Periodic table (crystal structure)

For elements that are solid at standard temperature and pressure the first table gives the crystalline structure of the most thermodynamically stable form(s) in those conditions. Each element is shaded by a color representing its respective Bravais lattice, except that all orthorhombic lattices are grouped together.

Crystal structure of elements in the periodic table at standard temperature and pressure[1]
1 H																		2 He
3 Li W	4 Be Mg												5 B β-B	6 C g-C	7 N	8 O	9 F	10 Ne
11 Na W	12 Mg Mg												13 Al Cu	14 Si d-C	15 P b-P	16 S α-S	17 Cl	18 Ar
19 K W	20 Ca Cu		21 Sc Mg	22 Ti Mg	23 V W	24 Cr W	25 Mn α-Mn	26 Fe W	27 Co Mg	28 Ni Cu	29 Cu Cu	30 Zn Mg	31 Ga α-Ga	32 Ge d-C	33 As α-As	34 Se γ-Se	35 Br	36 Kr
37 Rb W	38 Sr Cu		39 Y Mg	40 Zr Mg	41 Nb W	42 Mo W	43 Tc Mg	44 Ru Mg	45 Rh Cu	46 Pd Cu	47 Ag Cu	48 Cd Mg	49 In In	50 Sn β-Sn	51 Sb α-As	52 Te γ-Se	53 I Cl	54 Xe
55 Cs W	56 Ba W		71 Lu Mg	72 Hf Mg	73 Ta W	74 W W	75 Re Mg	76 Os Mg	77 Ir Cu	78 Pt Cu	79 Au Cu	80 Hg	81 Tl Mg	82 Pb Cu	83 Bi α-As	84 Po α-Po	85 At	86 Rn
87 Fr	88 Ra W		103 Lr	104 Rf	105 Db	106 Sg	107 Bh	108 Hs	109 Mt	110 Ds	111 Rg	112 Cn	113 Nh	114 Fl	115 Mc	116 Lv	117 Ts	118 Og
			57 La α-La	58 Ce α-La	59 Pr α-La	60 Nd α-La	61 Pm α-La	62 Sm α-Sm	63 Eu W	64 Gd Mg	65 Tb Mg	66 Dy Mg	67 Ho Mg	68 Er Mg	69 Tm Mg	70 Yb Cu
			89 Ac Cu	90 Th Cu	91 Pa α-Pa	92 U α-U	93 Np α-Np	94 Pu α-Pu	95 Am α-La	96 Cm α-La	97 Bk α-La	98 Cf α-La	99 Es Cu	100 Fm	101 Md	102 No

The second table gives the most stable structure of each element at its melting point. (H, He, N, O, F, Ne, Cl, Ar, Kr, Xe, and Rn are gases at STP; Br and Hg are liquids at STP.) Note that helium does not have a melting point at atmospheric pressure, but it adopts a magnesium-type hexagonal close-packed structure under high pressure.

