An understanding of the origin of elastic strain is extremely important for both crystalline materials and amorphous materials. Owing to the lack of a long range order in their structure, it is arduous to dynamically study the elastic mechanism of amorphous materials experimentally at atomic scale compared with their crystalline counterparts. Here, the elastic deformation mechanism of amorphous silica nanowires (NWs) has been studied for the first time via in situ elastic tensile tests in a transmission electron microscope. Radial distribution functions (RDFs) calculated from the corresponding selected area electron diffraction patterns (SAEDPs) at different strains were used to reconstruct a structural model based on the reverse Monte-Carlo (RMC) method. The result interestingly indicates that the elastic strain of silica glass NWs can be mainly attributed to the elastic elongation of the bond length accompanied by a change in the bond angle distribution. This work is useful for understanding the high strength of amorphous materials.The two most crucial properties of a structural material are its elastic strain limit and plasticity. Plasticity is the property indicating the flexibility of a material, while the elastic strain limit represents the maximum stress that the material can withstand before yielding. The development of materials with high elastic strain limit and excellent plasticity is an urgent target for researchers [1−4]. Amorphous materials such as oxide glasses and metallic glasses are widely used in military applications. Unlike for their crystalline counterparts, there is still inadequate comprehension of the extraordinary behaviors of such glasses [5−10]. In nano-sized objects, smaller is stronger, owing to the combination of their decreased defect density and increased strength and elastic strain. Experimental elastic strain limits of more than 7.8% for ZnO nanowires (NWs) [11,12] the size of such glasses minimizes flaw size and maximizes their strength (i.e., elastic strain). Elimination of extrinsic flaws and decreased internal structural defects can lead to an outstanding large elastic strain limit of more than 3-6% for submicro-sized glasses [16−19], in which shear bands are suppressed owing to the reduction in size [16]. The ultimate strength of silica NWs is higher than 10 GPa and increases with decreasing NW diameter. The reduced possibility of having large cracks in small samples is the main reason for their high strength [20]. Molecular dynamic simulations also indicate such a size-dependent elasticity for amorphous silica NWs originating from coupling between core softening and surface stiffening of each NW the structure of which is different from its bulk counterpart [21]. In our systematic studies, an approximately 13% elastic strain limit for silica NWs with diameters around 50 nm was confirmed. The uniaxial tensile stress corresponding to such an elastic strain limit would be 9.5 GPa (assuming a Young's modulus of 73 GPa for silica NWs [22]). Recent results have revealed that the...