Porous Carbon for CO 2 Capture Technology: Unveiling Fundamentals and Innovations

: Porous carbon is an emerging material for the capture of CO 2 from point sources of emissions due to its high structural, mechanical, and chemical stability, along with reusability advantages. Currently, research efforts are mainly focused on high-or medium-pressure adsorption, rather than low-pressure or DAC (direct air capture) conditions. Highly porous and functionalized carbon, containing heteroatoms (N, O, etc.), is synthesized using different activation synthesis routes, such as hard template, soft template, and chemical activation, to achieve high CO 2 capture efﬁciency at various temperatures and pressure ranges. Fundamental pore formation mechanisms with different activation routes have been evaluated and explored. Higher porosity alone can be ineffective without the presence of proper saturated diffusion pathways for CO 2 transfer. Therefore, it is imperative to emphasize more rational multi-hierarchical macro-/meso-/micro-/super-/ultra-pore design strategies to achieve a higher utilization efﬁciency of these pores. Moreover, the present research primarily focuses on powder-based hierarchical porous carbon materials, which may reduce the efﬁciency of the capture performance when shaping the powder into pellets or ﬁxed-bed shapes for applications considered. Therefore, it is imperative to develop a synthesis strategy for pelletized porous carbon and to explore its mechanistic synthesis route and potential for CO 2 capture.


Introduction
The industrialization and urbanization of humans have resulted in a significant increase in CO 2 emissions, estimated to be over 36 billion tons at present [1].As a consequence, the current CO 2 concentration levels in the environment have reached ~420 ppm, compared to ~280 ppm during preindustrial times (Figure 1) [2,3].This increase is certain to cause hugely detrimental effects on human life through climate change.It requires immediate efforts to adopt a net-zero strategy to mitigate CO 2 effects by efficiently capturing CO 2 from point sources (such as oil refineries, heavy industries, cement, fossil fuel power plants, and industrial process plants) or through direct air capture (DAC) [4][5][6].
Over the years, CO 2 capture or separation from flue gases has seen the development of the chemical absorption technique utilizing liquid alkanolamine solution process (scrubbing) on an industrial scale [7,8].The liquid amine absorption technique has reached an industrial state-level advancement with considerable CO 2 capture capacity (1.5 mmol g −1 ) and absorption rate (0.05-0.18 mol m −2 s −1 ) at a 4-25 vol.% concentration level [7,9,10].Primary and secondary amines form carbamate with comparatively higher reaction kinetics with CO 2 , requiring high enthalpy absorption reactions of 80-90 and 70-75 kJ mol −1 CO 2 , respectively.In the case of tertiary amines, they form bicarbonate with CO 2 with sluggish reaction kinetics, requiring 40-55 kJ mol −1 CO 2 absorption enthalpy through a base-catalyzed hydration mechanism [11][12][13].
Surfaces 2023, 6 317 Surfaces 2023, 6, FOR PEER REVIEW 2 with sluggish reaction kinetics, requiring 40-55 kJ mol −1 CO2 absorption enthalpy through a base-catalyzed hydration mechanism [11][12][13].Consequently, solvent regeneration (stripping) requires a huge amount of energy (3-5 GJ t −1 CO2 captured), leading to large-scale industrial energy consumption and adding to the 70% additional cost, which is the main obstacle.However, the acceptable value for industrial application is 0.4-0.7 GJ t −1 CO2 [14 -16].Furthermore, the liquid amine absorption process faces other hurdles, such as liquid amine degradation due to high heating, solvent loss, equipment corrosion of reactors (steel/carbon), production of carcinogenic toxic products (nitramines, nitrosamines), and the utilization of large amounts of NaOH or KOH to restore CO2 absorption capacity of amines, resulting in a secondary pollutant to alkaline wastewater [17,18].
One of the technical criteria for solid adsorbent capture is the consideration of capture under dry conditions to ensure a reasonable capture efficiency.However, most of the Consequently, solvent regeneration (stripping) requires a huge amount of energy (3-5 GJ t −1 CO 2 captured), leading to large-scale industrial energy consumption and adding to the 70% additional cost, which is the main obstacle.However, the acceptable value for industrial application is 0.4-0.7 GJ t −1 CO 2 [14][15][16].Furthermore, the liquid amine absorption process faces other hurdles, such as liquid amine degradation due to high heating, solvent loss, equipment corrosion of reactors (steel/carbon), production of carcinogenic toxic products (nitramines, nitrosamines), and the utilization of large amounts of NaOH or KOH to restore CO 2 absorption capacity of amines, resulting in a secondary pollutant to alkaline wastewater [17,18].
One of the technical criteria for solid adsorbent capture is the consideration of capture under dry conditions to ensure a reasonable capture efficiency.However, most of the post-combustion flue gas remains wet (5-7 vol.% water) at 40-80 • C, necessitating an energy-intensive drying process to remove moisture from the multi-component flue gas flow [27,28].Ultimately, removing moisture from the gas flow or drying it backfires in terms of technical feasibility on an industrial scale.Additionally, wet condition CO 2 capture significantly reduces the efficiency of MOF-, COF-, and zeolite-based solid adsorbents due to lower hydrothermal stability [27,29].In comparison, carbon-based materials exhibit comparable stability under moisture and thermal conditions due to the structural and mechanical rigidity of the carbon structure.
Among the solid adsorbents, carbon-based adsorbents are considered promising candidates for CO 2 capture technology due to their abundant sources, low cost, and scalable preparation process [30].Additionally, carbon-based materials are known for their good thermal and chemical stability, low energy regeneration, and ability to maintain adsorption performance even under high moisture conditions [31,32].They also offer the benefit of tunable opportunities for textural properties and surface functionalization [33].

Carbon as a Promising Candidate for CO 2 Capture Technology
Carbon is considered a promising candidate for CO 2 capture technology due to its capacity to offer a clean surface for reutilization, along with its thermal, mechanical, chemical, and moisture stability [34].Its simple preparation strategy and low cost make it suitable for industrial applications [35].
Various templating methods, including gas templates, hard templates, soft templates, and chemical activation, are employed to design ultra-super-micropores for low-pressure CO 2 capture and macro-mesopores for high-pressure CO 2 capture [1].Heteroatom doping on carbon and surface modification induces hetero-surface functionalized groups on the carbon structure to control surface chemistry [38,39].CO 2 molecules, being of acidic nature and possessing a quadrupole moment, have a competitive advantage over other gases for surface sorption due to the surface chemistry.Essentially, weak van der Waals forces induce the physisorption of CO 2 molecules on the surface, which can be intensified by functional groups, such as acid-base interactions, H-bonds, or electrostatic interactions.As a result, this leads to a higher adsorption capacity for CO 2 compared to other gas mixtures, making it more selective towards CO 2 molecules [40,41].
During carbonization, a higher degree of aromaticity imparts a hydrophobic nature to carbon, allowing it to function effectively under hydrated conditions [42].However, while heteroatom doping reduces polyaromatic condensation and reduce mechanical and chemical stability, it is essential to seek a rational design strategy for synthesizing carbon materials [43,44].