Crystal structures of elements at their melting points at atmospheric pressure
1 H 13 K Mg																		2 He *
3 Li 453 K W	4 Be 1560 K W												5 B 2349 K β-B	6 C 3800 K g-C	7 N 63 K β-N	8 O 54 K γ-O	9 F 53 K γ-O	10 Ne 24 K Cu
11 Na 370 K W	12 Mg 923 K Mg												13 Al 933 K Cu	14 Si 1687 K d-C	15 P 883 K b-P	16 S 393 K β-S	17 Cl 171 K Cl	18 Ar 83 K Cu
19 K 336 K W	20 Ca 1115 K W		21 Sc 1814 K W	22 Ti 1941 K W	23 V 2183 K W	24 Cr 2180 K W	25 Mn 1519 K W	26 Fe 1811 K W	27 Co 1768 K Cu	28 Ni 1728 K Cu	29 Cu 1357 K Cu	30 Zn 692 K Mg	31 Ga 302 K α-Ga	32 Ge 1211 K d-C	33 As 1090 K b-P	34 Se 494 K γ-Se	35 Br 265 K Cl	36 Kr 115 K Cu
37 Rb 312 K W	38 Sr 1050 K W		39 Y 1799 K W	40 Zr 2128 K W	41 Nb 2750 K W	42 Mo 2896 K W	43 Tc 2430 K Mg	44 Ru 2607 K Mg	45 Rh 2237 K Cu	46 Pd 1828 K Cu	47 Ag 1234 K Cu	48 Cd 594 K Mg	49 In 429 K In	50 Sn 505 K β-Sn	51 Sb 903 K α-As	52 Te 722 K γ-Se	53 I 386 K Cl	54 Xe 161 K Cu
55 Cs 301 K W	56 Ba 1000 K W		71 Lu 1925 K Mg	72 Hf 2506 K W	73 Ta 3290 K W	74 W 3695 K W	75 Re 3459 K Mg	76 Os 3306 K Mg	77 Ir 2719 K Cu	78 Pt 2041 K Cu	79 Au 1337 K Cu	80 Hg 234 K α-Hg	81 Tl 557 K W	82 Pb 600 K Cu	83 Bi 544 K α-As	84 Po 527 K β-Po	85 At 575 K? ?	86 Rn 202 K ?
87 Fr 281 K? ?	88 Ra 973 K W		103 Lr 1900 K? ?	104 Rf ?	105 Db ?	106 Sg ?	107 Bh ?	108 Hs ?	109 Mt ?	110 Ds ?	111 Rg ?	112 Cn ?	113 Nh ?	114 Fl ?	115 Mc ?	116 Lv ?	117 Ts ?	118 Og ?
			57 La 1193 K W	58 Ce 1068 K W	59 Pr 1208 K W	60 Nd 1297 K W	61 Pm 1315 K W	62 Sm 1345 K W	63 Eu 1099 K W	64 Gd 1585 K W	65 Tb 1629 K W	66 Dy 1680 K W	67 Ho 1734 K Mg	68 Er 1802 K Mg	69 Tm 1818 K Mg	70 Yb 1097 K W
			89 Ac 1323 K Cu	90 Th 2115 K W	91 Pa 1841 K W	92 U 1405 K W	93 Np 917 K W	94 Pu 912 K W	95 Am 1449 K W	96 Cm 1613 K Cu	97 Bk 1259 K Cu	98 Cf 1173 K Cu	99 Es 1133 K Cu	100 Fm 1800 K? ?	101 Md 1100 K? ?	102 No 1100 K? ?

Predictions are given for elements 85–87, 100–113 and 118; all but radon^[2] have not been produced in bulk. Probably Cn and Fl would be liquids at STP (ignoring radioactive self-heating concerns). Calculations have difficulty replicating the experimentally known bcc structures of the stable alkali metals, and the same problem affects Fr (87);^[3] nonetheless, it is probably also bcc.^[4] The latest predictions for Fl (114) could not distinguish between face-centred cubic and hexagonal close-packed structures, which were predicted to be close in energy.^[5] No predictions are available for elements 115–117.

Predicted crystal structures of highly unstable elements
1 H																		2 He
3 Li	4 Be												5 B	6 C	7 N	8 O	9 F	10 Ne
11 Na	12 Mg												13 Al	14 Si	15 P	16 S	17 Cl	18 Ar
19 K	20 Ca		21 Sc	22 Ti	23 V	24 Cr	25 Mn	26 Fe	27 Co	28 Ni	29 Cu	30 Zn	31 Ga	32 Ge	33 As	34 Se	35 Br	36 Kr
37 Rb	38 Sr		39 Y	40 Zr	41 Nb	42 Mo	43 Tc	44 Ru	45 Rh	46 Pd	47 Ag	48 Cd	49 In	50 Sn	51 Sb	52 Te	53 I	54 Xe
55 Cs	56 Ba		71 Lu	72 Hf	73 Ta	74 W	75 Re	76 Os	77 Ir	78 Pt	79 Au	80 Hg	81 Tl	82 Pb	83 Bi	84 Po	85 At [Cu][6]	86 Rn [Cu][7]
87 Fr [W][4]	88 Ra		103 Lr [Mg][8]	104 Rf [Mg][8]	105 Db [W][8]	106 Sg [W][8]	107 Bh [Mg][8]	108 Hs [Mg][9]	109 Mt [Cu][8]	110 Ds [W][8]	111 Rg [W][8]	112 Cn [Mg][10]	113 Nh [Mg][11]	114 Fl	115 Mc	116 Lv	117 Ts	118 Og [Cu][7]
			57 La	58 Ce	59 Pr	60 Nd	61 Pm	62 Sm	63 Eu	64 Gd	65 Tb	66 Dy	67 Ho	68 Er	69 Tm	70 Yb
			89 Ac	90 Th	91 Pa	92 U	93 Np	94 Pu	95 Am	96 Cm	97 Bk	98 Cf	99 Es	100 Fm [Cu][12]	101 Md [Cu][12]	102 No [Cu][12]

The following is a list of structure types which appear in the tables above. Regarding the number of atoms in the unit cell, structures in the rhombohedral lattice system have a rhombohedral primitive cell and have trigonal point symmetry but are also often also described in terms of an equivalent but nonprimitive hexagonal unit cell with three times the volume and three times the number of atoms.

