Two-dimensional (2D) metallic states formed on the ZnO(1010) surface by hydrogen adsorption have been investigated using angle-resolved photoelectron spectroscopy (ARPES). The observed metallic state is characterized by a peak-dip-hump structure at just below the Fermi level and a long tail structure extending up to 600 meV in binding energy. The peak and hump positions are separated by about 70 meV, a value close to the excitation energy of longitudinal optical (LO) phonons. Spectral functions formulated on the basis of the 2D electron-phonon coupling well reproduce the ARPES intensity distribution of the metallic states. This spectral analysis suggests that the 2D electrons accumulated on the ZnO surface couple to the LO phonons and that this coupling is the origin of the anomalous long tail. Our results indicate that the 2D electrons at the ZnO surface are described as the electron liquid model. A characteristic difference among the 2DESs with different orbital character is the many-body effects of the electronic system such as electron-phonon (e-ph) and electron-plasmon interactions. Recent ARPES studies have reported that the many-body interactions in the 2DESs on SrTiO 3 (001) are inevitable and the 2DESs should be described in terms of the electron liquid [10,13]. In these 2DESs, the tails that accompany the two-dimensional (2D) metallic band have been attributed to energy loss structures by the e-ph coupling interaction. A similar enhanced spectral weight has also been observed for the 2DESs on anatase TiO 2 surfaces [16]. On the other hand, no such anomalous spectral weight has been reported for the s-orbital derived 2D metallic bands on ZnO(1010) [3][4][5], ZnO(0001) [2,3], In 2 O 3 (111) [6], and CdO(001) surfaces [7,8]. This systematic difference implies that the e-ph coupling strength might be weaker for the s electrons than the d electrons. However, this difference is against the theoretical predictions [17] that the orbital character should have little effect on the e-ph coupling. Therefore, the solution of this discrepancy is one of the challenging subjects for the 2DESs on oxide surfaces.In the present study, the electronic structure of the 2DES developed on the H-dosed ZnO(1010) surface was examined by ARPES. The detailed measurements have allowed us to successfully extract 2D quasiparticle (2DQP) bands and the e-ph satellites from the measured broad band, which has been regarded as a single metallic band in the previous studies [2][3][4][5]18]. The spectral analysis reveals the e-ph coupling strength of α = 0.30 − 0.34, indicating a sufficient e-ph coupling in the 2DES on the ZnO(1010) surface.Single-crystal ZnO(1010) was cleaned in situ by wellestablished procedures [19, 20]. H 2 molecules were cracked by hot tungsten filaments and dosed on the surface at room temperature. By these procedures, surfacelocalized O 2p dangling-bond state is suppressed and a 2DES is induced at the surface [5]. The ARPES measurements were performed at BL-1 of a compact electronstorage ring (HiSOR) at Hiroshima Uni...