Carbon Products Preparation Mechanism
A carbon synthesis technique utilizes various technical processes such as pyrolysis (400-1100 • C), sol-gel, and hydrothermal processes [45].Hydrothermal technology utilizes water as a medium in a closed reactor vessel to undergo processes such as hydrolysis, dehydration, decarboxylation, concentration polymerization, and aromatization [46].It aligns with the principles of thermochemical conversion, making it a sustainable and green process similar to the natural formation of carbon.Hydrothermal methods offer the opportunity to produce various initial intermediate products that can later be combined with the general pyrolysis process, enabling the diversification of morphological and structural properties [47,48].Pyrolysis is a thermochemical conversion process where materials decompose into solid (char), liquid (oil), and gas (syngas) as the temperature increases.The properties of pyrolysis products depend on various factors, including temperature, residence time, heating rate, and whether fast or slow pyrolysis is employed.In the con-ventional pyrolysis process, a furnace's heating wall transfers heat to the material's surface, resulting in a higher yield of char compared to microwave pyrolysis [49,50].
Fundamental carbon formation mechanisms bear the dehydration, intramolecular condensation, decarboxylation, and polymerization for oxygen-containing functional groups in the different temperature ranges (Figure 2) [1,51].Various techniques or different sources are utilized in the formation of different intermediate products to provide the different characteristic carbon products.Initially, various sources or technical processes yield diverse intermediate products through dehydration, intramolecular condensation, or initial polymerization, resulting in an intermediate structural framework [52].With increasing temperature, aromatic polycondensation steps occur, generating multiple gas components like NH 3 , CH 4 , CO, CO 2 , H 2 , water vapor, or structural degradation, which create structural, internal, and surface pores.Additionally, pressure modifies or influences the shape of the carbon [53,54].
opportunity to produce various initial intermediate products that can later be combined with the general pyrolysis process, enabling the diversification of morphological and structural properties [47,48].Pyrolysis is a thermochemical conversion process where materials decompose into solid (char), liquid (oil), and gas (syngas) as the temperature increases.The properties of pyrolysis products depend on various factors, including temperature, residence time, heating rate, and whether fast or slow pyrolysis is employed.In the conventional pyrolysis process, a furnace's heating wall transfers heat to the material's surface, resulting in a higher yield of char compared to microwave pyrolysis [49,50].
Fundamental carbon formation mechanisms bear the dehydration, intramolecular condensation, decarboxylation, and polymerization for oxygen-containing functional groups in the different temperature ranges (Figure 2) [1,51].Various techniques or different sources are utilized in the formation of different intermediate products to provide the different characteristic carbon products.Initially, various sources or technical processes yield diverse intermediate products through dehydration, intramolecular condensation, or initial polymerization, resulting in an intermediate structural framework [52].With increasing temperature, aromatic polycondensation steps occur, generating multiple gas components like NH3, CH4, CO, CO2, H2, water vapor, or structural degradation, which create structural, internal, and surface pores.Additionally, pressure modifies or influences the shape of the carbon [53,54].

Factors Influencing CO2 Adsorption on the Carbon Surface
The number of CO2 molecules adsorbed on the surface depends on several factors, including surface area, cumulative pore volume, pore sizes, pore interconnectivity, pore shape, and surface chemistry [55].The low-pressure or high-pressure capture efficiency depends on the textural properties of the adsorbents.It is suggested that low-pressure conditions are overwhelmed by ultra-micropores (0.35-0.70 nm) to super-micropores (0.70-0.90 nm).At high-pressure conditions, pores size greater than micropores is more favorable [56,57].Also, it is important to consider the competition among the different gases (CO2, N2, NOx, SO2, H2O vapor, etc.) to be separated or captured at a point source [58].The kinetic diameter of CO2 (0.33 nm) is smaller than the kinetic diameters of nitrogen (0.36 nm) and oxygen (0.34 nm); CO2 adsorption favors the smaller than micro-size pores

Factors Influencing CO 2 Adsorption on the Carbon Surface
The number of CO 2 molecules adsorbed on the surface depends on several factors, including surface area, cumulative pore volume, pore sizes, pore interconnectivity, pore shape, and surface chemistry [55].The low-pressure or high-pressure capture efficiency depends on the textural properties of the adsorbents.It is suggested that low-pressure conditions are overwhelmed by ultra-micropores (0.35-0.70 nm) to super-micropores (0.70-0.90 nm).At high-pressure conditions, pores size greater than micropores is more favorable [56,57].Also, it is important to consider the competition among the different gases (CO 2 , N 2 , NO x , SO 2 , H 2 O vapor, etc.) to be separated or captured at a point source [58].The kinetic diameter of CO 2 (0.33 nm) is smaller than the kinetic diameters of nitrogen (0.36 nm) and oxygen (0.34 nm); CO 2 adsorption favors the smaller than micro-size pores (<2 nm), while N 2 adsorption is more favorable at mesoporous volumes (>2 nm) [59].Surface chemistry of the adsorbents influences the CO 2 sorption amounts, selectivity, dynamic kinetics due to CO 2 molecule polarizability, and quadrupole nature.A CO 2 molecule has higher polarizability (26.3 [10,20,26]. CO 2 physisorption on a carbon surface occurs due to the weak van der Waals force.Heteroatoms or heteroatom-containing functional groups influence the CO 2 adsorption on the surface of carbon, leading to more adsorption potential, depending on the types of in-teractions (H-bond, electrostatic interaction, Lewis acid-base interaction) (Figure 3) [60][61][62].There is still an ongoing debate about which types of interactions mainly occur or which forces are important in the CO 2 physisorption on the carbon surface.It can be assumed that higher polarizability and quadrupole moment of CO 2 molecules are more favorable for CO 2 molecules to separate from the other gases (N 2 , O 2 , H 2 , CH 4 , etc.) [63].
CO2 physisorption on a carbon surface occurs due to the weak van der Waals force.Heteroatoms or heteroatom-containing functional groups influence the CO2 adsorption on the surface of carbon, leading to more adsorption potential, depending on the types of interactions (H-bond, electrostatic interaction, Lewis acid-base interaction) (Figure 3) [60][61][62].There is still an ongoing debate about which types of interactions mainly occur or which forces are important in the CO2 physisorption on the carbon surface.It can be assumed that higher polarizability and quadrupole moment of CO2 molecules are more favorable for CO2 molecules to separate from the other gases (N2, O2, H2, CH4, etc.) [63].

Strategies for Modifying Carbon Structures
A three-dimensional interconnected porous carbon synthesis strategy has been developed over the years to enhance the surface area, porosity, and gas diffusion rate of the components [37].Various activation techniques for the carbon structure have been explored, including chemical activation, soft and hard template methods, and in situ metal ion activation strategies.The basic synthesis strategy, challenges, and minute factors that influence the structure of carbon are discussed in the following section.

Chemical Activation
To produce highly porous and efficient carbon products, chemical activation of the carbon during carbonization has shown a potential utilization technique [65].In the process, carbon precursors or carbon sources are simply mixed with an activating agent, and carbonization proceeds through different temperatures (350~800 °C) to achieve a porous carbon.Different acidic (e.g., HCl, FeCl3, ZnCl2, H3PO4, H2SO4, and HNO3), alkaline (e.g., KOH, NaOH, CaCO3 and K2CO3), or oxidant substances (e.g., H2O2, and KMnO4) have previously been utilized as activating agents to activate the carbon during carbonization [66][67][68].Utilizing such an activating agent provides a very effective way to reduce the

Strategies for Modifying Carbon Structures
A three-dimensional interconnected porous carbon synthesis strategy has been developed over the years to enhance the surface area, porosity, and gas diffusion rate of the components [37].Various activation techniques for the carbon structure have been explored, including chemical activation, soft and hard template methods, and in situ metal ion activation strategies.The basic synthesis strategy, challenges, and minute factors that influence the structure of carbon are discussed in the following section.

