The photoelectron spectra of ClO2 and its negative ion are investigated theoretically by a time-dependent wave-packet method. The near equilibrium MRCI potential energy surfaces of Peterson and Werner [J. Chem. Phys. 99, 302 (1993)] are employed in the nuclear dynamical simulations. The theoretical findings are in good agreement with the experimental results. In the experimental recording, excitations along the symmetric stretching and bending vibrational modes of ClO2 were observed. The excitation along the asymmetric stretching vibrational mode is absent in the experimental results. Considering these observations, and utilizing the available electronic structure results, we in our dynamical study focused on the C-2v nuclear arrangements of the system. The relevant intial wave function to describe the photoelectron transition is prepared in both ways by the Hamiltonian matrix diagonalization using the ab initio potential energy surface of the ground electronic state, as well as in terms of the dimensionless normal coordinates of the electronic ground state of ClO2. The stick vibronic spectra are calculated by solving the time-independent Schrodinger equation employing a basis set expansion approach and the Lanczos algorithm. The resulting vibrational eigenvalues are compared with the experimental results and are discussed. The inclusion of the asymmetric stretching vibration and the possible role of the nonadiabatic couplings in the nuclear dynamics are also emphasized.