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Bohr magneton

The Bohr magneton (symbol: μB) is a fundamental physical constant representing the natural unit of magnetic moment for an electron arising from either its orbital angular momentum or intrinsic spin. It is defined by the formula μB = e ħ / (2 me), where e is the elementary charge, ħ is the reduced Planck's constant, and me is the mass of the electron. The currently accepted value, based on the 2022 CODATA recommendations, is 9.2740100657(29) × 10−24 J/T (joules per tesla), with the uncertainty in the final two digits. Introduced as part of Niels Bohr's seminal 1913 model of the , the concept linked quantized to magnetic properties, providing a quantum unit for orbits that resolved inconsistencies in classical electromagnetism. The term "Bohr magneton" was formally coined in 1920 by , who derived it explicitly from Bohr's theory while contrasting it with experimental units of . This constant quantizes the orbital of an as μz = −μB ml (where ml is the ) and plays a central role in phenomena like the , where external magnetic fields split atomic energy levels. In , the Bohr magneton extends beyond Bohr's original semi-classical framework to describe spin magnetic moments (with a g-factor of approximately 2 for electrons) and serves as a for measuring and molecular . It is notably smaller than the (by a factor of about , due to the proton's greater mass) and is essential in fields such as electron paramagnetic resonance, magnetochemistry, and the study of ferromagnetic materials. Experimental verifications, including precise measurements of the electron g-factor, confirm its value to high accuracy, underscoring its foundational status in .

Definition and Properties

Definition

The Bohr magneton, denoted by the symbol \mu_B, is a that serves as the natural unit of for an arising from its orbital . It quantifies the intrinsic moment associated with the electron's orbital motion in atomic systems, where the magnetic moment is proportional to the angular momentum. The value of the Bohr magneton is given by the expression \mu_B = \frac{e \hbar}{2 m_e}, where e is the elementary charge, \hbar is the reduced Planck's constant, and m_e is the rest mass of the electron. This constant acts as the quantum of magnetic moment in atomic physics, representing the smallest unit of orbital magnetic moment in quantized systems, such as those described by angular momentum quantum numbers. The term "Bohr magneton" is named after the Danish physicist , whose early atomic model provided the conceptual foundation for understanding orbits and their associated magnetic properties, though the unit itself emerged in the context of developments in the early .

Numerical Value and Units

The current CODATA-recommended value for the Bohr magneton, as determined in the 2022 adjustment and published in 2024, is \mu_B = 9.2740100657(29) \times 10^{-24} J/T, with a relative standard uncertainty of $3.1 \times 10^{-10}. This value is derived from the defining relation \mu_B = e \hbar / (2 m_e), incorporating precise measurements of the e, reduced \hbar, and m_e. In Gaussian cgs units, the Bohr magneton is expressed as \mu_B \approx 9.274 \times 10^{-21} erg/G. In units of electronvolts per , it is \mu_B = 5.7883817982(18) \times 10^{-5} /T, with a relative of $3.1 \times 10^{-10}. In , where the unit of is e \hbar / m_e, the Bohr magneton has the value \mu_B = 1/2. The precision of this CODATA value reflects improvements from recent experiments on the electron's magnetic properties, particularly high-accuracy measurements of the electron anomaly a_e = (g_e - 2)/2. A key contribution came from the 2023 measurement by the group, which reported a_e^\text{(exp)} = 1.15965218059(13) \times 10^{-3} with a relative of $1.1 \times 10^{-10}, enhancing resolution by a factor of 2.2 compared to prior results and supporting further refinements of the \alpha in subsequent adjustments. Earlier measurements, such as those from 2018 and 2020, further supported these refinements by providing consistent determinations of \alpha with uncertainties around $1 \times 10^{-10}. Conversion between SI and Gaussian cgs units for the Bohr magneton requires multiplying the SI value (in ) by $10^3, since $1J =10^7 erg and $1 T = $10^4 exactly. For conversion to eV/T, divide the SI value by the in coulombs times the in (or equivalently, use $1J\approx 6.241509074 \times 10^{18}eV), yielding the factor\mu_B^\text{(eV/T)} = \mu_B^\text{(J/T)} / 1.602176634 \times 10^{-19}$. These factors ensure consistency across unit systems for computational applications.

