Molecular Geometry & Bonding
what the shape decides
Concept

Defect state — where it appears

A level pulled out of a band by a site whose energy differs from its neighbours', with a wavefunction that decays away from that site. Its position and its extent are both fixed by how deep the defect is, and at a high enough concentration the levels of many defects spread into a band of their own.

Named by 9 essays across 2 fields — each of them below, with the objects they name alongside it.

A 6×5 patch with one site missing. A 6 by 5 patch of a square structure with one site removed, the two colours of the bipartite structure drawn differently. The disc areas show where the level at zero has its amplitude: entirely on one colour.

A vacancy is not an impurity

An impurity is a site whose energy has been changed, and everything about the level it produces depends on by how much. A vacancy is a site that is not there, and the levels it leaves sit at exactly zero for a reason that cannot be tuned, weakened or moved — the count of them is a difference between two numbers of atoms, and two vacancies do not split however far apart they are put.

solids · Defect One impurity is a level; many are a band. The impurity levels of a ring of 160 with sites of depth -3, drawn as a bar from the lowest to the highest, against the fraction of sites that are impurities. At the lowest concentration every level is at the same energy and the bar has no height at all. By 30 per cent the levels span 2.44 and have closed to within 0.25 of the host band, which is shaded.

One defect is a level, many are a band

A single deepened site in a chain pulls one state out of the band to −√(h² + 4), exactly, and holds it on 1.42 sites. Put in more and the levels spread: at one site in ten they span 1.45 in the same units and have closed to within 0.69 of the host band, and above one site in eight the count of levels stops matching the count of defects, because two defects on neighbouring sites push one of their pair back into the band.

solids · Defect The whole difference lives at the two ends. The energy difference between the two dimerisations of an open chain, held at the same distortion, multiplied by the number of sites. It settles on a constant — 1.09 in units of the hopping — so the difference per site falls as one over the length, with a fitted exponent of -1. An end is a bond that is not there, and it is worth the same amount whatever it is attached to.

The distortion the ends decide

A chain of an even number of sites has an odd number of bonds, so its two dimerisations are different molecules rather than one molecule translated. Held at the same distortion they differ by 1.08715 in units of the hopping, whatever the length — a fixed amount of energy living at the two ends, with the per-site difference falling as one over the length at a fitted exponent of −0.99986. And below a hundred and twenty-eight sites the second dimerisation does not exist at all.

applied · Peierls distortion Where the two halves of an alloy come apart. The gap at the centre of a binary alloy's band against the contrast between its two components, for a chain of 2048 sites arranged three ways. The ordered arrangement's gap is exactly twice the contrast and opens at once; the segregated one's is exactly the contrast less the band width and opens at 2; and the random one, which has no closed form, opens a little before the segregated one and stays a little wider. Below the openings the curves sit at one level spacing rather than at zero, which is what a finite chain has instead of a gap.

Two bands, if the chain is short enough

Take a chain, raise half its sites and lower the other half, and ask when the band comes apart into two. The ordered arrangement splits at once, the segregated one at a contrast equal to the band width, and the random one splits earlier than either — and then closes again as the chain is made longer, because a long chain contains a long run of like atoms and a long run is a narrow sub-band.

solids · Defect The chain distorts hardest where it stops. The alternation of each bond along a relaxed chain of 64, at four elastic constants, with the bulk value of each drawn as a dashed line. Every chain alternates more at its end than in its middle — by 1.21 times at the stiffest and 3.15 at the softest — and the excess dies away over a handful of bonds. The uniform alternation usually assumed is the flat part of these curves.

The chain distorts hardest where it stops

Holding the alternation uniform is what made the end energy a clean constant, and it is the one assumption the end-energy calculation had to make. Letting every bond find its own value shows the distortion is largest at the end and decays inwards over a measurable length — one and a half bonds in a strongly dimerised chain, five in a weak one.

solids · Peierls distortion Where the coupling overtakes the spacing. Two quantities that both depend on the chain length, for runs of 6. The coupling is the splitting of the closest pair of runs, which rises as the chain grows because a longer chain brings some pair closer together. The spacing is the mean separation of the gap levels in energy, which falls as the chain grows because there are more of them. They cross at 8,675 sites, and a set of levels coupled more strongly than they are spaced is a band.

The length at which levels become a band

Two runs of low sites share a state when they are close enough, and the splitting falls exponentially over two sites. A longer chain brings some pair closer while spreading its levels thinner, so the two quantities run against each other and cross — at about a thousand sites for runs of four and eighty thousand for runs of eight. Chains of four hundred sites are far below that, which is why every gap state on them is a box.

solids · Defect The coupling at the closest pair, and at the typical one. For runs of four to eight low sites at half concentration: the splitting between two runs one site apart, which is the largest coupling any chain can produce, and the splitting at the separation two runs typically have. Both on a logarithmic axis spanning 173 decades. A band width taken from the second is not a small number; it is not a number.

A band that is a hundred and seventy decades of nothing

The chain length at which a defect's levels become a band can be located by asking when the coupling between the closest pair exceeds the level spacing. A band also has a width, and a width is set by the typical coupling rather than the closest one. For runs of eight at half concentration those two numbers differ by a hundred and seventy-three orders of magnitude.

solids · Defect The count, for five run lengths. The fraction of runs whose nearest neighbour of the same length is coupled more strongly than a threshold, against how many decades below the closest possible coupling that threshold sits. Every curve is a straight line over this range, because the fraction is small and the geometric tail is linear in the separation there. The slope is what the next figure is about: it is the whole content of the distribution, and it is a product of two numbers.

A count rather than an average

Two couplings quoted from one distribution sit a hundred and seventy decades apart. Neither is a summary of it. The quantity that decides how much of a spectrum near a box level is resonant pairs is a count of pairs above a threshold — and it has a closed form, which is a density times a reach times the logarithm of ten.

solids · Defect The resonant share is not a straight line; it bends over and saturates. The share of runs of six in a resonant pair against the logarithm of the chain length, from a thousand sites to 10⁵⁰, at five concentrations of low sites. Dashed lines carry the slope from 10³ to 10¹² straight on. At x = 0.5 the share is 16.1 per cent at 10¹² and 57.7 per cent at 10⁵⁰, where the straight line would be at 78.6. At x = 0.75, the concentration with the most runs of six, it passes 76 per cent by 10³⁰.

The share that was read as a line

The share of defect runs sitting in a resonant pair was read as a straight line in the logarithm of the chain length, rising by a density times a reach per decade and never saturating. The exact rise is that amount times the share of runs not yet resonant. At the concentration first studied the difference is small over nine decades and large beyond them; swept to the concentration with the most runs, the rise falls to a third, and half of all runs are resonant ten orders of magnitude later than the straight line says.

solids · Defect

Named alongside it

The objects these essays reach for when they reach for this one.

Thermodynamic limitTight-binding modelsModel limitClosed formLocalisationBands in a solidBand gapDisorderExact diagonalisationBand edgeEnergy per siteLevel spacing

All concepts