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Some properties for almost cellular algebras

  • Received: 01 April 2020 Revised: 01 June 2020 Published: 24 August 2020
  • 16W70, 20C08

  • In this paper, we will investigate some properties for almost cellular algebras. We compare the almost cellular algebras with quasi-hereditary algebras, which are known to carry any homological and categorical structures. We prove that any almost cellular algebra is the iterated inflation and obtain some sufficient and necessary conditions for an almost cellular algebra A to be quasi-hereditary.

    Citation: Yongjie Wang, Nan Gao. Some properties for almost cellular algebras[J]. Electronic Research Archive, 2021, 29(1): 1681-1689. doi: 10.3934/era.2020086

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  • In this paper, we will investigate some properties for almost cellular algebras. We compare the almost cellular algebras with quasi-hereditary algebras, which are known to carry any homological and categorical structures. We prove that any almost cellular algebra is the iterated inflation and obtain some sufficient and necessary conditions for an almost cellular algebra A to be quasi-hereditary.



    Cellular algebras were introduced by J. Graham and G. Lehrer in [6]. Their definition is based on the existence of a certain basis with some special properties motivated by KazhdanšCLusztig bases of Hecke algebras and is applicable to other families of algebras like Brauer algebras [6], cyclotomic Temperley-Lieb algebras [6,8], cyclotomic Birman-Murakami-Wenzl algebras [5,14], and so on. An equivalent definition of the cellular algebra was given by S. König and C.C. Xi in terms of cell ideals and a filtration by two-sided ideals [10]. Two different equivalent definitions have different advantages. The first one can be used to check concrete examples. The second one, however, is often more handy for theoretical and structural purposes (see [10], [11] and their references). One of the advantages of the concept of cellularity is that it provides a way to parametrize irreducible modules. The problem of determining a parameter set for, or even constructing bases of irreducible modules, is in this way reduced (but of course not solved in general) to questions of linear algebra. The relation between the cellular algebras and quasi-hereditary algebras was investigated by S. König and C.C. Xi. Precisely they obtained some sufficient and necessary conditions for a cellular algebra to be quasi-hereditary (More details could be found in [11,Theorem 3.1]).

    There are several generalizations of cellular algebras. For example, affine cellular algebras if we extend the framework of cellular algebras to algebras that need not be finite dimensional over a field [13], relative cellular algebras if we allow different partial orderings relative to fixed idempotents [4], standardly based algebra by constructing a nice bases satisfy some conditions [3] and almost cellular algebras if we remove the compatible anti-involution from the definition of cellularity [7]. In this paper, we focus on the third generalization. Motivated by Schur-Weyl duality, the authors introduce the quantum walled Brauer-Clifford superalgebras BCr,s(q), the quantum deformation of the walled Brauer-Clifford superalgebra BCr,s, which is the centralizer superalgebra of the action of Uq(q(n)) on the mixed tensor space under some mild condition [1]. The Howe duality for quantum queer superalgebras was given [2]. Because of their similarity with Hecke-Clifford (super)algebras, the quantum walled Brauer-Clifford (super)algebras are not the cellular algebras since the absence of an anti-involution with the property that it fixes isomorphism classes of irreducible modules. However, these algebras also have many of the properties of cellular algebras, which belong to a large class of algebras, removing the anti-involution from the definition of cellularity, called almost cellular algebras1 [7].

    1When equipped with a compatible anti-involution, the almost cellular algebras are cellular algebras, so called them almost cellular algebras.

    The aim of this paper is to study the structure of almost cellular algebras and determine some sufficient and necessary conditions for an almost cellular algebra to be quasi-hereditary, which is inspired by S. König and C. C. Xi's papers [10,11]. In section two we review the definition of almost cellular algebras, and some examples. We end this section by determining the possibilities for a factor JA of an almost cellular algebra A. In last section, we give a list of homological properties of a factor and show the difference between cellular algebras and almost cellular algebras see Proposition 3.4, we prove that the determinant of the Cartan matrix C of an almost algebra A is a positive integer, and obtain some sufficient and necessary conditions for an almost cellular algebra to be quasi-hereditary.

    Throughout the paper the symbols R and k stand for an arbitrary Noetherian commutative integral domain and a field, respectively. Denote the abelian group of two elements by Z2={¯0,¯1}.

