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For independent bond percolation of density $0<p<1$ on the cubic lattice in dimension $d\ge 2$, let ${\beta }_n$ be the one-arm probability for reaching maximum-norm distance $n$. The weighted BK boundary-splitting estimate gives ${\beta }_{m+n}\le |\partial {\Lambda }_n|{\beta }_m{\beta }_n$. Since the logarithm of this boundary size is $o(n)$, the asymmetrically almost-subadditive sequence argument applies to $\log {\beta }_n$. The rate exists and lies in $[0,-\log p]$; positive rate gives exponential decay.

For bond percolation on the square lattice, put $g_n={\mathbb{P}}_p(0\leftrightarrow \partial [-n,n{]}^2)$. Splitting an open self-avoiding walk at its first visit to the radius-$m$ boundary gives disjoint certificates for reaching a boundary graph vertex and then reaching radius $n$ about that graph vertex. The Van den Berg-Kesten inequality and the union bound give $g_{m+n}\le 8m{g}_m{g}_n$ for positive $m,n$. With $g_0=1$ and $|\partial {\Lambda }_0|=1$, the boundary-cardinality form holds for zero indices as well.

Independent bond percolation on ${\mathbb{Z}}^2$ has at most one infinite percolation cluster at every parameter, including a possible critical parameter. The number of infinite percolation clusters is constant almost surely by translation ergodicity of Bernoulli percolation. A finite constant larger than one is impossible: a box meeting two clusters can be made entirely open, joining them and decreasing that number with positive probability by finite modification of Bernoulli percolation.

If infinitely many clusters existed, a box would meet three with positive probability. Preserve one infinite exterior arm from each and replace the finitely many interior and boundary edges by a three-armed tree joining them, closing the remaining edges. Its branch graph vertex becomes a trifurcation vertex in percolation. Translation invariance therefore gives a positive density $q$. But the trifurcation boundary-counting lemma gives $q|W|\le |{\partial }^{+}W|$ for every large box, contradicting vanishing boundary-to-volume ratio. This proves uniqueness without assuming absence of an infinite percolation cluster at criticality.

The multiplicative factor $q$ assigned to each connected component of a graph in a finite random-cluster measure. At fixed edge probability, the weight of a configuration with $k$ components includes $q^k$. For $q=1$ this reduces to independent bond percolation; increasing $q$ at fixed $p$, for $q\ge 1$, suppresses increasing events by random-cluster weight monotonicity.

For critical site percolation on the triangular lattice, scaling-limit crossing probabilities transform naturally under conformal maps between planar domains. This rigorously established property supports descriptions of interfaces by SLE and calculations of planar percolation critical exponents. Transferring it to a different lattice or to bond percolation requires a separate universality argument.

For nearest-neighbour bond percolation with $0<p<1$ on the strip $T_k=\mathbb{Z}\times \{-k,\dots ,k\}$, put $q_k(n)={\mathbb{P}}_p((0,0)\leftrightarrow (n,0)\text{ in }{T}_k)$. The Harris-FKG inequality and translation invariance imply $q_k(n+m)\ge q_k(n)q_k(m)$. Thus $-\log q_k(n)$ is a subadditive sequence, and the Fekete lemma givesThe direct horizontal graph path gives $0\le f_k(p)\le -\log p$. Enlarging the strip increases every percolation two-point connection probability, so $f_k(p)$ is nonincreasing in $k$ and has a nonnegative limit of a sequence.

For independent bond percolation on a transitive locally finite lattice, let $c_n$ count rooted self-avoiding walks and let $\mu =\lim c_n^{1/n}$ be the connective constant. An infinite open percolation cluster supplies an open walk of every length. The union bound gives $\theta (p)\le c_n{p}^n$, which tends to zero when $p\mu <1$. Thus $p_c\ge 1/\mu$.

Independent bond percolation on the square lattice satisfies $p_c\le 1-{\mu }^{-1}$, where $\mu$ is its connective constant. If $(1-p)\mu <1$, closed dual graph cycles have a summable large-length tail: their counts are bounded by a polynomial factor times the count of self-avoiding walks. Conditioning a sufficiently large finite box to be open excludes short enclosing graph cycles without changing the law of the remaining edges. With positive conditional probability no enclosing closed dual graph cycle remains, so the origin belongs to an infinite percolation cluster.

In bond percolation on a directed graph, independently open each directed edge with probability $p$. The out-cluster of $x$ consists of vertices reachable by open directed paths. In site percolation, independently open vertices and require every vertex of the directed path, including $x$, to be open. The same definitions allow a multigraph. The orientation matters: an infinite underlying connected graph need not contain an infinite out-cluster from a specified root.