Prototype	Strukturbericht	Diagram	Lattice system	Space group	Atoms per unit cell	Coordination	notes
α-Pu	(none)		Monoclinic	P21/m (No. 11)	16		slightly distorted hexagonal structure. Lattice parameters: a = 618.3 pm, b = 482.2 pm, c = 1096.3 pm, β = 101.79° [13][14]
β-S	(none)		Monoclinic	P21/c (No. 14)	32
α-Np	Ac		Orthorhombic	Pnma (No. 62)	8		highly distorted bcc structure. Lattice parameters: a = 666.3 pm, b = 472.3 pm, c = 488.7 pm [15][16]
α-U	A20		Orthorhombic	Cmcm (No. 63)	4	Each atom has four near neighbours, 2 at 275.4 pm, 2 at 285.4 pm. The next four at distances 326.3 pm and four more at 334.2 pm.[17]	Strongly distorted hcp structure.
α-Ga	A11		Orthorhombic	Cmce (No. 64)	8	each Ga atom has one nearest neighbour at 244 pm, 2 at 270 pm, 2 at 273 pm, 2 at 279 pm.[18]	The structure is related to that of iodine.
b-P	A17		Orthorhombic	Cmce (No. 64)	8		Specifically the black phosphorus form of phosphorus.
Cl	A14		Orthorhombic	Cmce (No. 64)	8
α-S	A16		Orthorhombic	Fddd (No. 70)	16
In	A6		Tetragonal	I4/mmm (No. 139)	2		Identical symmetry to the α-Pa type structure. Can be considered slightly distorted from an ideal Cu type face-centered cubic structure[18] which has ${\displaystyle c/a={\sqrt {2}}}$.
α-Pa	Aa		Tetragonal	I4/mmm (No. 139)	2		Identical symmetry to the In type structure. Can be considered slightly distorted from an ideal W type body centered cubic structure which has ${\displaystyle c/a=1}$.
β-Sn	A5		Tetragonal	I41/amd (No. 141)	4	4 neighbours at 302 pm; 2 at 318 pm; 4 at 377 pm; 8 at 441 pm [18]	white tin form (thermodynamical stable above 286.4 K)
β-B	(none)		Rhombohedral	R3m (No. 166)	105 (rh.) 315 (hex.)		Partly due to its complexity, whether this structure is the ground state of Boron has not been fully settled.
α-As	A7		Rhombohedral	R3m (No. 166)	2 (rh.) 6 (hex.)	in grey metallic form, each As atom has 3 neighbours in the same sheet at 251.7pm; 3 in adjacent sheet at 312.0 pm.[18] each Bi atom has 3 neighbours in the same sheet at 307.2 pm; 3 in adjacent sheet at 352.9 pm.[18] each Sb atom has 3 neighbours in the same sheet at 290.8pm; 3 in adjacent sheet at 335.5 pm.[18]	puckered sheet
α-Sm	(none)		Rhombohedral	R3m (No. 166)	3 (rh.) 9 (hex.)	12 nearest neighbours	complex hcp with 9-layer repeat: ABCBCACAB....[19]
α-Hg	A10		Rhombohedral	R3m (No. 166)	1 (rh.) 3 (hex.)	6 nearest neighbours at 234 K and 1 atm (it is liquid at room temperature and thus has no crystal structure at ambient conditions!)	Identical symmetry to the β-Po structure, distinguished based on details about the basis vectors of its unit cell. This structure can also be considered to be a distorted hcp lattice with the nearest neighbours in the same plane being approx 16% farther away [18]
β-Po	Ai		Rhombohedral	R3m (No. 166)	1 (rh.) 3 (hex.)		Identical symmetry to the α-Hg structure, distinguished based on details about the basis vectors of its unit cell.
γ-Se	A8		Hexagonal	P321 (No. 154)	3
Mg	A3		Hexagonal	P63/mmc (No. 194)	2	Zn has 6 nearest neighbors in same plane: 6 in adjacent planes 14% farther away[18] Cd has 6 nearest neighbours in the same plane- 6 in adjacent planes 15% farther away[18]	If the unit cell axial ratio is exactly ${\textstyle 2{\sqrt {\frac {2}{3}}}\approx 1.633}$ the structure would be a mathematical hexagonal close packed (HCP) structure. However, in real materials there are deviations from this in some metals where the unit cell is distorted in one direction but the structure still retains the hcp space group—remarkable all the elements have a ratio of lattice parameters c/a < 1.633 (best are Mg and Co and worst Be with c/a ~ 1.568). In others like Zn and Cd the deviations from the ideal change the symmetry of the structure and these have a lattice parameter ratio c/a > 1.85.
g-C	A9		Hexagonal	P63/mmc (No. 194)	4		Specifically the graphite form of carbon.
α-La	A3'		Hexagonal	P63/mmc (No. 194)	4		The Double hexagonal close packed (DHCP) structure. Similar to the ideal hcp structure, the perfect dhcp structure should have a lattice parameter ratio of ${\textstyle {\frac {c}{a}}=4{\sqrt {\frac {2}{3}}}\approx 3.267.}$ In the real dhcp structures of 5 lanthanides (including β-Ce) ${\textstyle c/2a}$ variates between 1.596 (Pm) and 1.6128 (Nd). For the four known actinides dhcp lattices the corresponding number vary between 1.620 (Bk) and 1.625 (Cf).[20]
β-N	(none)		Hexagonal	P63/mmc (No. 194)	4
α-Po	Ah		Cubic	Pm3m (No. 221)	1	6 nearest neighbours	simple cubic lattice. The atoms in the unit cell are at the corner of a cube.
γ-O	(none)		Cubic	Pm3n (No. 223)	16		Closely related to the β-W structure, except with a diatomic oxygen molecule in place of each tungsten atom. The molecules can rotate in place, but the direction of rotation for some of the molecules is restricted.
α-Mn	A12		Cubic	I43m (No. 217)	58	Unit cell contains Mn atoms in 4 different environments.[18]	Distorted bcc
W	A2		Cubic	Im3m (No. 229)	2		The Body centered cubic structure (BCC). It is not a close packed structure. In this each metal atom is at the centre of a cube with 8 nearest neighbors, however the 6 atoms at the centres of the adjacent cubes are only approximately 15% further away so the coordination number can therefore be considered to be 14 when these are on one 4 fold axe structure becomes face-centred cubic (cubic close packed).
Cu	A1		Cubic	Fm3m (No. 225)	4		The face-centered cubic (cubic close packed) structure. More content relating to number of planes within structure and implications for glide/slide e.g. ductility.
d-C	A4		Cubic	Fd3m (No. 227)	8		The diamond cubic (DC) structure. Specifically the diamond form of Carbon.

