Hydrogen is becoming the center piece in the global de-carbonatization efforts in multiple industrial sectors. Gaseous hydrogen at high pressures in gas tanks is the most common approach for H2 storage, transportation and hydrogen refueling for fuel cell vehicles. Gaseous hydrogen at high pressures is also heavily used in the Haber process for ammonia production and hydro-cracking of heavy petroleum. In the long term, low-cost high pressure H2 will also play a critical role in the future long-duration grid storage for deep decarbonization and improved resilience.In this talk, I will share some recent development on a hybrid electrochemical/catalytic approach for direct generation of high-pressure H2 in collaboration with Pacific Northwest National Laboratory (PNNL). The hybrid system oxidizes water to oxygen at the anode, reduces V3+ to V2+ at the cathode, and stores proton in the catholyte during the “electrochemical charging” step. We demonstrated that the charged catholyte is then capable of generating H2 at >350 bar in the subsequent “catalytic discharging” step without any additional energy input. This concept leverages the electrochemical Nernst potential difference between the redox couple (V2+/3+) and the hydrogen evolution reaction and delivers a unique system that is capable of generating H2 at demand and at high pressure without any mechanical or electrochemical compression. We estimate a cost of <$0.19/kg-H2 for compression, representing >80% of the cost reduction compared to the traditional multi-stage compressor approach.