Strongâacid COâ electrolysis, boosted by iodideâmodified copper, is turning waste carbon into valuable multiâcarbon fuelsâusing PEMâstyle stacks you already know.
Most companies chasing net-zero targets are stuck on the same bottleneck: COâ is cheap to capture but hard to monetize. You can pay to store it underground, or you can turn it into something the market actually wantsâfuels and chemicals. The catch is doing that efficiently, at scale, and in real industrial conditions.
A recent wave of research, capped by new work on iodideâtuned COâ electroreduction in strong acid, points to a serious upgrade: converting COâ into multiâcarbon products (like ethylene and ethanol) in compact, protonâexchangeâmembrane (PEM)âstyle reactors. Thatâs the same basic architecture that already underpins gigawatts of hydrogen electrolysers.
This matters because it connects directly to where green technology is going in 2025: AIâoptimized grids feeding power into modular electrochemical units that make fuels, polymers, and solvents on demand. COâ electroreduction in strong acid doesnât just clean up emissions; it can plug into existing PEM stacks, supply chains, and balanceâofâplant systems.
In this post, Iâll break down what this new iodideâenabled chemistry actually does, why âstrong acidâ is such a big deal, and how it could reshape green technology strategies for utilities, chemicals producers, and climateâtech startups.
What COâ Electroreduction Is Really Trying To Solve
The core goal of COâ electroreduction is straightforward: use renewable electricity to turn COâ into energyâdense molecules. Those molecules can be:
- C1 products like CO, formate, or methane
- C2+ (multiâcarbon) products like ethylene, ethanol, propanol, and acetate
From a green technology and business perspective, multiâcarbon products are where the economics get interesting:
- Ethylene is the backbone for plastics and is a >200 million tonne per year market.
- Ethanol and propanol are highâvalue fuels and chemical intermediates.
If you can make C2+ products directly from COâ with cheap renewable power, youâre not just avoiding emissionsâyouâre replacing steam crackers and fossil syngas units.
The reality? Traditional COâ electrolysis has three big problems:
- Alkaline systems donât match industrial hardware. Most highâselectivity COâ electrolysers run in alkaline or neutral media, which donât integrate cleanly with mature PEM technology used for hydrogen.
- Carbonate loss kills efficiency. In alkaline environments, COâ reacts with hydroxide to form carbonate and bicarbonate. You lose COâ, waste energy, and complicate separation.
- Hydrogen wins the competition. In acidic media, protons are abundant, so the hydrogen evolution reaction (HER) outcompetes COâ reduction. You end up making Hâ, not ethylene.
So the field has been stuck: alkaline systems work but are awkward industrially; acid systems match PEM infrastructure but usually donât make useful carbon products.
Why Strong Acid Is So Attractive â And So Hard
If youâre thinking in terms of scalable green technology, strong acid (think sulfuric acid or similar pH ~0 environments) has clear advantages:
- Compatibility with PEM membranes and stacks. Thatâs the tech already being deployed for green hydrogen at multiâMW scale.
- High conductivity and compact designs. You can push higher current densities and shrink reactor footprints.
- Simpler water management. Acidic PEM systems are wellâunderstood and backed by decades of fuelâcell engineering.
But strong acid also brings a brutal challenge:
In strong acid, hydrogen evolution is the default reaction; COâ reduction is the underdog.
On a copper catalystâstill the workhorse for multiâcarbon productsâprotons crowd the surface, and electrons preferentially reduce them to Hâ instead of reducing COâ or CO. Thatâs why COââtoâC2+ in strong acid was long considered unrealistic.
Over the last few years, though, several breakthroughs have changed that story:
- Electricâfield engineering with alkali cations to reshape the interfacial environment
- Microenvironment control (hydrophobic layers, ionomers, local pH pockets)
- Tandem catalyst designs that first make CO, then upgrade CO to C2+ products
The new insight from iodideâmodified copper in strong acid adds another piece: the anion at the surface isnât just a passive spectator; it can be a powerful director of both selectivity and stability.
How SurfaceâAdsorbed Iodide Boosts MultiâCarbon Products
The key takeaway from the latest research is simple but powerful:
A thin layer of adsorbed iodide ions on copper can tilt a strongly acidic environment away from hydrogen and toward multiâcarbon COâ reduction.
Hereâs whatâs going on beneath that statement.
1. Iodide reshapes the catalyst surface
Halides like chloride, bromide, and iodide are known to interact strongly with copper. Iodide, in particular, can:
- Adsorb onto the copper surface
- Form transient CuâI phases
- Influence which crystal facets are exposed and how they reconstruct under potential
Those structural changes matter because CâC coupling, the step that turns two CO units into a C2 product, is highly sensitive to surface geometry. The right arrangement of Cu atoms lowers the barrier for making C2 intermediates.
2. Iodide engineers the interfacial electric field
The narrow region where electrode, electrolyte, and gas meetâthe electrochemical double layerâcontrols which molecules get stabilized or repelled.
Surfaceâadsorbed iodide:
- Alters the local electric field orientation and magnitude
- Changes how cations (like Kâș, Csâș, etc.) pack near the surface
- Affects the degree of hydration of these cations
Those shifts change how COâ, CO, and key intermediates (like *CO and *OCCO) bind and react. Studies over the past decade show that stronger electric fields and hydrophobic microenvironments promote CO accumulation and CâC coupling. Iodide helps construct exactly that kind of microenvironmentâeven in strong acid.
3. Iodide suppresses hydrogen evolution (enough)
You wonât completely shut down hydrogen evolution in strong acid. But you donât need to. You just need to:
- Block some of the most active hydrogen sites
- Keep enough COâderived intermediates on the surface long enough to couple
Iodide does both. It competes for sites that would otherwise produce Hâ, while simultaneously favoring CO adsorption and dimerization pathways on copper. The net effect: a higher Faradaic efficiency toward C2+ products at industrially relevant current densities.