Chemical Activation
To produce highly porous and efficient carbon products, chemical activation of the carbon during carbonization has shown a potential utilization technique [65].In the process, carbon precursors or carbon sources are simply mixed with an activating agent, and carbonization proceeds through different temperatures (350~800 • C) to achieve a porous carbon.Different acidic (e.g., HCl, FeCl 3 , ZnCl 2 , H 3 PO 4 , H 2 SO 4 , and HNO 3 ), alkaline (e.g., KOH, NaOH, CaCO 3 and K 2 CO 3 ), or oxidant substances (e.g., H 2 O 2 , and KMnO 4 ) have previously been utilized as activating agents to activate the carbon during carbonization [66][67][68].Utilizing such an activating agent provides a very effective way to reduce the carbonization temperature and induce porosity or shape modification during the formation process.However, it cannot omit the extra step of removing the corrosive chemical from the structure using water.
Different groups have tried to determine the activation mechanism, nearly in complete agreement.Most commonly, KOH was used as the chemical activation agent, being a strong base [65,69].Most groups predict the carbonization reaction as Equation ( 1) [70]: Afterward, some groups have shown that volatile groups from the precursor (CO, CO 2 , and H 2 O), upon heating, react with KOH and form K 2 CO 3 : The metallic potassium (K), resulting from the reaction of the K 2 CO 3 with the carbon species, as well as its spatial positioning or penetration into the internal structure of carbon, promotes porosity.This internal porosity, upon removal during the washing step, provides the internal pore network: A proper ratio of precursors to activating agents influences the textural, mechanical, and structural properties of the carbon products.An optimally high ratio of the activating agent (approximately 4) enhances the porosity of the carbon by intercalating its structure and resulting in expansion of the pores.However, with a higher ratio (>6), the excessive enhancement breaks the pore walls and reduces the overall porosity.A carbon nanosphere was hydrothermally prepared from glucose [71].This process controlled the spherical shape of the precursor.Subsequent heat treatment and activation using a KOH solution were employed to introduce finely tuned ultra-micropores into the structure (Figure 4).carbonization temperature and induce porosity or shape modification during the formation process.However, it cannot omit the extra step of removing the corrosive chemical from the structure using water.
Different groups have tried to determine the activation mechanism, nearly in complete agreement.Most commonly, KOH was used as the chemical activation agent, being a strong base [65,69].Most groups predict the carbonization reaction as Equation ( 1) [70]: Afterward, some groups have shown that volatile groups from the precursor (CO, CO2, and H2O), upon heating, react with KOH and form K2CO3: The metallic potassium (K), resulting from the reaction of the K2CO3 with the carbon species, as well as its spatial positioning or penetration into the internal structure of carbon, promotes porosity.This internal porosity, upon removal during the washing step, provides the internal pore network: A proper ratio of precursors to activating agents influences the textural, mechanical, and structural properties of the carbon products.An optimally high ratio of the activating agent (approximately 4) enhances the porosity of the carbon by intercalating its structure and resulting in expansion of the pores.However, with a higher ratio (˃6), the excessive enhancement breaks the pore walls and reduces the overall porosity.A carbon nanosphere was hydrothermally prepared from glucose [71].This process controlled the spherical shape of the precursor.Subsequent heat treatment and activation using a KOH solution were employed to introduce finely tuned ultra-micropores into the structure (Figure 4).

Physical Activation
Physical activation is environmentally friendly, cheaper, simpler and requires no chemical agent.The gas template controls the textural properties [72,73].During pyrolysis (300-1100 • C), degradation products generate different kinds of gas, such as CO 2 , CO, CH 4 , NO, H 2 O, and NH 3 , depending on the precursor's source [37].Sometimes, external sources of media like CO 2 , NH 3 , steam, He, Ar, air, or a mixture of gases (binary mixture) are utilized to activate the carbon surface (Figure 5) [74][75][76].Several efforts have been made to increase the pore volume and surface area by utilizing external steam during pyrolysis [77].Steam, along with the pyrolysis temperature, interacts with carbon to produce C(O) and H 2 , which are sources of various activated gases such as CO, CO 2 , and CH 4 .Consequently, this process promotes the formation of new pores and the expansion of pore sizes (Figure 5) [64,78].The steam activation mechanism of the carbon surface is described in the following reactions [36,79]: a.Os d. 5s (1) Volatiles release and react with atmosphere.
(2) Steam and oxygen diffuse into and reaction with carbon te>.iure.Jung-Heo showed that steam activation of carbon from cellulose fiber expanded the existing ultra-micropores and produced additional ultra-micropores (Figure 6) [80].The graphitic structure shattered due to the activation process, resulting in the size of the pores being larger than 2 nm.The activation process increased the specific surface area and pore volume to 1018 m 2 g −1 and 0.43 cm 3 g −1 from 452 m 2 g −1 and 0.199 cm 3 g −1 , respectively.Consequently, the CO 2 capture performance reached 4.41 mmol g −1 at 0 • C, 1 bar (1.21 mmol g −1 at 25 • C, 15% CO 2 ) compared to without activation, which was 3.18 mmol g −1 at 0 • C, 1 bar [80].mmol g −1 at 25 °C, 15% CO2) compared to without activation, which was 3.18 mmol g −1 at 0 °C, 1 bar [80].Air activation is one of the efficient ways to simultaneously produce micropores and mesopores on the carbon surface while inducing O-containing functional groups such as C=O, C-O, -OH, and -COOH [81,82].It is important to choose the activation time carefully.Initially, micropore formation on the carbon surface occurs predominantly, and, over time, it leads to an increase in mesopores due to the destruction of micropores [81,83].The air activation mechanism of the carbon surface is described in the following reactions [84]: In comparison to chemical activation, physical activation has less control over porosity development than chemical activation.The flow rate of N2 or other gases influences the textural properties of the carbonized products (10-200 mL min −1 ).During the carbonization process, the gas template of the degradation products provides the basic porosity and shapes of the carbonized products [85].The faster or slower removal of the gas template depends on the gas flow rate of the carbonization medium.The effects of the flow rate on textural properties and shapes need to be explored.Additionally, the activation time (0.5~72 h) plays a crucial role in determining the textural properties, as higher activation time and degree promote higher porosity in the structure.At the same time, the porosity range differs based on the activation time or temperature range of carbonization.Smaller pores (ultra-to-micropores, ultra-pores: 0.35-0.70nm, super-micropores: 0.70-0.90nm, micropores: 0.90-2 nm) tend to shift to the range of higher pores with increasing temperature due to pore wall breakages that induce the conversion of super-micropores to mesopores [34,85].

Metal Ion Activation
The chemical and physical activation strategies are highly efficient for microporous carbon synthesis.Pores smaller than 1 nm (ultra-to-super-micropores) are particularly effective for low pressure CO2 uptake.Several research efforts have focused on the singleion activation route to produce carbon with ultra-micropores in the structure [86].In this Air activation is one of the efficient ways to simultaneously produce micropores and mesopores on the carbon surface while inducing O-containing functional groups such as C=O, C-O, -OH, and -COOH [81,82].It is important to choose the activation time carefully.Initially, micropore formation on the carbon surface occurs predominantly, and, over time, it leads to an increase in mesopores due to the destruction of micropores [81,83].The air activation mechanism of the carbon surface is described in the following reactions [84]: In comparison to chemical activation, physical activation has less control over porosity development than chemical activation.The flow rate of N 2 or other gases influences the textural properties of the carbonized products (10-200 mL min −1 ).During the carbonization process, the gas template of the degradation products provides the basic porosity and shapes of the carbonized products [85].The faster or slower removal of the gas template depends on the gas flow rate of the carbonization medium.The effects of the flow rate on textural properties and shapes need to be explored.Additionally, the activation time (0.5~72 h) plays a crucial role in determining the textural properties, as higher activation time and degree promote higher porosity in the structure.At the same time, the porosity range differs based on the activation time or temperature range of carbonization.Smaller pores (ultra-to-micropores, ultra-pores: 0.35-0.70nm, super-micropores: 0.70-0.90nm, micropores: 0.90-2 nm) tend to shift to the range of higher pores with increasing temperature due to pore wall breakages that induce the conversion of super-micropores to mesopores [34,85].

