THE ATOM BOHR MODEL QUANTUM COMPARISON SIMULATOR MOLECULES BUILD NUCLEUS
Atoms · Molecules · Nuclei — Real-Time 3D Quantum Simulation

QUANTUM ATOM

Everything you can see, touch, and breathe is made of atoms.
Yet for centuries, no one could see inside one.
This simulator changes that — rendering electron orbitals, molecular bonds, and the nucleus itself in real-time 3D.

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118
Elements Simulated
52
Molecules Modeled
10
Orbital Sub-Shells
28K
Points Per Orbital
3
Companion Tools
1926
Year QM Was Born

The Basics

What is an atom?

An atom is the smallest unit of ordinary matter that retains the chemical properties of an element. The word comes from the Greek atomos — meaning "uncuttable" — coined by Democritus around 400 BCE, who theorized that all matter was made of indivisible particles in an infinite void.

He was wrong about one thing: atoms are absolutely cuttable. Every atom consists of a dense central nucleus — packed with positively charged protons and neutral neutrons — surrounded by a cloud of negatively charged electrons that define its chemistry, its bonds, and its behavior.

The nucleus is extraordinarily dense. If an atom were the size of a football stadium, the nucleus would be a marble at the center. Everything else is mostly empty space — or more precisely, a quantum probability field where electrons exist as smeared-out wave functions rather than definite point particles.

It took humanity over 2,400 years — from Democritus to Schrödinger — to develop an accurate picture of atomic structure. Each model was a revolution that shattered the previous one. The journey is one of the greatest intellectual adventures in human history.

HYDROGEN ATOM · QUANTUM PROBABILITY DENSITY
99.9%
Empty Space
If you removed the empty space from every atom in the human body, all matter would fit in a sugar cube — yet weigh the same.
10⁻¹⁵m
Nucleus Diameter
The nucleus is 100,000 times smaller than the atom itself. Nuclear density is approximately 2.3 × 10¹⁷ kg/m³.
118
Known Elements
Each element is defined by its number of protons. Change the proton count and you change the element entirely — that's nuclear transmutation.

History of Atomic Theory

2,400 years
of discovery

Every model of the atom was once the cutting edge of human knowledge — and every model was eventually proved incomplete. This is how science works.

~400 BCE
Democritus · Greece
The Atomist Hypothesis
Democritus proposed that all matter is composed of tiny, indivisible, indestructible particles called atoms. Different atoms have different sizes and shapes, explaining different materials. Pure philosophy — no experiments, no math. Yet astonishingly prescient.
PHILOSOPHICAL MODEL
1804
John Dalton · England
The Billiard Ball Model
Dalton's atomic theory put numbers on atoms for the first time. Elements are made of identical atoms; atoms of different elements have different masses; compounds form when atoms combine in fixed ratios. The atom was a solid, indivisible sphere — a billiard ball of matter.
SOLID SPHERE
1897
J.J. Thomson · England
The Plum Pudding Model
Thomson discovered the electron — the first subatomic particle — using cathode ray tubes. His model placed electrons (the "plums") embedded in a diffuse ball of positive charge (the "pudding"). Atoms had internal structure for the first time. Nobel Prize 1906.
PLUM PUDDING
1911
Ernest Rutherford · New Zealand/England
The Nuclear Model
Rutherford's gold foil experiment shattered the plum pudding model. Most alpha particles passed straight through — but some bounced back at extreme angles. "It was as if you fired artillery shells at tissue paper and they came back and hit you." The nucleus was born. Most of the atom is empty space.
NUCLEAR DISCOVERY
1913
Niels Bohr · Denmark
The Bohr Planetary Model
Bohr quantized the atom. Electrons orbit the nucleus in fixed circular shells at discrete energy levels. When electrons jump between levels they absorb or emit photons of specific frequencies — explaining the hydrogen spectrum perfectly. Revolutionary, but still wrong about electron shape. Nobel Prize 1922.
QUANTIZED ORBITS
1924
Louis de Broglie · France
Wave-Particle Duality
De Broglie proposed that if light (waves) could behave as particles (photons), then particles like electrons could behave as waves. Every moving particle has a wavelength λ = h/mv. This was the conceptual seed of quantum mechanics. Nobel Prize 1929.
MATTER WAVES
1925–26
Heisenberg · Schrödinger · Born
Quantum Mechanics Born
Heisenberg developed matrix mechanics; Schrödinger developed wave mechanics; Born gave the probability interpretation of the wavefunction. Together they created quantum mechanics — the most accurate physical theory ever devised. Electrons don't orbit — they exist as probability densities described by wavefunctions ψ.
QUANTUM REVOLUTION
Today
Quantum Atom Simulator
See It For Yourself
For the first time in history, anyone with a browser can visualize real quantum mechanical orbital shapes in three dimensions — rendered in real-time from the actual probability density mathematics. The invisible, finally visible.
THIS SIMULATOR