    Definition 2.1. Suppose A,A1,,Ak are unital associative rings. We say A has a sandwich filtration over A1,,Ak if it has a filtration by two-sided ideals

    0=J0J1Jk=A

    such that Ji/Ji1ViAiWi as an (A,A)-bimodule for some nonzero (A,Ai)-bimodule Vi and (Ai,A)-bimodule Wi, both free of finite rank over Ai. We call ViAiWi the factors of A. In particular, a factor JA means the first layer in a sandwich filtration, that is, J is a two-sided ideal of A and JV1A1W1 as (A,A)-bimodules. If the rings A1,,Ak all coincide, we simply say that A has a sandwich filtration over A1. If A admits a sandwich filtration, we call A an almost cellular algebra.

    Remark 2.2. The relationship between almost cellular algebras and cellular algebras is as follows: a cellular algebra admits a sandwich filtration over the base field and has a compatible anti-involution. The definition above is analogous to the iterated inflations in [12], since it allows each Ai to be an arbitrary ring. It is interesting to find an equivalent definition based on the bases for an almost cellular algebra, which can help us to determine whether an algebra is an almost cellular algebra or not?

    Typical examples of almost cellular algebras can be found in [7].

    Example 2.3. Cellular algebras and affine cellular algebras are almost cellular algebras.

    Example 2.4. The finite Hecke-Clifford algebra HCn(q) is the unital associative algebra over C(q) generated by elements ti for 1in1 and elements ci for 1in which satisfy the relations:

    (tiq)(ti+q1)=0,i=1,,n1,titj=tjti,|ij|2,titi+1ti=ti+1titi+1,i=1,,n2,c2i=1,cicj=cjci,1ijn,tici=ci+1ti,titj=tjti,ji,i+1.

    Example 2.5. The q-walled Brauer-Clifford algebra WBCr,s(q) is the unital associative algebra over R generated by elements

    t1,,tr1,c1,cr,¯t1,,¯ts1,¯c1,,¯cs,and e.

    The elements t1,,tr1,c1,cr satisfy the relations of finite Hecke-Clifford algebra HCr(q), and the elements ¯t1,,¯ts1,¯c1,,¯cs satisfy the relations of finite Hecke-Clifford algebra HCs(q) except that ¯c2i=1. Moreover t1,,tr1,c1,cr supercommute with ¯t1,,¯ts1,¯c1, ,¯cs. The generator e commutes with

    t1,,tr2,c1,cr1,¯t2,,¯ts1,¯c2,,¯cs,

    and satisfies

    e2=0,  etr1e=e=e¯t1e,  cre=¯c1e,  ecr=e¯c1,  ecre=0,
    et1r1¯t1etr1=et1r1¯t1e¯t1,  tr1e¯t1r1¯t1e=¯t1et1r1¯t1e.

    Remark 2.6. 1. The Hecke-Clifford algebra HCn(q) and the q-walled Brauer-Clifford algebra WBCr,s(q) are almost cellular algebras. Moreover, roughly speaking, the q-walled Brauer-Clifford algebra WBCr,s(q) has a sandwich filtration over the finite Hecke-Clifford algebras HCrl(q)HCsl(q) for 0lmin(r,s).

    2. The finite Hecke-Clifford algebra HCn(q) and the q-walled Brauer-Clifford algebra WBCr,s(q) become Z2-graded algebras if we define |ti|=|¯tj|=|e|=ˉ0 and |ck|=|¯cl|=ˉ1 for all possible i,j,k,l.

    Lemma 2.7. ([7,Lemma 2]) Let R be a Noetherian commutative integral domain and A be an R-algebra. Suppose we have an (A,A)- bimodule injection VRWA, where V is an (A,R)-bimodule, W is an (R,A)-bimodule, and V and W are both free over R. Then the multiplication map

    (VRW)A(VRW)VRW

    induced by this injection is given by

    (vRw)(vRw)=vφ(wv)Rw,

    where φ:WAVR is an (R,R)-bimodule homomorphism uniquely determined by this formula.

    Proposition 2.8. Let A be an almost cellular algebra over a field k and JA a factor of A. Then J satisfies one of the following conditions

    1. J has square zero.

    2. There exists a primitive idempotent eA such that JAeAAeeAeeA as (A,A)-bimodules, and eAek. In particular, J=J2 is a heredity ideal.

    Proof. By assumption, we may write JVkW as (A,A)-bimodules, where V is a left A-module, W is a right A-module, V and W are finite-dimensional k-vector spaces. By Lemma 2.2, if φ(wv)=0 for all wW and vV, then we have the situation (i).