Metal Ion Activation
The chemical and physical activation strategies are highly efficient for microporous carbon synthesis.Pores smaller than 1 nm (ultra-to-super-micropores) are particularly effective for low pressure CO 2 uptake.Several research efforts have focused on the singleion activation route to produce carbon with ultra-micropores in the structure [86].In this process, monodispersed alkali metal ions (Li + , K + , Na + , Rb + , Cs + ) are introduced into the carbon precursors of phenolic resin through a reaction between alkali hydroxide and the acidic groups of the resin during the solution process [87].Monodispersed metal ions induce ultra-micropores in the carbon structure and provide the opportunity to tune pore sizes at the angstrom or sub-angstrom level (0.6-0.76 nm), depending on their individual activation strength and metal ionic size.The technique of metal ion activation has made significant progress through the in situ homogeneous activation process.In this method, metal salts are combined with organic precursors, such as alkali metal salts of carboxylic phenolic resin, through a hydrothermal process to produce xerogel.Under a temperature of 400 • C, these compounds undergo decomposition, resulting in the creation of metal carbonate (M 2 CO 3 ), accompanied by the release of water vapor and CO 2 gas, which act as templates.Moreover, the subsequent thermal decomposition of the metal carbonate (M 2 CO 3 ) facilitates the generation of metal oxide (M 2 O) through a redox reaction between the metal carbonate (M 2 CO 3 ) and carbon.This reaction is depicted by the equation Furthermore, the metal oxide (M 2 O) significantly etches the carbon framework through a vigorous redox interaction between the metal oxide and the carbon framework.This is illustrated by the equation M 2 O + C → 2M + CO.As a result, the produced metallic component intercalates the crystalline graphitic lattice of the carbon.Consequently, this process leads to the expansion of the interlayer spacing within the lattice, thereby stabilizing the carbon structure.Subsequent to the washing process, in which the metallic portion is removed by water, the structure no longer reverts to its previous nonporous state.Instead, it retains the expanded lattice configuration, resulting in nanopores smaller than 1 nm.The precise size of these pores (spacing) can be finely tuned based on the dimensions of the metal ion, allowing for adjustment from Li + to Cs + .Zhou et al. produced N-doped, uniformly ultra-microporous carbon material of approximately 0.5 nm using a metal activation process on K + -exchanged meta-aminophenol-formaldehyde resin [86].This process led to a notable CO 2 capture performance of 1.67 mmol g −1 under low pressure (0.15 bar, 25 • C).

Hard Template Activation
A hard template is utilized to associate with gaseous and solid carbon structures during high-temperature pyrolysis by duplicating or molecular printing on the surface of the template structure.The carbon can maintain its microstructure during the activation treatment process.Hard templates such as zeolites (zeolite x/y), porous metals (Zn-Co, Cu-Ni, Ni-Mn, etc.), metal powder (Ni/Cu powder), metal foam (Ni, Cu, Fe, etc.), silica (silica sphere, SBA-15, MCM-48), and MOFs (MOF-5, ZIF-8) have been explored to produce interconnected porous carbon structures [88,89].Hard templates can provide effective and stable effects under confined conditions in spaces.In general, zeolites (0.1-10 nm), MOFs (0.1-50 nm), silica (10-1000 nm), salts (1 nm-10 µm), porous metals (100 nm-10 µm), metal powder (100 nm-1 µm), and metal foam (1 µm-10 µm) are utilized to infuse various ranges of porosity into the carbon structure [89].Recently, Joseph et al. successfully synthesized interconnected hierarchical carbon by utilizing Coca-Cola, a soft drink, combined with the hard template KIT-6 (mesoporous silica nanoparticles) and activating the carbon using ZnCl 2 [90].This method resulted in an impressively high specific surface area of 2003 m 2 g −1 .In this process, the hard template acts as the source of the mesoporous structure, while ZnCl 2 plays a pivotal role in enhancing micropores within the carbon structure and reducing the number of mesopores.However, an excessive use of the activation agent ZnCl 2 can potentially lead to damage in both mesopore and micropore structures (Figure 7).A molten salt, or a eutectic mixture of salts such as LiBr/KBr (348 °C), LiI/KI (275 °C), LiCl/KCl (353 °C), is utilized as a high-temperature solvent to synthesize porous carbon (Figure 8) [52,[91][92][93].In the synthesis process, the solvent intermediate products are carbonized under diluted conditions, resembling water under hydrothermal conditions, providing the opportunity for the formation of structured carbon [94].Carbohydrate polymerization in the presence of strongly interacting metal ionic species creates nanopores in the carbon material, and the pore size can be tuned depending on the ionic species or the precursor-to-salt ratio.A proper choice of cation and counter anion controls the pore size.Additionally, the miscibility in the reaction medium with intermediate products, depending on their polarizability, influences the textural properties [95].In situ hard salt templates of NaCl, ZnCl2, Na2CO3, and CaCO3 are utilized to enable large-scale production of carbon from glucose, sucrose, and biomass.This is due to their cheap and simple removal process through water washing steps.The silica and zeolite templates require HF or NaOH, while metal powder, porous metal, metal foam, and MOFs need an acidic solution for removal after shaping the carbon structure.Such types of aggressive removal steps sometimes damage the objective pores' structure to some extent [89,96].
Overall, hard template carbon offers greater mechanical stability and robustness when compared to reactive or soft template synthesis carbon.This type of carbon displays elevated surface area and structural integrity.Moreover, it enables the production of various ordered structures, including thin-walled carbon layers, sieving-specific pore sizes, ordered mesoporous carbon, and close-packed ordered hexagonal or cubic mesoporous carbon.It also leads to carbon with bimodal porosity [97,98].Nonetheless, the utilization of hard-templated carbon comes with notable drawbacks.A significant challenge involves the necessity of eliminating the hard template from the carbon through etching, achieved A molten salt, or a eutectic mixture of salts such as LiBr/KBr (348 • C), LiI/KI (275 • C), LiCl/KCl (353 • C), is utilized as a high-temperature solvent to synthesize porous carbon (Figure 8) [52,[91][92][93].In the synthesis process, the solvent intermediate products are carbonized under diluted conditions, resembling water under hydrothermal conditions, providing the opportunity for the formation of structured carbon [94].Carbohydrate polymerization in the presence of strongly interacting metal ionic species creates nanopores in the carbon material, and the pore size can be tuned depending on the ionic species or the precursor-to-salt ratio.A proper choice of cation and counter anion controls the pore size.Additionally, the miscibility in the reaction medium with intermediate products, depending on their polarizability, influences the textural properties [95].A molten salt, or a eutectic mixture of salts such as LiBr/KBr (348 °C), LiI/KI (275 °C), LiCl/KCl (353 °C), is utilized as a high-temperature solvent to synthesize porous carbon (Figure 8) [52,[91][92][93].In the synthesis process, the solvent intermediate products are carbonized under diluted conditions, resembling water under hydrothermal conditions, providing the opportunity for the formation of structured carbon [94].Carbohydrate polymerization in the presence of strongly interacting metal ionic species creates nanopores in the carbon material, and the pore size can be tuned depending on the ionic species or the precursor-to-salt ratio.A proper choice of cation and counter anion controls the pore size.Additionally, the miscibility in the reaction medium with intermediate products, depending on their polarizability, influences the textural properties [95].In situ hard salt templates of NaCl, ZnCl2, Na2CO3, and CaCO3 are utilized to enable large-scale production of carbon from glucose, sucrose, and biomass.This is due to their cheap and simple removal process through water washing steps.The silica and zeolite templates require HF or NaOH, while metal powder, porous metal, metal foam, and MOFs need an acidic solution for removal after shaping the carbon structure.Such types of aggressive removal steps sometimes damage the objective pores' structure to some extent [89,96].
Overall, hard template carbon offers greater mechanical stability and robustness when compared to reactive or soft template synthesis carbon.This type of carbon displays elevated surface area and structural integrity.Moreover, it enables the production of various ordered structures, including thin-walled carbon layers, sieving-specific pore sizes, ordered mesoporous carbon, and close-packed ordered hexagonal or cubic mesoporous carbon.It also leads to carbon with bimodal porosity [97,98].Nonetheless, the utilization of hard-templated carbon comes with notable drawbacks.A significant challenge involves the necessity of eliminating the hard template from the carbon through etching, achieved In situ hard salt templates of NaCl, ZnCl 2 , Na 2 CO 3 , and CaCO 3 are utilized to enable large-scale production of carbon from glucose, sucrose, and biomass.This is due to their cheap and simple removal process through water washing steps.The silica and zeolite templates require HF or NaOH, while metal powder, porous metal, metal foam, and MOFs need an acidic solution for removal after shaping the carbon structure.Such types of aggressive removal steps sometimes damage the objective pores' structure to some extent [89,96].
Overall, hard template carbon offers greater mechanical stability and robustness when compared to reactive or soft template synthesis carbon.This type of carbon displays elevated surface area and structural integrity.Moreover, it enables the production of various ordered structures, including thin-walled carbon layers, sieving-specific pore sizes, ordered mesoporous carbon, and close-packed ordered hexagonal or cubic mesoporous carbon.It also leads to carbon with bimodal porosity [97,98].Nonetheless, the utilization of hard-templated carbon comes with notable drawbacks.A significant challenge involves the necessity of eliminating the hard template from the carbon through etching, achieved by an aggressive acid removal process like, when using a silica template, washing with HF or HCl.This extra step consumes time and resources.Additionally, hard-templated carbon is constrained in terms of pore size range, which becomes critical when aiming for a multi-hierarchical pore structure [97,99,100].It is worth noting that even a high-surface-area carbon product lacking multi-hierarchical porosity may not deliver efficient gas capture performance [1,101]