Historical Development

Early Concepts

In the early 20th century, efforts to understand atomic spectra and magnetic properties led to initial proposals for quantized atomic magnetic moments, predating structured quantum models of the atom. Walther Ritz, in 1907, suggested that atoms could act as elementary permanent magnets to account for the regularities in spectral lines, such as those described by the Balmer formula, implying that quantized energy levels might produce discrete magnetic effects through oscillating electric currents within atoms. In 1911, Pierre Weiss introduced the concept of the "molecular magneton" to explain , positing that atoms in ferromagnetic materials possess intrinsic magnetic moments that align under an internal "molecular field," leading to below a critical . Weiss derived an empirical value for this unit of approximately 1.853 × 10^{-24} J/T, based on measurements of saturation magnetization in materials like iron and , which he termed the Weiss magneton. Building on classical electron orbit models, Richard Gans calculated in 1911 a magnetic moment for orbiting electrons that was twice the value later established as the Bohr magneton, by assuming the electron's orbital was quantized in units of ħ = h / 2π but using a of e / m_e (without the conventional 1/2 factor), resulting in μ = e ħ / m_e. This semi-classical approach highlighted discrepancies between classical expectations and experimental paramagnetic susceptibilities. At the First in 1911, derived an expression for the atomic in the context of , proposing μ = e ħ / (2 m_e), where ħ = h / (2π), by quantizing the electron's orbital in units of ħ and applying to the alignment of these moments in a . Independently, in 1913, Romanian physicist Ștefan Procopiu arrived at the same expression using Planck's to determine the molecular , assuming quantized levels for electrons in atoms and linking it to observed paramagnetic behaviors.

Introduction in Atomic Theory

In Niels Bohr's seminal 1913 atomic model, the concept of the emerged as a fundamental unit linking the quantized of to their orbital . Bohr postulated that the L of an in stable orbits around the is quantized as L = n \hbar, where n is a positive and \hbar = h / 2\pi is the reduced Planck's constant. From classical electrodynamics, the \mu associated with this orbital motion is given by \mu = \frac{e}{2 m_e} L, where e is the and m_e is the mass. Substituting the quantization condition yields \mu = n \mu_B, with \mu_B = \frac{e \hbar}{2 m_e} defining the as the basic unit of atomic for orbital contributions. This theoretical framework was formalized in Bohr's third paper of the 1913 , where he applied it to explain aspects of spectra and magnetic properties, building on earlier classical ideas but introducing quantum restrictions to resolve inconsistencies in radiation theory. The model's prediction that magnetic moments are integer multiples of \mu_B provided a natural scale for magnetism, distinct from bulk phenomenological units. Pre-Bohr contributions from researchers like Pierre Weiss had proposed smaller empirical magnetons for ferromagnetic materials, but Bohr's unit was specifically tailored to individual orbits in atoms. In 1920, formalized the terminology by naming this theoretical unit the "Bohr magneton" in his work on the anomalous , explicitly distinguishing it from the smaller "Weiss magneton" derived from early experimental studies of in solids. Pauli's adoption highlighted the unit's role in bridging and observed spectral splittings under magnetic fields. Independently, physicist Ștefan Procopiu had derived the same expression for the electron's in 1913, based on quantum considerations of molecular elements, predating widespread recognition of Bohr's work in some contexts; this led to the alternative designation "Bohr–Procopiu magneton" in certain scientific literature. Early experimental validations of the Bohr magneton came through observations of the in atomic spectra, where magnetic fields split spectral lines in patterns consistent with orbital magnetic moments quantized in units of \mu_B. For instance, measurements of line splittings in vapors during the 1910s aligned with Bohr's predictions for hydrogen-like systems, confirming the scale of \mu_B and supporting the model's quantization hypothesis against classical expectations. These validations, building on pre-1913 Zeeman data, underscored the unit's physical reality in atomic structure.

