Developing functional, cleavable two-dimensional materials for use in next generation devices has recently become a topic of considerable interest due to their unique properties. Of particular interest, transition metal halides CrI3 and CrCl3 have shown to be good contenders for tunable and cleavable magnetic materials due to their unique magnetic properties in the monolayer. Here, electron spin resonance spectroscopy is used to pinpoint the atomic origins and underlying mechanisms of magnetic interactions as a function of temperature (5-500 K) and microwave frequency (9.43, 120 GHz) on CrI3 and CrCl3 bulk single crystals. ESR signals from CrI3 due to Cr3+ were observed to decay at 460 K, while ESR signals from CrCl3 remain up to 500 K. In the case of CrCl3, the temperature dependences of signal behavior, line width and g-value show characteristic signatures of ferromagnetic fluctuations at around 40 K, near to the antiferromagnetic phase transition at 17 K.

In this work, we report on the electron spin resonance (ESR) studies performed on few-layered nanocrystalline (NCs) MoS2, WS2, and TiS2 prepared using hydrothermal and vapor transport methods. From the temperature dependent ESR spectra collected from MoS2 NCs, we have identified adsorbed oxygen species, sulphur vacancies, thio- and oxo-Mo5+ related paramagnetic defect centers. WS2 NCs have exhibited W+3 and oxo-W+5 paramagnetic defect spin species. TiS2 NCs showed defects such as Fe3+ (unwanted), oxygen and sulfur vacancies. This work demonstrates the usage of spin-sensitive spectroscopy such as ESR in unravelling the defects which contain unpaired electron spin centers in layered NCs two-dimensional materials.

ABSRTACTIn this article, we report low-temperature electron spin resonance (ESR) investigations carried out on solution processed three-layer inverted solar cell structures: PC61BM/CH3NH3PbI3/PEDOT:PSS/Glass, where PC61BM and PEDOT:PSS act as electron and hole transport layers, respectively. ESR measurements were conducted on ex-situ light (1 Sun) illuminated samples. We find two distinct ESR spectra. First ESR spectra resembles a typical powder pattern, associated with gx = gy = 4.2; gz = 9.2, found to be originated from Fe3+ extrinsic impurity located in the glass substrate. Second ESR spectra contains a broad (peak-to-peak line width ∼ 10 G) and intense ESR signal appearing at g = 2.008; and a weak, partly overlapped, but much narrower (peak-to-peak line width ∼ 4 G) ESR signal at g = 2.0022. Both sets of ESR spectra degrade in intensity upon light illumination. The latter two signals were found to stem from light-induced silicon dangling bonds and oxygen vacancies, respectively. Our controlled measurements confirm that these centers were generated during UV-ozone treatment of the glass substrate –a necessary step to be performed before PEDOT:PSS is spin coated. This work forms a significant step in understanding the light-induced- as well as extrinsic defects in perovskite solar cell materials.