The interactions
among magnetic ions exhibit a significant dependence
on their geometric arrangements within crystalline lattices. In the
research presented herein, we detail the synthesis, structural elucidation,
and examination of the magnetic properties of a novel compound, KHoSe2. This compound is synthesized by utilizing the KCl salt flux
technique. Through both X-ray and neutron powder diffraction analyses,
we determine that KHoSe2 adopts a trigonal crystal structure
within the R3̅m space group
(S.G.166), featuring a layered architecture. Within this structure,
Ho3+ ions are arranged in a triangular lattice. Magnetic
susceptibility measurements conducted down to T =
1.8 K reveal no evidence of long-range magnetic order. Additionally,
neutron powder diffraction studies across various temperatures corroborate
the absence of long-range magnetic ordering at temperatures exceeding
10 K. An anomalous feature in the specific heat capacity near T = 3.5 K, which has not been observed in other materials
in this family, is observed. Furthermore, the specific heat capacity
investigations also suggest an effective spin (S
eff) of 1/2 for KHoSe2, which deviates from the
anticipated value for an isolated Ho3+ ion. These findings
propose that KHoSe2 may function as a significantly frustrated
magnet, potentially paralleling the foundational states observed in
quintessential quantum spin liquid candidates featuring Yb3+ ions with S = 1/2, such as KYbSe2.