of their properties vary considerably across different models. [1] [63] In 2024, a team of researchers at the JINR observed one decay chain of the known isotope 289Mc as a product in the p2n channel of the reaction between 242Pu and 50Ti, an experiment targeting neutron-deficient livermorium isotopes. This was the first successful report of a charged-particle exit channel in a hot fusion reaction between an actinide target and a projectile with Z ≥ 20. [103]
The process of slow neutron capture used to produce nuclides as heavy as 257 Fm is blocked by short-lived isotopes of fermium that undergo spontaneous fission (for example, 258Fm has a half-life of 370 μs); this is known as the "fermium gap" and prevents the synthesis of heavier elements in such a reaction. It might be possible to bypass this gap, as well as another predicted region of instability around A = 275 and Z = 104–108, in a series of controlled nuclear explosions with a higher neutron flux (about a thousand times greater than fluxes in existing reactors) that mimics the astrophysical r-process. [63] First proposed in 1972 by Meldner, such a reaction might enable the production of macroscopic quantities of superheavy elements within the island of stability; [1] the role of fission in intermediate superheavy nuclides is highly uncertain, and may strongly influence the yield of such a reaction. [88]
It may also be possible to generate isotopes in the island of stability such as 298Fl in multi-nucleon transfer reactions in low-energy collisions of actinide nuclei (such as 238U and 248Cm). [97] This inverse quasifission (partial fusion followed by fission, with a shift away from mass equilibrium that results in more asymmetric products) mechanism [104] may provide a path to the island of stability if shell effects around Z = 114 are sufficiently strong, though lighter elements such as nobelium and seaborgium (Z = 102–106) are predicted to have higher yields. [63] [105] Preliminary studies of the 238U + 238U and 238U + 248Cm transfer reactions have failed to produce elements heavier than mendelevium (Z = 101), though the increased yield in the latter reaction suggests that the use of even heavier targets such as 254Es (if available) may enable production of superheavy elements. [106] This result is supported by a later calculation suggesting that the yield of superheavy nuclides (with Z ≤ 109) will likely be higher in transfer reactions using heavier targets. [98] A 2018 study of the 238U + 232Th reaction at the Texas A&M Cyclotron Institute by Sara Wuenschel et al. found several unknown alpha decays that may possibly be attributed to new, neutron-rich isotopes of superheavy elements with 104 < Z < 116, though further research is required to unambiguously determine the atomic number of the products. [98] [107] This result strongly suggests that shell effects have a significant influence on cross sections, and that the island of stability could possibly be reached in future experiments with transfer reactions. [107]
Further shell closures beyond the main island of stability in the vicinity of Z = 112–114 may give rise to additional islands of stability. Although predictions for the location of the next magic numbers vary considerably, two significant islands are thought to exist around heavier doubly magic nuclei; the first near 354126 (with 228 neutrons) and the second near 472164 or 482164 (with 308 or 318 neutrons). [34] [75] [108] Nuclides within these two islands of stability might be especially resistant to spontaneous fission and have alpha decay half-lives measurable in years, thus having comparable stability to elements in the vicinity of flerovium. [34] Other regions of relative stability may also appear with weaker proton shell closures in beta-stable nuclides; such possibilities include regions near 342126 [109] and 462154. [110] Substantially greater electromagnetic repulsion between protons in such heavy nuclei may greatly reduce their stability, and possibly restrict their existence to localized islands in the vicinity of shell effects. [111] This may have the consequence of isolating these islands from the main chart of nuclides, as intermediate nuclides and perhaps elements in a "sea of instability" would rapidly undergo fission and essentially be nonexistent. [108] It is also possible that beyond a region of relative stability around element 126, heavier nuclei would lie beyond a fission threshold given by the liquid drop model and thus undergo fission with very short lifetimes, rendering them essentially nonexistent even in the vicinity of greater magic numbers. [109]
It has also been posited that in the region beyond A > 300, an entire "continent of stability" consisting of a hypothetical phase of stable quark matter, comprising freely flowing up and down quarks rather than quarks bound into protons and neutrons, may exist. Such a form of matter is theorized to be a ground state of baryonic matter with a greater binding energy per baryon than nuclear matter, favoring the decay of nuclear matter beyond this mass threshold into quark matter. If this state of matter exists, it could possibly be synthesized in the same fusion reactions leading to normal superheavy nuclei, and would be stabilized against fission as a consequence of its stronger binding that is enough to overcome Coulomb repulsion. [112]
Bohrium is a synthetic chemical element; it has symbol Bh and atomic number 107. It is named after Danish physicist Niels Bohr. As a synthetic element, it can be created in particle accelerators but is not found in nature. All known isotopes of bohrium are highly radioactive; the most stable known isotope is 270Bh with a half-life of approximately 2.4 minutes, though the unconfirmed 278Bh may have a longer half-life of about 11.5 minutes.
