Isotopes of oganesson
Oganesson (Og), with atomic number 118, is a synthetic superheavy element whose isotopes are all highly unstable, radioactive, and produced only in particle accelerators, exhibiting half-lives on the order of milliseconds or less.[1] The sole confirmed isotope is ^{294}Og, which has a half-life of approximately 0.58 milliseconds (with uncertainties ranging from 0.40 to 1.02 ms across measurements) and primarily undergoes alpha decay to ^{290}Lv (livermorium-290), with a minor branch to spontaneous fission.[2] Theoretical models predict additional isotopes such as ^{293}Og and ^{295}Og, but these remain unconfirmed experimentally, with earlier claims of their synthesis retracted due to insufficient evidence.[3] The discovery of oganesson isotopes stemmed from efforts to extend the periodic table through hot fusion reactions involving heavy-ion bombardment. In 2002, a collaborative team from the Joint Institute for Nuclear Research (JINR) in Dubna, Russia, and the Lawrence Livermore National Laboratory in the United States first synthesized ^{294}Og (along with its decay daughter ^{290}Lv) by accelerating ^{48}Ca ions onto a ^{249}Cf target, producing three decay events.[2] This result was confirmed in 2005 with three additional events at JINR, providing the robust evidence required for official recognition by the International Union of Pure and Applied Chemistry (IUPAC) and International Union of Pure and Applied Physics (IUPAC) in 2015, leading to the element's naming as oganesson in 2016 after nuclear physicist Yuri Oganessian.[4] To date, only a handful of ^{294}Og atoms—fewer than six—have been produced in total, highlighting the extreme challenges in superheavy element synthesis due to low cross-sections (on the order of picobarns) and fleeting existence times.[5] Research on oganesson isotopes focuses on nuclear structure, decay chains, and potential chemical properties, though the sub-millisecond half-lives preclude conventional chemistry experiments. ^{294}Og undergoes alpha decay (with energy around 11.8 MeV) to ^{290}Lv, which further decays by alpha emission to ^{286}Fl (flerovium-286) and continues through the chain to lighter superheavy nuclides.[2] Theoretical studies suggest that isotopes nearer the predicted "island of stability" (around mass numbers 296–298) could have longer half-lives, possibly seconds or more, enabling future investigations into relativistic effects on group 18 element behavior, such as deviations from noble gas inertness.[6] Ongoing experiments at facilities like JINR and GSI Helmholtz Centre aim to produce more events and probe heavier isotopes, but progress remains limited by accelerator capabilities and detection sensitivities.[7]Known isotopes
List of known isotopes
Oganesson (Og), atomic number 118, has only a single confirmed isotope, ^{294}Og, synthesized through fusion reactions involving calcium-48 and californium-249 targets.[8] The known properties of this isotope are summarized in the following table. Due to the extremely limited number of production events—only five atoms observed as of 2025—the half-life measurement carries significant uncertainty, reflecting statistical limitations from the small sample size.[8][9]| Isotope | Mass number (A) | Half-life | Decay mode(s) | Daughter product(s) |
|---|---|---|---|---|
| ^{294}Og | 294 | 0.58^{+0.44}_{-0.18} ms | α decay (dominant), SF | ^{290}Lv (α), no observed SF daughter |
Nuclear properties of oganesson-294
Oganesson-294, the only confirmed isotope of oganesson, was synthesized through the hot fusion reaction of a ^{48}Ca beam with a ^{249}Cf target, producing the compound nucleus ^{297}Og that evaporates three neutrons to yield ^{294}Og. Evaporation residues were separated in flight using the Dubna Gas-Filled Recoil Separator (DGFRS) at the Joint Institute for Nuclear Research (JINR) and implanted into a position-sensitive silicon detector array, where subsequent alpha decay sequences were recorded to genetically link parent-daughter relationships. This detection method allowed identification of decay chains consistent with Z=118 assignment based on matching energies and half-lives with known descendants.