Cellular homology provides a powerful and efficient method for computing the homology groups of CW complexes. It relies on a chain complex constructed directly from the cells of the CW structure.
The relative homology group is given by:
where denotes the free abelian group generated by the -cells.
For , the homology group .
The inclusion map induces a map on homology which is an isomorphism for and surjective for .
Proof Sketch
The pair is a good pair, and the quotient space is a wedge sum of -spheres, one for each n-cell of . Thus, , which gives the result.
This is shown by considering the long exact sequence for the pair and using induction on .
This follows from considering the long exact sequence of the pair . Any cycle in is compact and can be deformed into some finite skeleton , which allows us to relate to the homology of its skeletons.
We can now define a chain complex based on the structure of a CW complex .
Cellular Chain Groups
The cellular chain group is the free abelian group generated by the -cells of . By the lemma above, we have an isomorphism:
The cellular boundary map is defined as the composite of maps from the long exact sequence of the pair :
where is the mystery map and is induced by inclusion.
Lemma
The composition of two consecutive cellular boundary maps is zero, i.e., . Thus, forms a chain complex.
Proof The composition involves the segment . This is a portion of the long exact sequence for the pair , so the composition . The full map is . Since , the entire composition is zero.
Cellular Homology
The -th cellular homology group of is the homology of this chain complex:
The key result is that this new homology theory is naturally isomorphic to the singular homology.
Theorem
For a CW complex , the cellular homology is isomorphic to the singular homology:
Proof The situation is summarized by the following commutative diagram:
where the arrows with same colors come from the same section of the long exact sequence.
Define as follows: Take , since is surjective, there exists such that . Define .
We need to check that is well-defined. Firstly, because . Thus, . Secondly, we need to show that does not depend on the choice of . If there is another such that , then , so for some . Thus, , which implies . And clearly that is a homomorphism, so it is well-defined.
Next, we show that is injective. If , then for some . Since is injective, , which implies . Thus, and is injective.
Finally, we show that is surjective. For any with , so that . Since is injective, , which implies . Thus, there exists such that . Define , then . So is surjective.
Cellular Boundary Formula
To compute the boundary maps in practice, we use a formula based on the degrees of maps.
Cellular Boundary Formula
If we denote the -cells by and the -cells by , the boundary map is given by:
The coefficient is the degree of the composite map:
where is the attaching map of the cell , is the quotient map, and is the projection onto the sphere corresponding to the cell .
Proof Observe that the following diagram commute:
Following the blue route, will be sent to , while following the red route, will be sent to , which is the coefficient of in . Since the diagram commutes, these two must be equal.
Comparison with Simplicial Homology
For simplicial homology, the chain group is the free abelian group on the -simplices of . The coefficients of the boundary map are always or .
Example: Real Projective Space
The real projective space has a CW structure with exactly one -cell in each dimension for . The cell is attached to the -skeleton via the standard 2-sheeted covering map .
The cellular chain complex is for and otherwise.
The boundary map is determined by the degree of the composite map: Let’s call this composite map . To find its degree, we can sum the local degrees over the preimage of a regular point . The preimage under consists of two points, which we can identify with and its antipode in the domain .
Near , the map is a local homeomorphism that preserves orientation. The local degree is +1.
Near , the map is a composition of the antipodal map (which has degree ) and an orientation-preserving local homeomorphism. The local degree is .
Therefore, the total degree is . The boundary map is multiplication by this integer:
Homology of
Let’s compute the homology of . The chain complex is: Substituting and the computed boundary maps: The homology groups are:
for .
So, we have:
In general, the homology of is:
Example: Surface of Genus g
A standard CW structure for the orientable surface of genus , , has:
1 0-cell (a point).
1-cells, denoted .
1 2-cell, , attached along the path .
The cellular chain complex is .
The map is the zero map because the boundary of each 1-cell is the single 0-cell, mapping to .
To compute , we find the degree of the attaching map projection. For each , the attaching map traverses once forward and once backward (). The corresponding degrees cancel out, so . The same logic applies to the ‘s, so .
Therefore, both and are zero maps.
The homology groups are then the chain groups themselves:
Example: Complex Projective Space
The complex projective space has a CW structure with one cell in each even dimension for . The chain complex consists of in even dimensions and 0 in odd dimensions:All boundary maps must be zero since they map from or to a zero group.
The homology groups are therefore the chain groups themselves: