Cellular algebra

This article is about the cellular algebras of Graham and Lehrer. For the cellular algebras of Weisfeiler and Lehman, see association scheme.

In abstract algebra, a cellular algebra is a finite-dimensional associative algebra A with a distinguished cellular basis which is particularly well-adapted to studying the representation theory of A.

History

The cellular algebras discussed in this article were introduced in a 1996 paper of Graham and Lehrer.[1] However, the terminology had previously been used by Weisfeiler and Lehman in the Soviet Union in the 1960s, to describe what are also known as association schemes. [2][3]

Definitions

Let R be a fixed commutative ring with unit. In most applications this is a field, but this is not needed for the definitions. Let also A be a R-algebra.

The concrete definition

A cell datum for A is a tuple (\Lambda,i,M,C) consisting of

C: \dot{\bigcup}_{\lambda\in\Lambda} M(\lambda)\times M(\lambda) \to A
The images under this map are notated with an upper index \lambda\in\Lambda and two lower indices \mathfrak{s},\mathfrak{t}\in M(\lambda) so that the typical element of the image is written as C_\mathfrak{st}^\lambda.

and satisfying the following conditions:

  1. The image of C is a R-basis of A.
  2. i(C_\mathfrak{st}^\lambda)=C_\mathfrak{ts}^\lambda for all elements of the basis.
  3. For every \lambda\in\Lambda, \mathfrak{s},\mathfrak{t}\in M(\lambda) and every a\in A the equation
aC_\mathfrak{st}^\lambda \equiv \sum_{\mathfrak{u}\in M(\lambda)} r_a(\mathfrak{u},\mathfrak{s}) C_\mathfrak{ut}^\lambda \mod A(<\lambda)
with coefficients r_a(\mathfrak{u},\mathfrak{s})\in R depending only on a,\mathfrak{u} and \mathfrak{s} but not on \mathfrak{t}. Here A(<\lambda) denotes the R-span of all basis elements with upper index strictly smaller than \lambda.

This definition was originally given by Graham and Lehrer who invented cellular algebras.[1]

The more abstract definition

Let i:A\to A be an anti automorphism of R-algebras with i^2=id (just called "involution" from now on).

A cell ideal of A w.r.t. i is a two-sided ideal J\subseteq A such that the following conditions hold:

  1. i(J)=J.
  2. There is a left ideal \Delta\subseteq J that is free as a R-module and an isomorphism
\alpha: \Delta\otimes_R i(\Delta) \to J
of A-A-bimodules such that \alpha and i are compatible in the sense that
\forall x,y\in\Delta: i(\alpha(x\otimes i(y))) = \alpha(y\otimes i(x))

A cell chain for A w.r.t. i is defined as a direct decomposition

A=\bigoplus_{k=1}^m U_k

into free R-submodules such that

  1. i(U_k)=U_k
  2. J_k:=\bigoplus_{j=1}^k U_j is a two-sided ideal of A
  3. J_k/J_{k-1} is a cell ideal of A/J_{k-1} w.r.t. to the induced involution.

Now (A,i) is called a cellular algebra if it has a cell chain. One can show that the two definitions are equivalent.[4] Every basis gives rise to cell chains (one for each topological ordering of \Lambda) and choosing a basis of every left ideal \Delta/J_{k-1}\subseteq J_k/J_{k-1} one can construct a corresponding cell basis for A.

Examples

Polynomial examples

R[x]/(x^n) is cellular. A cell datum is given by i=id and

A cell-chain in the sense of the second, abstract definition is given by

0 \subseteq (x^{n-1}) \subseteq (x^{n-2}) \subseteq \ldots \subseteq (x^1) \subseteq (x^0)=R

Matrix examples

R^{d\times d} is cellular. A cell datum is given by i(A)=A^T and

A cell-chain (and in fact the only cell chain) is given by

 0 \subseteq R^{d\times d}

In some sense all cellular algebras "interpolate" between these two extremes by arranging matrix-algebra-like pieces according to the poset \Lambda.

Further examples

Modulo minor technicalities all Iwahori–Hecke algebras of finite type are cellular w.r.t. to the involution that maps the standard basis as T_w\mapsto T_{w^{-1}}.[5] This includes for example the integral group algebra of the symmetric groups as well as all other finite Weyl groups.

A basic Brauer tree algebra over a field is cellular if and only if the Brauer tree is a straight line (with arbitrary number of exceptional vertices).[4]

Further examples include q-Schur algebras, the Brauer algebra, the Temperley–Lieb algebra, the Birman–Murakami–Wenzl algebra, the blocks of the Bernstein–Gelfand–Gelfand category \mathcal{O} of a semisimple Lie algebra.[4]

Representations

Cell modules and the invariant bilinear form

Assume A is cellular and (\Lambda,i,M,C) is a cell datum for A. Then one defines the cell module W(\lambda) as the free R-module with basis \lbrace C_\mathfrak{s} | \mathfrak{s}\in M(\lambda)\rbrace and multiplication

aC_\mathfrak{s} := \sum_{\mathfrak{u}} r_a(\mathfrak{u},\mathfrak{s}) C_\mathfrak{u}

where the coefficients r_a(\mathfrak{u},\mathfrak{s}) are the same as above. Then W(\lambda) becomes an A-left module.

These modules generalize the Specht modules for the symmetric group and the Hecke-algebras of type A.

There is a canonical bilinear form \phi_\lambda: W(\lambda)\times W(\lambda)\to R which satisfies

C_\mathfrak{st}^\lambda C_\mathfrak{uv}^\lambda \equiv \phi_\lambda(C_\mathfrak{t},C_\mathfrak{u}) C_\mathfrak{sv}^\lambda \mod A(<\lambda)

for all indices s,t,u,v\in M(\lambda).

One can check that \phi_\lambda is symmetric in the sense that

\phi_\lambda(x,y) = \phi_\lambda(y,x)

for all x,y\in W(\lambda) and also A-invariant in the sense that

\phi_\lambda(i(a)x,y)=\phi_\lambda(x,ay)

for all a\in A,x,y\in W(\lambda).

Simple modules

Assume for the rest of this section that the ring R is a field. With the information contained in the invariant bilinear forms one can easily list all simple A-modules:

Let \Lambda_0:=\lbrace \lambda\in\Lambda | \phi_\lambda\neq 0\rbrace and define L(\lambda):=W(\lambda)/\operatorname{rad}(\phi_\lambda) for all \lambda\in\Lambda_0. Then all L(\lambda) are absolute simple A-modules and every simple A-module is one of these.

These theorems appear already in the original paper by Graham and Lehrer.[1]

Properties of cellular algebras

Persistence properties

If R is an integral domain then there is a converse to this last point:

  1. (A,i) is cellular.
  2. (A_1,i) and (A_2,i) are cellular.

If one further assumes R to be a local domain, then additionally the following holds:

Other properties

Assuming that R is a field (though a lot of this can be generalized to arbitrary rings, integral domains, local rings or at least discrete valuation rings) and A is cellular w.r.t. to the involution i. Then the following hold

  1. A is semisimple.
  2. A is split semisimple.
  3. \forall\lambda\in\Lambda: W(\lambda) is simple.
  4. \forall\lambda\in\Lambda: \phi_\lambda is nondegenerate.
  1. A is quasi-hereditary (i.e. its module category is a highest-weight category).
  2. \Lambda=\Lambda_0.
  3. All cell chains of (A,i) have the same length.
  4. All cell chains of (A,j) have the same length where j:A\to A is an arbitrary involution w.r.t. which A is cellular.
  5. \det(C_A)=1.

References

  1. 1 2 3 4 Graham, J.J; Lehrer, G.I. (1996), "Cellular algebras", Inventiones Mathematicae 123: 1–34, doi:10.1007/bf01232365
  2. Weisfeiler, B. Yu.; A. A., Lehman (1968). "Reduction of a graph to a canonical form and an algebra which appears in this process". Scientific-Technological Investigations. 2 (in Russian) 9: 1216.
  3. Cameron, Peter J. (1999). Permutation Groups. London Mathematical Society Student Texts (45). Cambridge University Press. ISBN 0-521-65378-9.
  4. 1 2 3 4 König, S.; Xi, C.C. (1996), "On the structure of cellular algebras", Algebras and modules II. CMS Conference Proceedings: 365–386
  5. Geck, Meinolf (2007), "Hecke algebras of finite type are cellular", Inventiones Mathematicae 169: 501–517, doi:10.1007/s00222-007-0053-2
  6. König, S.; Xi, C.C. (1999-06-24), "Cellular algebras and quasi-hereditary algebras: A comparison", Electronic Research Announcements of the American Mathematical Society 5: 71–75
  7. König, S.; Xi, C.C. (1999), "Cellular algebras: inflations and Morita equivalences", Journal of the London Mathematical Society 60: 700–722, doi:10.1112/s0024610799008212
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