Mixed
tin–lead halide perovskites have recently emerged
as highly promising materials for efficient single- and multi-junction
photovoltaic devices. This Focus Review discusses the optoelectronic
properties that underpin this performance, clearly differentiating
between intrinsic and defect-mediated mechanisms. We show that from
a fundamental perspective, increasing tin fraction may cause increases
in attainable charge-carrier mobilities, decreases in exciton binding
energies, and potentially a slowing of charge-carrier cooling, all
beneficial for photovoltaic applications. We discuss the mechanisms
leading to significant bandgap bowing along the tin–lead series,
which enables attractive near-infrared bandgaps at intermediate tin
content. However, tin-rich stoichiometries still suffer from tin oxidation
and vacancy formation which often obscures the fundamentally achievable
performance, causing high background hole densities, accelerating
charge-carrier recombination, lowering charge-carrier mobilities,
and blue-shifting absorption onsets through the Burstein–Moss
effect. We evaluate impacts on photovoltaic device performance, and
conclude with an outlook on remaining challenges and promising future
directions in this area.