Wietfeldt Henry, Meana-Pañeda Rubén, Machello Chiara, Reboul Cyril F, Van Cong T S, Kim Sungin, Heo Junyoung, Kim Byung Hyo, Kang Sungsu, Ercius Peter, Park Jungwon, Elmlund Hans
Center for Structural Biology, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.
Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, Australia.
Commun Chem. 2024 Jan 3;7(1):4. doi: 10.1038/s42004-023-01087-x.
In situ structures of Platinum (Pt) nanoparticles (NPs) can be determined with graphene liquid cell transmission electron microscopy. Atomic-scale three-dimensional structural information about their physiochemical properties in solution is critical for understanding their chemical function. We here analyze eight atomic-resolution maps of small (<3 nm) colloidal Pt NPs. Their structures are composed of an ordered crystalline core surrounded by surface atoms with comparatively high mobility. 3D reconstructions calculated from cumulative doses of 8500 and 17,000 electrons/pixel, respectively, are characterized in terms of loss of atomic densities and atomic displacements. Less than 5% of the total number of atoms are lost due to dissolution or knock-on damage in five of the structures analyzed, whereas 10-16% are lost in the remaining three. Less than 5% of the atomic positions are displaced due to the increased electron irradiation in all structures. The surface dynamics will play a critical role in the diverse catalytic function of Pt NPs and must be considered in efforts to model Pt NP function computationally.
铂(Pt)纳米颗粒(NPs)的原位结构可以通过石墨烯液体池透射电子显微镜来确定。关于其在溶液中的物理化学性质的原子尺度三维结构信息对于理解其化学功能至关重要。我们在此分析了八个小尺寸(<3nm)胶体Pt NPs的原子分辨率图谱。它们的结构由一个有序的晶体核心组成,周围是具有相对较高迁移率的表面原子。分别根据8500和17000电子/像素的累积剂量计算出的三维重建,通过原子密度损失和原子位移来表征。在所分析的五个结构中,由于溶解或撞击损伤而损失的原子总数不到5%,而在其余三个结构中损失的原子数为10-16%。在所有结构中,由于电子辐照增加,不到5%的原子位置发生了位移。表面动力学将在Pt NPs的多种催化功能中起关键作用,并且在通过计算模拟Pt NP功能的努力中必须予以考虑。