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In materials science, chemical force microscopy (CFM) is a variation of atomic force microscopy (AFM) which has become a versatile tool for characterization of materials surfaces. With AFM, structural morphology is probed using simple tapping or contact modes that utilize van der Waals interactions between tip and sample to maintain a constant probe deflection amplitude (constant force mode) or maintain height while measuring tip deflection (constant height mode). CFM, on the other hand, uses chemical interactions between functionalized probe tip and sample. Choice chemistry is typically gold-coated tip and surface with thiols attached, R being the functional groups of interest. CFM enables the ability to determine the chemical nature of surfaces, irrespective of their specific morphology, and facilitates studies of basic chemical bonding enthalpy and surface energy. Typically, CFM is limited by thermal vibrations within the cantilever holding the probe. This limits force measurement resolution to ~1 pN which is still very suitable considering weak interactions are ~20 pN per pair. Hydrophobicity is used as the primary example throughout this consideration of CFM, but certainly any type of bonding can be probed with this method. CFM has been primarily developed by Charles Lieber at Harvard University in 1994. The method was demonstrated using hydrophobicity where polar molecules (e.g. COOH) tend to have the strongest binding to each other, followed by nonpolar (e.g. CH3-CH3) bonding, and a combination being the weakest. Probe tips are functionalized and substrates patterned with these molecules. All combinations of functionalization were tested, both by tip contact and removal as well as spatial mapping of substrates patterned with both moieties and observing the complementarity in image contrast. Both of these methods are discussed below. The AFM instrument used is similar to the one in Figure 1. This is the simpler mode of CFM operation where a functionalized tip is brought in contact with the surface and is pulled to observe the force at which separation occurs, F_{ad} (see Figure 2).