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Monolayer MoS 2 has long been considered as the most promising candidate for wearable photovoltaic devices. However, its photovoltaic efficiency is restricted by its large band gap (2.0 eV). Though the band gap can be reduced by increasing the number of layers, the indirect band gap nature of the resulting multilayer MoS 2 is unfavorable. Herein, we report a theoretical discovery of the hitherto unknown symmetry-broken phase (denoted as 1T d ) of monolayer MoS 2 through a swarm structure search. The 1T d phase has a distorted octahedral coordinated pattern of Mo, and its direct band gap of 1.27 eV approaches the optimal value of 1.34 eV that gives the Shockley–Queisser limit for photovoltaic efficiency. Importantly, the direct band gap nature persists in thin films with multilayers owing to extremely weak vdW forces between adjacent 1T d layers. The theoretical photovoltaic efficiency at 30 nm thickness reaches ∼33.3%, which is the highest conversion efficiency among all the thin-film solar cell absorbers known thus far. Furthermore, several feasible strategies including appropriate electron injection and annealing methods were proposed to synthesize the 1T d phase. Once synthesized, the superior photovoltaic properties of the 1T d phase may lead to the development of an entirely new line of research for transition metal dichalcogenide solar cells.