    Thus we may assume that there exists one φ(wv)0 for some wW, vV. Then there exists a non-zero k0k such that (vw)(vw)=k0(vw). Hence J contains a primitive idempotent e, and Ae is a left ideal which is contained in J. Then JV(dimkW) as a left A-module. However, Ae is a submodule of J, and so J=AeJ(1e). It follows that V=AeM for some left A-module M, and we can decompose J=(Ae)mMm, where m=dimkW. Since (Ae)m is contained in the trace X of Ae inside J, it follows that it is contained in the trace AeA of Ae in A. But the dimension of AeA is less than or equal to the product of the dimension of Ae with the dimension of eA. This implies dimkWdimk(eA).

    On the other hand, eA is a right ideal which is contained in J. Then JW(dimkV) as a right A-module. Thus J=(1e)JeA. It follows that W=NeA for some right A-module N and we can decompose J=Nn(eA)n, where n=dimkV. Since (eA)n is contained in the trace AeA of eA in A, we get that dimkVdimk(Ae). By above arguments, we have the following inequalities

    dimkAedimkVdimkAe,dimkeAdimkWdimkeA.

    Hence, dimkV=dimkAe and dimkW=dimkeA. This means that V=Ae and W=eA. Since the multiplication AekeAAeA is always surjective and dim(Ae)mdimAeA, it must be an isomorphism. Hence JAeA and eAek.

    Remark 2.9. The proof of this proposition is a slight difference with the corresponding one of cellular algebra [10,Proposition 4.1].

    The following corollary is immediately given.

    Corollary 2.10. Let A be an almost cellular k-algebra with a sandwich filtration

    0=J0J1Jn=A,andJi/Ji1VikWi.

    If all the square of Ji/Ji1 are nonzero in A/Ji1, then A is a quasi-hereditary algebra and above sandwich filtration yields a heredity chain of A.

    Proof. By definition Ji/Ji1A/Ji1 is a factor of A/Ji1 and Ji/Ji1 is an (A/Ji1,A/Ji1) -bimodule. By induction on the length of the sandwich filtration and Proposition 1 we get that A is a quasi-hereditary algebra and above sandwich filtration yields a heredity chain of A.

    In section two, we have seen that for a factor JA of an almost cellular algebra A there is exactly two possibilities, i.e., J2=0 or J2=J. In this section, we investigate some homological properties for an almost cellular algebra A.

    Lemma 3.1. ([10,Proposition 6.1]) For any ideal J in a k-algebra A, the following two assertions are equivalent:

    1. J2=0,

    2. TorA2(A/J,A/J)JAJ.

    Proposition 3.2. Let A be an almost cellular k-algebra and JA a nilpotent factor of A such that JVkW as (A,A)-bimodules. Let D:=Homk(,k). Then the space TorA2(A/J,A/J) is not zero if and only if HomA(V,DW)0. In particular, if W=DV, then TorA2(A/J,A/J)0.

    Proof. Note from Lemma 3.1 that J2=0 if and only if TorA2(A/J,A/J)JAJ. Since J is isomorphic to VkW, we get an isomorphism of k-vector spaces JAJVk(WAV)kW. Thus the Tor space TorA2(A/J,A/J)0, provided that WAV is not zero. Since the latter space is the k-dual of HomA(V,DW), it shows the assertion.

    In particular, if W=DV, then 0idVHomA(V,DW). Thus TorA2(A/J,A/J)0.

    Lemma 3.3. Let A be a k-algebra with an anti-involution i and JΔki(Δ) be a cell ideal of A, where ΔJ is a left ideal of A. Let e be an idempotent of A such that ΔJe. Then eJe is a cell ideal of eAe with eJeeΔki(eΔ).

    Proof. Since i2=idA, we have that i can be regarded as an anti-involution of eAe, and i(eJe)=eJe. By assumptions Δ is finite-dimensional and ΔJe, we obtain that eΔ is finite-dimensional and eΔeJe. Moreover, eJeeAAΔki(Δ)AAeeΔki(eΔ) making the following diagram commutative, where α is the isomorphism JΔki(Δ),

    0=J0J1Jn=A,andJi/Ji1VikWi.

    Remark 3.4. It is known from [10,Proposition 4.3] that given a cellular algebra (A,i) and an idempotent e with i(e)=e, then (eAe,i) is a cellular algebra. It does mean that eAe is not necessarily cellular, which we also refer to [12,Section 7]. For example: let k be a commutative ring and A be the k-algebra of two-by-two matrices. Let i be an involution of A given by

    i(abcd)=(dbca).

