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Tuning Fe–Se Tetrahedral Frameworks by a Combination of [Fe(en)3]2+ Cations and Cl Anions

Journal Article · · Inorganic Chemistry
 [1];  [2];  [2];  [3];  [4];  [1];  [1];  [1];  [5];  [1]
  1. Ames Lab., and Iowa State Univ., Ames, IA (United States)
  2. Univ. of California, Davis, CA (United States)
  3. Univ. of Tennessee Space Inst., Tullahoma, TN (United States); Middle Tennessee State Univ., Murfreesboro, TN (United States)
  4. Florida State Univ., Tallahassee, FL (United States)
  5. Florida State Univ., Tallahassee, FL (United States); Florida State Univ., Tallahassee, FL (United States). National High Magnetic Field Lab. (MagLab)
A one-dimensional (1D) chain compound (en = ethylenediamine), featuring tetrahedral FeSe2 chains separated by [Fe(en)3]2+ cations and Cl anions, has been synthesized by a low temperature solvothermal method using simple starting materials. The degree of distortion in the Fe–Se backbone is similar to previously reported compounds with isolated 1D FeSe2 chains. 57Fe Mössbauer spectroscopy reveals the mixed-valent nature of [Fe(en)3]3(FeSe2)4Cl2 with Fe3+ centers in the [FeSe2]- chains and Fe2+ centers in the [Fe(en)3]2+ complexes. SQUID magnetometry indicates that is paramagnetic with a reduced average effective magnetic moment, μeff = 9.51 μB per formula unit, and a negative Weiss constant, θ = -10.9(4) K, indicating antiferromagnetic (AFM) nearest neighbor interactions within the [FeSe2]- chains. Furthermore, weak antiferromagnetic coupling between chains, combined with rather strong intrachain AFM coupling, leads to spin-glass behavior at low temperatures, as indicated by a frequency shift of the peak observed at 3 K in AC magnetic measurements. A combination of [Fe(en)3]2+ and Cl ions is also capable of stabilizing mixed-valent 2D Fe–Se puckered layers in the crystal structure of [Fe(en)3]4(Fe14Se21)Cl2, where Fe14Se21 layers have a unique topology with large open pores. Property measurements of [Fe(en)3]4(Fe14Se21)Cl2 could not be performed due to the inability to either grow large crystals or synthesize this material in single-phase form.
Research Organization:
Ames Laboratory (AMES), Ames, IA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF)
Grant/Contract Number:
AC02-07CH11358; AC02-06CH11357
OSTI ID:
1668259
Alternate ID(s):
OSTI ID: 1734914
Report Number(s):
IS-J--10,299
Journal Information:
Inorganic Chemistry, Journal Name: Inorganic Chemistry Journal Issue: 18 Vol. 59; ISSN 0020-1669
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English

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