Small-slope elastic membrane energy

For a nearly flat membrane represented by height $h(x)$, the quadratic bending-and-tension energy per invariant transverse length isIts free equilibrium equation is $k_c{h}_{xxxx}-\sigma h_{xx}=0$.

For a tension-dominated membrane with internal dimension $D$, the massless Gaussian height covariance has spectrum $k_{B}T/(\sigma q^2)$. Removing the uniform translation mode leaves the height difference well-defined. Its variance grows linearly with distance for $D=1$, logarithmically for $D=2$, and approaches a cutoff-dependent constant for $D>2$. A microscopic cutoff is necessary when the short-distance integral diverges. This distinguishes rough positional order from a failure of the local small-slope approximation.

Adding positive quadratic confinement $t\int h^2/2$ to the membrane energy changes its height spectrum to $k_{B}T/(\sigma q^2+t)$. The continuous height-shift symmetry is explicitly broken. Connected correlation function decay on the finite length $\xi$ and the height-difference variance saturates for every internal dimension, although its saturation value can depend on a microscopic cutoff. A negative confinement coefficient gives an unstable quadratic model rather than pinning.

For a membrane of bending modulus $k_c$ adhering with energy per area $\mathcal{U}$ to a cylinder of radius $R$, $U=R^2\mathcal{U}/k_c$ compares adhesion with bending cost.

A membrane-mediated interaction potential is the separation-dependent energy produced when deformation fields around two membrane-bound objects overlap. Its sign and range depend on membrane tension, bending stiffness, inclusion geometry, and which side of the membrane each object occupies.