[10][11] Five atoms of ^{294}Og have been observed across experiments conducted in 2002, 2005, 2018, and a 2023 irradiation at FLNR-JINR, where the fifth event was recorded after 9 days of beam time, all decaying via alpha emission.[10][11][12] The measured half-life from these events is 0.58^{+0.44}_{-0.18} ms. The alpha decay energy is 11.65 ± 0.06 MeV, with no observed spontaneous fission (SF) events among the limited statistics, suggesting a dominant alpha decay mode (observed branching ratio ≈100%); however, SF is theoretically possible due to the high fissility of superheavy nuclei, with an upper limit on the SF branching ratio estimated below 20% based on non-observation.[10][11] The alpha decay of ^{294}Og proceeds through the chain ^{294}Og → ^{290}Lv → ^{286}Fl → ^{282}Cn → ^{278}Ds → ^{274}Hs, with each step primarily via alpha emission except where SF competes in lighter daughters. Representative values include: ^{290}Lv with half-life ≈8.3 ms and α energy ≈10.8 MeV; ^{286}Fl with half-life ≈110 ms (α branching ≈60%, SF ≈40%) and α energy ≈10.3 MeV; ^{282}Cn with half-life ≈1.0 ms and α energy ≈9.9 MeV; ^{278}Ds with half-life ≈1.7 ms and α energy ≈9.7 MeV; and ^{274}Hs with half-life ≈54 ms and α energy ≈9.3 MeV, often terminating in SF of subsequent seaborgium daughters. These properties highlight the rapid succession of decays, limiting opportunities for chemical studies, and confirm the even-even nature of ^{294}Og consistent with enhanced stability against immediate fission.[10][11]Nucleosynthesis
Hot fusion reactions
Hot fusion reactions, utilizing neutron-rich projectiles such as ^{48}Ca on actinide targets, have been the primary method for synthesizing isotopes of oganesson, enabling the production of relatively neutron-rich superheavy nuclei near the predicted island of stability. These reactions involve complete fusion followed by evaporation of neutrons to form the compound nucleus ^{297}Og, which de-excites primarily through the 3n channel to yield ^{294}Og. The successful synthesis of oganesson was achieved via the reaction ^{249}Cf(^{48}Ca,3n)^{294}Og at the Joint Institute for Nuclear Research (JINR) in Dubna, Russia. In the initial 2002 experiment, one atom of ^{294}Og was produced, followed by two more atoms in a 2005 confirmation run, establishing the discovery of element 118. These experiments employed a ^{48}Ca beam at an energy of approximately 243 MeV in the laboratory system, corresponding to a compound nucleus excitation energy of about 29 MeV, with a measured cross section of 0.3–0.9 pb for the 3n evaporation channel. The total beam dose across both runs was 2.5×10^{19} ions. The experimental apparatus utilized the Dubna Gas-Filled Recoil Separator (DGFRS), which separates recoil products from the intense beam and scattered particles based on their charge-to-mass ratio in a helium-filled chamber, allowing detection of individual decay chains. Only the 3n evaporation channel was observed, producing ^{294}Og; despite searches, no confirmed events were detected in the 2n or 1n channels leading to ^{295}Og or ^{293}Og, attributable to their significantly lower cross sections below 0.1 pb. Efforts to synthesize heavier oganesson isotopes have included attempts using enriched ^{250}Cf and ^{251}Cf targets in reactions such as ^{250}Cf(^{48}Ca,3n)^{295}Og and ^{251}Cf(^{48}Ca,3n)^{296}Og, aimed at approaching the neutron magic number N=184. However, no decays attributable to these isotopes have been detected as of 2025, despite beam doses exceeding 10^{19} ions in recent experiments at JINR.Cold and other fusion reactions
