“…Since the oxyanion metalloids such as As(III)/As(V), Se(VI), and Cr(VI) are electronegative, they can be preferentially attracted to or chemically bound to the shell of iron (hydr)oxide before they are reduced by the iron core. With the progress in the reaction, the adsorbed metalloids can be reduced via the sacrificial oxidation of the iron inner core, and the reduced metalloids can transport across the defects of the iron (hydr)oxide shell simultaneously, ,,,− thereby forming the metalloid “subshell” beneath the shell of an iron nanoparticle (Figure b). ,,, As for the As-subshell, As was predominantly accumulated at the subsurface (∼3 nm from the shell) of the iron nanoparticle, and the thickness was in the range of 1.0–2.3 nm. , Zhang’s group revealed that the reaction of an iron nanoparticle with As(V) was capable of generating the As(III)-subshell and then converting into As(0)-subshell in solutions. ,,,,, Correspondingly, the Fe species of the As-laden iron nanoparticle could be well stratified from the outermost Fe(III) (hydr)oxide periphery to a mixed Fe(III)/Fe(II) interlayer, then Fe(II) and pure Fe(0) phases . Compared to the reduction of As(III) to As(0), which was strongly dependent on the loading of Fe 0 , it should be noted that the As(III) could be oxidized back to As(V) in the presence of iron nanoparticles and oxygen .…”