including low sliding friction and strong bonding to the bone. [2,3] In contrast, synthetic hydrogels usually have an isotropic and amorphous structure, resulting in the absence of anisotropic optical and mechanical properties. Inspired by the nature, there are many efforts to develop anisotropic hydrogels by different strategies, [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21] including molecular self-assembly, [5,6] electric/magnetic field-directed orientation, [7][8][9][10][11][12][13][14] and diffusion-induced orientation, [15][16][17] to form ordered structures before or during the gelation process. For instance, Thomas and co-workers prepared photonic hydrogels by molecular self-assembly of a block copolymer to form a uniform lamellar structure, which was subsequently fixed by chemical cross-linking. [5] The resultant hydrogel showed iridescent colors under different ionic strength owing to the Bragg diffraction of the light with a specific wavelength. Aida, Miyamoto, and their coworkers applied magnetic and electric fields to orient the charged nanosheets followed by in situ polymerization of the precursor solution to fabricate monodomain nanocomposite hydrogels, which showed anisotropic optical and mechanical properties, as well as anisotropic actuation under external stimulations. [7][8][9] Dobashi and co-workers have developed anisotropic physical hydrogels by dialyzing the solution of curdlan or DNA in the solution of multivalent metallic ions, in which the diffusion of ions induced molecular orientation and gelation of the negatively charged, rigid biomacromolecules. [15,16] Although big progress has been achieved in designing monodomain hydrogels, it still remains a big challenge to develop anisotropic gels with intricate ordered structures, because of lacking efficient approach to control the local orientation of molecules or nanoparticles at different regions. Recently, Studart and co-workers fabricated composite hydrogels by multistep polymerization with a magnetic field to orient the nanofillers along a specific direction. [22,23] The integrated hydrogels with complex ordered structures showed programmed deformations under external stimulations. However, the fabrication process was time-consuming because the separate domains with specific orientations should be completed step-wisely to form the composite hydrogel. A facile and efficient strategy is really desired to prepare hydrogels with intricate anisotropic superstructures, which is an important step to develop biomimetic materials with versatile functions. A straightforward idea is to simultaneously modulate the external field with independent Most soft biotissues possess intricate anisotropic superstructures, which afford living organism versatile functionalities. However, it remains a big challenge to develop such complex ordered structures in synthetic hydrogels. Here a simple and efficient strategy to fabricate periodically patterned hydrogels with complex anisotropic structures by diffusion-induced orientation and g...