Model 1 of 2

The Bohr Model

Niels Bohr's 1913 model was the first to successfully predict the hydrogen spectrum. It was a triumph — and a stepping stone to something far stranger.

BOHR MODEL · HYDROGEN
BOHR ENERGY LEVELS
Eₙ = −13.6 eV / n²
ORBITAL ANGULAR MOMENTUM
L = n · ℏ
The Core Idea
Bohr proposed that electrons can only occupy specific, discrete energy levels — called shells or orbits — labeled by the principal quantum number n = 1, 2, 3... Electrons in lower shells have lower energy. They cannot exist "between" shells.
Quantum Jumps
When an electron absorbs a photon of exactly the right energy, it jumps to a higher shell (excitation). When it falls back down, it emits a photon whose frequency exactly matches the energy difference: ΔE = hf. This explained the hydrogen emission spectrum perfectly.
What It Got Right
Hydrogen's spectral lines (Lyman, Balmer, Paschen series) were predicted with extraordinary precision. The concept of quantized energy levels — that electrons don't exist at all energies — was profoundly correct and remains a cornerstone of chemistry.
Where It Broke Down
The Bohr model fails for multi-electron atoms, cannot explain chemical bonding, predicts incorrect orbital shapes, violates the Heisenberg Uncertainty Principle (electrons can't have both defined position and momentum), and incorrectly assumes circular planetary orbits. It's a useful approximation — not reality.

Model 2 of 2

The Quantum
Cloud Model

Quantum mechanics replaced orbits with orbitals — not paths, but probability clouds defined by wavefunctions. Electrons don't travel in circles. They exist everywhere at once, with some places more probable than others.

In quantum mechanics, the state of an electron is described by a wavefunction ψ(r, θ, φ). The wavefunction itself has no direct physical meaning — but its square, |ψ|², gives the probability density of finding the electron at any point in space. This is Born's rule.

An orbital is not an orbit. It is a three-dimensional region of space where an electron is most likely to be found — typically defined as the volume containing 90% of the electron probability. The shapes of these orbitals — spheres, dumbbells, cloverleaves, toroids — emerge directly from the mathematics of the Schrödinger equation.

This means electrons are fundamentally delocalized. An electron in a 2p orbital isn't "spinning around the nucleus" — it genuinely has some probability of being in one lobe, the other lobe, or anywhere in between, simultaneously. Only when you measure it does it "collapse" to a definite position.

This weirdness is not a flaw — it is the source of everything: chemical bonds, solid matter, semiconductors, DNA, life itself. The quantum atom is why chemistry works.

Quantum Numbers
n
Principal Quantum Number
Determines the electron's energy level and the size of the orbital. Higher n = higher energy = larger, more diffuse orbital.
n = 1, 2, 3, 4, 5...
ℓ
Angular Momentum Number
Defines the shape of the orbital. ℓ=0 gives spherical s-orbitals; ℓ=1 gives dumbbell p-orbitals; ℓ=2 gives d-orbitals.
ℓ = 0 to (n−1)
m
Magnetic Quantum Number
Specifies the orientation of the orbital in space. A p subshell has 3 orientations (px, py, pz); d has 5.
m = −ℓ to +ℓ
s
Spin Quantum Number
Electrons have intrinsic angular momentum called spin. Each orbital can hold at most 2 electrons — one spin-up, one spin-down. This is the Pauli Exclusion Principle.
s = +½ or −½
"The more precisely the position is determined, the less precisely the momentum is known — and this is not a measurement problem. It is a fundamental property of reality."
— Werner Heisenberg, 1927 · Uncertainty Principle
Δx · Δp ≥ ℏ/2
Position uncertainty × Momentum uncertainty ≥ Reduced Planck constant / 2

Side by Side

Bohr vs. Quantum
Mechanical Model

Both models agree on energy levels for hydrogen. But quantum mechanics goes far deeper — explaining shapes, bonding, chemistry, and ultimately all of physical reality.

Bohr Model
Proposed 1913
Niels Bohr
Electron Path
Circular orbits at fixed radii
Electron Location
Defined position on orbit
Orbital Shape
Circles only — incorrect
Energy Levels (H)
Correct for hydrogen
Multi-Electron Atoms
Fails completely
Chemical Bonding
Cannot explain
Heisenberg Uncertainty
Violates it
Quantum Numbers Used
n only (1 quantum number)
Spectral Lines
Hydrogen series correct
What It's Good For
Teaching, rough energy estimates
VS
Quantum Mechanical
Developed 1925–1926
Schrödinger · Heisenberg · Born
Electron Path
No defined path — probability cloud
Electron Location
Probability density |ψ|²
Orbital Shape
Spheres, dumbbells, cloverleaves, toroids
Energy Levels (H)
Correct for all atoms
Multi-Electron Atoms
Full treatment
Chemical Bonding
Completely explained
Heisenberg Uncertainty
Built-in, fundamental
Quantum Numbers Used
n, ℓ, m, s (4 quantum numbers)
Spectral Lines
All elements, fine structure, Zeeman effect
What It's Good For
Everything in chemistry and materials

Why It Matters

What quantum atoms
explain

The quantum mechanical model isn't just an academic exercise. It is the foundation of every technology that defines the modern world.

01
Chemical Bonding
Why do atoms bond? Because overlapping orbital wavefunctions form constructive interference — lowering total energy when electron clouds merge. Covalent bonds, ionic bonds, metallic bonding — all emerge from orbital overlap. Without quantum orbitals, we cannot explain why H₂O is a molecule at all.
Solved by orbital overlap theory
02
Semiconductors & Electronics
The transistor — the atom of the digital age — works because silicon's electron orbitals form energy bands with a gap that can be controlled by doping. Every chip, phone, and computer exists because engineers can manipulate quantum orbital behavior. There is no classical explanation for why silicon conducts selectively.
Enabled the entire digital revolution
03
DNA & Molecular Biology
The double helix is held together by hydrogen bonds and π-stacking — both quantum orbital phenomena. The base pairing specificity (A-T, G-C) that encodes all genetic information is a consequence of orbital geometry. Life itself is quantum mechanical at its foundation.
Explains the molecular basis of life
04
Atomic Spectra & Lasers
Every element has a unique spectral fingerprint because its electrons can only exist in discrete energy levels. When they fall between levels, they emit photons of specific wavelengths — which is how we know what distant stars are made of, and how lasers achieve coherent light amplification by stimulated emission.
Foundation of spectroscopy and laser physics
05
MRI & Medical Imaging
Magnetic Resonance Imaging exploits nuclear spin — a purely quantum mechanical property with no classical analogue. The spin quantum number (s = ±½) of hydrogen nuclei in water molecules is manipulated by radio waves to produce detailed images of soft tissue. MRI saves millions of lives annually.
No quantum mechanics → no MRI
06
The Periodic Table Explained
Why does the periodic table have its specific shape — 2, 8, 18, 32 elements per period? Because of shell filling: s-orbitals hold 2, p hold 6, d hold 10, f hold 14. The entire structure of chemistry, the reactivity trends, the metallic and non-metallic properties — all arise from orbital filling rules.
Predicts all chemical properties

