The tin atoms have a distorted tetrahedralcoordination geometry.
中心锡原子为畸变四面体配位构型。
2
Based on our results, to design better performing electrolytes, future computational models will need to move beyond tetrahedralcoordination structures.
根据我们的研究结果去设计性能更好的电解质，未来的计算模型，将会超越四面体配位结构。
3
This contradicts numerous theoretical studies which indicated a primarily tetrahedralcoordination structure with a solvation number near 2 or 3, depending on the prevalence of ion pairing.