Soft Template Activation
A soft template, derived from an organic co-polymer along with carbon precursors, is employed in the preparation of meso-/macroporous carbon products [102].This soft template results in a supramolecular arrangement, combining carbon precursors, block copolymers, and polymers to form a mesophase.The stability of this mesophase is achieved through either a catalytic or thermal treatment.Subsequent thermal decomposition removes the template, inducing porosity in the carbon structure.To create the mesophase, a carbon donor or carbon precursor is combined with a structure-directing organic or co-polymeric agent.Both components are necessary for mesophase formation.It is crucial for the template to withstand the thermal carbonization process while also facilitating the crosslinking of carbon with polymers [102][103][104].
The size and morphology of carbon mesopores can be readily controlled through the implementation of soft templating effects.The creation of supramolecular products, assembled through molecular cooperation, can be regulated in terms of their size, shape, and orientation by adjusting the ratio of carbon donors to directing co-polymers [105].Additionally, factors such as the solubility of components in the solution, the solution ratio, and polarizability effects play crucial roles in the modification of soft templating products [106,107].
The mesophase structure primarily forms through hydrogen bonding between template polymers and carbon precursors.For instance, the hydrogen-bonded molecular cooperative assembled complex of melamine and cyanuric acid (MCA), along with various other complexes like MCA and glucose (MG), Pluronic F108, Pluronic F127, P123, and ZIF-8, contribute to the formation of the mesophase structure through H-bonding [1,108,109].Subsequent thermal treatment leads to the compaction and shrinkage of materials, resulting in the isotropic formation of mesopores ranging from 3 to 30 nm in size.The template is either partially or completely removed at temperatures between 300 and 400 • C. Simultaneously, the carbonization process also involves the aromatic polycondensation of carbon products [1,110].