    Then the k-algebra A together with the involution i is cellular. Note that a two-by-two matrix is an idempotent matrix if and only if (abcd)=(abcd)2 if and only if the following equations are satisfied

    a=a2+bc,  b=b(a+d),  c=c(a+d),  d=d2+bc.

    Therefore, there is no idempotent matrix fixed by the above involution i when the character of k is 2, in this case, the k-algebra A together with the involution i is not a cellular algebra. In the case of the character of k is not 2, then the matrix e=(21212121) is a primitive idempotent matrix which also fixed by the involution i, thus the k-algebra A together with the involution i is a cellular algebra.

    The next proposition shows the difference with those of almost cellular algebras.

    Proposition 3.5. Let A,A1,A2,,An be k-algebras. Let A be an almost cellular algebra with a sandwich filtration

    0=J0J1Jn=A,andJi/Ji1ViAiWi,

    for all 1in. Let e be an idemponent of A. Then eAe is an almost cellular algebra.

    Proof. Let s be the biggest integer such that eJse=0 and let t be the smallest integer such that eJte=eJt+1e. Then

    eJle/eJl1ee(Jl/Jl1)eeVlAlWle,for all s+1lt.

    Note that eVl is an (eAe,Al)-bimodule and Wle is an (Al,eAe)-bimodule, both free of finite rank over Al. Thus by above arguments eAe is an almost cellular algebra with a sandwich filtration

    0=eJseeJs+1eeJte=eAe, and eJie/eJi1eeViAiWie,

    for all s+1lt.

    From now on, we assume that R is a Noetherian commutative integral domain. Given an associative R-algebra B, two finitely generated free R-modules V and W, and a bilinear form φ:VRWB with values in B, we define an associative algebra A as follows: as an R-module, A=VRWRB. The multiplication is defined by

    (abx)(cdy):=adxφ(c,b)y. (1)

    Proposition 3.6. This definition makes A into an associative R-algebra.

    Proof. Since B is an associative algebra, we have

    ((abx)(cdy))(efz)=(adxφ(c,b)y)(efz)=afxφ(c,b)yφ(e,d)z

    equals to

    (abx)((cdy)(efz))=(abx)(cfyφ(e,d)z)=afxφ(c,b)yφ(e,d)z.

    Lemma 3.7. Let A be an R-algebra with a factor J=A. Then A is isomorphic to a full matrix ring over the ground ring R.

    Proof. By the assumption A=VRW for some free R-modules V and W. So there is an R-bimodule isomorphism

    AHomA(A,A)HomA(VRW,A)HomR(W,HomA(V,A))

    Denote the R-ranks of the free R-module V and W by n and m respectively. Then A has R-rank n×m, and as a left module, A is isomorphic to m copies of V. Hence, HomA(V,A) has R-rank at least n. But by the above isomorphism it can not have larger rank. This means that the A-endomorphism ring E of V has rank one and is exactly R. We complete the proof.

    Definition 3.8. Let C be any algebra and let B be an algebra of the form VRWRR with the multiplication defined in (3.1). Let A=CB such that B is a factor of A and A/B is isomorphic to C. Then we call A an inflation of C along B.

    Theorem 3.9. Any almost cellular algebra A over R with a sandwich filtration is the iterated inflation of finitely many copies of R.

    Proof. First we regard a factor JA as an algebra, which is always an inflation of the ground ring R. In fact, by Lemma 2.2 there exists an (R,R)-bimodule morphism φ:WAVR and we can identify J with LRLRR for two free R-modules L and L having the same R-rank as V and W, respectively. Thus we can write J as an inflation.

    Now we prove the theorem by induction on the length of the sandwich filtration. An almost cellular R-algebra A which is a factor in itself is just a full matrix ring over R of size n×m by Lemma 3.3. Choose L and L to be free R-modules of rank n and m respectively, which we identify with V=Ae and W=eA, where e is a primitive idempotent. In this case, we identify eAe with R.

    Using the above observation, we can rewrite matrix multiplication ARAA as

    ARA(AeReA)R(AeReA)AeReAeReAAeReAA, (2)

    where all maps are (A,A)-bimodule homomorphisms. Thus, it provides us a bilinear form φ:LRLR and also shows how to write A as inflation of R along L and L.

    Now we assume that A is an almost cellular algebra with a sandwich chain of length greater than 1. We fix a factor JA. By induction, the quotient algebra B=A/J is an iterated inflation of copies of R. Now we claim that A is an inflation of B along J. Indeed, we use the facts that J is an inflation of R by the first paragraph and JA is a factor of A.

