The growth behavior of anodic porous alumina formed via anodizing in a new electrolyte, squaric acid (3,4-dihydroxy-3-cyclobutene-1,2-dione), is reported for the first time. A high-purity aluminum foil was anodized in a 0.1 M squaric acid solution at 293 K and a constant applied potential of 100-150 V. Anodic oxides grew on the aluminum foil at applied potentials of 100-120 V, but a burned oxide film was formed at higher voltage. Anodic porous alumina with a cell size of approximately 200-400 nm and sub-100-nm-scale pore diameter was successfully fabricated by anodizing in squaric acid. The cell size of the anodic oxide increased with anodizing time because of the uneven growth of the porous layer. The anodic porous alumina obtained by squaric acid anodizing consists of amorphous Al 2 O 3 containing 5-6 at% carbon from the electrolyte. Fig. 1). The morphology of anodic porous alumina, especially its cell size (identical meaning to interpore distance) and pore diameter in the porous layer, is limited by the electrolyte and voltage (electrochemical potential) applied during anodizing [23,24]. Fig. 1 summarizes the anodizing electrolytes that have been reported to date for porous alumina fabrication. Sulfuric (H 2 SO 4 ), oxalic ((COOH) 2 ), and phosphoric (H 3 PO 4 ) acids are well-known, self-ordering anodizing solutions for porous alumina fabrication, and highly ordered porous alumina can be obtained by anodizing in these solutions at constant voltages of 18-25 V, 40 V, and 160-195 V, respectively [24-29]. Malonic acid (HOOC-CH 2 -COOH) and tartaric acid (HOOC-(CHOH) 2 -COOH), typical dicarboxylic acids, have also been reported to support the fabrication of highly ordered porous alumina fabrication at 120 V and 195 V, respectively [30,31]. In addition, several other electrolytes, such as chromic (H 2 CrO 4 ) [32,33], malic (HOOC-CH(OH)-CH 2 -COOH) [23,34], citric (HOCO-CH 2 -C(OH)(COOH)-COOH)) [23], and glycolic (CH 2 OH-COOH) [23] acids, have been reported as anodizing electrolytes to date. However, the formation of thick porous alumina with straight nanopores by anodizing in chromic acid is difficult because of branching and colony-forming nanopores [35]. Although citric acid anodizing has already been used for nanostructure fabrication [36], other organic electrolytes, including malic and glycolic acid solutions, cause the formation of non-uniform anodic porous alumina [23,34]. Therefore, five self-ordering electrolytes, namely, sulfuric, oxalic, and phosphoric acids, are generally selected for anodic porous alumina fabrication by many researchers.In recent years, new anodizing procedures using an effective experimental approach and optimal anodizing conditions have been reported by several researchers to control the nano-scale features of anodic porous alumina. Lee et al. studied the rapid formation of ordered porous alumina by a hard anodizing procedure involving a powerful cooling stage and obtained an ultra-high aspect ratio (>1,000) of anodic porous alumina by anodizing in oxalic acid at 120-150...