Significant Role of Surface Functional Groups in Porous Carbon
The surface functional group on the carbon structure plays a critical role in CO 2 capture technology.Pure carbon bears adsorption energy of 6.6 kJ mol −1 for CO 2 , which is not sufficient to capture CO 2 molecules and separate them from a mixture of gases (flue gas), even though CO 2 molecules have a higher quadrupole moment.This becomes particularly important at low pressure or during direct air capture, where higher adsorption energy is required to effectively compete with other gases and moisture [101,111].It is essential to introduce exposed heteroatom functional groups (such as N, B, O, P, S, etc.) on the surfaces of micro-/meso-/macropores of the carbon to enhance the amount of CO 2 captured and the kinetics [22,[112][113][114].
Different precursors or mixtures of hetero-precursors are utilized to prepare and induce various surface functional groups on the carbon [115,116].Built-in functional groups efficiently improve the adsorption of CO 2 molecules through acid-base interactions, H-bond interactions, or electrostatic quadrupole interactions.Numerical quantification shows that O-containing, N-containing, and N-/O-co-modified functional groups on carbon improve the CO 2 adsorption energy to −14.3 to −22.6 kJ mol −1 , −22.1 to −27.1 kJ mol −1 , and −28.9 kJ mol −1 , respectively [117][118][119].
Heteroatom doping or impregnation on the carbon structure influences its structural and mechanical stability.Heteroatom insertion counterbalances the structural or mechanical properties of the carbon by reducing the degree of polyaromatic condensation during carbonization at over 600 • C and destroying the pore structure, which poses challenges for maintaining the chemical, mechanical, and thermal stability of the carbon framework [1,120].
Xing et al. demonstrated the importance of H-bonding in N-doped activated carbon [31].The CO 2 adsorption capacity is roughly proportional to the N content of the activated carbon.The presence of the N atom on the carbon lattice modifies the electronic state of the hydrogen atom in the graphene layer, intensifying the interaction between the CO 2 molecules and the carbon surface.The affinity for CO 2 molecules through H-bonding is measured by the binding energy ∆E (kJ mol −1 ), where a higher value of binding energy denotes a stronger affinity for CO 2 molecules.A CO 2 molecule's binding energy without N-containing carbon is 1.26 kJ mol −1 , which is much lower than the average binding energy of N-containing carbon, which is 7.84 kJ mol −1 .The binding energies with NH 2 , pyridinic N, and CH are 11.2, 10.5, and 9.1 kJ mol −1 , respectively.The findings of this study cannot correlate with or explain the traditional acid-base interaction of CO 2 molecules with carbon surfaces [31].
Wu et al., through DFT analysis, compared the importance of configuration types of N and O atoms in the carbon structure for the CO 2 physisorption mechanism on the carbon surface at the molecular level [118]; the pyridinic carbon surface shows the highest attraction to CO 2 molecules (E ads = −21.4kJ mol −1 ) (Figure 9).Additionally, they explored O doping on the carbon structure, which enhances the CO 2 adsorption energy (E ads = −9.7 to -17.0 kJ mol −1 ) compared to bare carbon (E ads = −5.4kJ mol −1 ).They also observed a charge density difference with and without the N/O functional group, indicating no significant electron transfer between a CO 2 molecule and a carbon surface, which establishes physisorption as the adsorption nature of functionalized carbon.
Surfaces 2023, 6, FOR PEER REVIEW 1 Heteroatom doping or impregnation on the carbon structure influences its structura and mechanical stability.Heteroatom insertion counterbalances the structural or mechan ical properties of the carbon by reducing the degree of polyaromatic condensation durin carbonization at over 600 °C and destroying the pore structure, which poses challenge for maintaining the chemical, mechanical, and thermal stability of the carbon framewor [1,120].
Xing et al. demonstrated the importance of H-bonding in N-doped activated carbo [31].The CO2 adsorption capacity is roughly proportional to the N content of the activated carbon.The presence of the N atom on the carbon lattice modifies the electronic state o the hydrogen atom in the graphene layer, intensifying the interaction between the CO molecules and the carbon surface.The affinity for CO2 molecules through H-bonding i measured by the binding energy ΔE (kJ mol −1 ), where a higher value of binding energ denotes a stronger affinity for CO2 molecules.A CO2 molecule's binding energy withou N-containing carbon is 1.26 kJ mol −1 , which is much lower than the average binding energ of N-containing carbon, which is 7.84 kJ mol −1 .The binding energies with NH2, pyridini N, and CH are 11.2, 10.5, and 9.1 kJ mol −1 , respectively.The findings of this study canno correlate with or explain the traditional acid-base interaction of CO2 molecules with car bon surfaces [31].
Wu et al., through DFT analysis, compared the importance of configuration types o N and O atoms in the carbon structure for the CO2 physisorption mechanism on the car bon surface at the molecular level [118]; the pyridinic carbon surface shows the highes attraction to CO2 molecules (Eads = −21.4kJ mol −1 ) (Figure 9).Additionally, they explored O doping on the carbon structure, which enhances the CO2 adsorption energy (Eads = -9.to -17.0 kJ mol −1 ) compared to bare carbon (Eads = -5.4kJ mol −1 ).They also observed charge density difference with and without the N/O functional group, indicating no sig nificant electron transfer between a CO2 molecule and a carbon surface, which establishe physisorption as the adsorption nature of functionalized carbon.Bari et al. investigated the precise role of surface functional groups in CO 2 sorption on the carbon surface using the CO 2 temperature-programmed desorption profile (CO 2 -TPD) [1].Initially, the study adsorbed CO 2 at 0.2 bar and desorbed all physiosorbed CO 2 from the porous carbon by purging with helium gas for an hour.The experiment then compared the roles of N-and O-containing functional groups in the temperature range of 50-400 • C through temperature-programmed desorption (Figure 10).
Bari et al. investigated the precise role of surface functional groups in CO2 sorption on the carbon surface using the CO2 temperature-programmed desorption profile (CO2-TPD) [1].Initially, the study adsorbed CO2 at 0.2 bar and desorbed all physiosorbed CO2 from the porous carbon by purging with helium gas for an hour.The experiment then compared the roles of N-and O-containing functional groups in the temperature range of 50-400 °C through temperature-programmed desorption (Figure 10).
N-containing functional groups (pyridinic N, pyrrolic N, graphitic N, and oxidized N) in the carbon desorb approximately 24% of CO2 within the temperature range of 60-180 °C due to weak intermolecular interactions such as hydrogen bonding, acid-amine, or electrostatic interactions.They also demonstrate that O-containing functional groups (C-OH, (CO)OR, R= H, C) act as active sites for CO2 uptake by forming bicarbonate, carbamic acid, and carbamate due to strong chemical bonds (~100 kJ mol −1 ) [121].Such chemisorbed CO2 is desorbed at temperatures above 200 °C [122][123][124].Jianfei et al. successfully synthesized N-and P-co-doped porous carbon by employing chitosan aerogel, phytic acid, and dicyandiamide as precursor materials.Subsequently, they activated the carbon using NaNO3, thereby circumventing the need for the utilization of harsh alkalis like NaOH or KOH (Figure 11) [125].This innovative method yielded an impressive CO2 capture performance of 5.31 mmol g −1 at a pressure of 1 bar and a temperature of 25 °C.Notably, when examining the carbon sample lacking P doping, a CO2 capture capacity of 1.89 mmol g −1 was observed at 1 bar and 25 °C.These results Jianfei et al. successfully synthesized N-and P-co-doped porous carbon by employing chitosan aerogel, phytic acid, and dicyandiamide as precursor materials.Subsequently, they activated the carbon using NaNO 3 , thereby circumventing the need for the utilization of harsh alkalis like NaOH or KOH (Figure 11) [125].This innovative method yielded an impressive CO 2 capture performance of 5.31 mmol g −1 at a pressure of 1 bar and a temperature of 25 • C. Notably, when examining the carbon sample lacking P doping, a CO 2 capture capacity of 1.89 mmol g −1 was observed at 1 bar and 25 • C.These results strongly suggest that the synergistic interaction between N-and P-doping induces modifications in the surface chemistry, consequently augmenting the CO 2 capture performance [125].
electrostatic charge, while the carbon atom withdraws bonding electrons.Simultaneously, due to the larger atomic radius of phosphorus, the graphene structure of carbon experiences more significant distortion upon interaction.The distribution of the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) is predominantly centered around the phosphorus atom.This arrangement greatly facilitates Lewis acid-base interactions with CO2 molecules, thereby contributing significantly to the overall CO2 capture performance [126].A hydrochar-based carbon material was synthesized through the combination of glucose and ethylene diamine, and it exhibited efficient CO2 capture performance compared to carbon derived from urea activation by KOH and carbon derived from urea activation by ZIF8, specifically in the low-pressure range of 0 to 1 bar (Figure 12b) [127].To assess the influence of pore structure and chemical properties on CO2 adsorption capacity, a machine learning approach was employed using a dataset comprising 1594 CO2 adsorption data points.The findings of the study highlight that, under low-pressure conditions (0.1-1 bar), ultra-micropores and carbon-containing nitrogen (N) functional groups have the most significant impact on CO2 capture performance (Figure 12c,d).As the pore size increases, the amount of CO2 adsorption decreases, as smaller pore sizes provide a greater likelihood of interaction between the pore walls and CO2 molecules.Notably, the machine learning outcomes emphasize that pore sizes smaller than 0.7 nm play a critical role in capturing CO2 at 1 bar.Regarding functional groups, N-containing groups such as pyri- Similarly, Davood et al. conducted a study involving the incorporation of various heteroatoms (B, N, P, S) into activated porous carbon to enhance CO 2 capture performance [126].A comparison was made among these elements in terms of their impact.Among the considered elements (B, N, P, and S), phosphorus (P)-doping exhibited the highest efficiency in enhancing CO 2 capture, yielding an uptake of 7.13 mmol g −1 at 1 bar and 20 • C (Figure 12a).In this context, it is worth noting that the carbon atom (C) has a higher electronegativity (2.5) than the phosphorus (P) atom (2.1), which stands in contrast to the situation in C-N interactions, where the nitrogen (N) atom possesses an electronegativity of 3.0.This discrepancy results in the phosphorus atom displaying a relatively more positive electrostatic charge, while the carbon atom withdraws bonding electrons.Simultaneously, due to the larger atomic radius of phosphorus, the graphene structure of carbon experiences more significant distortion upon interaction.The distribution of the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) is predominantly centered around the phosphorus atom.This arrangement greatly facilitates Lewis acid-base interactions with CO 2 molecules, thereby contributing significantly to the overall CO 2 capture performance [126].
A hydrochar-based carbon material was synthesized through the combination of glucose and ethylene diamine, and it exhibited efficient CO 2 capture performance compared to carbon derived from urea activation by KOH and carbon derived from urea activation by ZIF8, specifically in the low-pressure range of 0 to 1 bar (Figure 12b) [127].To assess the influence of pore structure and chemical properties on CO 2 adsorption capacity, a machine learning approach was employed using a dataset comprising 1594 CO 2 adsorption data points.The findings of the study highlight that, under low-pressure conditions (0.1-1 bar), ultra-micropores and carbon-containing nitrogen (N) functional groups have the most significant impact on CO 2 capture performance (Figure 12c,d).As the pore size increases, the amount of CO 2 adsorption decreases, as smaller pore sizes provide a greater likelihood of interaction between the pore walls and CO 2 molecules.Notably, the machine learning outcomes emphasize that pore sizes smaller than 0.7 nm play a critical role in capturing CO 2 at 1 bar.Regarding functional groups, N-containing groups such as pyridinic N, pyrrolic N, and quaternary N exhibit substantial effects on CO 2 uptake, surpassing the effects of O-containing functional groups like hydroxyls, carboxylic acids, and ketones [127].
Surfaces 2023, 6, FOR PEER REVIEW dinic N, pyrrolic N, and quaternary N exhibit substantial effects on CO2 uptake, su sing the effects of O-containing functional groups like hydroxyls, carboxylic acids ketones [127].