An attempt to synthesize isotopes of oganesson via cold fusion involved bombarding a ^{208}Pb target with ^{86}Kr ions to form the compound nucleus ^{294}Og^{*}, potentially leading to ^{294-x}Og + x n for x = 0–3.[13] This experiment, conducted at Lawrence Berkeley National Laboratory in April–May 2001, delivered a beam dose of 2.6 \times 10^{18} ions but observed no decay events attributable to oganesson isotopes.[13] The resulting upper limits on the production cross section were 0.9 pb at a magnetic rigidity of 2.00 Tm and 0.6 pb at 2.12 Tm, indicating cross sections below 1 pb.[13] As an alternative to the successful ^{48}Ca-induced hot fusion, researchers explored the reaction ^{248}Cm(^{50}Ti, x n)^{298-x}Og (x = 0–4) to access more neutron-rich oganesson isotopes.[14] This effort, performed at the RIKEN Nishina Center using the GARIS-II separator, spanned 39 days with a total beam dose of 4.93 \times 10^{18} ^{50}Ti projectiles but yielded no correlated decay chains.[14] An upper limit of 0.50 pb (1\sigma) was established for the cross section, limited by achievable beam intensities and the low reaction rates typical of such asymmetric systems.[14] Other proposed routes, such as ^{238}U(^{50}Ti, x n) or multinucleon transfer reactions in heavy-ion collisions (e.g., ^{238}U + ^{238}U or ^{136}Xe + ^{248}Cm), remain unattempted for oganesson production as of 2025, with no observed yields due to insufficient experimental validation.[15][16] These failures stem from higher fusion barriers in cold fusion reactions, which increase with atomic number and reduce fusion probabilities exponentially beyond Z = 113, and lower neutron evaporation probabilities that limit survival against fission compared to neutron-richer hot fusion pathways.[17][3]Theoretical predictions
Predicted isotopes and stability
Theoretical models, including semi-microscopic calculations based on the Skyrme-SLy4 interaction and deformed Woods-Saxon potentials, predict the existence of oganesson isotopes spanning a mass range from ^{288}Og to ^{308}Og, with potential extensions to higher masses up to ^{313}Og in broader superheavy surveys.[18] These predictions indicate that lighter isotopes like ^{293}Og may have alpha decay half-lives around 0.1 ms, while mid-range ones such as ^{295}Og could reach up to 45 ms, marking it as relatively more stable within the series.[18] Heavier isotopes, including those approaching or reaching the neutron number N=184 (e.g., ^{302}Og), are expected to exhibit enhanced stability due to shell closure effects, though overall half-lives remain in the millisecond range owing to the high proton number Z=118, which promotes rapid decay. Macroscopic-microscopic approaches, such as the shell-effect induced generalized liquid-drop model combined with clustering effects, further refine these estimates by predicting dominant alpha decay for isotopes up to ^{303}Og, with half-lives for ^{295}Og and ^{296}Og near 0.4 ms.[19] For ^{297}Og, similar models forecast an alpha decay half-life of approximately 0.16 ms, transitioning toward spontaneous fission dominance in isotopes beyond ^{304}Og, where fission barriers lower significantly. These trends highlight oganesson's position near the periphery of the predicted "island of stability" centered around Z ≈ 114 and N = 184, where shell closures might otherwise prolong lifetimes, but the increasing Coulomb repulsion at high Z limits half-lives to milliseconds rather than seconds or longer. Relativistic effects play a dual role in oganesson isotopes: in nuclear structure, relativistic mean-field models account for enhanced binding near shell closures, supporting the stability trends, while in atomic physics, strong relativistic stabilization of the 7p_{1/2} orbital deviates from the behavior of lighter homologs like radon (Z=86), potentially rendering oganesson less noble-gas-like and more reactive or even solid at room temperature. Despite these predictions, no oganesson isotopes beyond the verified ^{294}Og have been detected, with its measured half-life of 0.7 ms serving as a benchmark for model validation.[18] Ongoing and future experiments at upgraded facilities, such as enhanced heavy-ion accelerators, aim to probe these heavier, theoretically more stable isotopes to test the boundaries of the island of stability.[20]| Isotope | Predicted Half-Life | Dominant Decay Mode | Model/Reference |
|---|---|---|---|
| ^{293}Og | ~0.1 ms | α-decay | Semi-microscopic (Skyrme-SLy4) |
| ^{295}Og | ~1–45 ms | α-decay | Semi-microscopic (Skyrme-SLy4) |
| ^{297}Og | ~0.16 ms | α-decay | Two-potential approach |
| ^{302}Og | ~1–10 ms (est.) | α-decay/SF | GLDM + shell effects |