In Their Own Words

The physicists
who saw it first

"
Anyone who is not shocked by quantum theory has not understood it.
Niels Bohr
Father of the Bohr Model · Nobel Prize 1922
"
The more I think about the physical portion of Schrödinger's theory, the more repulsive I find it. What Schrödinger writes about the visualizability of his theory is probably not quite right, in other words it's crap.
Werner Heisenberg
Uncertainty Principle · Nobel Prize 1932
"
God does not play dice with the universe.
Albert Einstein
On quantum probability — he was wrong about this one
"
The electron is not as simple as it looks.
W.L. Bragg
X-Ray Crystallography · Nobel Prize 1915
"
I think I can safely say that nobody understands quantum mechanics.
Richard Feynman
Quantum Electrodynamics · Nobel Prize 1965
"
If quantum mechanics hasn't profoundly shocked you, you haven't understood it yet. Everything we call real is made of things that cannot be regarded as real.
Niels Bohr
Copenhagen Interpretation · 1927 Solvay Conference
"
The underlying physical laws necessary for the mathematical theory of a large part of physics and the whole of chemistry are thus completely known, and the difficulty is only that the exact application of these laws leads to equations much too complicated to be soluble.
— Paul Dirac · Quantum Mechanics of Many-Electron Systems, 1929

Purpose

Why this
simulator exists

Textbook diagrams of orbitals are flat. Verbal descriptions are abstract. Neither prepares you for the strangeness and beauty of quantum reality. Seeing changes everything.

Intuition Building
Reading that a 2p orbital is "dumbbell-shaped" is one thing. Watching it rotate in 3D, seeing its lobes, understanding its orientation relative to other orbitals — that's real comprehension. The simulator builds spatial intuition that no textbook can.
The Invisible, Visible
Atoms are 10,000 times smaller than the wavelength of visible light. You cannot see an atom with a microscope. Yet we know the exact shape of every orbital from mathematics. This simulator renders that math into something your visual cortex can grasp.
Chemistry Comes Alive
When you see that two p-orbitals on adjacent atoms can overlap sideways to form a π-bond, bonding theory stops being memorization and becomes geometry. The shapes of molecules, their reactivity, their properties — all encoded in orbital shapes you can now see.
Math Made Concrete
The Schrödinger equation's solutions are abstract functions of (r, θ, φ). This simulator samples those functions using Monte Carlo methods — turning pure mathematics into point clouds. The probability density |ψ|² becomes visible as the density of glowing dots.
Education Democratized
High-end molecular visualization software costs thousands of dollars and requires specialist training. This simulator runs in any browser, on any device, for free. Anyone curious about quantum mechanics — anywhere in the world — can explore the atom immediately.
d-Orbital Geometry
The five d-orbital shapes — dz², dxy, dxz, dyz, dx²-y² — are notoriously difficult to visualize from flat diagrams. The simulator renders all five in 3D with distinct color coding per sub-lobe, including the dz² torus ring that appears nowhere else in atomic structure.