Envisioning Future Research Prospects and Forging a Focused Strategy
It is interesting to note that, until now, the development of multi-hierarchical po carbon has mainly focused on powder-based highly efficient carbon products (Table

Envisioning Future Research Prospects and Forging a Focused Strategy
It is interesting to note that, until now, the development of multi-hierarchical porous carbon has mainly focused on powder-based highly efficient carbon products (Table 1).However, for practical industrial-scale applications, it is necessary to shape the powder into pellets [147].Achieving a well-defined fixed shape and particle size before practical application requires additional fabrication steps, such as extrusion, granulation, pressing, and binder inclusion [148].
After shaping the powder into fixed pellets for practical use, there is a high concern for pressure drops across the reactor bed, which can limit mass and heat transfer [149][150][151][152].Moreover, the inclusion of a binder or other fabrication processes can lead to changes or reductions in surface area, pore size, and pore volume [153][154][155].This can also cause a significant reduction in the amount of active components and efficient functional activity, thereby affecting structural and material stability [156,157].
To overcome these drawbacks, research trends require a shift towards a pelletizationbased synthesis strategy as the ultimate solution to obtain well-preserved fixed-shaped and functionally hierarchical porous carbon products [158,159].However, only a few research efforts have focused on this approach, and they are still far from achieving practical efficient performance [160].
It could be assumed that pelletized-state carbonization, rather than powder state carbonization or pyrolysis, will effectively improve, modify, or influence the morphological state of carbon products, due to the close contact with the carbon intermediate.It could also be assumed that the gas template is more aggressively utilized at the molecular level during the precursor's carbonization.
Figure 13 shows that, when precursors are carbonized at higher temperatures in powder form, the self-degraded or mass-loss gas template may be able to escape easily from the pyrolyzed medium.On the other hand, in a close-packed or void-filling state, the degradation products of the gas template interact more intensely and effectively at the molecular level, occupying the space left by the mass loss and providing more efficient textural properties.The proposed synthesis mechanism could reduce the technical complexity of activation by chemical or secondary physical activation (hard template, soft organic template, steam, air, NH 3 , He, Ar, etc.) processes.Alternatively, it could be combined with the existing processes to explore new possibilities for obtaining more efficient carbon products.
Surfaces 2023, 6, FOR PEER REVIEW To overcome these drawbacks, research trends require a shift towards a pellet based synthesis strategy as the ultimate solution to obtain well-preserved fixedand functionally hierarchical porous carbon products [158,159].However, only a search efforts have focused on this approach, and they are still far from achieving p efficient performance [160].
It could be assumed that pelletized-state carbonization, rather than powder st bonization or pyrolysis, will effectively improve, modify, or influence the morpho state of carbon products, due to the close contact with the carbon intermediate.I also be assumed that the gas template is more aggressively utilized at the molecul during the precursor's carbonization.
Figure 13 shows that, when precursors are carbonized at higher temperat powder form, the self-degraded or mass-loss gas template may be able to escap from the pyrolyzed medium.On the other hand, in a close-packed or void-filling st degradation products of the gas template interact more intensely and effectively molecular level, occupying the space left by the mass loss and providing more e textural properties.The proposed synthesis mechanism could reduce the technic plexity of activation by chemical or secondary physical activation (hard template, ganic template, steam, air, NH3, He, Ar, etc.) processes.Alternatively, it could b bined with the existing processes to explore new possibilities for obtaining more e carbon products.2).Achieving a multi-hierarchical porous carbon is crucial when ering CO2 capture efficiency, selectivity, kinetics, and a wide pressure range (in DAC, medium, and high pressures).To optimize low-pressure capture efficie abundance of ultra-to-super-micropores is highly anticipated, while high-pressure ios tend to benefit from the presence of meso-/macropores.
To ensure both swift capture efficiency and effective utilization of ultra-micr it is essential to integrate them harmoniously with meso-/macropores in the overa phological design or engineering.Furthermore, the inclusion of heteroatom-con compositions is paramount in creating an efficient and selective adsorbent, leverag face chemistry.This task is challenging, as it requires the introduction of functional Different activation processes come with their own set of advantages and disadvantages (Table 2).Achieving a multi-hierarchical porous carbon is crucial when considering CO 2 capture efficiency, selectivity, kinetics, and a wide pressure range (including DAC, medium, and high pressures).To optimize low-pressure capture efficiency, an abundance of ultra-to-super-micropores is highly anticipated, while high-pressure scenarios tend to benefit from the presence of meso-/macropores.
To ensure both swift capture efficiency and effective utilization of ultra-micropores, it is essential to integrate them harmoniously with meso-/macropores in the overall morphological design or engineering.Furthermore, the inclusion of heteroatom-containing compositions is paramount in creating an efficient and selective adsorbent, leveraging surface chemistry.This task is challenging, as it requires the introduction of functional groups while maintaining a high degree of aromatic condensation within carbon products, in order to achieve a structurally stable carbon end-product.Combining all necessary conditions within a single-pot synthesis strategy proves to be a formidable challenge, both Surfaces 2023, 6 333 in terms of attainment and the engineering of an efficient pore structure.Combining metal ion activation with soft templating and pelletization followed by carbonization in a one-pot process has the potential to produce multi-hierarchical carbon products.