Hassium is a synthetic chemical element; it has symbol Hs and atomic number 108. It is highly radioactive: its most stable known isotopes have half-lives of approximately ten seconds. One of its isotopes, 270Hs, has magic numbers of protons and neutrons for deformed nuclei, giving it greater stability against spontaneous fission. Hassium is a superheavy element; it has been produced in a laboratory in very small quantities by fusing heavy nuclei with lighter ones. Natural occurrences of the element have been hypothesised but never found.
Rutherfordium is a synthetic chemical element; it has symbol Rf and atomic number 104. It is named after physicist Ernest Rutherford. As a synthetic element, it is not found in nature and can only be made in a particle accelerator. It is radioactive; the most stable known isotope, 267Rf, has a half-life of about 48 minutes.
Darmstadtium is a synthetic chemical element; it has symbol Ds and atomic number 110. It is extremely radioactive: the most stable known isotope, darmstadtium-281, has a half-life of approximately 14 seconds. Darmstadtium was first created in November 1994 by the GSI Helmholtz Centre for Heavy Ion Research in the city of Darmstadt, Germany, after which it was named.
Roentgenium is a synthetic chemical element; it has symbol Rg and atomic number 111. It is extremely radioactive and can only be created in a laboratory. The most stable known isotope, roentgenium-282, has a half-life of 130 seconds, although the unconfirmed roentgenium-286 may have a longer half-life of about 10.7 minutes. Roentgenium was first created in December 1994 by the GSI Helmholtz Centre for Heavy Ion Research near Darmstadt, Germany. It is named after the physicist Wilhelm Röntgen, who discovered X-rays. Only a few roentgenium atoms have ever been synthesized, and they have no practical application.
Livermorium is a synthetic chemical element; it has symbol Lv and atomic number 116. It is an extremely radioactive element that has only been created in a laboratory setting and has not been observed in nature. The element is named after the Lawrence Livermore National Laboratory in the United States, which collaborated with the Joint Institute for Nuclear Research (JINR) in Dubna, Russia, to discover livermorium during experiments conducted between 2000 and 2006. The name of the laboratory refers to the city of Livermore, California, where it is located, which in turn was named after the rancher and landowner Robert Livermore. The name was adopted by IUPAC on May 30, 2012. Six isotopes of livermorium are known, with mass numbers of 288–293 inclusive; the longest-lived among them is livermorium-293 with a half-life of about 80 milliseconds. A seventh possible isotope with mass number 294 has been reported but not yet confirmed.
Oganesson is a synthetic chemical element; it has symbol Og and atomic number 118. It was first synthesized in 2002 at the Joint Institute for Nuclear Research (JINR) in Dubna, near Moscow, Russia, by a joint team of Russian and American scientists. In December 2015, it was recognized as one of four new elements by the Joint Working Party of the international scientific bodies IUPAC and IUPAP. It was formally named on 28 November 2016. The name honors the nuclear physicist Yuri Oganessian, who played a leading role in the discovery of the heaviest elements in the periodic table. It is one of only two elements named after a person who was alive at the time of naming, the other being seaborgium, and the only element whose eponym is alive as of 2024.
Unbinilium, also known as eka-radium or element 120, is a hypothetical chemical element; it has symbol Ubn and atomic number 120. Unbinilium and Ubn are the temporary systematic IUPAC name and symbol, which are used until the element is discovered, confirmed, and a permanent name is decided upon. In the periodic table of the elements, it is expected to be an s-block element, an alkaline earth metal, and the second element in the eighth period. It has attracted attention because of some predictions that it may be in the island of stability.
Moscovium is a synthetic chemical element; it has symbol Mc and atomic number 115. It was first synthesized in 2003 by a joint team of Russian and American scientists at the Joint Institute for Nuclear Research (JINR) in Dubna, Russia. In December 2015, it was recognized as one of four new elements by the Joint Working Party of international scientific bodies IUPAC and IUPAP. On 28 November 2016, it was officially named after the Moscow Oblast, in which the JINR is situated.
Tennessine is a synthetic chemical element; it has symbol Ts and atomic number 117. It has the second-highest atomic number and joint-highest atomic mass of all known elements and is the penultimate element of the 7th period of the periodic table. It is named after the U.S. state of Tennessee, where key research institutions involved in its discovery are located.
An extended periodic table theorizes about chemical elements beyond those currently known and proven. The element with the highest atomic number known is oganesson (Z = 118), which completes the seventh period (row) in the periodic table. All elements in the eighth period and beyond thus remain purely hypothetical.
