ronment without mechanical parts, longlasting, maintenance-free, portable, etc. Therefore, TEGs are especially suitable for applications in self-powered electronic systems. [4][5][6] Most high-performance TE materials are inorganic semiconductors, which show high figure of merit values [7,8] and have irreplaceable applications as power supply systems in space exploration, such as radioisotope TE generators. [9,10] Nevertheless, traditional inorganic TE materials are mechanically rigid and fragile, thus are not compatible with heat sources with complex surfaces, obstructing their applications in distributed power supply systems, especially wearable electronics.Two main strategies have been developed to address these issues. One strategy used intrinsically flexible TE materials, including conducting polymers, [11][12][13] carbon-based materials, [14,15] and highly plastic semiconductors. [16,17] Despite these attractive developments, the intrinsically flexible TE materials still suffered inferior TE properties, and the TEGs based on these films were usually constructed using in-plane configurations that made them difficult to build matched thermal impedance when harvesting heat from human body. Quite recently, ionic TE materials as another candidate for thermal energy conversion, showed a magnitude larger temperature gradient driven voltage based on Soret effect than typical electronic TE materials based on electrons/holes diffusion. [18,19] However, most of the ionic TEGs only functioned Direct energy conversion based on thermoelectric (TE) materials is a longterm and maintenance-free energy harvesting technique, and therefore is very promising for self-powered wearable electronics. Yet, it is challenging to achieve high-performance stretchable, healable, and even recyclable thermoelectric generators (TEGs) without compromising TE conversion performance due to the intrinsic mechanical rigidity and brittleness of the inorganic TE materials. Herein, recyclable, healable, and stretchable TEGs (RHS-TEGs) are reported that are assembled from commercial Bi 2 Te 3 and Sb 2 Te 3 TE legs generating superior power density via the use of liquid metal as interconnects and dynamic covalent thermoset polyimine as encapsulation. The TEGs fabricated using this strategy are endowed with excellent TE performance, mechanical compliance, and healing and recycling capabilities. The normalized output power density and mechanical stretchability can reach up to 1.08 µW cm −2 •K 2 and 50%, respectively. After healing and recycling, the TEGs show output performance comparable to the original devices. The TEGs also exhibit high reliability and stability under cyclic deformation. This study paves the way for sustainable application of TEGs as energy harvesters to power wearable electronics using body heat.