High-temperature water–rock interaction experiments show that Fe-solution react with calcite and magnesite to produce magnetite and release H2. At ambient temperatures, H2 is produced by a previously unrecognized mineral self-organization mechanism capable of generating sustained redox gradients. Time-resolved analyses show that membrane-forming mineral structures create localized chemically reactive microenvironments even when the surrounding system is not strongly reducing. A quantitative reactive transport model reproduces mineral growth, diffusion and redox evolution, linking experimental observations with theoretical predictions. The broader implications of this mineral-driven energy generation mechanism are currently being evaluated internally to assess its technological scope and applicability, while dedicated scientific publications are in preparation. Together, these results provide experimental evidence that mineral-mediated processes could have supplied both energy and compartmentalization relevant to early chemical evolution. At the same time, systematic investigations of silica solubility and nucleation across a wide pH range have revealed deviations from classical alkaline solubility models, refining current understanding of silica speciation. Advanced analytical approaches will allow exploring the role of early-stage silica clusters and polymerization dynamics, including biomorph formation with carbonates and Fe(II). Newly developed microfluidic reactors enable controlled diffusion-driven mineral growth and real-time observation of biomorph formation and silica–metal membrane development. These experiments demonstrate that purely physicochemical processes can generate complex tubular and vesicle-like morphologies, highlighting the importance of robust abiotic reference frameworks when interpreting potential biosignatures. Prebiotic chemistry experiments further expand this integrated approach. A time-resolved Miller-type reactor has been developed to continuously monitor gas-phase chemistry during spark-discharge simulations. The results show that prebiotic synthesis unfolds as a dynamic reaction network rather than a simple linear pathway, characterized by rapid methane consumption, accumulation of reduced species, transient hydrocarbon intermediates and sustained formation of oxidized carbon compounds. Solid organic films produced under these conditions have been characterized spectroscopically, and ongoing research explores mineral catalytic effects and isotopic signatures.