The electronically unsaturated three-coordinated hydridoborenium cations [LBH](+) [HB(C6F5)(3)](-) (1) and [LBH](+)[B(C6F5)(4)](-) (2), supported by a bis(phosphinimino)amide ligand, were found to be excellent catalysts for hydrosilylation of a range of aliphatic and aromatic aldehydes and ketones under mild reaction conditions (L = [{(2,4,6-Me3C6H2N)P(Ph-2)}(2)N]). The key steps of the catalytic cycle for hydrosilylation of PhCHO were monitored via in situ multinuclear NMR measurements for catalysts 1 and 2. The combined effect of carbonyl activation via the Lewis acidic hydridoborenium cation and the hydridic nature of the borate counteranion in 1 makes it a more efficient catalyst in comparison to that of carbonyl activation via the predominant Lewis acid activation pathway operating with catalyst 2. The catalytic cycle of 1 showed hydride transfer from the borate moiety [HB(C6F5)(3)](-) to PhCHO in the first step, forming [PhCH2-O-B(C6F5)(3)](-), which subsequently underwent sigma-bond metathesis with Et3SiH to form the product, PhCH2-O-SiEt3. Quantum chemical calculations also support the borate anion mediated mechanism with 1. In contrast, the reaction catalyzed by 2 proceeds predominantly via the Lewis acid activation of the carbonyl group involving [LB(H)<- OC(H)Ph](+)[B(C6F5)(4)](-) as the transition state and [LBOCH2Ph](+)[B(C6F5)(4)](-) as the intermediate.