From a system design perspective, that translates directly to:
- More carbon converted into valuable products instead of waste Hâ
- Smaller and potentially cheaper downstream separation units
What This Means For Green Technology And Industry
If youâre planning a green technology roadmapâfor a utility, a chemicals company, or a climateâtech startupâthis chemistry unlocks several strategic advantages.
1. COââtoâchemicals in PEMâcompatible stacks
The most immediate implication: COâ electroreduction in strong acid can now start to look like PEM hydrogen electrolysis in terms of:
- Stack architecture (membraneâelectrode assemblies, gasâdiffusion electrodes)
- Balance of plant (water circulation, compression, power electronics)
- Operational parameters (current densities approaching or exceeding 1 A cmâ»ÂČ)
That alignment is huge. It means you can:
- Reuse engineering knowâhow and supply chains from PEM Hâ
- Coâlocate COâ and Hâ production in modular plants
- Scale faster because major components are already industrialized
2. Higher singleâpass COâ utilization
Strongâacid, membraneâelectrodeâassembly designs have already hit singleâpass COâ conversion efficiencies approaching 90% in some demonstrations. Add in an iodideâengineered catalyst that directs more of that carbon into C2+ products, and you get:
- Less recycle of unreacted COâ
- Lower compression and separation energy
- Better overall energy and carbon efficiency for the plant
For gridâconnected systems using variable renewables, that efficiency makes flexible, onâoff operation less punishing.
3. Cleaner, AIâoptimizible process signals
One underâdiscussed benefit: strongâacid COâ electrolysis creates cleaner datasets for AI process control.
- Fewer competing side reactions from carbonate chemistry
- More stable ionic composition of the electrolyte
- Clearer correlations between potential, current, and product distribution
Thatâs fertile ground for AI models that adjust current density, temperature, and feed composition in real time to maximize C2+ yield and minimize degradation. For operators already using AI to manage electrolyser fleets, acidic COâ reduction slots into existing analytics and control pipelines more naturally than wonky alkaline chemistries.
Practical Considerations For Companies And Developers
If youâre thinking, âWhat would it take to actually implement this?â, hereâs a pragmatic checklist.
1. Technology readiness and pilots
Weâre not at full commercial deployment yet. But the trajectory is clear:
- Labâscale: Detailed mechanistic studies (like the iodide work) clarifying active sites, intermediates, and degradation.
- Benchâscale: Flow cells and small MEAs hitting high current density with meaningful C2+ selectivities.
- Pilotâscale: 10â100 kW systems integrated with COâ capture units and renewable power.
If your organization runs an R&D or innovation program, the realistic nearâterm move is joint development or pilot participation, not buying a turnkey plant tomorrow.
2. Integration with existing green tech assets
Companies already deploying green technologyâespecially electrolytic hydrogenâhave a head start. Acidic COâ electroreduction can:
- Share power infrastructure and DC bus with Hâ electrolysers
- Use similar stack housing and assembly designs
- Plug into existing AIâbased asset management systems for predictive maintenance and optimization
In my experience, firms that treat COâ electrolysis as an extension of their PEM stack portfolio, rather than a totally separate technology, move faster and spend less.
3. Product strategy: what do you actually want to make?
The iodideâenhanced approach helps with a mix of C2+ productsâoften ethylene, ethanol, acetate, and others. From a business lens, you should be explicit about:
- Target product slate: fuels, monomers, or oxygenates?
- Market access: do you have offtake agreements or internal use cases?
- Separation and purification: gaseous vs liquid products, required purity, regulatory constraints.
Electrochemistry is only half the story. Downstream processing and market positioning can make or break the economics.
Where AI Fits In The Future Of Acidic COâ Electrolysis
Since this post sits in a green technology series with a strong AI angle, itâs worth calling out how AI actually helps hereânot as a buzzword, but as a concrete toolset.
Here are three highâimpact roles I see:
-
Catalyst discovery and optimization
Models informed by densityâfunctionalâtheory data and experimental results can screen halide combinations, cation choices, and surface structures far faster than trialâandâerror. -
Digital twins for electrolysers
Highâfidelity process models, trained on real plant data, can predict how iodideâmodified catalysts age, when performance drifts, and how to adjust operation to compensate. -
Gridâaware dispatch
COââtoâfuel plants wonât run flat out 24/7 on renewables. AI scheduling can align highâintensity operation with lowâcost, lowâcarbon hours while still hitting production targets.
The bottom line: acidic COâ electrolysis is exactly the kind of highâdimensional, tightly coupled system where AI control pays offâand the new iodideâdriven chemistry makes that system far more attractive to build in the first place.
Where This Leaves You In 2025
Hereâs the thing about COâ electroreduction in strong acid: five years ago, it was mostly a curiosity. Today, with detailed insights into how surfaceâadsorbed iodide ions and tailored microenvironments steer copper toward multiâcarbon products, itâs becoming a serious candidate for largeâscale deployment.
For organizations building green technology strategies, the smart move now is to:
- Track and engage with pilot projects using acidic, PEMâstyle COâ electrolysers.
- Start evaluating coâlocation scenarios with existing capture and renewable assets.
- Build internal capabilityâoften AIâdrivenâfor monitoring, optimization, and productâslate control in electrochemical processes.
COâ isnât just a liability any more; with the right electrochemistry, itâs feedstock. The companies that learn to run these iodideâtuned, strongly acidic systems efficiently will own a critical part of the next generation of green industrial infrastructure.