Unfortunately, the question as stated is thermodynamically impossible. Let's look at the proposed reaction:
$$\ce{CO2(g) -> CO(g) + O(g)}$$
This reaction is simply a bond dissociation (specifically, a carbon-oxygen covalent double bond is broken). We can look up the enthalpy change associated with it. From a table of values on Wikipedia, we find in the row for carbon dioxide that this reaction has an enthalpy change of $\mathrm{+532\ kJ\ mol^{-1}}$ at $\mathrm{298\ K}$. The proposed reaction is therefore heavily endothermic. That is to say, it must absorb energy. Interestingly, it's true that the extreme strength of the bond in carbon monoxide has a measurable effect, making this process more favourable than expected. However, it is still overall extremely unfavourable, and therefore requires a large input of energy. I stress that this is unavoidable, no matter how fancy your machine - if the end result is the reaction stated above, then you must pay the energy cost somehow.
Part of the problem, though, is that we have monoatomic oxygen as a product, which is a very reactive, high energy species - it doesn't actually exist except in special conditions. A simple adjustment therefore is to have molecular dioxygen, $\ce{O2}$ (the kind in the atmosphere that you breathe). The reaction then becomes:
$$\ce{2 CO2(g) -> 2 CO(g) + O2(g)}$$
So what's the enthalpy change associated with this reaction? Looking up another table, this turns out to be $\mathrm{+283\ kJ\ mol^{-1}}$ at $\mathrm{298\ K}$. Again, this reaction is endothermic, though much less so than the first one. Regardless, once more this reaction is an energy sink.
If you want more visceral confirmation of this fact, consider the following. It is well known that pure carbon monoxide burns in an oxygen atmosphere. The reaction is self-sustaining and releases considerable heat. If you pay close attention, the reaction in the video is the exact inverse of the second equation. By chemical thermodynamics, if the combustion of $\ce{CO}$ to $\ce{CO2}$ releases heat, then it is necessarily true that cleaving $\ce{CO2}$ to form $\ce{CO}$ and $\ce{O2}$ will consume energy.
As a last point, there are ways to make the production of $\ce{CO}$ from $\ce{CO2}$ feasible, but it requires changing the products. For example, if hydrogen gas is used as a reagent, the following becomes possible:
$$\ce{CO2(g) + H2(g) -> CO(g) + H2O(g)}$$
The enthalpy change for this reaction is $\mathrm{+41\ kJ\ mol^{-1}}$ at $\mathrm{298\ K}$ , which is still endothermic, but approaching the break-even point. This is not too surprising, as hydrogen gas can behave as a reductant, and the bonds in water molecules are strong, pushing the reaction forwards. Let us make one last tiny modification:
$$\ce{CO2(g) + H2(g) -> CO(g) + H2O\color{red}{(l)}}$$
By assuming the water produced is in the liquid state as opposed to a gas, the reaction surrenders a little more energy, and the calculated reaction enthalpy becomes $\mathrm{-3\ kJ\ mol^{-1}}$ at $\mathrm{298\ K}$. This reaction is very mildly exothermic, which is to say it releases heat (admittedly, so little that it's within margin of error, and slightly different conditions could make the reaction overall endothermic).
If you're not dead-set on having carbon monoxide as a product, then there are further options still. For example, here is the complete reduction of $\ce{CO2}$ to methane ($\ce{CH4}$), a considerably exothermic process with a reaction enthalpy of $\mathrm{-253\ kJ\ mol^{-1}}$ at $\mathrm{298\ K}$:
$$\ce{CO2(g) + 4H2(g) -> CH4(g) + 2 H2O(l)}$$
Methane is not an ideal product, as it too is a greenhouse gas and is a low value chemical feedstock due to its abundance and relative lack of useful chemistry. There is much more interest in conversion of $\ce{CO2}$ to compounds such as methanol $\ce{CH3OH}$ and formic acid $\ce{HCOOH}$. These two particular reactions are also exothermic.
There are several issues with using hydrogen reduction of $\ce{CO2}$ as a carbon capture strategy to combat climate change, but perhaps the main one is a real-world factor: most hydrogen we currently produce is derived from fossil fuels, notably from the partial combustion of fossil methane (natural gas) with water at high temperatures, known as steam reforming. Therefore, while alternative sources of hydrogen gas using renewable low-carbon intensity energy are not available, this is a poor strategy to remove anthropogenic $\ce{CO2}$ from the atmosphere.