Simulator Capabilities

Every feature,
explained

Monte Carlo Point Clouds
Each orbital renders thousands of points sampled from the actual wavefunction probability density. Dense regions appear brighter; sparse regions dimmer. The visual pattern you see is not artistic — it's the electron probability distribution plotted directly.
PHYSICS-ACCURATE
Packed Nuclear Model
The nucleus is built from individual proton (red) and neutron (blue) spheres packed via Fibonacci sphere distribution. Nuclear radius scales as R ∝ A^(1/3), matching real nuclear physics. A glowing halo approximates the strong nuclear force field.
REALISTIC NUCLEUS
Smooth Orbital Mode
Alternative render where point alpha is directly proportional to |ψ|² at that location. Dense wavefunction regions accumulate brightness naturally. Switch between grainy Monte Carlo and smooth density visualization to build different intuitions.
WAVEFUNCTION DENSITY
Real Image Mode
Warm monochromatic palette mimicking how electron density maps look in electron microscopy and spectroscopic imaging. Toggle between the colorful educational view and the scientifically realistic appearance.
SCIENTIFIC PALETTE
Cartesian Reference Grid
XZ horizontal and XY vertical reference planes help orient orbital lobes in 3D space. Essential for understanding p-orbital axis alignments (px vs py vs pz) and the diagonal orientations of dxy/dxz/dyz orbitals.
SPATIAL ORIENTATION
Anomalous Configurations
Chromium [Ar] 3d⁵4s¹ and Copper [Ar] 3d¹⁰4s¹ are special-cased with their correct electron configurations. Half-filled and fully-filled d subshells are extra stable — a quantum mechanical phenomenon that the simulator models accurately.
AUFBAU EXCEPTIONS
Antimatter Mode
Charge-conjugate any element or molecule on the fly. Electrons render as positrons, protons and neutrons as antiprotons and antineutrons, with identical orbital geometry to the matter version. The entire UI retints into its own pink/violet and electric-blue palette, and the data panel relabels live with an ANTI- prefix and overline notation.
CHARGE CONJUGATION
Ultra Mode
Switches orbital rendering from point clouds to mesh-based surfaces with a Fresnel shader — a transparent center and a glowing rim — for a smooth "glass bubble" look with zero point grain. A different way to build intuition than the grainy Monte Carlo default.
FRESNEL SHADER
Excited State Mode
Promotes an electron to a higher orbital and shows the transition path live in the data panel — the actual quantum jump behind atomic emission spectra. Available for atoms; not applicable in Molecule Mode.
ATOMS ONLY
Spherical Mode
A simplified, teaching-friendly stand-in for p, d, and f lobes — rounded, dumbbell-like blobs instead of the mathematically precise lobe geometry. Toggles independently of Real Image, Smooth, and Ultra modes, so it combines with any of them.
SCHEMATIC LOBES

Orbital Geometry

The five shapes
of quantum reality

Each orbital type has a distinct geometry arising from the angular part of the wavefunction. These shapes determine everything about how atoms bond and react.

s
Sharp Orbital · ℓ = 0
Spherical Shell
1s · 2s · 3s · 4s · 5s

The s-orbital is a perfect sphere of electron probability centered on the nucleus. Every direction is equally likely — the angular wavefunction Y₀⁰ is a constant. What changes with shell number is the radial distribution: higher n orbitals have nodes (spherical shells of zero probability) and peak density farther from the nucleus. The 2s orbital has one radial node; 3s has two.

SHAPEPerfect sphere
ANGULAR NODES0
MAX ELECTRONS2 (per orbital)
SHELLS PRESENTn = 1, 2, 3, 4, 5
p
Principal Orbital · ℓ = 1
Dumbbell Lobes
2p · 3p · 4p (3 sub-orbitals each)

P-orbitals have two lobes extending in opposite directions along one axis. The angular wavefunction Y₁ᵐ is proportional to cos(θ) or sin(θ)·cos/sin(φ), which gives the characteristic dumbbell shape. There are three degenerate p-orbitals in each shell — px, py, pz — oriented along the three Cartesian axes. A nodal plane passes through the nucleus perpendicular to the lobe axis.

SHAPETwo-lobe dumbbell
ANGULAR NODES1 (nodal plane)
MAX ELECTRONS6 per subshell (2×3)
SUB-ORBITALSpx · py · pz
d
Diffuse Orbital · ℓ = 2
Cloverleaf & Torus
3d · 4d (5 sub-orbitals each)

D-orbitals come in five distinct geometries. Four of them (dxy, dxz, dyz, dx²-y²) are four-lobe cloverleaf shapes between or along the axes. The fifth — dz² — is unique: two polar lobes along the z-axis plus a distinctive equatorial torus (donut ring) in the xy-plane. D-orbitals are responsible for the rich chemistry of transition metals and their colorful compounds.

