作者
Junhua Liu,Liang Si,Q. Zhang,Xiao Wang,Jens Freese,Grant Harris,Mei Wu,Xinxin Zhang,Tsung-Han Lin,Ronny Sutarto,Javier Herrero‐Martín,Charles Guillemard,Manuel Valvidares,Li Lin,Xiao-Fei Gao,Yaoyao Ji,Zhong‐Liang Deng,Yuhao Hong,Long Wei,Yulin Gan,Lingfei Wang,Guanglei Cheng,Peng Gao,Lin Gu,Jiandi Zhang,Zhiwei Hu,Liu Hao Tjeng,Robert J. Green,Kai Chen,Zhaoliang Liao
摘要
Abstract Perovskite LaCoO 3 is a subject of extensive and ongoing investigation due to the delicate competition between high‐spin (HS) and low‐spin (LS) states of Co 3+ . On the other hand, their indistinct free energy boundary poses a significant challenge to annihilate the magnetically/electrically inert LS Co 3+ for yielding fully HS state. Here, electronic transformation from the conventional isovalent mixed HS/LS state () into an unprecedented aliovalent fully HS state () is demonstrated in monolayer LaCoO 3 confined by 5d SrIrO 3 slabs via atomically constructing SrIrO 3 /LaCoO 3 superlattices. Excitingly, this emergent fully HS monolayer exhibits not only remarkable 2D ferromagnetism beyond the Mermin–Wagner restriction, but also larger magnetization (≈1.8µ B /Co) and higher Curie temperature (above 100 K) than that of conventional thick film and any previously reported oxide‐based monolayer ferromagnets. Furthermore, Ir/Co hybridization driven orbital reconstruction with polarization beyond standard crystal field expectations is observed, which is supported by DFT calculations. The findings not only expand the electronic phase domains of LCO into fully HS state, but also provide a fresh platform for investigating the 2D magnetic physics under strongly spin‐orbit coupled regime and developing new 2D spintronic devices.