In planar bond percolation, declare a dual edge open exactly when the primal edge it crosses is closed. Independent primal parameter $p$ then gives independent dual parameter $1-p$.

In bond percolation on the square lattice, the outer boundary of a finite percolation cluster, after filling its holes, consists of closed bonds. Their crossing edges in the planar dual graph form a connected enclosing contour, and hence belong to a single dual bond percolation cluster $K$. If $|K|=m$, both its coordinate widths are at most $m-1$, so the enclosed primal cluster contains at most $m^2$ vertices. A contour enclosing the origin also places every vertex of $K$ within distance $m+1$ of the origin. An exponential volume tail for the subcritical dual bond percolation clusters thus gives a bound $C{e}^{-c\sqrt{n}}$ for a finite primal cluster of size at least $n$.

For independent bond percolation on ${\mathbb{Z}}^d$ below the percolation critical probability, there are $K,c>0$ such that ${\mathbb{P}}_p(|C(x)|\ge n)\le K{e}^{-cn}$, uniformly in $x$. This concerns the number of vertices in a percolation cluster, a stronger conclusion than decay of its radius alone.

If an increasing event $A$ depends on $m$ sites or edges, the uniform-label monotone coupling of Bernoulli percolation and the union bound give $0\le {\mathbb{P}}_q(A)-{\mathbb{P}}_p(A)\le m(q-p)$ for $p\le q$. A change of the event requires a coordinate with label in $(p,q]$. For bond percolation from the origin to the boundary of $[-n,n{]}^2$, first-hit graph paths use the $4n(2n+1)$ internal edges, so the same count bounds the parameter sensitivity.

The percolation critical probability of independent bond percolation on the infinite square lattice is exactlyIn this model, $\theta (p)=0$ for $p\le 1/2$ and $\theta (p)>0$ for $p>1/2$. The particular graph, independent edge decisions, and distinction between bond percolation and site percolation matter: this value is not a universal threshold for arbitrary random networks. The equality of open and closed edge probabilities at $1/2$ suggests a relation to dual bond percolation, but that symmetry alone is not a proof of long-distance connectivity.

Harris established the lower bound, including absence of an infinite percolation cluster at $p=1/2$, in 1960. Kesten completed the equality in 1980. His original paper states the threshold result as Theorem 1 and the positive/zero percolation probability alternatives as Theorem 2: ^[ref]. These are claims about the infinite square lattice, rather than deductions from a simulated finite sample.

Suppose every vertex of a directed graph has at most $\Delta$ incoming bonds. In bond percolation with parameter $q$, open a site whenever at least one incoming bond is open. Incoming bond sets have different heads and hence are disjoint, so these site indicators are independent random variables. Supplement their probabilities to $r=1-(1-q{)}^{\Delta }$. Every vertex reached by a nontrivial open directed path is now open. Conditioning the root to be open gives ${\theta }_s(r)\ge r{\theta }_b(q)$, since a simple directed path from the root never uses a bond entering the root. Thus $p_H^s\le 1-(1-p_H^b{)}^{\Delta }$.

Closed dual graph cycles in disjoint square rings depend on disjoint primal edge sets. In independent bond percolation their barrier events are independent. If each event has probability at least $\delta >0$, an open graph path from the origin across $k$ rings has probability at most $(1-\delta {)}^k$. A geometric sequence of radii turns this estimate into the polynomial critical one-arm upper bound.

The martini lattice is obtained from the honeycomb lattice by replacing every vertex in one of its two vertex classes by a triangle, attaching its three former incident bonds to the triangle's three vertices. It is a periodic degree-three planar graph, with triangular faces and nine-sided faces. Each decorated vertex and its incident bonds is a three-terminal cell with three internal triangle bonds and three terminal spokes. Its independent bond percolation threshold is $1/\sqrt{2}$, as follows from three-terminal cell partition duality.

Suppose a planar bond percolation model has critical one-arm probability at most $C{n}^{-\alpha }$ with $\alpha >0$, and a finite-radius connection event depends on $O(n^2)$ edges. The finite-box comparison for percolation parameters gives $\theta (p_c+\epsilon )\le C{n}^{-\alpha }+C^{\prime }\epsilon n^2$. Balancing at $n\asymp {\epsilon }^{-1/(\alpha +2)}$ gives $\theta (p_c+\epsilon )\le A{\epsilon }^{\alpha /(\alpha +2)}$. For the square lattice use $p_c=1/2$ and the polynomial critical one-arm upper bound.

A bond percolation law is one-independent if the bond states in any two sets with disjoint endpoint sets are independent as collections. In particular, states of bonds in a matching in a graph are mutually independent. The law need not be invariant under translations or positively associated.