SHAPECloverleaf · dz² torus
ANGULAR NODES2
MAX ELECTRONS10 per subshell (2×5)
SUB-ORBITALSdz² · dxy · dxz · dyz · dx²-y²
f
Fundamental Orbital · ℓ = 3
Multi-Lobed Complex
4f · 5f (7 sub-orbitals each)

F-orbitals are the most geometrically complex shapes the simulator renders — each sub-orbital has six or eight lobes arranged around the nucleus rather than the simple two- or four-lobe patterns of p and d. There are seven degenerate f-orbitals per shell: fz³, fxz², fyz², fxyz, fz(x²-y²), fx(x²-3y²), fy(3x²-y²). They first appear at 4f, where they're responsible for the lanthanide contraction — the reason 4f electrons sit spatially inside the already-filled 6s shell rather than extending beyond it. 5f plays the same role for the actinides.

SHAPE6–8 lobe complex
ANGULAR NODES3
MAX ELECTRONS14 per subshell (2×7)
SUB-ORBITALSfz³ · fxz² · fyz² · fxyz · fz(x²-y²) · fx(x²-3y²) · fy(3x²-y²)
dz²
Special Case · m = 0
The Torus Ring
Most unusual orbital shape in chemistry

The dz² orbital is chemically notorious. Unlike the other four d-orbitals, it has two axial lobes along z and a donut-shaped ring of probability density in the equatorial plane. This unique geometry arises because dz² is technically a linear combination of d(z²-x²) and d(z²-y²). It plays a starring role in octahedral crystal field splitting and the axial bonding of square planar complexes like cisplatin.

UNIQUE FEATUREEquatorial torus ring
KEY ROLECrystal field theory
IMPORTANT INTransition metal complexes
SYMMETRYCylindrical (C∞v)

Molecule Mode

Watch atoms
become molecules

Flip from Atoms to Molecules and individual electron clouds fuse into real chemical structures. Bond angles and geometry come from genuine VSEPR theory, not hard-coded guesses — the shapes you see are the shapes molecules actually take.

52 Curated Molecules
From simple diatomics like H₂ and O₂ to shapes every chemistry student has drawn by hand: bent H₂O, trigonal pyramidal NH₃, tetrahedral CH₄, trigonal bipyramidal PF₅, octahedral SF₆, and more.
VSEPR-ACCURATE
DNA Double Helix
A full B-form double helix, one complete turn — 10 base pairs, all-atom detail including explicit hydrogens, 588 atoms rendered with per-atom orbital clouds rather than a schematic ribbon.
588 ATOMS · ALL-ATOM
Sigma & Pi Bonds
Single, double, and triple bonds render distinctly — including crossed pi-lobe geometry for alkynes and a narrowed sigma core — built directly from bond-aware orbital sampling, not a generic cylinder between atoms.
BOND-AWARE RENDERING
Antimatter Molecules
Antimatter Mode works in Molecule Mode too — charge-conjugating every atom in the structure at once, so you can compare an entire antimatter molecule against its matter counterpart, geometry unchanged.
WHOLE-MOLECULE CONJUGATION
Instanced Nuclei at Scale
Large molecules share two GPU-instanced meshes for every proton and neutron across the whole structure, giving full per-nucleon color detail — even at nearly 6,000 nucleons — in just two draw calls.
GPU-INSTANCED
Real Bond Geometry, Not Guesses
Bond angles are computed from real VSEPR theory — electron pair repulsion, lone pairs, and hybridization — so a bent water molecule and a linear CO₂ emerge from the same underlying physics, not separate hard-coded shapes.
PHYSICS-DERIVED

Build Mode

Type it.
Watch it exist.

A third mode alongside Atoms and Molecules: type the name of any element or compound — organic, inorganic, simple, or complex — and the simulator resolves it into real 3D geometry. Not limited to the 52 curated molecules; this is open-ended.