Theoretical Foundations

Derivation in Bohr Model

In Niels Bohr's 1913 atomic model for hydrogen-like atoms, the electron is postulated to execute stable circular motion around the under the Coulomb attraction, with the key assumption of quantized orbital given by L = n \hbar, where n is a positive integer (the principal ) and \hbar = h / 2\pi is the reduced Planck's constant. This quantization condition ensures discrete energy levels and stable orbits, distinguishing the model from classical electrodynamics. The orbiting constitutes a , as its charge motion generates a time-averaged . The magnitude of this equivalent is I = \frac{e v}{2 \pi r}, where e > 0 is the magnitude, v is the electron's speed, and r is the orbital radius. The area enclosed by this loop is A = \pi r^2, so the orbital moment has magnitude \mu_\mathrm{orbital} = I A = \left( \frac{e v}{2 \pi r} \right) (\pi r^2) = \frac{e v r}{2}. In vector terms, \vec{\mu}_\mathrm{orbital} = \frac{e}{2 m_e} \vec{L} (with the yielding an antiparallel direction for the electron's negative charge), but the magnitude relation holds directly from the classical expression for a . The orbital is defined as L = m_e v r, where m_e is the rest mass. Substituting v r = L / m_e into the expression yields \mu_\mathrm{orbital} = \frac{[e](/page/E!)}{2 m_e} L. Applying the quantization condition L = n \hbar, the orbital becomes \mu_\mathrm{orbital} = n \left( \frac{[e](/page/E!) \hbar}{2 m_e} \right). The quantity \mu_B = \frac{[e](/page/E!) \hbar}{2 m_e} represents the natural unit of orbital in the model, termed the Bohr magneton after its in Bohr's ; for the (n = 1), L = \hbar and \mu_\mathrm{orbital} = \mu_B. Bohr noted the proportionality between the and in circular orbits, linking it to spectroscopic phenomena, though the explicit unit emerged from this semi-classical analysis.

Quantum Mechanical Perspective

In , the orbital arises from the interaction of the electron's orbital with an external . The operator for the orbital is given by \vec{\mu}_L = -\frac{\mu_B}{[\hbar](/page/H-bar)} \vec{L}, where \vec{L} is the orbital and \mu_B = \frac{[e](/page/Elementary_charge) \hbar}{2m_e} is the Bohr magneton, with e the magnitude, [\hbar](/page/H-bar) the reduced Planck's constant, and m_e the . For eigenstates of the orbital with quantum numbers l and m_l (ranging from -l to +l), the z-component eigenvalue is - m_l \mu_B, reflecting the quantized projections along the field direction. The spin magnetic moment introduces a distinct quantum mechanical feature, described by \vec{\mu}_S = -g_e \frac{\mu_B}{\hbar} \vec{S}, where \vec{S} is the and g_e \approx 2 is the . For a single with S = \hbar/2, the magnitude of the spin magnetic moment is approximately \mu_B, twice the naive classical expectation due to the relativistic , which naturally incorporates as an intrinsic with twice that of the orbital case. This factor of 2 resolves the observed in atomic spectra and is a cornerstone of relativistic quantum mechanics. In multi-electron atoms, the total magnetic moment combines orbital and spin contributions through the total angular momentum \vec{J} = \vec{L} + \vec{S}, yielding \vec{\mu}_J = -g_J \frac{\mu_B}{\hbar} \vec{J}, where g_J is the , given by g_J = 1 + \frac{J(J+1) + S(S+1) - L(L+1)}{2J(J+1)} in LS coupling. This formalism accounts for the vector coupling of angular momenta and explains the splitting patterns in weak magnetic fields, such as the anomalous . The Bohr magneton thus serves as the fundamental unit scaling these moments. The spin g-factor g_e receives quantum electrodynamic (QED) corrections beyond the Dirac value of exactly 2, arising from virtual photon interactions. The leading correction is \Delta g_e = \frac{\alpha}{2\pi}, where \alpha is the , first computed by Schwinger using renormalization techniques in perturbative . Higher-order terms further refine g_e - 2 \approx 0.001159652, influencing fine-structure splittings via spin-orbit (where the orbital motion produces an effective interacting with the moment) and hyperfine interactions ( electron and nuclear moments, scaled by \mu_B). These QED effects validate the Dirac framework while highlighting radiative corrections essential for precision .