Flerovium is a synthetic chemical element; it has symbol Fl and atomic number 114. It is an extremely radioactive, superheavy element, named after the Flerov Laboratory of Nuclear Reactions of the Joint Institute for Nuclear Research in Dubna, Russia, where the element was discovered in 1999. The lab's name, in turn, honours Russian physicist Georgy Flyorov. IUPAC adopted the name on 30 May 2012. The name and symbol had previously been proposed for element 102 (nobelium), but was not accepted by IUPAC at that time.
In nuclear physics, a magic number is a number of nucleons such that they are arranged into complete shells within the atomic nucleus. As a result, atomic nuclei with a "magic" number of protons or neutrons are much more stable than other nuclei. The seven most widely recognized magic numbers as of 2019 are 2, 8, 20, 28, 50, 82, and 126.
Unbibium, also known as element 122 or eka-thorium, is a hypothetical chemical element; it has placeholder symbol Ubb and atomic number 122. Unbibium and Ubb are the temporary systematic IUPAC name and symbol respectively, which are used until the element is discovered, confirmed, and a permanent name is decided upon. In the periodic table of the elements, it is expected to follow unbiunium as the second element of the superactinides and the fourth element of the 8th period. Similarly to unbiunium, it is expected to fall within the range of the island of stability, potentially conferring additional stability on some isotopes, especially 306Ubb which is expected to have a magic number of neutrons (184).
Darmstadtium (110Ds) is a synthetic element, and thus a standard atomic weight cannot be given. Like all synthetic elements, it has no stable isotopes. The first isotope to be synthesized was 269Ds in 1994. There are 11 known radioisotopes from 267Ds to 281Ds and 2 or 3 known isomers. The longest-lived isotope is 281Ds with a half-life of 14 seconds. However, the unconfirmed 282Ds might have an even longer half-life of 67 seconds.
Flerovium (114Fl) is a synthetic element, and thus a standard atomic weight cannot be given. Like all synthetic elements, it has no stable isotopes. The first isotope to be synthesized was 289Fl in 1999. Flerovium has six known isotopes, along with the unconfirmed 290Fl, and possibly two nuclear isomers. The longest-lived isotope is 289Fl with a half-life of 1.9 seconds, but 290Fl may have a longer half-life of 19 seconds.
In nuclear physics, the valley of stability is a characterization of the stability of nuclides to radioactivity based on their binding energy. Nuclides are composed of protons and neutrons. The shape of the valley refers to the profile of binding energy as a function of the numbers of neutrons and protons, with the lowest part of the valley corresponding to the region of most stable nuclei. The line of stable nuclides down the center of the valley of stability is known as the line of beta stability. The sides of the valley correspond to increasing instability to beta decay. The decay of a nuclide becomes more energetically favorable the further it is from the line of beta stability. The boundaries of the valley correspond to the nuclear drip lines, where nuclides become so unstable they emit single protons or single neutrons. Regions of instability within the valley at high atomic number also include radioactive decay by alpha radiation or spontaneous fission. The shape of the valley is roughly an elongated paraboloid corresponding to the nuclide binding energies as a function of neutron and atomic numbers.
Unbiunium, also known as eka-actinium or element 121, is a hypothetical chemical element; it has symbol Ubu and atomic number 121. Unbiunium and Ubu are the temporary systematic IUPAC name and symbol respectively, which are used until the element is discovered, confirmed, and a permanent name is decided upon. In the periodic table of the elements, it is expected to be the first of the superactinides, and the third element in the eighth period. It has attracted attention because of some predictions that it may be in the island of stability. It is also likely to be the first of a new g-block of elements.
Unbiquadium, also known as element 124 or eka-uranium, is a hypothetical chemical element; it has placeholder symbol Ubq and atomic number 124. Unbiquadium and Ubq are the temporary IUPAC name and symbol, respectively, until the element is discovered, confirmed, and a permanent name is decided upon. In the periodic table, unbiquadium is expected to be a g-block superactinide and the sixth element in the 8th period. Unbiquadium has attracted attention, as it may lie within the island of stability, leading to longer half-lives, especially for 308Ubq which is predicted to have a magic number of neutrons (184).
Unbihexium, also known as element 126 or eka-plutonium, is a hypothetical chemical element; it has atomic number 126 and placeholder symbol Ubh. Unbihexium and Ubh are the temporary IUPAC name and symbol, respectively, until the element is discovered, confirmed, and a permanent name is decided upon. In the periodic table, unbihexium is expected to be a g-block superactinide and the eighth element in the 8th period. Unbihexium has attracted attention among nuclear physicists, especially in early predictions targeting properties of superheavy elements, for 126 may be a magic number of protons near the center of an island of stability, leading to longer half-lives, especially for 310Ubh or 354Ubh which may also have magic numbers of neutrons.