    In the following subsection, we show sufficient and necessary conditions for an almost cellular algebra A to be quasi-hereditary.

    Denote the simple A-modules L(1),,L(m) and their projective covers by P(1),, P(m). Let C=(cij) be the Cartan matrix of an algebra A, where the entry cij is the composition multiplicity [P(i):L(j)]. The determinant of C is called the Cartan determinant. In general this can be any integer. But the Cartan determinant of a cellular algebra is a positive integer. For our situation, we also have

    Proposition 3.10. Let A,A1,,An be R-algebras over R. Let A be an almost cellular algebra with a sandwich filtration

    0=J0J1Jn=A,andJi/Ji1ViAiWi=Δ(i).

    Then the determinant det(C) of the Cartan matrix C of A is a positive integer.

    Proof. Denote the number of isomorphism classes of simple Ai-modules by mi. Then the number of isomorphism classes of simple A-modules is mm1+mn by [7,Theorem 3] and Vi is of finite Ai-rank. Let da,b=[Δ(a):L(b)], the composition multiplicity of the simple module L(b) in the standard module Δ(a), and D=(da,b) the corresponding matrix. Then D is an n×m-matrix with integer entries. By the characterization of simple A-modules, we may assume that D=(D1D2), where D1 and D2 are integer matrices and D2 (whose rows correspond to those indices i such that J2iJi1) is a square matrix by again by [7,Theorem 3]. Note that D2 is a lower triangular matrix with all diagonal entries equal to one. This implies that det(D2)=1.

    The Cartan matrix C of A satisfies C=DTD, where DT is the transpose matrix of D. Indeed, the composition multiplicity [Δ(a):L(b)] equals to dimkWae(b), where e(b) is the primitive idempotent corresponding to L(b). Now,

    CT=(DT1DT2)(D1D2)=(DT1D1+DT2D2),

    so hence det(C)=det(I+(DT2D2)1DT1D1) by det(DT2D2)=1. Note that DT2D2 is positive definitive and DT1D1 is positive semi-definitive. Then we can decompose DT2D2 with DT2D2=Z2 for some symmetric matrix Z, and furthermore, B=Z1DT1D1Z1 and (DT2D2)1DT1D1 have the same eigenvalues. Since B is symmetric and its eigenvalues λ are non-negative real numbers, it follows that C=I+(DT2D2)1DT1D1 has the eigenvalues of the form 1+λ, and therefore det(C) is a positive integer.

    König and Xi obtained some equivalent conditions for a cellular algebra to be quasi-hereditary (see [11,Theorem 3.1]). Inspired by their work and combined with the above proposition, we have the following theorem.

    Theorem 3.11. Let A,A1,,An be R-algebras over R. Let A be an almost cellular algebra. Then the following are equivalent:

    1. There is a sandwich filtration of A over A1,An whose length equals the sum of the numbers of isomorphism classes of simple Ai-modules.

    2. The determinant det(C) of Cartan matrix C of A is equal to one.

    In particular, if R is a field, then det(C)=1 if and only if each Ai=R and A is quasi-hereditary algebra with the sandwich filtration to be exactly the heredity chain.

    Proof. From Proposition 5 we get that det(C) is equal to one if λ=0 if and only if for the given sandwich filtration we have n=m. This means that (i)(ii).

    If R is a field, then from [7,Theorem 3] we get that the statement (i) holds if and only if each Ai=R. Thus we complete the proof.

    Future Directions There are a number of interesting questions yet to be considered. For example, is there an equivalent definition based on the bases for an almost cellular algebra, which can help us to determine whether an algebra is an almost cellular algebra or not? An affine quasi-hereditary algebra with a balanced split involution is an affine cellular algebra [9,Proposition 9.8], and given an affine cellular algebra with an affine cell chain of ideals, one can ask how to decide whether it is affine quasi-hereditary? Furthermore, when is an almost cellular algebra with a sandwich filtration to be affine quasi-hereditary? So far as the authors are aware, this theory has yet to be developed.

    We would like to express our debt to Prof. ChangChang Xi for his suggestion. We are very grateful to referees for their insightful comments which helped us to improve the paper considerably. This paper was partially written up during the first author take part in the international conference of Lie theory and representations held in Shanghai University, from which we gratefully acknowledge the support and excellent working environment. N. Gao was supported by the National Natural Science Foundation of China No. 11771272. Y. Wang also thanks the support of National Natural Science Foundation of China No. 11901146.



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