stimuli, such as UV-vis light irradiation, [ 18,19 ] heating, [ 20,21 ] or special chemical environments, [ 22,23 ] are required to trigger the healing process because the substance migration of coatings is hindered by the substrates. [ 26 ] Among intrinsic self-healing coatings, water-enabled self-healing coatings are especially promising because the healing is accomplished by simply soaking the coatings in water or exposing them to moisture, [27][28][29][30][31][32][33][34][35][36] without using any special devices or chemicals. Lyon and co-workers [ 25,36 ] fi rst developed hydrogel thin fi lms/coatings on polydimethylsiloxane by layer-by-layer (LBL) assembly of submicrometer-sized polyanionic gel particles and linear polycations; these fi lms can rapidly heal micrometer-sized defects after exposed to water. Subsequently, Sun and co-workers have fabricated various kinds of water-enabled self-healing coatings by LBL assembly of polyelectrolyte multilayers. [ 11,[27][28][29][30] Up to now, all water-enabled self-healing coatings are prepared by LBL assembly. [ 11,[24][25][26][27][28][29][30][31][32][33][34][35][36] This method is advantageous in easy preparation and fi ne control over the coating structures. However, pretreatment of the substrates is usually needed for the subsequent LBL assembly; the resulting coatings cannot bind tightly to different materials. In addition, it is time-consuming especially in fabricating micrometer-thick coatings which are required for effi cient healing of severe damages [ 27 ] and compensation for the lost substance in the coatings. [ 30 ] Therefore, it is desirable to develop a universal approach with high time and cost effi ciency to fabricate mechanically robust water-enabled self-healing coatings on a wide range of substrates.Here we report a versatile yet facile method to fabricate waterenabled self-healing coatings on various substrates, by precipitating hydrogen-bonded complexes of tannic acid (TA) and polyethylene glycol (PEG) in aqueous solution. TA, a natural polyphenol, endows the coatings with high binding affi nity to different substrates [37][38][39][40][41][42][43] and antioxidant capacities. [ 38,46 ] TAs associate with PEGs into stable micrometer-sized complexes through intermolecular hydrogen bond in neutral or acidic aqueous solution. [ 44,45 ] With addition of NaCl, these complexes rapidly precipitate onto substrates under gravity and coalesce with each other to generate uniform soft coatings via hydrogen bonding. After drying, the hydrogen-bonding will be enhanced to produce mechanically robust coatings with strong adhesion to different substrates. However, the coatings become soft and Recent years have witnessed the rapid developments of self-healing coatings because they can protect materials from diverse risks and are able to autonomously heal after being physically damaged. Here, a universal yet facile method is reported with high time and cost effi ciency to fabricate transparent water-enabled self-healing coatings on various substrates by precipitat...