Iron sulfide nanocomposites have been prepared through reactions of bis[bis(trimethylsilyl)amido]iron(II) or zerovalent iron nanoparticles (NPs) with hydrogen sulfide gas. The chemical composition of these materials was analyzed by TEM, XRD, WAXS and Mö ssbauer measurements. Decomposition of bis[bis(trimethylsilyl)amido]iron(II) under an H 2 S atmosphere in the presence of palmitic acid produces thin iron sulfide nanoflakes, which seemingly consist of Fe 2 S 2 and Fe 7 S 8 . The sulfidation of 9 nm zerovalent iron NPs with H 2 S yields thin nano flakes exhibiting the same iron sulfide phases and residual iron. Remarkably, treatment of slightly larger iron NPs (13 nm) with H 2 S (or alternatively benzylthiol) yields wellshaped iron-iron sulfide core-shell particles. These particles exhibit a crystalline iron core and an amorphous iron sulfide shell, which likely consists of Fe 2 S 2 , Fe 7 S 8 and Fe 1ÀX S. Magnetic measurements on these core-shell particles show a decrease of the total magnetization (compared to bulk iron) coming along with the sulfidation process. Owing to the partially preserved ferromagnetic character these iron-iron sulfide core-shell particles were found to have magnetic heating properties.[a] Dr.