Applications and Significance

In Atomic and Molecular Physics

In , the Bohr magneton serves as the fundamental unit of for , enabling the quantitative description of how external interact with atomic energy levels and influence observable phenomena such as splitting and magnetic susceptibilities. A key application is the , where an applied causes the splitting of degenerate atomic energy levels, leading to the observed in atomic spectra. In the normal Zeeman effect, primarily involving orbital , the energy shift for a level with m_l is given by \Delta E = \mu_B B m_l, where B is the strength. For the more general anomalous Zeeman effect, which incorporates , the splitting is \Delta E = g_j \mu_B B m_j, with g_j as the and m_j the ; this accounts for the majority of observed splittings in atoms due to spin-orbit coupling. These shifts arise from the interaction energy -\vec{\mu} \cdot \vec{B}, where the \vec{\mu} is proportional to the Bohr magneton. The Bohr magneton also underpins the magnetic susceptibilities of atoms and molecules, distinguishing paramagnetic from diamagnetic behaviors. In paramagnetism, unpaired electron spins align with an external field, leading to a positive susceptibility that follows Curie's law: \chi \propto \frac{\mu_B^2}{kT}, where k is Boltzmann's constant and T the temperature; this reflects the thermal averaging of spin orientations, with the Curie constant incorporating the squared magnetic moment per atom. Diamagnetism, conversely, arises from induced orbital currents opposing the field, yielding a weak negative susceptibility independent of temperature. Electron spin resonance (ESR) spectroscopy relies on the Bohr magneton to probe unpaired s in atoms and molecules by inducing transitions between spin states in a . The resonance condition for transitions between m_s = \pm 1/2 states is h \nu = g \mu_B B, where h is Planck's constant, \nu the microwave frequency, g the electron g-factor (approximately 2), and B the field; this energy splitting allows detection of properties with high sensitivity. Electronic magnetic effects dominate atomic and molecular magnetism because the Bohr magneton \mu_B = \frac{e \hbar}{2 m_e} is much larger than the \mu_N = \frac{e \hbar}{2 m_p} \approx \frac{\mu_B}{1836}, due to the proton's mass being about 1836 times that of the , rendering nuclear contributions negligible in most atomic-scale phenomena.

In Modern Technologies

In (MRI), proton s interact with hyperfine fields generated by unpaired s, where the energy scale is governed by the ratio of the to the proton (|γ_e / γ_p| ≈ 658), enabling enhanced polarization transfer and high-resolution studies of - coupling. This ratio underpins (DNP) techniques, such as Overhauser DNP, which exploit the much larger to boost nuclear polarization by factors up to 658, improving MRI sensitivity for biomedical imaging applications like proton double imaging (PEDRI). In quantum computing, the Bohr magneton plays a key role in controlling spins as s, particularly in quantum dots and nitrogen-vacancy () centers in . For quantum dots, initialization of states requires magnetic fields where the Zeeman energy |g μ_B B| greatly exceeds k_B T, ensuring alignment to the for reliable operations. In NV centers, external fields of around 20 mT induce splittings via the term g_e μ_B B in the (with g_e ≈ 2), facilitating manipulation through optical and addressing, while coherence times reach up to 15 ms with dynamical techniques, limited in part by magnetic interactions scaling with g μ_B μ_0. Electron paramagnetic resonance (EPR) spectroscopy utilizes the Bohr magneton to quantify g-factors and hyperfine splittings, providing insights into the electronic structure and local environments of paramagnetic materials for advanced . The resonance condition h ν = g μ_B B directly relates the applied field B to the observed ν, allowing precise determination of g (typically near 2 for free electrons) and splittings from interactions, which reveal bonding and coordination details in catalysts, biomolecules, and . Recent innovations in nanoscale EPR sensors, such as those employing superconducting flux qubits or NV centers, achieve detection volumes as small as 50 fL with sensitivities down to 400 spins·Hz⁻¹/², enabling spatially resolved measurements in quantum devices and biological systems. Precision measurements involving the Bohr magneton contribute to refining fundamental constants through comparisons of spin precession and cyclotron frequencies in Penning trap experiments with single electrons. These ratios yield the electron g-factor anomaly (g-2), which, combined with the cyclotron frequency q B / (2π m_e), informs the value of μ_B = e ħ / (2 m_e) with uncertainties below 10^{-12}. Such data were integral to the 2022 CODATA adjustment, updating μ_B to 9.2740100657(29) × 10^{-24} J T^{-1}, with ongoing experiments poised to support the anticipated 2026 revision for even higher accuracy in metrology and quantum standards.

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