Developed by teams led by Prof. Li Can at the Chinese Academy of Sciences and Prof. Jian Liu at Inner Mongolia University, the sunlight-driven catalyst systems mimic biological structures to improve energy conversion efficiency.
Living cells execute complex biochemical tasks with remarkable precision by compartmentalizing components inside tightly regulated internal spaces. Scientists working in nanocell engineering try to replicate these biological systems inside synthetic nanomaterials. A research team at the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS), working alongside Prof. Jian Liu’s group at Inner Mongolia University, constructed a hollow CdS@polydopamine nanoreactor to imitate key biological functions, as reported in scientific documentation.
Mimicking Cellular Redox Activity and Compartmentalization
The newly engineered nanoreactor incorporates two distinct biomimetic elements designed to handle complex chemical reactions. First, the polydopamine shell features a dynamic catechol/o-benzoquinone redox pair. Instead of acting as an active proton pump, this chemical pair functions as a proton relay. By continually accepting and releasing protons, it accelerates proton-coupled electron transfer, a mechanism where proton and electron movements are tightly synchronized.
Second, the structure relies on compartmentalization. A nanoscale hollow cavity sits inside a porous shell, establishing a confined environment where reactants accumulate. This architecture facilitates molecular diffusion and captures incoming photons, allowing light-driven reactions to proceed more efficiently under natural illumination.
Photosynthesis Rates and Recyclable Hydrogel Integration
By combining in situ spectroscopy, photochemical analysis, finite element simulations, and theoretical calculations, the researchers identified a Z-scheme heterojunction-based photocatalytic mechanism powering the system. Under visible-light illumination in an aqueous solution, the nanoreactor achieved an H2O2 photosynthesis rate of 3.24 mmol gcat.-1 h-1 alongside a solar-to-chemical conversion efficiency of 1.2 percent.

To make the material practical for continuous use, the team embedded the nanoreactors within an environmentally benign sodium alginate hydrogel matrix. This technique produced solid, recyclable photocatalysts capable of continuous H2O2 synthesis under natural sunlight while keeping performance stable over time.
Alternative Organelle-Mimetic Designs for Solar Fuel Co-Production
Parallel developments in organelle-mimetic architecture expand upon these cell-inspired principles. Researchers elsewhere constructed a ZIF-67@CoS/CdS nanoreactor that mimics natural metalloproteins and organelle structures to enable directional charge transport and hydrogen-bond microenvironment regulation.
Characterizations show that an established interfacial electric field accelerates charge migration, while the catalyst lowers energy barriers for water dissociation and hydrogen formation by modifying hydrogen bonds. This optimized catalyst delivers a molar-level H2 activity of 1457.1 mmol m−2 over a five-hour test across 1,000 square centimeters under sunlight, achieving a pyruvic acid selectivity of 91.2 percent.
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