Type Anything
A search box that accepts any of the 118 elements or any compound name — "caffeine," "sodium chloride," "aniline" — and resolves it on the spot, with quick-example chips for common organic molecules to try first.
FREEFORM SEARCH
Instant Offline Chemistry
Straight and singly-branched alkanes, monocyclic cycloalkanes, and simple alcohol, amine, or ether substitutions resolve instantly with real tetrahedral bond geometry — no internet required, computed live in the browser.
TIER 2 · OFFLINE ENGINE
Real Compounds via PubChem
Anything past the offline engine's scope — alkenes, alkynes, aromatics, carboxylic acids, inorganic salts, and deep fused-ring systems — is fetched live from PubChem's public database as real, published 3D coordinates.
TIER 3 · LIVE LOOKUP
"Did You Mean...?"
Misspell a compound name and Build suggests the closest match — checked first against the local library, then against PubChem's own autocomplete — instead of just failing silently.
TYPO-TOLERANT
Every Mode Still Works
A Build result is pushed straight into the same live registry the 52 curated molecules live in — so Ultra Mode, Antimatter Mode, Smooth Orbitals, and Spherical Mode all apply to anything you build automatically, for free.
NO SPECIAL-CASING
Organic and Inorganic, Simple and Complex
From a lone element to a small organic solvent to a genuinely complex, deeply fused-ring molecule — Build doesn't distinguish; it just resolves whatever you type against the tier that can handle it.
NO CURATION REQUIRED

Companion Tool

Keep zooming.
It doesn't stop at protons.

The Nucleus Explorer does one thing no textbook diagram can: lets you zoom in forever. Start at the whole nucleus and keep scrolling in — reached from the nucleus icon inside the Simulator's toolbar.

Zoom Without Limit
Start at the whole nucleus and keep scrolling in. First individual protons and neutrons resolve into view, then nucleons themselves dissolve into quarks bound by gluons — the actual bottom of the visible matter stack.
Pion Exchange Overlay
Toggle a visualization of pion exchange — the mechanism physicists use to describe how the strong nuclear force binds protons and neutrons together inside the nucleus.
Gluon Field Overlay
Zoom past the nucleons and toggle the gluon field — the force carriers that bind quarks together, an endless exchange with no classical analogue at all.
Down to Quarks
Keep going past the nucleons entirely and reach quarks — the actual bottom of the visible matter stack, rendered as distinct particles rather than an abstract diagram.
Step Through Elements
Previous/next controls step through the periodic table one element at a time, or jump straight to any element from the built-in picker — the nucleus rebuilds instantly with the correct proton and neutron count.
?
Legend & Help Panel
A built-in color legend and help panel explain exactly what you're looking at at every scale, so the jump from "ball of protons" to "quarks and gluons" never leaves you guessing.

Element Coverage

H through Og

All 118 elements from Hydrogen (Z=1) to Oganesson (Z=118) — the complete periodic table, spanning all 7 periods and every s, p, d, and f orbital filling in the Aufbau sequence.

Period 1
Period 2
Period 3
Period 4 (incl. 3d transition metals)
Period 5 (incl. 4d transition metals)
Period 6 (incl. lanthanides & 5d metals)
Period 7 (incl. actinides & superheavy elements)

Under the Hood

From equation
to pixels

The simulator translates quantum mechanical mathematics directly into real-time 3D graphics. Three steps from Schrödinger to screen.

01
Aufbau Configuration
Selects the element. Calculates which orbital subshells are occupied and how many electrons each contains, using the Aufbau principle (lowest energy first), Hund's rule (maximize unpaired spins), and the Pauli Exclusion Principle. Special cases for Cr and Cu handle their real anomalous configurations.
02
Wavefunction Sampling
Each orbital type has a custom sampler. S-orbitals: radial Gaussian shell at radius R with falloff. P-orbitals: teardrop lobe geometry per axis using the angular factor cos²(θ). D-orbitals: full five-lobe model — cloverleafs via orthonormal basis lobes, dz² torus via toroidal coordinate sampling. All 3D positions weighted by probability density.
03
WebGL Rendering
Up to 28,000 points per orbital uploaded to the GPU as buffer geometry. A custom GLSL vertex shader sizes each point by distance; a fragment shader renders it as a soft Gaussian disc. Additive blending means dense regions appear brighter, sparse regions dimmer — naturally encoding probability density as visual brightness.
"
Not only is the universe stranger than we think — it is stranger than we can think.
— Werner Heisenberg · Across the Frontiers, 1974

Ready to see
the quantum world?

118 elements. 10 orbital types. Real-time 3D.
No installation. No account. Just open it and explore.