Summary
Porous carbon-based materials surpass many limitations and exhibit outstanding CO 2 adsorption/desorption capabilities, as well as excellent clean surface cycling durability, mechanical strength, chemical resistance, and moisture stability.Various fundamental strategies have been developed to induce the efficient formation of hierarchical porous carbon products.However, applying different pressure ranges to capture CO 2 within multi-porosity structures poses a challenging task.This is because ultra-/super-micropores are favorable for low-pressure and low-quantity CO 2 adsorption, while meso-/macropores are more suited for high-pressure conditions.
Additionally, when considering the selectivity of ultra-to-micropores for CO 2 adsorption, the meso-/macropores region competes with other gases.Considering the molecular sieve effects, even with a higher surface area and a large number of ultra-/super-micropores, there is an unfortunate limitation in their ability to provide effective adsorption and proper kinetics due to improper diffusion pathways.Therefore, it becomes essential to devise a proper and rational design strategy to achieve a multi-hierarchical pore structure encompassing macro-/meso-/micro-/super-/ultra-pores.Moreover, the use of heteroatomcontaining sources, along with inappropriate strategies for activation and templating, hinders the degree of aromatic condensation during carbonization, leading to unbalanced formation of macro-/mesopores.
The concept of merging soft templates and metal ion activation, alongside the innovative pelletization method, holds the prospect of promising potential across a diverse spectrum of practical applications (Figure 14).The ability of a soft template to direct the structure helps in incorporating heteroatoms into the carbon structure from diverse multicomponent precursor sources.This plays a crucial role in maintaining the appropriate level of carbon polycondensation during the carbonization process, contributing to the mechanical strength of the structure and facilitating the development of meso-and macropores.The effectiveness of capturing CO 2 and performing low-pressure capture relies on the presence of ultra-to-super-micropores. Metal ion activation, in this context, facilitates the efficient creation of these ultra-to-super-micropores within the structure.Additionally, the challenges related to structural and functional degradation that often arise when shaping synthesized efficient powder for application can effectively be addressed through the proposed pre-pelletization strategy.It can be inferred that the pre-pelletization strategy makes effective use of gas templates, which share similarities with the physical activation strategy.This approach holds the potential to provide a solution to the limitations associated with post-synthesis shaping while preserving the desired structural and functional attributes.
macropores.The effectiveness of capturing CO2 and performing low-pressure capture relies on the presence of ultra-to-super-micropores. Metal ion activation, in this context, facilitates the efficient creation of these ultra-to-super-micropores within the structure.Additionally, the challenges related to structural and functional degradation that often arise when shaping synthesized efficient powder for application can effectively be addressed through the proposed pre-pelletization strategy.It can be inferred that the pre-pelletization strategy makes effective use of gas templates, which share similarities with the physical activation strategy.This approach holds the potential to provide a solution to the limitations associated with post-synthesis shaping while preserving the desired structural and functional attributes.

Figure 2 .
Figure 2. A schematic representation elucidating the mechanisms of carbon formation.

Figure 2 .
Figure 2. A schematic representation elucidating the mechanisms of carbon formation.

Figure 3 .
Figure 3. Graphical illustration that shows the CO2 capture mechanisms on the carbon surface [64].Adapted with permission from ref., copyright (2020) Elsevier Ltd.

Figure 3 .
Figure 3. Graphical illustration that shows the CO 2 capture mechanisms on the carbon surface [64].Adapted with permission from ref., copyright (2020) Elsevier Ltd.

Figure 5 .
Figure 5. Schematic diagram showing the mechanisms of pore formation within the carbon structure during the physical activation process; (a-d) activation reaction time: 0, 1, 3, and 5 s, consecutively [78].Adapted with permission from ref., copyright (2019) Elsevier Ltd.

Figure 6 .
Figure 6.A schematic show of carbon surface activation by steam [80].Adapted with permission from ref., copyright (2015) Elsevier Ltd.

Figure 6 .
Figure 6.A schematic show of carbon surface activation by steam [80].Adapted with permission from ref., copyright (2015) Elsevier Ltd.

Figure 7 .
Figure 7. Diagram illustrating the synthesis process of interconnected hierarchical carbon using the KIT-6 hard template and ZnCl2 activation.[90].Adapted with permission from ref., copyright (2023) Elsevier Ltd.

Figure 8 .
Figure 8. Hierarchical porous carbon synthesis from glucose utilizing LiBr/KBr molten salt and an organic reactive template of melamine-cyanuric acid complex [1].Adapted with permission from ref., copyright (2023) Springer Nature.

Figure 7 .
Figure 7. Diagram illustrating the synthesis process of interconnected hierarchical carbon using the KIT-6 hard template and ZnCl 2 activation.[90].Adapted with permission from ref., copyright (2023) Elsevier Ltd.

Figure 8 .
Figure 8. Hierarchical porous carbon synthesis from glucose utilizing LiBr/KBr molten salt and an organic reactive template of melamine-cyanuric acid complex [1].Adapted with permission from ref., copyright (2023) Springer Nature.

Figure 8 .
Figure 8. Hierarchical porous carbon synthesis from glucose utilizing LiBr/KBr molten salt and an organic reactive template of melamine-cyanuric acid complex [1].Adapted with permission from ref., copyright (2023) Springer Nature.

Figure 10 .
Figure 10.CO 2 -TPD profiles of carbon samples (a) without or (b) with CO 2 pre-adsorption, (c) deconvolution of CO 2 -TPD profile of MG-Br-600 with CO 2 pre-adsorption, and (d) multi-cycle profiles of CO 2 -TPD results of MG-Br-600 [1].Adapted with permission from ref., copyright (2023) Springer Nature.N-containing functional groups (pyridinic N, pyrrolic N, graphitic N, and oxidized N) in the carbon desorb approximately 24% of CO 2 within the temperature range of 60-180 • C due to weak intermolecular interactions such as hydrogen bonding, acid-amine, or electrostatic interactions.They also demonstrate that O-containing functional groups (C-OH, (CO)OR, R = H, C) act as active sites for CO 2 uptake by forming bicarbonate, carbamic acid, and carbamate due to strong chemical bonds (~100 kJ mol −1 ) [121].Such chemisorbed CO 2 is desorbed at temperatures above 200 • C [122-124].Jianfei et al. successfully synthesized N-and P-co-doped porous carbon by employing chitosan aerogel, phytic acid, and dicyandiamide as precursor materials.Subsequently, they activated the carbon using NaNO 3 , thereby circumventing the need for the utilization of harsh alkalis like NaOH or KOH (Figure11)[125].This innovative method yielded an impressive CO 2 capture performance of 5.31 mmol g −1 at a pressure of 1 bar and a temperature of 25 • C. Notably, when examining the carbon sample lacking P doping, a CO 2 capture capacity of 1.89 mmol g −1 was observed at 1 bar and 25 • C.These results strongly suggest that the synergistic interaction between N-and P-doping induces modifications in the surface chemistry, consequently augmenting the CO 2 capture performance[125].

Figure 13 .
Figure 13.A schematic representation comparing powder and fixed-shape state carbonizati egies for the effective utilization of the gas template from the carbon degradation products Different activation processes come with their own set of advantages and vantages (Table2).Achieving a multi-hierarchical porous carbon is crucial when ering CO2 capture efficiency, selectivity, kinetics, and a wide pressure range (in DAC, medium, and high pressures).To optimize low-pressure capture efficie abundance of ultra-to-super-micropores is highly anticipated, while high-pressure ios tend to benefit from the presence of meso-/macropores.To ensure both swift capture efficiency and effective utilization of ultra-micr it is essential to integrate them harmoniously with meso-/macropores in the overa phological design or engineering.Furthermore, the inclusion of heteroatom-con compositions is paramount in creating an efficient and selective adsorbent, leverag face chemistry.This task is challenging, as it requires the introduction of functional

Figure 13 .
Figure 13.A schematic representation comparing powder and fixed-shape state carbonization strategies for the effective utilization of the gas template from the carbon degradation products.

Figure 14 .
Figure 14.Charting a potential route: pathways to crafting pelletized porous carbon.

Table 1 .
Performance comparison of CO2 uptake, kinetics, heat of adsorption, and selectivity i bon materials from different sources and under various modification processes for carbon cap

Table 1 .
Performance comparison of CO 2 uptake, kinetics, heat of adsorption, and selectivity in carbon materials from different sources and under various modification processes for carbon capture.
Abbreviations: Carbon is denoted as C and Molten salt as MS in the Table.

Table 2 .
A comparison of the different activation processes.