The observed crystal structures of many metals can be described as a nearly mathematical close-packing of equal spheres. A simple model for both of these is to assume that the metal atoms are spherical and are packed together as closely as possible. In closest packing, every atom has 12 equidistant nearest neighbours, and therefore a coordination number of 12. If the close packed structures are considered as being built of layers of spheres, then the difference between hexagonal close packing and face-centred cubic is how each layer is positioned relative to others. The following types can be viewed as a regular buildup of close-packed layers:

• Mg type (hexagonal close packing) has alternate layers positioned directly above/below each other: A,B,A,B,...
• Cu type (face-centered cubic) has every third layer directly above/below each other: A,B,C,A,B,C,...
• α-La type (double hexagonal close packing) has layers directly above/below each other, A,B,A,C,A,B,A,C,.... of period length 4 like an alternative mixture of fcc and hcp packing.^[21]
• α-Sm type has a period of 9 layers A,B,A,B,C,B,C,A,C,...^[22]

Precisely speaking, the structures of many of the elements in the groups above are slightly distorted from the ideal closest packing. While they retain the lattice symmetry as the ideal structure, they often have nonideal c/a ratios for their unit cell. Less precisely speaking, there are also other elements are nearly close-packed but have distortions which have at least one broken symmetry with respect to the close-packed structure:

• In type is slightly distorted from a cubic close packed structure
• α-Pa type is distorted from a hexagonal close packed structure

• Crystal structure
• Allotropy

General

• P.A. Sterne; A. Gonis; A.A. Borovoi, eds. (July 1996). "Actinides and the Environment". Proc. of the NATO Advanced Study Institute on Actinides and the Environment. NATO ASI Series. Maleme, Crete, Greece: Kluver Academic Publishers. pp. 59–61. ISBN 0-7923-4968-7.
• L.R. Morss; Norman M. Edelstein; Jean Fuger, eds. (2007). The Chemistry of the Actinide and Transactinide Elements (3rd ed.). Springer. ISBN 978-1402035555.

• Strukturbericht Type A – structure reports for the pure elements
• Crystal Structures for the solid chemical elements at 1 bar